Early age–related atrophy of cutaneous lymph nodes precipitates an early functional decline in skin immunity in mice with aging

Author:

Sonar Sandip Ashok12ORCID,Uhrlaub Jennifer L.12ORCID,Coplen Christopher P.12,Sempowski Gregory D.3ORCID,Dudakov Jarrod A.4,van den Brink Marcel R. M.5,LaFleur Bonnie J.6,Jergović Mladen12ORCID,Nikolich-Žugich Janko126ORCID

Affiliation:

1. Department of Immunobiology, University of Arizona College of Medicine-Tucson, Tucson, AZ 85724

2. Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ 85724

3. Duke Human Vaccine Institute, Duke University, Durham, NC 27710

4. Program in Immunology, Fred Hutchinson Cancer Center, Department of Immunology, University of Washington, Seattle, WA 98109

5. Department of Immunology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021

6. BIO5 Institute, University of Arizona, Tucson, AZ 85719

Abstract

Significance Older adults are more vulnerable to infection and less capable of vigorously responding to vaccination. The contribution of peripheral T cell maintenance defects to these processes is incompletely understood. Here, we provide evidence that lymph nodes (LNs), which are critical for naive T (T N ) cell maintenance and initiation of new immune responses, age asynchronously. Skin-draining LNs undergo early (6 to 9 mo) and deeper LN and spleen late-life (18 mo) atrophy, characterized by reduced ability to maintain T N cells, structural and numerical loss of LN stromal cell microenvironments, and reduced immunity to cutaneous vaccination. These results highlight the critical role of age-related LN atrophy in functional immunity and immune homeostasis.

Funder

HHS | U.S. Public Health Service

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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