Reduced T cell immunity in unmedicated, comorbidity-free obsessive-compulsive disorder: An immunophenotyping study
Immune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients. Thirteen drug-naïve/free OCD patients and twenty-six age &...
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Published in | Journal of psychiatric research Vol. 137; pp. 521 - 524 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.05.2021
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ISSN | 0022-3956 1879-1379 1879-1379 |
DOI | 10.1016/j.jpsychires.2021.03.035 |
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Abstract | Immune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients.
Thirteen drug-naïve/free OCD patients and twenty-six age & sex matched healthy controls were recruited. Immunophenotyping was carried out by staining the whole blood specimens with fluorescent monoclonal antibodies against the cell surface markers such as CD45, CD3, CD16, CD56, CD8, CD4, CD28, CD25 and CD127, followed by data acquisition on BD FACSVerse™ flow cytometer. The proportions of CD4 and CD8 T cells; T regulatory (Tregs), Natural Killer (NK) cells and NK-T cells were compared between patients with OCD and healthy control subjects.
Significantly reduced percentage of T regulatory (Treg) cells was observed in individuals with OCD compared to healthy control subjects [1.0 ± 0.7 vs. 1.9 ± 1.4; p = 0.03, r = 0.33].
Treg cells play a crucial role in regulating the immune response, especially by suppressing the functional activities of T cells. In this study, decreased population of Treg cells essentially indicates a dysregulated T cell and/or T cell mediated immune activation in drug-naïve OCD patients. This preliminary observation might form the basis of further studies examining the immuno-inflammatory/autoimmune origin of OCD.
•Immune system aberrations play a significant role in the pathophysiology of Obsessive-compulsive disorder.•T-regulatory cells play a crucial role in regulating the immune response by suppressing the functional activities of T cells.•T-regulatory cell population essentially indicates a dysregulated T cell and/or T cell mediated immune activation. |
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AbstractList | Immune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients.
Thirteen drug-naïve/free OCD patients and twenty-six age & sex matched healthy controls were recruited. Immunophenotyping was carried out by staining the whole blood specimens with fluorescent monoclonal antibodies against the cell surface markers such as CD45, CD3, CD16, CD56, CD8, CD4, CD28, CD25 and CD127, followed by data acquisition on BD FACSVerse™ flow cytometer. The proportions of CD4 and CD8 T cells; T regulatory (Tregs), Natural Killer (NK) cells and NK-T cells were compared between patients with OCD and healthy control subjects.
Significantly reduced percentage of T regulatory (Treg) cells was observed in individuals with OCD compared to healthy control subjects [1.0 ± 0.7 vs. 1.9 ± 1.4; p = 0.03, r = 0.33].
Treg cells play a crucial role in regulating the immune response, especially by suppressing the functional activities of T cells. In this study, decreased population of Treg cells essentially indicates a dysregulated T cell and/or T cell mediated immune activation in drug-naïve OCD patients. This preliminary observation might form the basis of further studies examining the immuno-inflammatory/autoimmune origin of OCD.
•Immune system aberrations play a significant role in the pathophysiology of Obsessive-compulsive disorder.•T-regulatory cells play a crucial role in regulating the immune response by suppressing the functional activities of T cells.•T-regulatory cell population essentially indicates a dysregulated T cell and/or T cell mediated immune activation. Immune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients. Thirteen drug-naïve/free OCD patients and twenty-six age & sex matched healthy controls were recruited. Immunophenotyping was carried out by staining the whole blood specimens with fluorescent monoclonal antibodies against the cell surface markers such as CD45, CD3, CD16, CD56, CD8, CD4, CD28, CD25 and CD127, followed by data acquisition on BD FACSVerse™ flow cytometer. The proportions of CD4 and CD8 T cells; T regulatory (Tregs), Natural Killer (NK) cells and NK-T cells were compared between patients with OCD and healthy control subjects. Significantly reduced percentage of T regulatory (Treg) cells was observed in individuals with OCD compared to healthy control subjects [1.0 ± 0.7 vs. 1.9 ± 1.4; p = 0.03, r = 0.33]. Treg cells play a crucial role in regulating the immune response, especially by suppressing the functional activities of T cells. In this study, decreased population of Treg cells essentially indicates a dysregulated T cell and/or T cell mediated immune activation in drug-naïve OCD patients. This preliminary observation might form the basis of further studies examining the immuno-inflammatory/autoimmune origin of OCD. Immune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients.BACKGROUNDImmune system aberrations have been postulated to play a role in the pathophysiology of Obsessive-compulsive disorder (OCD). This study was aimed to examine