Expansions of peripheral blood CD8 T-lymphocyte subpopulations and an association with cytomegalovirus seropositivity in the elderly: the Swedish NONA immune study
- PMID: 11772532
- DOI: 10.1016/s0531-5565(01)00212-1
Expansions of peripheral blood CD8 T-lymphocyte subpopulations and an association with cytomegalovirus seropositivity in the elderly: the Swedish NONA immune study
Abstract
Results from a previous longitudinal study, the Swedish OCTO-Immune study, indicated that the combination of higher CD8 peripheral blood lymphocytes (PBLs), decreased CD4 PBLs, and poor proliferative response to mitogenic stimulation in very old humans were associated with an increased 2 year mortality. In follow up studies this combination of immune parameters was significantly associated with a CD4/CD8 ratio less than one and positive IgG serologic titers to cytomegalovirus (CMV). The present study, the Swedish NONA-Immune study, was an extension of that study, using a new sample of the very old. The results of this study confirmed the results of the previous study and extended the surface marker profile of the PBLs, indicating that the CD4/CD8 ratio change is associated with increased CD8 cells, decreased CD4 cells, and lymphocyte activation. The predominant phenotypes of the CD3+CD8+ cells were CD27-, CD28-, CD56+, and CD57+, CD45RA+, and double marked CD45RA+RO+. As in the OCTO study, the NONA-Immune data indicated that the changes are associated significantly with seropositive responses to CMV.
Similar articles
-
Age-related change in peripheral blood T-lymphocyte subpopulations and cytomegalovirus infection in the very old: the Swedish longitudinal OCTO immune study.Mech Ageing Dev. 2000 Dec 20;121(1-3):187-201. doi: 10.1016/s0047-6374(00)00210-4. Mech Ageing Dev. 2000. PMID: 11164473
-
Morbidity does not influence the T-cell immune risk phenotype in the elderly: findings in the Swedish NONA Immune Study using sample selection protocols.Mech Ageing Dev. 2003 Apr;124(4):469-76. doi: 10.1016/s0047-6374(03)00024-1. Mech Ageing Dev. 2003. PMID: 12714255
-
Large numbers of dysfunctional CD8+ T lymphocytes bearing receptors for a single dominant CMV epitope in the very old.J Clin Immunol. 2003 Jul;23(4):247-57. doi: 10.1023/a:1024580531705. J Clin Immunol. 2003. PMID: 12959217
-
T-cell dysregulation caused by chronic antigenic stress: the role of CMV in immunosenescence?Aging Clin Exp Res. 2006 Apr;18(2):171-3. doi: 10.1007/BF03327436. Aging Clin Exp Res. 2006. PMID: 16702790 Review.
-
The narrowing of the CD8 T cell repertoire in old age.Curr Opin Immunol. 2011 Aug;23(4):537-42. doi: 10.1016/j.coi.2011.05.005. Epub 2011 Jun 7. Curr Opin Immunol. 2011. PMID: 21652194 Free PMC article. Review.
Cited by
-
Late-life Attenuation of Cytomegalovirus-mediated CD8 T Cell Memory Inflation: Shrinking of the Cytomegalovirus Latency Niche.J Immunol. 2024 Oct 1;213(7):965-970. doi: 10.4049/jimmunol.2400113. J Immunol. 2024. PMID: 39150241
-
The Impact of Cytomegalovirus Infection on Natural Killer and CD8+ T Cell Phenotype in Multiple Sclerosis.Biology (Basel). 2024 Feb 28;13(3):154. doi: 10.3390/biology13030154. Biology (Basel). 2024. PMID: 38534424 Free PMC article.
-
Immunosenescence and Cytomegalovirus: Exploring Their Connection in the Context of Aging, Health, and Disease.Int J Mol Sci. 2024 Jan 6;25(2):753. doi: 10.3390/ijms25020753. Int J Mol Sci. 2024. PMID: 38255826 Free PMC article. Review.
-
Pre-transplant immune profile defined by principal component analysis predicts acute rejection after kidney transplantation.Front Immunol. 2023 Jul 11;14:1192440. doi: 10.3389/fimmu.2023.1192440. eCollection 2023. Front Immunol. 2023. PMID: 37497224 Free PMC article.
-
The effects of cytomegalovirus on brain structure following sport-related concussion.Brain. 2023 Oct 3;146(10):4262-4273. doi: 10.1093/brain/awad126. Brain. 2023. PMID: 37070698 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials