IFNγ−TNFα−IL2−MIP1α−CD107a+PRF1+CD8 pp65-Specific T-Cell Response Is Independently Associated With Time to Death in Elderly Humans
Year: 2014
Type: article
Study design: Observational Study
Abstract: Persistent cytomegalovirus (CMV) infection has been suggested to be a major driving force in the immune deterioration and an underlying source of age-related diseases in the elderly. CMV antibody titers are associated with lower responses to vaccination, cardiovascular diseases, frailty, and mortality. CMV infection is also associated with shorter T-cell telomeres and replicative senescence. Although an age-related deregulation of CMV-specific T-cell responses could be an underlying cause of the relationship between CMV and immune defects, strong and polyfunctional responses are observed in elderly individuals, casting uncertainty on their direct role in age-related immune frailty. In this study, we longitudinally followed a cohort of healthy donors aged over 50 years, assessing their mortality rates and time to death during a 2-year period. Specific T-cell responses to the immunodominant antigen pp65 (IFNγ, TNFα, IL2, MIP1α, CD107a, and perforin production) were analyzed at the beginning of the 2-year observation period. A cytotoxic CD8 pp65-specific T-cell response, without cytokine or chemokine coexpression, was independently associated with all-cause mortality in these elderly individuals. This pp65-specific CD8 T-cell response could be a useful tool to identify individuals with depressed immune function and a higher risk of death.
Institutions: Hospital General Universitario Gregorio Marañón, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío, Instituto de Investigación Sanitaria Gregorio Marañón, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Vaccine Research Center, Hospital San Juan de Dios del Aljarafe, Instituto Maimónides de Investigación Biomédica de Córdoba, Hospital Universitario Reina Sofía, University of Córdoba
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funder: National Institutes of Health
OpenAlex ID: W2140090688
