T Lymphocyte Subsets Associated With Prevalent Diabetes in Veterans With and Without Human Immunodeficiency Virus

Author:

Bailin Samuel S1ORCID,McGinnis Kathleen A2,McDonnell Wyatt J1,So-Armah Kaku3,Wellons Melissa1,Tracy Russell P4,Doyle Margaret F4,Mallal Simon1,Justice Amy C25ORCID,Freiberg Matthew S16,Landay Alan L7,Wanjalla Celestine1,Koethe John R16ORCID

Affiliation:

1. Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA

2. Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut, USA

3. Boston University School of Medicine, Boston, Massachusetts, USA

4. Department of Pathology and Laboratory Medicine, University of Vermont, Burlington, Vermont, USA

5. Department of Internal Medicine, Yale School of Medicine, West Haven, Connecticut, USA

6. Veterans Affairs Tennessee Valley Healthcare System, Nashville, Tennessee, USA

7. Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA

Abstract

Abstract Background A higher proportion of circulating memory CD4+ T cells is associated with prevalent diabetes mellitus in the general population. Given the broad changes in adaptive immunity, including memory T-cell expansion, and rising prevalence of diabetes in the human immunodeficiency virus (HIV) population, we assessed whether similar relationships were present in persons with HIV (PWH). Methods Multiple CD4+ and CD8+ T-cell subsets were measured by flow cytometry, and prevalent diabetes cases were adjudicated by 2 physicians for PWH and HIV-negative participants in the Veterans Aging Cohort Study. Multivariable logistic regression models evaluated the association of T-cell subsets and diabetes stratified by HIV status, adjusted for cytomegalovirus serostatus and traditional risk factors. Results Among 2385 participants (65% PWH, 95% male, 68% African American), higher CD45RO+ memory CD4+ T cells and lower CD38+ CD4+ T cells were associated with prevalent diabetes, and had a similar effect size, in both the PWH and HIV-negative (P ≤ .05 for all). Lower CD38+CD8+ T cells were also associated with diabetes in both groups. Conclusions The CD4+ and CD8+ T-cell subsets associated with diabetes are similar in PWH and HIV-negative individuals, suggesting that diabetes in PWH may be related to chronic immune activation.

Funder

National Institute on Alcohol Abuse and Alcoholism

COMpAAAS/Veterans Aging Cohort Study

National Institute of Diabetes and Digestive and Kidney Diseases

National Heart, Lung, and Blood Institute

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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