Combined Immune Checkpoint Blockade Enhances Antiviral Immunity against Bovine Leukemia Virus

Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical r...

Full description

Saved in:
Bibliographic Details
Published in:Journal of virology Vol. 97; no. 1; p. e0143022
Main Authors: Nakamura, Hayato, Konnai, Satoru, Okagawa, Tomohiro, Maekawa, Naoya, Sajiki, Yamato, Watari, Kei, Kamitani, Kana, Saito, Maya, Kato, Yukinari, Suzuki, Yasuhiko, Murata, Shiro, Ohashi, Kazuhiko
Format: Journal Article
Language:English
Published: United States American Society for Microbiology 31-01-2023
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical role in immunosuppression and disease progression during BLV infection. In addition, a preliminary study has suggested that another immunoinhibitory molecule, T-cell immunoglobulin domain and mucin domain-3 (TIM-3), is involved in immunosuppression during BLV infection. Therefore, this study was designed to further elucidate the immunoinhibitory role of immune checkpoint molecules in BLV infection. TIM-3 expression was upregulated on peripheral CD4 and CD8 T cells in BLV-infected cattle. Interestingly, in EBL cattle, CD4 and CD8 T cells infiltrating lymphomas expressed TIM-3. TIM-3 and PD-1 were upregulated and coexpressed in peripheral CD4 and CD8 T cells from BLV-infected cattle. Blockade by anti-bovine TIM-3 monoclonal antibody increased CD69 expression on T cells and gamma interferon (IFN-γ) production from peripheral blood mononuclear cells from BLV-infected cattle. A syncytium formation assay also demonstrated the antiviral effects of TIM-3 blockade against BLV infection. The combined inhibition of TIM-3 and PD-1 pathways significantly enhanced IFN-γ production and antiviral efficacy compared to inhibition alone. In conclusion, the combined blockade of TIM-3 and PD-1 pathways shows strong immune activation and antiviral effects and has potential as a novel therapeutic method for BLV infection. Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Previously, it was found that immune checkpoint molecules, such as PD-1, suppress BLV-specific Th1 responses as the disease progresses. To date, most studies have focused only on how PD-1 facilitates escape from host immunity in BLV-infected cattle and the antiviral effects of the PD-1 blockade. In contrast, how T-cell immunoglobulin domain and mucin domain-3 (TIM-3), another immune checkpoint molecule, regulates anti-BLV immune responses is rarely reported. It is also unclear why PD-1 inhibition alone was insufficient to exert anti-BLV effects in previous clinical studies. In this study, the expression profile of TIM-3 in T cells derived from BLV-infected cattle suggested that TIM-3 upregulation is a cause of immunosuppression in infected cattle. Based on these results, anti-TIM-3 antibody was used to experimentally evaluate its function in influencing immunity against BLV. Results indicated that TIM-3 upregulation induced by BLV infection suppressed T-cell activation and antiviral cytokine production. Some T cells coexpressed PD-1 and TIM-3, indicating that simultaneous inhibition of PD-1 and TIM-3 with their respective antibodies synergistically restored antiviral immunity. This study could open new avenues for treating bovine chronic infections.
AbstractList Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical role in immunosuppression and disease progression during BLV infection. In addition, a preliminary study has suggested that another immunoinhibitory molecule, T-cell immunoglobulin domain and mucin domain-3 (TIM-3), is involved in immunosuppression during BLV infection. Therefore, this study was designed to further elucidate the immunoinhibitory role of immune checkpoint molecules in BLV infection. TIM-3 expression was upregulated on peripheral CD4 and CD8 T cells in BLV-infected cattle. Interestingly, in EBL cattle, CD4 and CD8 T cells infiltrating lymphomas expressed TIM-3. TIM-3 and PD-1 were upregulated and coexpressed in peripheral CD4 and CD8 T cells from BLV-infected cattle. Blockade by anti-bovine TIM-3 monoclonal antibody increased CD69 expression on T cells and gamma interferon (IFN-γ) production from peripheral blood mononuclear cells from BLV-infected cattle. A syncytium formation assay also demonstrated the antiviral effects of TIM-3 blockade against BLV infection. The combined inhibition of TIM-3 and PD-1 pathways significantly enhanced IFN-γ production and antiviral efficacy compared to inhibition alone. In conclusion, the combined blockade of TIM-3 and PD-1 pathways shows strong immune activation and antiviral effects and has potential as a novel therapeutic method for BLV infection. Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Previously, it was found that immune checkpoint molecules, such as PD-1, suppress BLV-specific Th1 responses as the disease progresses. To date, most studies have focused only on how PD-1 facilitates escape from host immunity in BLV-infected cattle and the antiviral effects of the PD-1 blockade. In contrast, how T-cell immunoglobulin domain and mucin domain-3 (TIM-3), another immune checkpoint molecule, regulates anti-BLV immune responses is rarely reported. It is also unclear why PD-1 inhibition alone was insufficient to exert anti-BLV effects in previous clinical studies. In this study, the expression profile of TIM-3 in T cells derived from BLV-infected cattle suggested that TIM-3 upregulation is a cause of immunosuppression in infected cattle. Based on these results, anti-TIM-3 antibody was used to experimentally evaluate its function in influencing immunity against BLV. Results indicated that TIM-3 upregulation induced by BLV infection suppressed T-cell activation and antiviral cytokine production. Some T cells coexpressed PD-1 and TIM-3, indicating that simultaneous inhibition of PD-1 and TIM-3 with their respective antibodies synergistically restored antiviral immunity. This study could open new avenues for treating bovine chronic infections.
Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical role in immunosuppression and disease progression during BLV infection. In addition, a preliminary study has suggested that another immunoinhibitory molecule, T-cell immunoglobulin domain and mucin domain-3 (TIM-3), is involved in immunosuppression during BLV infection. Therefore, this study was designed to further elucidate the immunoinhibitory role of immune checkpoint molecules in BLV infection. TIM-3 expression was upregulated on peripheral CD4 + and CD8 + T cells in BLV-infected cattle. Interestingly, in EBL cattle, CD4 + and CD8 + T cells infiltrating lymphomas expressed TIM-3. TIM-3 and PD-1 were upregulated and coexpressed in peripheral CD4 + and CD8 + T cells from BLV-infected cattle. Blockade by anti-bovine TIM-3 monoclonal antibody increased CD69 expression on T cells and gamma interferon (IFN-γ) production from peripheral blood mononuclear cells from BLV-infected cattle. A syncytium formation assay also demonstrated the antiviral effects of TIM-3 blockade against BLV infection. The combined inhibition of TIM-3 and PD-1 pathways significantly enhanced IFN-γ production and antiviral efficacy compared to inhibition alone. In conclusion, the combined blockade of TIM-3 and PD-1 pathways shows strong immune activation and antiviral effects and has potential as a novel therapeutic method for BLV infection. IMPORTANCE Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Previously, it was found that immune checkpoint molecules, such as PD-1, suppress BLV-specific Th1 responses as the disease progresses. To date, most studies have focused only on how PD-1 facilitates escape from host immunity in BLV-infected cattle and the antiviral effects of the PD-1 blockade. In contrast, how T-cell immunoglobulin domain and mucin domain-3 (TIM-3), another immune checkpoint molecule, regulates anti-BLV immune responses is rarely reported. It is also unclear why PD-1 inhibition alone was insufficient to exert anti-BLV effects in previous clinical studies. In this study, the expression profile of TIM-3 in T cells derived from BLV-infected cattle suggested that TIM-3 upregulation is a cause of immunosuppression in infected cattle. Based on these results, anti-TIM-3 antibody was used to experimentally evaluate its function in influencing immunity against BLV. Results indicated that TIM-3 upregulation induced by BLV infection suppressed T-cell activation and antiviral cytokine production. Some T cells coexpressed PD-1 and TIM-3, indicating that simultaneous inhibition of PD-1 and TIM-3 with their respective antibodies synergistically restored antiviral immunity. This study could open new avenues for treating bovine chronic infections.
Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical role in immunosuppression and disease progression during BLV infection. In addition, a preliminary study has suggested that another immunoinhibitory molecule, T-cell immunoglobulin domain and mucin domain-3 (TIM-3), is involved in immunosuppression during BLV infection. Therefore, this study was designed to further elucidate the immunoinhibitory role of immune checkpoint molecules in BLV infection. TIM-3 expression was upregulated on peripheral CD4 + and CD8 + T cells in BLV-infected cattle. Interestingly, in EBL cattle, CD4 + and CD8 + T cells infiltrating lymphomas expressed TIM-3. TIM-3 and PD-1 were upregulated and coexpressed in peripheral CD4 + and CD8 + T cells from BLV-infected cattle. Blockade by anti-bovine TIM-3 monoclonal antibody increased CD69 expression on T cells and gamma interferon (IFN-γ) production from peripheral blood mononuclear cells from BLV-infected cattle. A syncytium formation assay also demonstrated the antiviral effects of TIM-3 blockade against BLV infection. The combined inhibition of TIM-3 and PD-1 pathways significantly enhanced IFN-γ production and antiviral efficacy compared to inhibition alone. In conclusion, the combined blockade of TIM-3 and PD-1 pathways shows strong immune activation and antiviral effects and has potential as a novel therapeutic method for BLV infection. IMPORTANCE Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Previously, it was found that immune checkpoint molecules, such as PD-1, suppress BLV-specific Th1 responses as the disease progresses. To date, most studies have focused only on how PD-1 facilitates escape from host immunity in BLV-infected cattle and the antiviral effects of the PD-1 blockade. In contrast, how T-cell immunoglobulin domain and mucin domain-3 (TIM-3), another immune checkpoint molecule, regulates anti-BLV immune responses is rarely reported. It is also unclear why PD-1 inhibition alone was insufficient to exert anti-BLV effects in previous clinical studies. In this study, the expression profile of TIM-3 in T cells derived from BLV-infected cattle suggested that TIM-3 upregulation is a cause of immunosuppression in infected cattle. Based on these results, anti-TIM-3 antibody was used to experimentally evaluate its function in influencing immunity against BLV. Results indicated that TIM-3 upregulation induced by BLV infection suppressed T-cell activation and antiviral cytokine production. Some T cells coexpressed PD-1 and TIM-3, indicating that simultaneous inhibition of PD-1 and TIM-3 with their respective antibodies synergistically restored antiviral immunity. This study could open new avenues for treating bovine chronic infections.
Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent studies have revealed that the expression of immunoinhibitory molecules, such as programmed death-1 (PD-1) and PD-ligand 1, plays a critical role in immunosuppression and disease progression during BLV infection. In addition, a preliminary study has suggested that another immunoinhibitory molecule, T-cell immunoglobulin domain and mucin domain-3 (TIM-3), is involved in immunosuppression during BLV infection. Therefore, this study was designed to further elucidate the immunoinhibitory role of immune checkpoint molecules in BLV infection. TIM-3 expression was upregulated on peripheral CD4+ and CD8+ T cells in BLV-infected cattle. Interestingly, in EBL cattle, CD4+ and CD8+ T cells infiltrating lymphomas expressed TIM-3. TIM-3 and PD-1 were upregulated and coexpressed in peripheral CD4+ and CD8+ T cells from BLV-infected cattle. Blockade by anti-bovine TIM-3 monoclonal antibody increased CD69 expression on T cells and gamma interferon (IFN-γ) production from peripheral blood mononuclear cells from BLV-infected cattle. A syncytium formation assay also demonstrated the antiviral effects of TIM-3 blockade against BLV infection. The combined inhibition of TIM-3 and PD-1 pathways significantly enhanced IFN-γ production and antiviral efficacy compared to inhibition alone. In conclusion, the combined blockade of TIM-3 and PD-1 pathways shows strong immune activation and antiviral effects and has potential as a novel therapeutic method for BLV infection. IMPORTANCE Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry worldwide. The molecular mechanisms of BLV-host interactions are complex. Previously, it was found that immune checkpoint molecules, such as PD-1, suppress BLV-specific Th1 responses as the disease progresses. To date, most studies have focused only on how PD-1 facilitates escape from host immunity in BLV-infected cattle and the antiviral effects of the PD-1 blockade. In contrast, how T-cell immunoglobulin domain and mucin domain-3 (TIM-3), another immune checkpoint molecule, regulates anti-BLV immune responses is rarely reported. It is also unclear why PD-1 inhibition alone was insufficient to exert anti-BLV effects in previous clinical studies. In this study, the expression profile of TIM-3 in T cells derived from BLV-infected cattle suggested that TIM-3 upregulation is a cause of immunosuppression in infected cattle. Based on these results, anti-TIM-3 antibody was used to experimentally evaluate its function in influencing immunity against BLV. Results indicated that TIM-3 upregulation induced by BLV infection suppressed T-cell activation and antiviral cytokine production. Some T cells coexpressed PD-1 and TIM-3, indicating that simultaneous inhibition of PD-1 and TIM-3 with their respective antibodies synergistically restored antiviral immunity. This study could open new avenues for treating bovine chronic infections.
Author Nakamura, Hayato
Murata, Shiro
Kato, Yukinari
Ohashi, Kazuhiko
Watari, Kei
Saito, Maya
Sajiki, Yamato
Kamitani, Kana
Suzuki, Yasuhiko
Okagawa, Tomohiro
Maekawa, Naoya
Konnai, Satoru
Author_xml – sequence: 1
  givenname: Hayato
  surname: Nakamura
  fullname: Nakamura, Hayato
  organization: Department of Disease Control, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 2
  givenname: Satoru
  orcidid: 0000-0002-3230-7109
  surname: Konnai
  fullname: Konnai, Satoru
  organization: Institute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan
– sequence: 3
  givenname: Tomohiro
  surname: Okagawa
  fullname: Okagawa, Tomohiro
  organization: Department of Advanced Pharmaceutics, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 4
  givenname: Naoya
  surname: Maekawa
  fullname: Maekawa, Naoya
  organization: Department of Advanced Pharmaceutics, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 5
  givenname: Yamato
  surname: Sajiki
  fullname: Sajiki, Yamato
  organization: Department of Disease Control, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 6
  givenname: Kei
  surname: Watari
  fullname: Watari, Kei
  organization: Department of Disease Control, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 7
  givenname: Kana
  surname: Kamitani
  fullname: Kamitani, Kana
  organization: Hokkaido Hayakita Meat Inspection Center, Hokkaido Government, Abira, Japan
– sequence: 8
  givenname: Maya
  surname: Saito
  fullname: Saito, Maya
  organization: Hokkaido Hayakita Meat Inspection Center, Hokkaido Government, Abira, Japan
– sequence: 9
  givenname: Yukinari
  surname: Kato
  fullname: Kato, Yukinari
  organization: Department of Molecular Pharmacology, Tohoku University Graduate School of Medicine, Sendai, Japan
– sequence: 10
  givenname: Yasuhiko
  surname: Suzuki
  fullname: Suzuki, Yasuhiko
  organization: Division of Bioresources, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan
– sequence: 11
  givenname: Shiro
  surname: Murata
  fullname: Murata, Shiro
  organization: Department of Advanced Pharmaceutics, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
– sequence: 12
  givenname: Kazuhiko
  surname: Ohashi
  fullname: Ohashi, Kazuhiko
  organization: Department of Advanced Pharmaceutics, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/36598199$$D View this record in MEDLINE/PubMed
BookMark eNp1kc9LwzAUx4Mo7ofePEuvgp1J2qbJRZhl6mDgRcWLhCRNt2xrMpq2sP_eanXowdM7vM_78t7njcCxdVYDcIHgBCFMb9atmUAURzDE-AgMEWQ0TBIUH4MhhBiHSUTfBmDk_Rp2WEziUzCISMIoYmwI3jNXSmN1HszLsrE6yFZabXbO2Dq42zq1EbkOZnYlrNI-mNratKYS25429T4QS2Gs72DXdjHBQjcbXRoRvJqq8WfgpBBbr8-_6xi83M-es8dw8fQwz6aLUCSY1qGiRKZEUqI0gUUU5UTqnDBCSEqZSBQplEhkKqVilBHGNCsoZjiHBKVYSxiNwW2fu2tkqXOlbd0tyXeVKUW1504Y_rdjzYovXcsZpRR38sbgug9QlfO-0sVhFkH-qZl3mvmXZo5xh1_1uPAl5mvXVLY77z_28vduh-CfH0Qf8sSKRA
CitedBy_id crossref_primary_10_1186_s12917_024_03977_1
crossref_primary_10_1016_j_vetimm_2023_110609
Cites_doi 10.4049/jimmunol.1900342
10.1292/jvms.63.703
10.3389/fimmu.2017.00650
10.1128/JVI.68.7.4589-4596.1994
10.1128/IAI.01014-15
10.1016/j.cimid.2012.09.005
10.1016/j.jhep.2009.12.005
10.1038/ni.2035
10.1292/jvms.16-0354
10.1016/j.vetimm.2014.10.006
10.1093/infdis/jiq153
10.1038/s41577-019-0224-6
10.1016/j.dci.2020.103847
10.1172/JCI43127
10.1371/journal.pone.0009504
10.1073/pnas.82.3.677
10.1128/JVI.70.4.2178-2183.1996
10.4049/immunohorizons.2000089
10.3389/fvets.2020.00012
10.1016/s0378-1135(03)00119-6
10.1172/JCI45138
10.4161/onci.23849
10.1016/j.vetimm.2011.08.018
10.1186/s12917-019-2082-7
10.1038/nri3790
10.3892/ol.2018.8835
10.1056/NEJMoa1200690
10.1128/JVI.72.8.6917-6921.1998
10.1371/journal.pone.0174916
10.1038/ni987
10.1073/pnas.1009731107
10.1186/1742-4690-4-18
10.1128/iai.00210-22
10.1038/ni988
10.1128/JVI.70.8.5706-5710.1996
10.1002/eji.200939274
10.1038/ni.1679
10.1292/jvms.20-0590
10.1016/j.it.2013.10.001
10.1038/nm.2871
10.1128/IAI.00910-17
10.1007/s00345-015-1656-7
10.1111/j.1348-0421.2010.00208.x
10.1056/NEJMoa1305133
10.1038/nri1111
10.1371/journal.pntd.0001030
10.1016/j.immuni.2007.01.016
10.1128/JVI.00639-09
10.1186/s12967-019-1917-0
10.1084/jem.20081398
10.1038/ni.2376
10.1186/1297-9716-42-103
10.1084/jem.20100643
10.1038/415536a
10.1084/jem.20100637
10.1002/iid3.93
10.1038/ni1271
10.1038/nature13848
10.1186/s13567-018-0543-9
10.1038/ncomms10501
10.1186/1297-9716-44-59
10.1128/IAI.00278-16
10.1080/2162402X.2016.1261779
10.1126/science.1148536
10.1186/1297-9716-43-45
10.14943/jjvr.68.2.77
ContentType Journal Article
Copyright Copyright © 2023 American Society for Microbiology.
