Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2009 Feb;64(2):183-6.
doi: 10.1093/gerona/gln068. Epub 2009 Feb 27.

Key research opportunities in immune system aging

Affiliations
Review

Key research opportunities in immune system aging

Susan L Swain et al. J Gerontol A Biol Sci Med Sci. 2009 Feb.

Abstract

A number of key advantages make the immune system uniquely suited for studies of aging. The understanding of loss of immune function with aging has advanced to allow incisive evaluations of general theories of aging. Specifically, the time is ripe for examination of mechanisms leading to age-associated molecular and cellular defects in the immune system and testing of strategies to reverse identified defects. These and other opportunities are discussed in the following, with special focus upon aging of the innate immune system, the role of commensal bacteria and inflammation in immune aging, and the need for better and more precise models in mice and primates to facilitate these studies and provide translation toward clinical application of immune rejuvenation.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Haynes L, Swain SL. Why aging T cells fail: implications for vaccination. Immunity. 2006;24:663–666. - PMC - PubMed
    1. Linton P-J, Dorshkind K. Age-related changes in lymphocyte development and function. Nat Immunol. 2004;5:133–139. - PubMed
    1. Renshaw M, Rockwell J, Engleman C, Gewirtz A, Katz J, Sambhara S. Cutting edge: impaired Toll-like receptor expression and function in aging. J Immunol. 2002;169:4697–4701. - PubMed
    1. Aydar Y, Balogh P, Tew JG, Szakal AK. Age-related depression of FDC accessory functions and CD21 ligand-mediated repair of co-stimulation. Eur J Immunol. 2002;32:2817–2826. - PubMed
    1. Murasko DM, Jiang J. Response of aged mice to primary virus infections. Immunol Rev. 2005;205:285–296. - PubMed