Evaluation of regulatory T lymphocytes and IL2Ra and FOXP3 gene expression in peripheral mononuclear cells from patients with amyotrophic lateral sclerosis

Background Loss of neuroprotective role of CD4 + helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the “rapidly progressive phase” of amyotrophic lateral sclerosis (ALS). Aim We aimed to investigate relative count of CD4 + and regulatory T lymph...

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Published in:Irish journal of medical science Vol. 187; no. 4; pp. 1065 - 1071
Main Authors: Rashid Chehreh Bargh, Sara, Tafakhori, Abbas, Masoumi, Farimah, Rahmani, Farzaneh, Ahmadi, Mona, Namdar, Afshin, Azimi, Maryam, Tavasolian, Parsova, Habibi, Sima, Zamani, Babak, Maserrat, Marziyeh, Sadr, Maryam, Noorbakhsh, Farshid, Rezaei, Nima
Format: Journal Article
Language:English
Published: London Springer London 01-11-2018
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Abstract Background Loss of neuroprotective role of CD4 + helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the “rapidly progressive phase” of amyotrophic lateral sclerosis (ALS). Aim We aimed to investigate relative count of CD4 + and regulatory T lymphocytes and expression level of IL2Ra and FOXP3 genes in peripheral blood mononuclear cells (PBMCs) from patients with ALS. Method We performed a flow cytometric analysis on PBMC from 38 patients with ALS and 32 controls to determine the count of CD4 + and CD4 + CD25 + cells. Quantitative real-time PCR analyses were implemented to determine the level of expression of FOXP3 and IL-2Rα (CD25) genes in the peripheral blood mononucleated cells. Results We found a significant higher proportion of CD4 + T cells ( p value < 0.001), along with a significantly reduced proportion of CD4 + CD25 + Treg cells ( p value  =  0.001, p value  =  0.02), in the peripheral blood of patient’s with ALS. Conclusion The results of our study are in line with the hypothesis that in the early phase of ALS, neuroprotective helper T cells infiltrate in the affected areas in the lumbar spinal cord. This was reflected in higher peripheral percentage of CD4 + helper T cells and higher expression of FOXP3 and IL-2Rα. The observed demise in the number of active CD4 + CD25 + regulatory T cells might indicate early signs of progression to later stages of ALS in our study group. Interestingly, disease duration was the sole independent significant determining factor that predicted CD4+CD25+ regulatory T cell counts in the peripheral blood of patients at various stages of ALS, according to a logistic regression model.
AbstractList Loss of neuroprotective role of CD4 helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the "rapidly progressive phase" of amyotrophic lateral sclerosis (ALS). We aimed to investigate relative count of CD4 and regulatory T lymphocytes and expression level of IL2Ra and FOXP3 genes in peripheral blood mononuclear cells (PBMCs) from patients with ALS. We performed a flow cytometric analysis on PBMC from 38 patients with ALS and 32 controls to determine the count of CD4 and CD4 CD25 cells. Quantitative real-time PCR analyses were implemented to determine the level of expression of FOXP3 and IL-2Rα (CD25) genes in the peripheral blood mononucleated cells. We found a significant higher proportion of CD4 T cells (p value < 0.001), along with a significantly reduced proportion of CD4 CD25 Treg cells (p value = 0.001, p value = 0.02), in the peripheral blood of patient's with ALS. The results of our study are in line with the hypothesis that in the early phase of ALS, neuroprotective helper T cells infiltrate in the affected areas in the lumbar spinal cord. This was reflected in higher peripheral percentage of CD4 helper T cells and higher expression of FOXP3 and IL-2Rα. The observed demise in the number of active CD4 CD25 regulatory T cells might indicate early signs of progression to later stages of ALS in our study group. Interestingly, disease duration was the sole independent significant determining factor that predicted CD4+CD25+ regulatory T cell counts in the peripheral blood of patients at various stages of ALS, according to a logistic regression model.
Background Loss of neuroprotective role of CD4 + helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the “rapidly progressive phase” of amyotrophic lateral sclerosis (ALS). Aim We aimed to investigate relative count of CD4 + and regulatory T lymphocytes and expression level of IL2Ra and FOXP3 genes in peripheral blood mononuclear cells (PBMCs) from patients with ALS. Method We performed a flow cytometric analysis on PBMC from 38 patients with ALS and 32 controls to determine the count of CD4 + and CD4 + CD25 + cells. Quantitative real-time PCR analyses were implemented to determine the level of expression of FOXP3 and IL-2Rα (CD25) genes in the peripheral blood mononucleated cells. Results We found a significant higher proportion of CD4 + T cells ( p value < 0.001), along with a significantly reduced proportion of CD4 + CD25 + Treg cells ( p value  =  0.001, p value  =  0.02), in the peripheral blood of patient’s with ALS. Conclusion The results of our study are in line with the hypothesis that in the early phase of ALS, neuroprotective helper T cells infiltrate in the affected areas in the lumbar spinal cord. This was reflected in higher peripheral percentage of CD4 + helper T cells and higher expression of FOXP3 and IL-2Rα. The observed demise in the number of active CD4 + CD25 + regulatory T cells might indicate early signs of progression to later stages of ALS in our study group. Interestingly, disease duration was the sole independent significant determining factor that predicted CD4+CD25+ regulatory T cell counts in the peripheral blood of patients at various stages of ALS, according to a logistic regression model.