Copyright © 2023 American Society for Microbiology. 2023 American Society for Microbiology
Copyright_xml – notice: Copyright © 2023 American Society for Microbiology.
– notice: Copyright © 2023 American Society for Microbiology. 2023 American Society for Microbiology
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
5PM
DOI 10.1128/jvi.01430-22
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
PubMed Central (Full Participant titles)
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
DatabaseTitleList MEDLINE
CrossRef


Database_xml – sequence: 1
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 1098-5514
Editor Kirchhoff, Frank
Editor_xml – sequence: 1
  givenname: Frank
  surname: Kirchhoff
  fullname: Kirchhoff, Frank
ExternalDocumentID 10_1128_jvi_01430_22
01430-22
36598199
Genre Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: MEXT | Japan Society for the Promotion of Science (JSPS)
  grantid: 22K19232
  funderid: https://doi.org/10.13039/501100001691
– fundername: National Agriculture and Food Research Organization (NARO)
  grantid: 26058 BC
  funderid: https://doi.org/10.13039/501100007172
– fundername: Japan Agency for Medical Research and Development (AMED)
  grantid: JP223fa627005
  funderid: https://doi.org/10.13039/100009619
– fundername: National Agriculture and Food Research Organization (NARO)
  grantid: 16817557
  funderid: https://doi.org/10.13039/501100007172
– fundername: Japan Agency for Medical Research and Development (AMED)
  grantid: JP21am0101078
  funderid: https://doi.org/10.13039/100009619
– fundername: Ministry of Agriculture, Forestry and Fisheries (MAFF)
  grantid: JPJ008617.17935709
  funderid: https://doi.org/10.13039/501100003993
– fundername: MEXT | Japan Society for the Promotion of Science (JSPS)
  grantid: 19KK0172
  funderid: https://doi.org/10.13039/501100001691
– fundername: MEXT | Japan Society for the Promotion of Science (JSPS)
  grantid: 22H02503
  funderid: https://doi.org/10.13039/501100001691
– fundername: Japan Agency for Medical Research and Development (AMED)
  grantid: JP22ama121008
  funderid: https://doi.org/10.13039/100009619
– fundername: ;
  grantid: 26058 BC
– fundername: ;
  grantid: JPJ008617.17935709
– fundername: ;
  grantid: 19KK0172
– fundername: ;
  grantid: JP223fa627005
– fundername: ;
  grantid: 22H02503
– fundername: ;
  grantid: 16817557
– fundername: ;
  grantid: 22K19232
– fundername: ;
  grantid: JP21am0101078
– fundername: ;
  grantid: JP22ama121008
GroupedDBID ---
-~X
0R~
18M
29L
2WC
39C
4.4
53G
5GY
5RE
5VS
85S
ABPPZ
ACGFO
ACNCT
ADBBV
AENEX
AGVNZ
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BTFSW
CGR
CS3
CUY
CVF
DIK
E3Z
EBS
ECM
EIF
F5P
FRP
GX1
H13
HYE
HZ~
IH2
KQ8
N9A
NPM
O9-
OK1
P2P
RHF
RHI
RNS
RPM
RSF
TR2
UCJ
UPT
W2D
W8F
WH7
WOQ
YQT
~02
~KM
8W4
ABFLS
ABPTK
ZA5
AAYXX
CITATION
5PM
ID FETCH-LOGICAL-a528t-c86b76b86ce60f33d6bed69666789a5c6fca5b7bbc989699e9f8292d06172eb03
IEDL.DBID RPM
ISSN 0022-538X
IngestDate Tue Sep 17 21:30:35 EDT 2024
Thu Nov 21 21:14:15 EST 2024
Tue Jan 31 21:35:08 EST 2023
Sat Sep 28 08:16:42 EDT 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords PD-L1
cattle
TIM-3
bovine leukemia virus
lymphoma
Language English
License All Rights Reserved. https://doi.org/10.1128/ASMCopyrightv2
All Rights Reserved.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a528t-c86b76b86ce60f33d6bed69666789a5c6fca5b7bbc989699e9f8292d06172eb03
Notes The authors declare no conflict of interest.
ORCID 0000-0002-3230-7109
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888214
PMID 36598199
PageCount 16
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_9888214
crossref_primary_10_1128_jvi_01430_22
asm2_journals_10_1128_jvi_01430_22
pubmed_primary_36598199
PublicationCentury 2000
PublicationDate 2023-01-31
PublicationDateYYYYMMDD 2023-01-31
PublicationDate_xml – month: 01
  year: 2023
  text: 2023-01-31
  day: 31
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: 1752 N St., N.W., Washington, DC
PublicationTitle Journal of virology
PublicationTitleAbbrev J Virol
PublicationTitleAlternate J Virol
PublicationYear 2023
Publisher American Society for Microbiology
Publisher_xml – name: American Society for Microbiology
References Chiba, S, Baghdadi, M, Akiba, H, Yoshiyama, H, Kinoshita, I, Dosaka-Akita, H, Fujioka, Y, Ohba, Y, Gorman, JV, Colgan, JD, Hirashima, M, Uede, T, Takaoka, A, Yagita, H, Jinushi, M (B11) 2012; 13
Ohira, K, Nakahara, A, Konnai, S, Okagawa, T, Nishimori, A, Maekawa, N, Ikebuchi, R, Kohara, J, Murata, S, Ohashi, K (B35) 2016; 4
Sajiki, Y, Konnai, S, Watari, K, Okagawa, T, Tanaka, A, Kawaji, S, Nagata, R, Maekawa, N, Suzuki, Y, Kato, Y, Murata, S, Mori, Y, Ohashi, K (B57) 2022; 90
Konnai, S, Murata, S, Ohashi, K (B39) 2017; 79
Wherry, EJ (B1) 2011; 12
Sakuishi, K, Ngiow, SF, Sullivan, JM, Teng, MW, Kuchroo, VK, Smyth, MJ, Anderson, AC (B59) 2013; 2
Okagawa, T, Konnai, S, Deringer, JR, Ueti, MW, Scoles, GA, Murata, S, Ohashi, K, Brown, WC (B54) 2016; 84
Sajiki, Y, Konnai, S, Cai, Z, Takada, K, Okagawa, T, Maekawa, N, Fujisawa, S, Kato, Y, Suzuki, Y, Murata, S, Ohashi, K (B65) 2020; 4
Pyeon, D, Splitter, GA (B33) 1998; 72
Jones, RB, Ndhlovu, LC, Barbour, JD, Sheth, PM, Jha, AR, Long, BR, Wong, JC, Satkunarajah, M, Schweneker, M, Chapman, JM, Gyenes, G, Vali, B, Hyrcza, MD, Yue, FY, Kovacs, C, Sassi, A, Loutfy, M, Halpenny, R, Persad, D, Spotts, G, Hecht, FM, Chun, TW, McCune, JM, Kaul, R, Rini, JM, Nixon, DF, Ostrowski, MA (B5) 2008; 205
Schwartz, I, Bensaid, A, Polack, B, Perrin, B, Berthelemy, M, Levy, D (B27) 1994; 68
Han, ZM, Huang, HM, Sun, YW (B17) 2018; 16
Suzuki, S, Konnai, S, Okagawa, T, Ikebuchi, R, Nishimori, A, Kohara, J, Mingala, CN, Murata, S, Ohashi, K (B46) 2015; 163
Zheng, Y, Li, Y, Lian, J, Yang, H, Li, F, Zhao, S, Qi, Y, Zhang, Y, Huang, L (B64) 2019; 17
Mengshol, JA, Golden-Mason, L, Arikawa, T, Smith, M, Niki, T, McWilliams, R, Randall, JA, McMahan, R, Zimmerman, MA, Rangachari, M, Dobrinskikh, E, Busson, P, Polyak, SJ, Hirashima, M, Rosen, HR (B22) 2010; 5
Gupta, S, Thornley, TB, Gao, W, Larocca, R, Turka, LA, Kuchroo, VK, Strom, TB (B58) 2012; 122
Okagawa, T, Konnai, S, Nishimori, A, Maekawa, N, Goto, S, Ikebuchi, R, Kohara, J, Suzuki, Y, Yamada, S, Kato, Y, Murata, S, Ohashi, K (B45) 2018; 49
Pyeon, D, O’Reilly, KL, Splitter, GA (B32) 1996; 70
Kabeya, H, Ohashi, K, Onuma, M (B30) 2001; 63
Huang, Y-H, Zhu, C, Kondo, Y, Anderson, AC, Gandhi, A, Russell, A, Dougan, SK, Petersen, B-S, Melum, E, Pertel, T, Clayton, KL, Raab, M, Chen, Q, Beauchemin, N, Yazaki, PJ, Pyzik, M, Ostrowski, MA, Glickman, JN, Rudd, CE, Ploegh, HL, Franke, A, Petsko, GA, Kuchroo, VK, Blumberg, RS (B12) 2015; 517
Goto, S, Konnai, S, Hirano, Y, Kohara, J, Okagawa, T, Maekawa, N, Sajiki, Y, Watari, K, Minato, E, Kobayashi, A, Gondaira, S, Higuchi, H, Koiwa, M, Tajima, M, Taguchi, E, Ishida, M, Uemura, R, Yamada, S, Kaneko, MK, Kato, Y, Yamamoto, K, Toda, M, Suzuki, Y, Murata, S, Ohashi, K (B56) 2020; 68