the profile of immune cell subsets in peripheral blood of un-medicated OCD patients.Thirteen drug-naïve/free OCD patients and twenty-six age & sex matched healthy controls were recruited. Immunophenotyping was carried out by staining the whole blood specimens with fluorescent monoclonal antibodies against the cell surface markers such as CD45, CD3, CD16, CD56, CD8, CD4, CD28, CD25 and CD127, followed by data acquisition on BD FACSVerse™ flow cytometer. The proportions of CD4 and CD8 T cells; T regulatory (Tregs), Natural Killer (NK) cells and NK-T cells were compared between patients with OCD and healthy control subjects.METHODThirteen drug-naïve/free OCD patients and twenty-six age & sex matched healthy controls were recruited. Immunophenotyping was carried out by staining the whole blood specimens with fluorescent monoclonal antibodies against the cell surface markers such as CD45, CD3, CD16, CD56, CD8, CD4, CD28, CD25 and CD127, followed by data acquisition on BD FACSVerse™ flow cytometer. The proportions of CD4 and CD8 T cells; T regulatory (Tregs), Natural Killer (NK) cells and NK-T cells were compared between patients with OCD and healthy control subjects.Significantly reduced percentage of T regulatory (Treg) cells was observed in individuals with OCD compared to healthy control subjects [1.0 ± 0.7 vs. 1.9 ± 1.4; p = 0.03, r = 0.33].RESULTSSignificantly reduced percentage of T regulatory (Treg) cells was observed in individuals with OCD compared to healthy control subjects [1.0 ± 0.7 vs. 1.9 ± 1.4; p = 0.03, r = 0.33].Treg cells play a crucial role in regulating the immune response, especially by suppressing the functional activities of T cells. In this study, decreased population of Treg cells essentially indicates a dysregulated T cell and/or T cell mediated immune activation in drug-naïve OCD patients. This preliminary observation might form the basis of further studies examining the immuno-inflammatory/autoimmune origin of OCD.CONCLUSIONTreg cells play a crucial role in regulating the immune response, especially by suppressing the functional activities of T cells. In this study, decreased population of Treg cells essentially indicates a dysregulated T cell and/or T cell mediated immune activation in drug-naïve OCD patients. This preliminary observation might form the basis of further studies examining the immuno-inflammatory/autoimmune origin of OCD. |
Author | Shivakumar, Venkataram Subbanna, Manjula Venkataswamy, Manjunath Ravi, Vasanthapuram Venkatasubramanian, Ganesan Debnath, Monojit Reddy, Y.C. Janardhan Narayanaswamy, Janardhanan C. Jose, Dania |
Author_xml | – sequence: 1 givenname: Manjula surname: Subbanna fullname: Subbanna, Manjula organization: Department of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 2 givenname: Venkataram orcidid: 0000-0003-0353-8597 surname: Shivakumar fullname: Shivakumar, Venkataram email: drshiv.nimhans@gmail.com organization: Department of Integrative Medicine, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 3 givenname: Dania surname: Jose fullname: Jose, Dania organization: Translational Psychiatry Laboratory, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 4 givenname: Manjunath surname: Venkataswamy fullname: Venkataswamy, Manjunath organization: Department of Neurovirology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 5 givenname: Monojit surname: Debnath fullname: Debnath, Monojit organization: Department of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 6 givenname: Vasanthapuram surname: Ravi fullname: Ravi, Vasanthapuram organization: Department of Neurovirology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 7 givenname: Y.C. Janardhan surname: Reddy fullname: Reddy, Y.C. Janardhan organization: OCD Clinic, Department of Psychiatry, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 8 givenname: Ganesan surname: Venkatasubramanian fullname: Venkatasubramanian, Ganesan organization: Translational Psychiatry Laboratory, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India – sequence: 9 givenname: Janardhanan C. surname: Narayanaswamy fullname: Narayanaswamy, Janardhanan C. organization: Translational Psychiatry Laboratory, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru-560029, India |
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Cites_doi | 10.1038/nm892 10.1001/archpsyc.1989.01810110048007 10.1177/0269881108089605 10.1016/S0165-0327(98)00072-X 10.1016/j.biopsych.2006.06.012 10.1136/jnnp.23.1.56 10.1111/cei.12804 10.1176/ajp.146.2.246 10.1016/j.bbi.2009.09.009 10.1016/0165-0327(88)90072-9 10.1038/nrn3746 10.1146/annurev.immunol.21.120601.141122 10.1007/s00787-017-1099-3 10.1016/j.autrev.2008.03.001 10.1186/s12974-017-1042-z 10.1007/s00213-020-05504-0 |
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Keywords | Autoimmunity Immunophenotyping Obsessive-compulsive disorder Inflammation T cells T regulatory cells |
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SubjectTerms | Autoimmunity Immunophenotyping Inflammation Obsessive-compulsive disorder T cells T regulatory cells |
Title | Reduced T cell immunity in unmedicated, comorbidity-free obsessive-compulsive disorder: An immunophenotyping study |
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