BACKGROUNDLoss of neuroprotective role of CD4+ helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the "rapidly progressive phase" of amyotrophic lateral sclerosis (ALS).AIMWe aimed to investigate relative count of CD4+ and regulatory T lymphocytes and expression level of IL2Ra and FOXP3 genes in peripheral blood mononuclear cells (PBMCs) from patients with ALS.METHODWe performed a flow cytometric analysis on PBMC from 38 patients with ALS and 32 controls to determine the count of CD4+ and CD4+CD25+ cells. Quantitative real-time PCR analyses were implemented to determine the level of expression of FOXP3 and IL-2Rα (CD25) genes in the peripheral blood mononucleated cells.RESULTSWe found a significant higher proportion of CD4+ T cells (p value < 0.001), along with a significantly reduced proportion of CD4+CD25+ Treg cells (p value = 0.001, p value = 0.02), in the peripheral blood of patient's with ALS.CONCLUSIONThe results of our study are in line with the hypothesis that in the early phase of ALS, neuroprotective helper T cells infiltrate in the affected areas in the lumbar spinal cord. This was reflected in higher peripheral percentage of CD4+ helper T cells and higher expression of FOXP3 and IL-2Rα. The observed demise in the number of active CD4+CD25+ regulatory T cells might indicate early signs of progression to later stages of ALS in our study group. Interestingly, disease duration was the sole independent significant determining factor that predicted CD4+CD25+ regulatory T cell counts in the peripheral blood of patients at various stages of ALS, according to a logistic regression model.
Author Sadr, Maryam
Tavasolian, Parsova
Maserrat, Marziyeh
Habibi, Sima
Zamani, Babak
Rezaei, Nima
Noorbakhsh, Farshid
Masoumi, Farimah
Rashid Chehreh Bargh, Sara
Tafakhori, Abbas
Namdar, Afshin
Azimi, Maryam
Rahmani, Farzaneh
Ahmadi, Mona
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  givenname: Nima
  surname: Rezaei
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  email: rezaei_nima@tums.ac.ir
  organization: Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Molecular Immunology Research Center, Tehran University of Medical Sciences, Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29574662$$D View this record in MEDLINE/PubMed
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Keywords Amyotrophic lateral sclerosis
IL-2Rα
CD25
FOXP3
T helper
Regulatory T cell
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Snippet Background Loss of neuroprotective role of CD4 + helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the...
Loss of neuroprotective role of CD4 helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the "rapidly...
BACKGROUNDLoss of neuroprotective role of CD4+ helper T cells, regulatory T cells, and M2 microglia constitutively results in the rapid neural death in the...
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SubjectTerms Adult
Aged
Amyotrophic Lateral Sclerosis - blood
Amyotrophic Lateral Sclerosis - genetics
Amyotrophic Lateral Sclerosis - immunology
Disease Progression
Family Medicine
Female
Forkhead Transcription Factors - biosynthesis
Forkhead Transcription Factors - blood
Forkhead Transcription Factors - genetics
Forkhead Transcription Factors - immunology
Gene Expression
General Practice
Humans
Interleukin-2 Receptor alpha Subunit - biosynthesis
Interleukin-2 Receptor alpha Subunit - blood
Interleukin-2 Receptor alpha Subunit - genetics
Interleukin-2 Receptor alpha Subunit - immunology
Internal Medicine
Leukocytes, Mononuclear - immunology
Leukocytes, Mononuclear - metabolism
Male
Medicine
Medicine & Public Health
Middle Aged
Original Article
T-Lymphocytes, Regulatory - immunology
T-Lymphocytes, Regulatory - metabolism
Title Evaluation of regulatory T lymphocytes and IL2Ra and FOXP3 gene expression in peripheral mononuclear cells from patients with amyotrophic lateral sclerosis
URI https://link.springer.com/article/10.1007/s11845-018-1793-2
https://www.ncbi.nlm.nih.gov/pubmed/29574662
https://search.proquest.com/docview/2018662725
Volume 187
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