Ndhlovu, LC, Leal, FE, Hasenkrug, AM, Jha, AR, Carvalho, KI, Eccles-James, IG, Bruno, FR, Vieira, RG, York, VA, Chew, GM, Jones, RB, Tanaka, Y, Neto, WK, Sanabani, SS, Ostrowski, MA, Segurado, AC, Nixon, DF, Kallas, EG (B50) 2011; 5
Wolf, Y, Anderson, AC, Kuchroo, VK (B14) 2020; 20
Sajiki, Y, Konnai, S, Okagawa, T, Nishimori, A, Maekawa, N, Goto, S, Watari, K, Minato, E, Kobayashi, A, Kohara, J, Yamada, S, Kaneko, MK, Kato, Y, Takahashi, H, Terasaki, N, Takeda, A, Yamamoto, K, Toda, M, Suzuki, Y, Murata, S, Ohashi, K (B42) 2019; 203
Okagawa, T, Konnai, S, Nishimori, A, Maekawa, N, Ikebuchi, R, Goto, S, Nakajima, C, Kohara, J, Ogasawara, S, Kato, Y, Suzuki, Y, Murata, S, Ohashi, K (B41) 2017; 8
Schietinger, A, Greenberg, PD (B3) 2014; 35
Zhu, C, Anderson, AC, Schubart, A, Xiong, H, Imitola, J, Khoury, SJ, Zheng, XX, Strom, TB, Kuchroo, VK (B9) 2005; 6
Shayan, G, Srivastava, R, Li, J, Schmitt, N, Kane, LP, Ferris, RL (B63) 2017; 6
Sabatos, CA, Chakravarti, S, Cha, E, Schubart, A, Sánchez-Fueyo, A, Zheng, XX, Coyle, AJ, Strom, TB, Freeman, GJ, Kuchroo, VK (B15) 2003; 4
Gillet, N, Florins, A, Boxus, M, Burteau, C, Nigro, A, Vandermeers, F, Balon, H, Bouzar, AB, Defoiche, J, Burny, A, Reichert, M, Kettmann, R, Willems, L (B31) 2007; 4
Goto, S, Konnai, S, Hirano, Y, Kohara, J, Okagawa, T, Maekawa, N, Sajiki, Y, Watari, K, Minato, E, Kobayashi, A, Gondaira, S, Higuchi, H, Koiwa, M, Tajima, M, Taguchi, E, Uemura, R, Yamada, S, Kaneko, MK, Kato, Y, Yamamoto, K, Toda, M, Suzuki, Y, Murata, S, Ohashi, K (B55) 2020; 7
Jin, HT, Anderson, AC, Tan, WG, West, EE, Ha, SJ, Araki, K, Freeman, GJ, Kuchroo, VK, Ahmed, R (B19) 2010; 107
McMahan, RH, Golden-Mason, L, Nishimura, MI, McMahon, BJ, Kemper, M, Allen, TM, Gretch, DR, Rosen, HR (B21) 2010; 120
Abdelbary, NH, Abdullah, HM, Matsuzaki, T, Hayashi, D, Tanaka, Y, Takashima, H, Izumo, S, Kubota, R (B49) 2011; 203
Sánchez-Fueyo, A, Tian, J, Picarella, D, Domenig, C, Zheng, XX, Sabatos, CA, Manlongat, N, Bender, O, Kamradt, T, Kuchroo, VK, Gutiérrez-Ramos, JC, Coyle, AJ, Strom, TB (B18) 2003; 4
Schwartz, I, Levy, D (B29) 1994; 25
Ikebuchi, R, Konnai, S, Shirai, T, Sunden, Y, Murata, S, Onuma, M, Ohashi, K (B37) 2011; 42
Nishimori, A, Konnai, S, Okagawa, T, Maekawa, N, Ikebuchi, R, Goto, S, Sajiki, Y, Suzuki, Y, Kohara, J, Ogasawara, S, Kato, Y, Murata, S, Ohashi, K (B40) 2017; 12
Hastings, WD, Anderson, DE, Kassam, N, Koguchi, K, Greenfield, EA, Kent, SC, Zheng, XX, Strom, TB, Hafler, DA, Kuchroo, VK (B16) 2009; 39
Ju, Y, Hou, N, Meng, J, Wang, X, Zhang, X, Zhao, D, Liu, Y, Zhu, F, Zhang, L, Sun, W, Liang, X, Gao, L, Ma, C (B7) 2010; 52
Monney, L, Sabatos, CA, Gaglia, JL, Ryu, A, Waldner, H, Chernova, T, Manning, S, Greenfield, EA, Coyle, AJ, Sobel, RA, Freeman, GJ, Kuchroo, VK (B4) 2002; 415
Okagawa, T, Konnai, S, Ikebuchi, R, Suzuki, S, Shirai, T, Sunden, Y, Onuma, M, Murata, S, Ohashi, K (B48) 2012; 43
Sakuishi, K, Apetoh, L, Sullivan, JM, Blazar, BR, Kuchroo, VK, Anderson, AC (B24) 2010; 207
Konnai, S, Usui, T, Ohashi, K, Onuma, M (B34) 2003; 94
Sajiki, Y, Konnai, S, Okagawa, T, Maekawa, N, Nakamura, H, Kato, Y, Suzuki, Y, Murata, S, Ohashi, K (B67) 2021; 114
Watari, K, Konnai, S, Maekawa, N, Okagawa, T, Suzuki, Y, Murata, S, Ohashi, K (B47) 2019; 15
Rangachari, M, Zhu, C, Sakuishi, K, Xiao, S, Karman, J, Chen, A, Angin, M, Wakeham, A, Greenfield, EA, Sobel, RA, Okada, H, McKinnon, PJ, Mak, TW, Addo, MM, Anderson, AC, Kuchroo, VK (B13) 2012; 18
Kuchroo, VK, Umetsu, DT, DeKruyff, RH, Freeman, GJ (B8) 2003; 3
Koyama, S, Akbay, EA, Li, YY, Herter-Sprie, GS, Buczkowski, KA, Richards, WG, Gandhi, L, Redig, AJ, Rodig, SJ, Asahina, H, Jones, RE, Kulkarni, MM, Kuraguchi, M, Palakurthi, S, Fecci, PE, Johnson, BE, Janne, PA, Engelman, JA, Gangadharan, SP, Costa, DB, Freeman, GJ, Bueno, R, Hodi, FS, Dranoff, G, Wong, KK, Hammerman, PS (B62) 2016; 7
Mirsky, ML, Olmstead, CA, Da, Y, Lewin, HA (B28) 1996; 70
Sagata, N, Yasunaga, T, Tsuzuku-Kawamura, J, Ohishi, K, Ogawa, Y, Ikawa, Y (B26) 1985; 82
Hamid, O, Robert, C, Daud, A, Hodi, FS, Hwu, WJ, Kefford, R, Wolchok, JD, Hersey, P, Joseph, RW, Weber, JS, Dronca, R, Gangadhar, TC, Patnaik, A, Zarour, H, Joshua, AM, Gergich, K, Elassaiss-Schaap, J, Algazi, A, Mateus, C, Boasberg, P, Tumeh, PC, Chmielowski, B, Ebbinghaus, SW, Li, XN, Kang, SP, Ribas, A (B61) 2013; 369
Cao, E, Zang, X, Ramagopal, UA, Mukhopadhaya, A, Fedorov, A, Fedorov, E, Zencheck, WD, Lary, JW, Cole, JL, Deng, H, Xiao, H, Dilorenzo, TP, Allison, JP, Nathenson, SG, Almo, SC (B10) 2007; 26
Topalian, SL, Hodi, FS, Brahmer, JR, Gettinger, SN, Smith, DC, McDermott, DF, Powderly, JD, Carvajal, RD, Sosman, JA, Atkins, MB, Leming, PD, Spigel, DR, Antonia, SJ, Horn, L, Drake, CG, Pardoll, DM, Chen, L, Sharfman, WH, Anders, RA, Taube, JM, McMiller, TL, Xu, H, Korman, AJ, Jure-Kunkel, M, Agrawal, S, McDonald, D, Kollia, GD, Gupta, A, Wigginton, JM, Sznol, M (B60) 2012; 366
Anderson, AC, Anderson, DE, Bregoli, L, Hastings, WD, Kassam, N, Lei, C, Chandwaskar, R, Karman, J, Su, EW, Hirashima, M, Bruce, JN, Kane, LP, Kuchroo, VK, Hafler, DA (B6) 2007; 318
Cai, C, Xu, YF, Wu, ZJ, Dong, Q, Li, MY, Olson, JC, Rabinowitz, YM, Wang, LH, Sun, Y (B25) 2016; 34
Ikebuchi, R, Konnai, S, Sunden, Y, Onuma, M, Ohashi, K (B36) 2010; 54
Blackburn, SD, Shin, H, Haining, WN, Zou, T, Workman, CJ, Polley, A, Betts, MR, Freeman, GJ, Vignali, DAA, Wherry, EJ (B66) 2009; 10
Golden-Mason, L, Palmer, BE, Kassam, N, Townshend-Bulson, L, Livingston, S, McMahon, BJ, Castelblanco, N, Kuchroo, V, Gretch, DR, Rosen, HR (B20) 2009; 83
Sajiki, Y, Konnai, S, Okagawa, T, Nishimori, A, Maekawa, N, Goto, S, Ikebuchi, R, Nagata, R, Kawaji, S, Kagawa, Y, Yamada, S, Kato, Y, Nakajima, C, Suzuki, Y, Murata, S, Mori, Y, Ohashi, K (B52) 2018; 86
Sajiki, Y, Konnai, S, Nagata, R, Kawaji, S, Nakamura, H, Fujisawa, S, Okagawa, T, Maekawa, N, Kato, Y, Suzuki, Y, Murata, S, Mori, Y, Ohashi, K (B53) 2021; 83
Konnai, S, Suzuki, S, Shirai, T, Ikebuchi, R, Okagawa, T, Sunden, Y, Mingala, CN, Onuma, M, Murata, S, Ohashi, K (B44) 2013; 36
Fourcade, J, Sun, Z, Benallaoua, M, Guillaume, P, Luescher, IF, Sander, C, Kirkwood, JM, Kuchroo, V, Zarour, HM (B23) 2010; 207
Shirai, T, Konnai, S, Ikebuchi, R, Okagawa, T, Suzuki, S, Sunden, Y, Onuma, M, Murata, S, Ohashi, K (B43) 2011; 144
Okagawa, T, Konnai, S, Nishimori, A, Ikebuchi, R, Mizorogi, S, Nagata, R, Kawaji, S, Tanaka, S, Kagawa, Y, Murata, S, Mori, Y, Ohashi, K (B51) 2016; 84
Nguyen, LT, Ohashi, PS (B2) 2015; 15
Ikebuchi, R, Konnai, S, Okagawa, T, Yokoyama, K, Nakajima, C, Suzuki, Y, Murata, S, Ohashi, K (B38) 2013; 44
e_1_3_2_26_2
e_1_3_2_49_2
e_1_3_2_28_2
e_1_3_2_41_2
e_1_3_2_64_2
e_1_3_2_20_2
e_1_3_2_43_2
e_1_3_2_62_2
e_1_3_2_22_2
e_1_3_2_45_2
e_1_3_2_68_2
e_1_3_2_24_2
e_1_3_2_47_2
e_1_3_2_66_2
e_1_3_2_60_2
e_1_3_2_9_2
e_1_3_2_16_2
e_1_3_2_37_2
e_1_3_2_7_2
e_1_3_2_18_2
e_1_3_2_39_2
e_1_3_2_54_2
e_1_3_2_10_2
e_1_3_2_31_2
