Search Results - "Jing, Weiqing"
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Programmed death receptor-1/programmed death receptor ligand-1 blockade after transient lymphodepletion to treat myeloma
Published in The Journal of immunology (1950) (01-06-2013)“…Early phase clinical trials targeting the programmed death receptor-1/ligand-1 (PD-1/PD-L1) pathway to overcome tumor-mediated immunosuppression have reported…”
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2
Pathogen boosted adoptive cell transfer immunotherapy to treat solid tumors
Published in Proceedings of the National Academy of Sciences - PNAS (24-01-2017)“…Because of insufficient migration and antitumor function of transferred T cells, especially inside the immunosuppressive tumor microenvironment (TME), the…”
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3
T Cells Deficient in Diacylglycerol Kinase ζ Are Resistant to PD-1 Inhibition and Help Create Persistent Host Immunity to Leukemia
Published in Cancer research (Chicago, Ill.) (15-10-2017)“…Efforts to improve the efficacy of adoptive T-cell therapies and immune checkpoint therapies in myelogenous leukemia are desired. In this study, we evaluated…”
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4
Combined immune checkpoint protein blockade and low dose whole body irradiation as immunotherapy for myeloma
Published in Journal for immunotherapy of cancer (20-01-2015)“…Multiple myeloma is characterized by the presence of transformed neoplastic plasma cells in the bone marrow and is generally considered to be an incurable…”
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Targeting transmembrane-domain-less MOG expression to platelets prevents disease development in experimental autoimmune encephalomyelitis
Published in Frontiers in immunology (27-10-2022)“…Multiple sclerosis (MS) is a chronic inflammatory autoimmune disease of the central nervous system with no cure yet. Here, we report genetic engineering of…”
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Depletion of CD4 T cells enhances immunotherapy for neuroblastoma after syngeneic HSCT but compromises development of antitumor immune memory
Published in Blood (30-04-2009)“…High-risk neuroblastoma remains a clinically challenging disease. Here, we report that a multifaceted immunotherapeutic approach including syngeneic…”
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Nongenotoxic antibody-drug conjugate conditioning enables safe and effective platelet gene therapy of hemophilia A mice
Published in Blood advances (24-09-2019)“…Gene therapy offers the potential to cure hemophilia A (HA). We have shown that hematopoietic stem cell (HSC)–based platelet-specific factor VIII (FVIII)…”
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1051 Noval IL-12 gene delivery vehicles for transformation of spontaneous canine soft-tissue sarcoma
Published in Journal for immunotherapy of cancer (01-11-2023)“…BackgroundInterleukin 12 (IL-12) is a highly inflammatory cytokine that has potent activity in cancer, which mediates its antitumor activity through both…”
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Depletion of CD25+ T cells from hematopoietic stem cell grafts increases posttransplantation vaccine-induced immunity to neuroblastoma
Published in Blood (23-06-2011)“…A multifaceted immunotherapeutic strategy that includes hematopoietic stem cell (HSC) transplantation, T-cell adoptive transfer, and tumor vaccination can…”
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10
Induction of activated T follicular helper cells is critical for anti-FVIII inhibitor development in hemophilia A mice
Published in Blood advances (22-10-2019)“…The development of neutralizing anti-FVIII antibodies (inhibitors) is a major complication of FVIII protein replacement therapy in patients with hemophilia A…”
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Adoptive cell therapy using PD-1 + myeloma-reactive T cells eliminates established myeloma in mice
Published in Journal for immunotherapy of cancer (20-06-2017)“…Adoptive cellular therapy (ACT) with cancer antigen-reactive T cells following lymphodepletive pre-conditioning has emerged as a potentially curative therapy…”
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CD25+ regulatory T cell inhibition enhances vaccine-induced immunity to neuroblastoma
Published in Journal of immunotherapy (1997) (01-02-2007)“…Evidence that CD4CD25 regulatory T (Treg) cells play a role in the progression of cancer continues to mount. There is a great deal of interest as to whether…”
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Discovery of YB-1 as a new immunological target in neuroblastoma by vaccination in the context of regulatory T cell blockade
Published in Acta biochimica et biophysica Sinica (01-12-2009)“…Neuroblastoma is one of the most common solid tumors in infancy and early childhood. Using the A/J mouse and a syngeneic neuroblastoma cell line AGN2a, we…”
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Evaluating clinically translatable conditioning for platelet gene therapy in murine hemophilia A with inhibitors
Published in Journal of thrombosis and haemostasis (01-11-2024)“…Platelet gene therapy is effective in hemophilia A (HA) mice even with inhibitors. Fludarabine (Flu), along with busulfan (Bu) or melphalan (Mel),…”
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The Tfh/Tfr Pathway Is Pivotal in FVIII Inhibitor Development in Mice
Published in Blood (02-11-2023)“…The development of neutralizing anti-FVIII antibodies (inhibitors) is one major complication of FVIII protein replacement therapy in hemophilia A patients. Our…”
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Melanoma patients respond to a new HLA‐A01‐presented antigenic ligand derived from a multi‐epitope region of melanoma antigen TRP‐2
Published in International journal of cancer (10-10-2005)“…Tyrosinase‐related protein‐2 (TRP‐2) is a known target antigen of spontaneous cytotoxic T cell responses in melanoma patients. Its frequent expression in…”
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Pre-Existing Anti-FVIII Immunity Alters Therapeutic Platelet-Targeted FVIII Engraftment in the System Preconditioned with Busulfan Alone through Cytotoxic CD8 T Cells
Published in Blood (23-11-2021)“…The development of anti-FVIII inhibitory antibodies (inhibitors) is a significant problem in FVIII protein replacement therapy in hemophilia A (HA). We have…”
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Pre-existing anti-factor VIII immunity alters therapeutic platelet-targeted factor VIII engraftment following busulfan conditioning through cytotoxic CD8 T cells
Published in Journal of thrombosis and haemostasis (01-03-2023)“…We previously demonstrated that busulfan preconditioning enabled sustained therapeutic platelet-derived factor VIII (FVIII) expression in naïve FVIIInull mice…”
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Fludarabine in Combination with Busulfan As Pretransplant Conditioning for Platelet Gene Therapy in Murine Hemophilia a with Inhibitors
Published in Blood (13-11-2019)“…Treatment of hemophilia A (HA) with inhibitors is costly, inconvenient, and incompletely effective. We have demonstrated that syngeneic transplantation of…”
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Induction of Activated T Follicular Helper Cells Is Critical for Anti-FVIII Inhibitor Development in Hemophilia a Mice
Published in Blood (13-11-2019)“…The development of neutralizing anti-FVIII antibodies (inhibitors) is one major complication of FVIII protein replacement therapy in hemophilia A patients…”
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