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Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study
OBJECTIVES: Cytomegalovirus infection is thought to affect the immune system and to impact general health during ageing. Higher CMV‐specific antibody levels in the elderly are generally assumed to reflect experienced viral reactivation during life. Furthermore, high levels of terminally differentiat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586993/ https://www.ncbi.nlm.nih.gov/pubmed/33133599 http://dx.doi.org/10.1002/cti2.1193 |
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author | Samson, Leonard Daniël van den Berg, Sara PH Engelfriet, Peter Boots, Annemieke MH Hendriks, Marion de Rond, Lia GH de Zeeuw‐Brouwer, Mary‐lène Verschuren, WM Monique Borghans, José AM Buisman, Anne‐Marie van Baarle, Debbie |
author_facet | Samson, Leonard Daniël van den Berg, Sara PH Engelfriet, Peter Boots, Annemieke MH Hendriks, Marion de Rond, Lia GH de Zeeuw‐Brouwer, Mary‐lène Verschuren, WM Monique Borghans, José AM Buisman, Anne‐Marie van Baarle, Debbie |
author_sort | Samson, Leonard Daniël |
collection | PubMed |
description | OBJECTIVES: Cytomegalovirus infection is thought to affect the immune system and to impact general health during ageing. Higher CMV‐specific antibody levels in the elderly are generally assumed to reflect experienced viral reactivation during life. Furthermore, high levels of terminally differentiated and CMV‐specific T cells are hallmarks of CMV infection, which are thought to expand over time, a process also referred to as memory inflation. METHODS: We studied CMV‐specific antibody levels over ~ 27 years in 268 individuals (aged 60–89 years at study endpoint), and to link duration of CMV infection to T‐cell numbers, CMV‐specific T‐cell functions, frailty and cardiovascular disease at study endpoint. RESULTS: In our study, 136/268 individuals were long‐term CMV seropositive and 19 seroconverted during follow‐up (seroconversion rate: 0.56%/year). CMV‐specific antibody levels increased slightly over time. However, we did not find an association between duration of CMV infection and CMV‐specific antibody levels at study endpoint. No clear association between duration of CMV infection and the size and function of the memory T‐cell pool was observed. Elevated CMV‐specific antibody levels were associated with the prevalence of cardiovascular disease but not with frailty. Age at CMV seroconversion was positively associated with CMV‐specific antibody levels, memory CD4(+) T‐cell numbers and frailty. CONCLUSION: Cytomegalovirus‐specific memory T cells develop shortly after CMV seroconversion but do not seem to further increase over time. Age‐related effects other than duration of CMV infection seem to contribute to CMV‐induced changes in the immune system. Although CMV‐specific immunity is not evidently linked to frailty, it tends to associate with higher prevalence of cardiovascular disease. |
format | Online Article Text |
id | pubmed-7586993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75869932020-10-30 Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study Samson, Leonard Daniël van den Berg, Sara PH Engelfriet, Peter Boots, Annemieke MH Hendriks, Marion de Rond, Lia GH de Zeeuw‐Brouwer, Mary‐lène Verschuren, WM Monique Borghans, José AM Buisman, Anne‐Marie van Baarle, Debbie Clin Transl Immunology Original Article OBJECTIVES: Cytomegalovirus infection is thought to affect the immune system and to impact general health during ageing. Higher CMV‐specific antibody levels in the elderly are generally assumed to reflect experienced viral reactivation during life. Furthermore, high levels of terminally differentiated and CMV‐specific T cells are hallmarks of CMV infection, which are thought to expand over time, a process also referred to as memory inflation. METHODS: We studied CMV‐specific antibody levels over ~ 27 years in 268 individuals (aged 60–89 years at study endpoint), and to link duration of CMV infection to T‐cell numbers, CMV‐specific T‐cell functions, frailty and cardiovascular disease at study endpoint. RESULTS: In our study, 136/268 individuals were long‐term CMV seropositive and 19 seroconverted during follow‐up (seroconversion rate: 0.56%/year). CMV‐specific antibody levels increased slightly over time. However, we did not find an association between duration of CMV infection and CMV‐specific antibody levels at study endpoint. No clear association between duration of CMV infection and the size and function of the memory T‐cell pool was observed. Elevated CMV‐specific antibody levels were associated with the prevalence of cardiovascular disease but not with frailty. Age at CMV seroconversion was positively associated with CMV‐specific antibody levels, memory CD4(+) T‐cell numbers and frailty. CONCLUSION: Cytomegalovirus‐specific memory T cells develop shortly after CMV seroconversion but do not seem to further increase over time. Age‐related effects other than duration of CMV infection seem to contribute to CMV‐induced changes in the immune system. Although CMV‐specific immunity is not evidently linked to frailty, it tends to associate with higher prevalence of cardiovascular disease. John Wiley and Sons Inc. 2020-10-14 /pmc/articles/PMC7586993/ /pubmed/33133599 http://dx.doi.org/10.1002/cti2.1193 Text en © 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Article Samson, Leonard Daniël van den Berg, Sara PH Engelfriet, Peter Boots, Annemieke MH Hendriks, Marion de Rond, Lia GH de Zeeuw‐Brouwer, Mary‐lène Verschuren, WM Monique Borghans, José AM Buisman, Anne‐Marie van Baarle, Debbie Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title | Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title_full | Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title_fullStr | Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title_full_unstemmed | Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title_short | Limited effect of duration of CMV infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
title_sort | limited effect of duration of cmv infection on adaptive immunity and frailty: insights from a 27‐year‐long longitudinal study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586993/ https://www.ncbi.nlm.nih.gov/pubmed/33133599 http://dx.doi.org/10.1002/cti2.1193 |
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