e_1_3_2_52_2
e_1_3_2_5_2
e_1_3_2_12_2
e_1_3_2_33_2
e_1_3_2_58_2
e_1_3_2_3_2
e_1_3_2_14_2
e_1_3_2_35_2
e_1_3_2_56_2
e_1_3_2_50_2
e_1_3_2_27_2
e_1_3_2_48_2
e_1_3_2_29_2
e_1_3_2_40_2
e_1_3_2_65_2
e_1_3_2_21_2
e_1_3_2_42_2
e_1_3_2_63_2
e_1_3_2_23_2
e_1_3_2_44_2
e_1_3_2_25_2
e_1_3_2_46_2
e_1_3_2_67_2
e_1_3_2_61_2
e_1_3_2_15_2
e_1_3_2_38_2
e_1_3_2_8_2
e_1_3_2_17_2
e_1_3_2_59_2
e_1_3_2_6_2
e_1_3_2_19_2
e_1_3_2_53_2
e_1_3_2_32_2
e_1_3_2_51_2
e_1_3_2_11_2
e_1_3_2_34_2
e_1_3_2_57_2
e_1_3_2_4_2
e_1_3_2_13_2
e_1_3_2_36_2
e_1_3_2_55_2
e_1_3_2_2_2
Schwartz I (e_1_3_2_30_2) 1994; 25
References_xml – volume: 203
  start-page: 1313
  year: 2019
  end-page: 1324
  ident: B42
  article-title: Prostaglandin E2-induced immune exhaustion and enhancement of antiviral effects by anti-PD-L1 antibody combined with COX-2 inhibitor in bovine leukemia virus infection
  publication-title: J Immunol
  doi: 10.4049/jimmunol.1900342
  contributor:
    fullname: Ohashi, K
– volume: 63
  start-page: 703
  year: 2001
  end-page: 708
  ident: B30
  article-title: Host immune responses in the course of bovine leukemia virus infection
  publication-title: J Vet Med Sci
  doi: 10.1292/jvms.63.703
  contributor:
    fullname: Onuma, M
– volume: 8
  start-page: 650
  year: 2017
  ident: B41
  article-title: Anti-bovine programmed death-1 rat-bovine chimeric antibody for immunotherapy of bovine leukemia virus infection in cattle
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2017.00650
  contributor:
    fullname: Ohashi, K
– volume: 68
  start-page: 4589
  year: 1994
  end-page: 4596
  ident: B27
  article-title: In vivo leukocyte tropism of bovine leukemia virus in sheep and cattle
  publication-title: J Virol
  doi: 10.1128/JVI.68.7.4589-4596.1994
  contributor:
    fullname: Levy, D
– volume: 84
  start-page: 77
  year: 2016
  end-page: 89
  ident: B51
  article-title: Bovine immunoinhibitory receptors contribute to suppression of Mycobacterium avium subsp. paratuberculosis-specific T-cell responses
  publication-title: Infect Immun
  doi: 10.1128/IAI.01014-15
  contributor:
    fullname: Ohashi, K
– volume: 36
  start-page: 63
  year: 2013
  end-page: 69
  ident: B44
  article-title: Enhanced expression of LAG-3 on lymphocyte subpopulations from persistently lymphocytotic cattle infected with bovine leukemia virus
  publication-title: Comp Immunol Microbiol Infect Dis
  doi: 10.1016/j.cimid.2012.09.005
  contributor:
    fullname: Ohashi, K
– volume: 52
  start-page: 322
  year: 2010
  end-page: 329
  ident: B7
  article-title: T cell immunoglobulin- and mucin-domain-containing molecule-3 (Tim-3) mediates natural killer cell suppression in chronic hepatitis B
  publication-title: J Hepatol
  doi: 10.1016/j.jhep.2009.12.005
  contributor:
    fullname: Ma, C
– volume: 12
  start-page: 492
  year: 2011
  end-page: 499
  ident: B1
  article-title: T cell exhaustion
  publication-title: Nat Immunol
  doi: 10.1038/ni.2035
  contributor:
    fullname: Wherry, EJ
– volume: 79
  start-page: 1
  year: 2017
  end-page: 5
  ident: B39
  article-title: Immune exhaustion during chronic infections in cattle
  publication-title: J Vet Med Sci
  doi: 10.1292/jvms.16-0354
  contributor:
    fullname: Ohashi, K
– volume: 163
  start-page: 115
  year: 2015
  end-page: 124
  ident: B46
  article-title: Increased expression of the regulatory T cell-associated marker CTLA-4 in bovine leukemia virus infection
  publication-title: Vet Immunol Immunopathol
  doi: 10.1016/j.vetimm.2014.10.006
  contributor:
    fullname: Ohashi, K
– volume: 203
  start-page: 948
  year: 2011
  end-page: 959
  ident: B49
  article-title: Reduced Tim-3 expression on human T-lymphotropic virus type I (HTLV-I) Tax-specific cytotoxic T lymphocytes in HTLV-I infection
  publication-title: J Infect Dis
  doi: 10.1093/infdis/jiq153
  contributor:
    fullname: Kubota, R
– volume: 20
  start-page: 173
  year: 2020
  end-page: 185
  ident: B14
  article-title: TIM3 comes of age as an inhibitory receptor
  publication-title: Nat Rev Immunol
  doi: 10.1038/s41577-019-0224-6
  contributor:
    fullname: Kuchroo, VK
– volume: 114
  start-page: 103847
  year: 2021
  ident: B67
  article-title: A TLR7 agonist activates bovine Th1 response and exerts antiviral activity against bovine leukemia virus
  publication-title: Dev Comp Immunol
  doi: 10.1016/j.dci.2020.103847
  contributor:
    fullname: Ohashi, K
– volume: 120
  start-page: 4546
  year: 2010
  end-page: 4557
  ident: B21
  article-title: Tim-3 expression on PD-1+ HCV-specific human CTLs is associated with viral persistence, and its blockade restores hepatocyte-directed in vitro cytotoxicity
  publication-title: J Clin Invest
  doi: 10.1172/JCI43127
  contributor:
    fullname: Rosen, HR
– volume: 5
  year: 2010
  ident: B22
  article-title: A crucial role for Kupffer cell-derived galectin-9 in regulation of T cell immunity in hepatitis C infection
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0009504
  contributor:
    fullname: Rosen, HR
– volume: 82
  start-page: 677
  year: 1985
  end-page: 681
  ident: B26
  article-title: Complete nucleotide sequence of the genome of bovine leukemia virus: its evolutionary relationship to other retroviruses
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.82.3.677
  contributor:
    fullname: Ikawa, Y
– volume: 70
  start-page: 2178
  year: 1996
  end-page: 2183
  ident: B28
  article-title: The prevalence of proviral bovine leukemia virus in peripheral blood mononuclear cells at two subclinical stages of infection
  publication-title: J Virol
  doi: 10.1128/JVI.70.4.2178-2183.1996
  contributor:
    fullname: Lewin, HA
– volume: 4
  start-page: 837
  year: 2020
  end-page: 850
  ident: B65
  article-title: Enhanced immunotherapeutic efficacy of anti-PD-L1 antibody in combination with an EP4 antagonist
  publication-title: Immunohorizons
  doi: 10.4049/immunohorizons.2000089
  contributor:
    fullname: Ohashi, K
– volume: 7
  start-page: 12
  year: 2020
  ident: B55
  article-title: Upregulation of PD-L1 expression by prostaglandin E2 and the enhancement of IFN-γ by anti-PD-L1 antibody combined with a COX-2 inhibitor in Mycoplasma bovis infection
  publication-title: Front Vet Sci
  doi: 10.3389/fvets.2020.00012
  contributor:
    fullname: Ohashi, K
– volume: 94
  start-page: 283
  year: 2003
  end-page: 294
  ident: B34
  article-title: The rapid quantitative analysis of bovine cytokine genes by real-time RT-PCR
  publication-title: Vet Microbiol
  doi: 10.1016/s0378-1135(03)00119-6
  contributor:
    fullname: Onuma, M
– volume: 122
  start-page: 2395
  year: 2012
  end-page: 2404
  ident: B58
  article-title: Allograft rejection is restrained by short-lived TIM-3+PD-1+Foxp3+ Tregs
  publication-title: J Clin Invest
  doi: 10.1172/JCI45138
  contributor:
    fullname: Strom, TB
– volume: 2
  year: 2013
  ident: B59
