| Literature DB >> 26459351 |
Axel Ronald Schulz1, Julia Nora Mälzer2, Cristina Domingo3, Karsten Jürchott4, Andreas Grützkau5, Nina Babel6, Mikalai Nienen6, Tomas Jelinek7, Matthias Niedrig3, Andreas Thiel2.
Abstract
Immunological competence declines progressively with age, resulting in increased susceptibility of the elderly to infection and impaired responses to vaccines. Underlying mechanisms remain largely obscure as they have been related to complex, individual systemic immune properties that are challenging to investigate. In this study, we explored age-related changes in human immunity during a primary virus infection experimentally induced by immunization with live-attenuated yellow fever (YF) vaccine. Applying detailed serology, advanced FACS analysis, and systems biology, we discovered that aged subjects developed fewer neutralizing Abs, mounted diminished YF-specific CD8(+) T cell responses, and showed quantitatively and qualitatively altered YF-specific CD4(+) T cell immunity. Among numerous immune signatures, low in vivo numbers of naive CD4(+) recent thymic emigrants and peripheral dendritic cells correlated well with reduced acute responsiveness and altered long-term persistence of human cellular immunity to YF vaccination. Hence, we reveal in this article that essential elements of immune responses such as recent thymic emigrants and dendritic cells strongly relate to productive immunity in the elderly, providing a conceivable explanation for diminished responsiveness to vaccination with neoantigens and infection with de novo pathogens in the aged population.Entities:
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Year: 2015 PMID: 26459351 DOI: 10.4049/jimmunol.1500598
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422