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Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection
INTRODUCTION: Previous research indicates that premature T cell senescence is a characteristic of major depressive disorder (MDD). However, known senescence inducing factors like cytomegalovirus (CMV) infection or, probably, childhood adversity (CA) have not been taken into consideration so far. OBJ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995284/ https://www.ncbi.nlm.nih.gov/pubmed/36909830 http://dx.doi.org/10.1016/j.bbih.2023.100608 |
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author | Simon, Maria S. Ioannou, Magdalini Arteaga-Henríquez, Gara Wijkhuijs, Annemarie Berghmans, Raf Musil, Richard Müller, Norbert Drexhage, Hemmo A. |
author_facet | Simon, Maria S. Ioannou, Magdalini Arteaga-Henríquez, Gara Wijkhuijs, Annemarie Berghmans, Raf Musil, Richard Müller, Norbert Drexhage, Hemmo A. |
author_sort | Simon, Maria S. |
collection | PubMed |
description | INTRODUCTION: Previous research indicates that premature T cell senescence is a characteristic of major depressive disorder (MDD). However, known senescence inducing factors like cytomegalovirus (CMV) infection or, probably, childhood adversity (CA) have not been taken into consideration so far. OBJECTIVE: Differentiation and senescent characteristics of T cells of MDD patients were investigated in relation to healthy controls (HC), taking the CMV seropositivity and CA into account. METHODS: 127 MDD and 113 HC of the EU-MOODSTRATIFICATION cohort were analyzed. Fluorescence activated cell sorting (FACS) analysis was performed to determine B, NK, and T cell frequencies. In a second FACS analysis, naïve, effector memory (Tem), central memory (Tcm), effector memory cells re-expressing RA (TEMRA), as well as CD28(+) and CD27(+) memory populations, were determined of the CD4(+) and CD8(+) T cell populations in a subsample (N = 35 MDD and N = 36 HC). CMV-antibody state was measured by IgG ELISA and CA by the Childhood Trauma Questionnaire. RESULTS: We detected a CMV-antibody positivity in 40% of MDD patients (35% HC, n. s.) with seropositive MDD cases showing a higher total childhood trauma score. Second, a higher inflation of memory CD4(+) T helper cells in CMV seronegative patients as compared to seronegative HC and reduced numbers of naïve CD4(+) T helper cells in CMV seropositive patients (not in CMV seropositive HC) were found. Third, a higher inflation of memory CD8(+) T cytotoxic cells in CMV seropositive cases as compared to CMV seropositive HC, particularly of the TEMRA cells, became apparent. Higher percentages of CD4(+) TEMRA and late stage CD27(−)CD28(−) TEMRA cells were similar in both HC and MDD with CMV seropositivity. Overall, apportioning of T cell subpopulations did not differ between CA positive vs negative cases. CONCLUSIONS: MDD patients show several signs of a CMV independent “MDD specific” premature T cell aging, such as a CMV independent increase in CD4(+) T memory cells and a latent naïve CD4 T-cell reduction and a latent CD8(+) T-cell increase. However, these two latent T cell senescence abnormalities only become evident with CMV infection (double hit). |
format | Online Article Text |
id | pubmed-9995284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99952842023-03-10 Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection Simon, Maria S. Ioannou, Magdalini Arteaga-Henríquez, Gara Wijkhuijs, Annemarie Berghmans, Raf Musil, Richard Müller, Norbert Drexhage, Hemmo A. Brain Behav Immun Health Full Length Article INTRODUCTION: Previous research indicates that premature T cell senescence is a characteristic of major depressive disorder (MDD). However, known senescence inducing factors like cytomegalovirus (CMV) infection or, probably, childhood adversity (CA) have not been taken into consideration so far. OBJECTIVE: Differentiation and senescent characteristics of T cells of MDD patients were investigated in relation to healthy controls (HC), taking the CMV seropositivity and CA into account. METHODS: 127 MDD and 113 HC of the EU-MOODSTRATIFICATION cohort were analyzed. Fluorescence activated cell sorting (FACS) analysis was performed to determine B, NK, and T cell frequencies. In a second FACS analysis, naïve, effector memory (Tem), central memory (Tcm), effector memory cells re-expressing RA (TEMRA), as well as CD28(+) and CD27(+) memory populations, were determined of the CD4(+) and CD8(+) T cell populations in a subsample (N = 35 MDD and N = 36 HC). CMV-antibody state was measured by IgG ELISA and CA by the Childhood Trauma Questionnaire. RESULTS: We detected a CMV-antibody positivity in 40% of MDD patients (35% HC, n. s.) with seropositive MDD cases showing a higher total childhood trauma score. Second, a higher inflation of memory CD4(+) T helper cells in CMV seronegative patients as compared to seronegative HC and reduced numbers of naïve CD4(+) T helper cells in CMV seropositive patients (not in CMV seropositive HC) were found. Third, a higher inflation of memory CD8(+) T cytotoxic cells in CMV seropositive cases as compared to CMV seropositive HC, particularly of the TEMRA cells, became apparent. Higher percentages of CD4(+) TEMRA and late stage CD27(−)CD28(−) TEMRA cells were similar in both HC and MDD with CMV seropositivity. Overall, apportioning of T cell subpopulations did not differ between CA positive vs negative cases. CONCLUSIONS: MDD patients show several signs of a CMV independent “MDD specific” premature T cell aging, such as a CMV independent increase in CD4(+) T memory cells and a latent naïve CD4 T-cell reduction and a latent CD8(+) T-cell increase. However, these two latent T cell senescence abnormalities only become evident with CMV infection (double hit). Elsevier 2023-02-27 /pmc/articles/PMC9995284/ /pubmed/36909830 http://dx.doi.org/10.1016/j.bbih.2023.100608 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Full Length Article Simon, Maria S. Ioannou, Magdalini Arteaga-Henríquez, Gara Wijkhuijs, Annemarie Berghmans, Raf Musil, Richard Müller, Norbert Drexhage, Hemmo A. Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title | Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title_full | Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title_fullStr | Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title_full_unstemmed | Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title_short | Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection |
title_sort | premature t cell aging in major depression: a double hit by the state of disease and cytomegalovirus infection |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995284/ https://www.ncbi.nlm.nih.gov/pubmed/36909830 http://dx.doi.org/10.1016/j.bbih.2023.100608 |
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