  article-title: TIM3+FOXP3+ regulatory T cells are tissue-specific promoters of T-cell dysfunction in cancer
  publication-title: Oncoimmunology
  doi: 10.4161/onci.23849
  contributor:
    fullname: Anderson, AC
– volume: 144
  start-page: 462
  year: 2011
  end-page: 467
  ident: B43
  article-title: Molecular cloning of bovine lymphocyte activation gene-3 and its expression characteristics in bovine leukemia virus-infected cattle
  publication-title: Vet Immunol Immunopathol
  doi: 10.1016/j.vetimm.2011.08.018
  contributor:
    fullname: Ohashi, K
– volume: 15
  start-page: 380
  year: 2019
  ident: B47
  article-title: Immune inhibitory function of bovine CTLA-4 and the effects of its blockade in IFN-γ production
  publication-title: BMC Vet Res
  doi: 10.1186/s12917-019-2082-7
  contributor:
    fullname: Ohashi, K
– volume: 15
  start-page: 45
  year: 2015
  end-page: 56
  ident: B2
  article-title: Clinical blockade of PD1 and LAG3 — potential mechanisms of action
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri3790
  contributor:
    fullname: Ohashi, PS
– volume: 16
  start-page: 1622
  year: 2018
  end-page: 1626
  ident: B17
  article-title: Effect of CEACAM-1 knockdown in human colorectal cancer cells
  publication-title: Oncol Lett
  doi: 10.3892/ol.2018.8835
  contributor:
    fullname: Sun, YW
– volume: 366
  start-page: 2443
  year: 2012
  end-page: 2454
  ident: B60
  article-title: Safety, activity, and immune correlates of anti-PD-1 antibody in cancer
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa1200690
  contributor:
    fullname: Sznol, M
– volume: 72
  start-page: 6917
  year: 1998
  end-page: 6921
  ident: B33
  article-title: Interleukin-12 p40 mRNA expression in bovine leukemia virus-infected animals: increase in alymphocytosis but decrease in persistent lymphocytosis
  publication-title: J Virol
  doi: 10.1128/JVI.72.8.6917-6921.1998
  contributor:
    fullname: Splitter, GA
– volume: 12
  year: 2017
  ident: B40
  article-title: In vitro and in vivo antivirus activity of an anti-programmed death-ligand 1 (PD-L1) rat-bovine chimeric antibody against bovine leukemia virus infection
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0174916
  contributor:
    fullname: Ohashi, K
– volume: 4
  start-page: 1093
  year: 2003
  end-page: 1101
  ident: B18
  article-title: Tim-3 inhibits T helper type 1-mediated auto- and alloimmune responses and promotes immunological tolerance
  publication-title: Nat Immunol
  doi: 10.1038/ni987
  contributor:
    fullname: Strom, TB
– volume: 107
  start-page: 14733
  year: 2010
  end-page: 14738
  ident: B19
  article-title: Cooperation of Tim-3 and PD-1 in CD8 T-cell exhaustion during chronic viral infection
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1009731107
  contributor:
    fullname: Ahmed, R
– volume: 4
  start-page: 18
  year: 2007
  ident: B31
  article-title: Mechanisms of leukemogenesis induced by bovine leukemia virus: prospects for novel anti-retroviral therapies in human
  publication-title: Retrovirology
  doi: 10.1186/1742-4690-4-18
  contributor:
    fullname: Willems, L
– volume: 90
  year: 2022
  ident: B57
  article-title: Prostaglandin E2-induced immune suppression via cytotoxic T-lymphocyte antigen 4 in paratuberculosis
  publication-title: Infect Immun
  doi: 10.1128/iai.00210-22
  contributor:
    fullname: Ohashi, K
– volume: 4
  start-page: 1102
  year: 2003
  end-page: 1110
  ident: B15
  article-title: Interaction of Tim-3 and Tim-3 ligand regulates T helper type 1 responses and induction of peripheral tolerance
  publication-title: Nat Immunol
  doi: 10.1038/ni988
  contributor:
    fullname: Kuchroo, VK
– volume: 70
  start-page: 5706
  year: 1996
  end-page: 5710
  ident: B32
  article-title: Increased interleukin-10 mRNA expression in tumor-bearing or persistently lymphocytotic animals infected with bovine leukemia virus
  publication-title: J Virol
  doi: 10.1128/JVI.70.8.5706-5710.1996
  contributor:
    fullname: Splitter, GA
– volume: 39
  start-page: 2492
  year: 2009
  end-page: 2501
  ident: B16
  article-title: TIM-3 is expressed on activated human CD4+ T cells and regulates Th1 and Th17 cytokines
  publication-title: Eur J Immunol
  doi: 10.1002/eji.200939274
  contributor:
    fullname: Kuchroo, VK
– volume: 10
  start-page: 29
  year: 2009
  end-page: 37
  ident: B66
  article-title: Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection
  publication-title: Nat Immunol
  doi: 10.1038/ni.1679
  contributor:
    fullname: Wherry, EJ
– volume: 83
  start-page: 162
  year: 2021
  end-page: 166
  ident: B53
  article-title: The enhancement of Th1 immune response by anti-PD-L1 antibody in cattle infected with Mycobacterium avium subsp. paratuberculosis
  publication-title: J Vet Med Sci
  doi: 10.1292/jvms.20-0590
  contributor:
    fullname: Ohashi, K
– volume: 35
  start-page: 51
  year: 2014
  end-page: 60
  ident: B3
  article-title: Tolerance and exhaustion: defining mechanisms of T cell dysfunction
  publication-title: Trends Immunol
  doi: 10.1016/j.it.2013.10.001
  contributor:
    fullname: Greenberg, PD
– volume: 18
  start-page: 1394
  year: 2012
  end-page: 1400
  ident: B13
  article-title: Bat3 promotes T cell responses and autoimmunity by repressing Tim-3-mediated cell death and exhaustion
  publication-title: Nat Med
  doi: 10.1038/nm.2871
  contributor:
    fullname: Kuchroo, VK
– volume: 86
  year: 2018
  ident: B52
  article-title: Prostaglandin E2 induction suppresses the Th1 immune responses in cattle with Johne’s disease
  publication-title: Infect Immun
  doi: 10.1128/IAI.00910-17
  contributor:
    fullname: Ohashi, K
– volume: 34
  start-page: 561
  year: 2016
  end-page: 567
  ident: B25
  article-title: Tim-3 expression represents dysfunctional tumor infiltrating T cells in renal cell carcinoma
  publication-title: World J Urol
  doi: 10.1007/s00345-015-1656-7
  contributor:
    fullname: Sun, Y
– volume: 54
  start-page: 291
  year: 2010
  end-page: 298
  ident: B36
  article-title: Molecular cloning and expression analysis of bovine programmed death-1
  publication-title: Microbiol Immunol
  doi: 10.1111/j.1348-0421.2010.00208.x
  contributor:
    fullname: Ohashi, K
– volume: 369
  start-page: 134
  year: 2013
  end-page: 144
  ident: B61
  article-title: Safety and tumor responses with lambrolizumab (anti-PD-1) in melanoma
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa1305133
  contributor:
    fullname: Ribas, A
– volume: 3
  start-page: 454
  year: 2003
  end-page: 462
  ident: B8
  article-title: The TIM gene family: emerging roles in immunity and disease
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri1111
  contributor:
    fullname: Freeman, GJ
– volume: 5
  year: 2011
  ident: B50
  article-title: HTLV-1 tax specific CD8+ T cells express low levels of Tim-3 in HTLV-1 infection: implications for progression to neurological complications
  publication-title: PLoS Negl Trop Dis
  doi: 10.1371/journal.pntd.0001030
  contributor:
    fullname: Kallas, EG
– volume: 26
  start-page: 311
  year: 2007
  end-page: 321
  ident: B10
  article-title: T cell immunoglobulin mucin-3 crystal structure reveals a galectin-9-independent ligand binding surface
  publication-title: Immunity
  doi: 10.1016/j.immuni.2007.01.016
  contributor:
    fullname: Almo, SC
– volume: 83
  start-page: 9122
  year: 2009
  end-page: 9130
  ident: B20
  article-title: Negative immune regulator Tim-3 is overexpressed on T cells in hepatitis C virus infection and its blockade rescues dysfunctional CD4+ and CD8+ T cells
  publication-title: J Virol
  doi: 10.1128/JVI.00639-09
  contributor:
    fullname: Rosen, HR
– volume: 17
  start-page: 165
  year: 2019
  ident: B64
  article-title: TNF-α-induced Tim-3 expression marks the dysfunction of infiltrating natural killer cells in human esophageal cancer
  publication-title: J Transl Med
  doi: 10.1186/s12967-019-1917-0
  contributor:
    fullname: Huang, L
– volume: 205
  start-page: 2763
  year: 2008
  end-page: 2779
  ident: B5
  article-title: Tim-3 expression defines a novel population of dysfunctional T cells with highly elevated frequencies in progressive HIV-1 infection
  publication-title: J Exp Med
  doi: 10.1084/jem.20081398
  contributor:
    fullname: Ostrowski, MA
– volume: 13
  start-page: 832
  year: 2012
  end-page: 842
  ident: B11
  article-title: Tumor-infiltrating DCs suppress nucleic acid-mediated innate immune responses through interactions between the receptor TIM-3 and the alarmin HMGB1
  publication-title: Nat Immunol
  doi: 10.1038/ni.2376
  contributor:
    fullname: Jinushi, M
– volume: 42
  start-page: 103
  year: 2011
  ident: B37
  article-title: Increase of cells expressing PD-L1 in bovine leukemia virus infection and enhancement of anti-viral immune responses in vitro via PD-L1 blockade
  publication-title: Vet Res
  doi: 10.1186/1297-9716-42-103
  contributor:
    fullname: Ohashi, K
– volume: 207
  start-page: 2187
  year: 2010
  end-page: 2194
  ident: B24
  article-title: Targeting Tim-3 and PD-1 pathways to reverse T cell exhaustion and restore anti-tumor immunity
  publication-title: J Exp Med
  doi: 10.1084/jem.20100643
  contributor:
    fullname: Anderson, AC
– volume: 415
  start-page: 536
  year: 2002
  end-page: 541
  ident: B4
  article-title: Th1-specific cell surface protein Tim-3 regulates macrophage activation and severity of an autoimmune disease
  publication-title: Nature
  doi: 10.1038/415536a
  contributor:
    fullname: Kuchroo, VK
– volume: 207
  start-page: 2175
  year: 2010
  end-page: 2186
  ident: B23
  article-title: Upregulation of Tim-3 and PD-1 expression is associated with tumor antigen-specific CD8+ T cell dysfunction in melanoma patients
  publication-title: J Exp Med
  doi: 10.1084/jem.20100637
  contributor:
    fullname: Zarour, HM
– volume: 4
  start-page: 52
  year: 2016
  end-page: 63
  ident: B35
  article-title: Bovine leukemia virus reduces anti-viral cytokine activities and NK cytotoxicity by inducing TGF-β secretion from regulatory T cells
  publication-title: Immun Inflamm Dis
  doi: 10.1002/iid3.93
  contributor:
    fullname: Ohashi, K
– volume: 6
  start-page: 1245
  year: 2005
  end-page: 1252
  ident: B9
  article-title: The Tim-3 ligand galectin-9 negatively regulates T helper type 1 immunity
  publication-title: Nat Immunol
  doi: 10.1038/ni1271
  contributor:
    fullname: Kuchroo, VK
– volume: 517
  start-page: 386
  year: 2015
  end-page: 390
  ident: B12
  article-title: CEACAM1 regulates TIM-3-mediated tolerance and exhaustion
  publication-title: Nature
  doi: 10.1038/nature13848
  contributor:
    fullname: Blumberg, RS
– volume: 49
  start-page: 50
  year: 2018
  ident: B45
  article-title: Cooperation of PD-1 and LAG-3 in the exhaustion of CD4+ and CD8+ T cells during bovine leukemia virus infection
  publication-title: Vet Res
  doi: 10.1186/s13567-018-0543-9
  contributor:
    fullname: Ohashi, K
– volume: 7
  start-page: 10501
  year: 2016
  ident: B62
  article-title: Adaptive resistance to therapeutic PD-1 blockade is associated with upregulation of alternative immune checkpoints
  publication-title: Nat Commun
  doi: 10.1038/ncomms10501
  contributor:
    fullname: Hammerman, PS
– volume: 25
  start-page: 521
  year: 1994
  end-page: 536
  ident: B29
  article-title: Pathobiology of bovine leukemia virus
  publication-title: Vet Res
  contributor:
    fullname: Levy, D
– volume: 44
  start-page: 59
  year: 2013
  ident: B38
  article-title: Blockade of bovine PD-1 increases T cell function and inhibits bovine leukemia virus expression in B cells in vitro
  publication-title: Vet Res
  doi: 10.1186/1297-9716-44-59
  contributor:
    fullname: Ohashi, K
– volume: 84
  start-page: 2779
  year: 2016
  end-page: 2790
  ident: B54
  article-title: Cooperation of PD-1 and LAG-3 contributes to T-cell exhaustion in Anaplasma marginale-infected cattle
  publication-title: Infect Immun
  doi: 10.1128/IAI.00278-16
  contributor:
    fullname: Brown, WC
– volume: 6
  year: 2017
  ident: B63
  article-title: Adaptive resistance to anti-PD1 therapy by Tim-3 upregulation is mediated by the PI3K-Akt pathway in head and neck cancer
  publication-title: Oncoimmunology
  doi: 10.1080/2162402X.2016.1261779
  contributor:
    fullname: Ferris, RL
– volume: 318
  start-page: 1141
  year: 2007
  end-page: 1143
  ident: B6
  article-title: Promotion of tissue inflammation by the immune receptor Tim-3 expressed on innate immune cells
  publication-title: Science
  doi: 10.1126/science.1148536
  contributor:
    fullname: Hafler, DA
– volume: 43
  start-page: 45
  year: 2012
  ident: B48
  article-title: Increased bovine Tim-3 and its ligand expressions during bovine leukemia virus infection
  publication-title: Vet Res
  doi: 10.1186/1297-9716-43-45
  contributor:
    fullname: Ohashi, K
– volume: 68
  start-page: 77
  year: 2020
  end-page: 90
  ident: B56
  article-title: Upregulation of PD-L1 expression by prostaglandin E2 and the enhancement of IFN-γ by anti-PD-L1 antibody combined with a COX-2 inhibitor in Mycoplasma bovis infection
  publication-title: Jpn J Vet Res
  doi: 10.14943/jjvr.68.2.77
  contributor:
    fullname: Ohashi, K
– ident: e_1_3_2_22_2
  doi: 10.1172/JCI43127
– ident: e_1_3_2_14_2
  doi: 10.1038/nm.2871
– ident: e_1_3_2_34_2
  doi: 10.1128/JVI.72.8.6917-6921.1998
– ident: e_1_3_2_32_2
  doi: 10.1186/1742-4690-4-18
– ident: e_1_3_2_18_2
  doi: 10.3892/ol.2018.8835
– ident: e_1_3_2_10_2
  doi: 10.1038/ni1271
– ident: e_1_3_2_35_2
  doi: 10.1016/s0378-1135(03)00119-6
– ident: e_1_3_2_65_2
  doi: 10.1186/s12967-019-1917-0
– ident: e_1_3_2_8_2
  doi: 10.1016/j.jhep.2009.12.005
– ident: e_1_3_2_54_2
  doi: 10.1292/jvms.20-0590
– ident: e_1_3_2_58_2
  doi: 10.1128/iai.00210-22
– ident: e_1_3_2_13_2
  doi: 10.1038/nature13848
– ident: e_1_3_2_66_2
  doi: 10.4049/immunohorizons.2000089
– ident: e_1_3_2_42_2
  doi: 10.3389/fimmu.2017.00650
– ident: e_1_3_2_21_2
  doi: 10.1128/JVI.00639-09
– ident: e_1_3_2_31_2
  doi: 10.1292/jvms.63.703
– ident: e_1_3_2_68_2
  doi: 10.1016/j.dci.2020.103847
– ident: e_1_3_2_43_2
  doi: 10.4049/jimmunol.1900342
– ident: e_1_3_2_52_2
  doi: 10.1128/IAI.01014-15
– ident: e_1_3_2_26_2
  doi: 10.1007/s00345-015-1656-7
– ident: e_1_3_2_15_2
  doi: 10.1038/s41577-019-0224-6
– ident: e_1_3_2_37_2
  doi: 10.1111/j.1348-0421.2010.00208.x
– ident: e_1_3_2_53_2
  doi: 10.1128/IAI.00910-17
– ident: e_1_3_2_2_2
  doi: 10.1038/ni.2035
– ident: e_1_3_2_5_2
  doi: 10.1038/415536a
– ident: e_1_3_2_59_2
  doi: 10.1172/JCI45138
– ident: e_1_3_2_44_2
  doi: 10.1016/j.vetimm.2011.08.018
– ident: e_1_3_2_48_2
  doi: 10.1186/s12917-019-2082-7
– ident: e_1_3_2_19_2
  doi: 10.1038/ni987
– ident: e_1_3_2_55_2
  doi: 10.1128/IAI.00278-16
– ident: e_1_3_2_3_2
  doi: 10.1038/nri3790
– ident: e_1_3_2_40_2
  doi: 10.1292/jvms.16-0354
– ident: e_1_3_2_45_2
  doi: 10.1016/j.cimid.2012.09.005
– ident: e_1_3_2_36_2
  doi: 10.1002/iid3.93
– ident: e_1_3_2_56_2
  doi: 10.3389/fvets.2020.00012
– ident: e_1_3_2_17_2
  doi: 10.1002/eji.200939274
– ident: e_1_3_2_50_2
  doi: 10.1093/infdis/jiq153
– ident: e_1_3_2_29_2
  doi: 10.1128/JVI.70.4.2178-2183.1996
– ident: e_1_3_2_27_2
  doi: 10.1073/pnas.82.3.677
– ident: e_1_3_2_28_2
  doi: 10.1128/JVI.68.7.4589-4596.1994
– ident: e_1_3_2_51_2
  doi: 10.1371/journal.pntd.0001030
– ident: e_1_3_2_12_2
  doi: 10.1038/ni.2376
– ident: e_1_3_2_49_2
  doi: 10.1186/1297-9716-43-45
– ident: e_1_3_2_16_2
  doi: 10.1038/ni988
– ident: e_1_3_2_41_2
  doi: 10.1371/journal.pone.0174916
– ident: e_1_3_2_46_2
  doi: 10.1186/s13567-018-0543-9
– ident: e_1_3_2_62_2
  doi: 10.1056/NEJMoa1305133
– ident: e_1_3_2_4_2
  doi: 10.1016/j.it.2013.10.001
– ident: e_1_3_2_63_2
  doi: 10.1038/ncomms10501
– ident: e_1_3_2_7_2
  doi: 10.1126/science.1148536
– ident: e_1_3_2_11_2
  doi: 10.1016/j.immuni.2007.01.016
– ident: e_1_3_2_9_2
  doi: 10.1038/nri1111
– ident: e_1_3_2_39_2
  doi: 10.1186/1297-9716-44-59
– ident: e_1_3_2_24_2
  doi: 10.1084/jem.20100637
– ident: e_1_3_2_20_2
  doi: 10.1073/pnas.1009731107
– ident: e_1_3_2_67_2
  doi: 10.1038/ni.1679
– ident: e_1_3_2_6_2
  doi: 10.1084/jem.20081398
– ident: e_1_3_2_64_2
  doi: 10.1080/2162402X.2016.1261779
– ident: e_1_3_2_61_2
  doi: 10.1056/NEJMoa1200690
– ident: e_1_3_2_60_2
  doi: 10.4161/onci.23849
– ident: e_1_3_2_33_2
  doi: 10.1128/JVI.70.8.5706-5710.1996
– ident: e_1_3_2_38_2
  doi: 10.1186/1297-9716-42-103
– ident: e_1_3_2_47_2
  doi: 10.1016/j.vetimm.2014.10.006
– ident: e_1_3_2_57_2
  doi: 10.14943/jjvr.68.2.77
– ident: e_1_3_2_23_2
  doi: 10.1371/journal.pone.0009504
– volume: 25
  start-page: 521
  year: 1994
  ident: e_1_3_2_30_2
  article-title: Pathobiology of bovine leukemia virus
  publication-title: Vet Res
  contributor:
    fullname: Schwartz I
– ident: e_1_3_2_25_2
  doi: 10.1084/jem.20100643
SSID ssj0014464
Score 2.487449
Snippet Bovine leukemia virus (BLV) is a retrovirus that causes enzootic bovine leukosis (EBL) in cattle and is widespread in many countries, including Japan. Recent...
Enzootic bovine leukosis caused by bovine leukemia virus (BLV) is an important viral disease in cattle, causing severe economic losses to the cattle industry...
SourceID pubmedcentral
crossref
asm2
pubmed
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage e0143022
SubjectTerms Animals
Cattle
CD8-Positive T-Lymphocytes - immunology
Enzootic Bovine Leukosis - immunology
Gene Expression Regulation - immunology
Immune Checkpoint Proteins - immunology
Immunology
Interferon-gamma - immunology
Leukemia Virus, Bovine - immunology
Mucins - immunology
Pathogenesis and Immunity
Programmed Cell Death 1 Receptor - immunology
Title Combined Immune Checkpoint Blockade Enhances Antiviral Immunity against Bovine Leukemia Virus
URI https://www.ncbi.nlm.nih.gov/pubmed/36598199
https://journals.asm.org/doi/10.1128/jvi.01430-22
https://pubmed.ncbi.nlm.nih.gov/PMC9888214
Volume 97
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1La9tAEF5qQ6GX0qQvt2lYSnuUba20r2PiOiT0QaEPciliH6NYcayYyC7033d2JZn40EvPGrFidpb5vtXMN4S8UwKkZZlNVJlxJChcJzpP84Q5yXgpp8rErrTzb_LLpfowDzI5vO-FiUX7zlbj-mY1rqtFrK1cr9ykrxObfP0800jbWJpPBmSA2LCn6N2vA-Q3eS8Rjqf5sq92Z2py_bsaBz27acLCFJtMcK2i6uvQNCu2l5l26Wi_VPJe7jl7Qh53oJGetB93QB5AfUgetmMk_zwlv_BQI8EFTy9CtwfQ2QLccn1b1Rt6islqaTzQeb0IG9zQkzoMjMBVWmtE4dRcmQphIj0N1wtAP8F2CavK0J_V3bZ5Rn6czb_PzpNubEJiOFObxClhpbBKOBDTMsu8sOAF0hrMS9pwJ0pnuJXWOq200Bp0qZhmPoIZsNPsORnWtzW8JNSG8-pSAzL1uU7BWJ5ary2CFmd9LkfkbfBc0cV9U0RKwVSBni6ipwvGRuR979di3Upo_MPuRevrnVW_QSMi93ZhZxC0sfefYMhEjewuRF7995uvyaMwWT7ctmTpERlu7rbwhgwavz1G5H3x8ThG3V_q5dp8
link.rule.ids 230,315,729,782,786,887,27934,27935,53802,53804
linkProvider National Library of Medicine
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF7RIASXUh6FFFpWCI5O7LX3dWxDqlRNKyQK6gVZ-xgTE-JGdVKp_57dtR2RA5eedyyt_O145lvPfIPQJ8GAa5LqSBQpdQSFykhmSRYRwwkteCxU6EqbfOOX1-LL2Mvk0K4XJhTtG10Oqj-LQVXOQm3lcmGGXZ3Y8OvFSDraRpJsuIMeO3-NSUfS258HjuFknUi4W7_u6t2JGP6-Kwde0S6OiJ9jkzIqRdB97al6QbZi0yYgbRdL_hN9Tp8_cN97aLdNN_Fxs_wCPYLqJXrSDKC8f4V-us-Bo8Zg8ZnvEwE8moGZL2_KaoVPXJibKwt4XM380ajxceVHTbjdNdYuf8fqlypdgolP_MUE4Cms57AoFf5R3q7r1-j76fhqNInagQuRokSsIiOY5kwLZoDFRZpapsEyR4hcRJOKGlYYRTXX2kghmZQgC0EksSENAh2n-6hX3VTwFmHtPd0kCnhiM5mA0jTRVmqX7hhtM95HH_0bz1uPqfNARojIHUJ5QCgnpI8-d3jky0Z84z92bxqMNlYdsH3Et9DbGHhV7e0VB1pQ125BOnjwkx_Q08nVxTSfnl2ev0PP_Hx6f2eTJu9Rb3W7hkO0U9v1UTizfwEYpu8V
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1bT9swFLZGp017AXYBOmCzpu0xTeIkvjxCaQUaQ0i7iJcp8uWEZqWhIi3S_j22k1T0gZft2SeSlc_OOZ9z_H0IfeYUmCKJCniRZJagZCIQaZwGRDOSFSzi0t9KO_3OLq74ycjJ5KysvnzTvlbloLqZDapy4nsr5zMddn1i4eW3obC0jcRpODdFuIGe2z0bpR1Rb38gWJaTdkLhdvyq63knPPxzXw6cql0UEOdlk9BMcK_92pP1jKzlp1VSWm-YfJSBxlv_MfdttNmWnfioCXmNnkH1Br1ojCj_vkW_7WfBUmQw-MzdFwE8nICezm_LaoGPbbqbSgN4VE3cEqnxUeUsJ-wMm2hbx2N5LUtbaOJjd0AB-ByWU5iVEv8q75b1O_RzPPoxPA1a44VAZoQvAs2pYlRxqoFGRZIYqsBQS4xsZhMy07TQMlNMKS24oEKAKDgRxPhyCFSU7KBedVvBHsLK7XgdS2CxSUUMUmWxMkLZskcrk7I--uTeet7unDr3pITw3KKUe5RyQvroS4dJPm9EOJ6I221wWkV14PYRW0NwFeDUtddHLHBeZbsF6v0_P_kRvbw8GefnZxdf99ErZ1Pvjm6S-AD1FndLOEQbtVl-8Mv2AbAL8ZU
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Combined+Immune+Checkpoint+Blockade+Enhances+Antiviral+Immunity+against+Bovine+Leukemia+Virus&rft.jtitle=Journal+of+virology&rft.au=Nakamura%2C+Hayato&rft.au=Konnai%2C+Satoru&rft.au=Okagawa%2C+Tomohiro&rft.au=Maekawa%2C+Naoya&rft.date=2023-01-31&rft.pub=American+Society+for+Microbiology&rft.issn=0022-538X&rft.eissn=1098-5514&rft.volume=97&rft.issue=1&rft_id=info:doi/10.1128%2Fjvi.01430-22&rft_id=info%3Apmid%2F36598199&rft.externalDBID=PMC9888214
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-538X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-538X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-538X&client=summon