Longitudinal Analysis of Nursing Home Residents’ T-Cell Responses After SARS-CoV-2 mRNA Vaccinations Shows Influence of Biological Sex and Infection History

Author:

Smith Carson L1,Didion Elise2,Aung Htin2,Tamilselvan Banumathi3,Bej Taissa4,Oyebanji Oladayo A2,Shive Carey L14,Wilson Brigid M45,Cameron Mark6,Cameron Cheryl3,Gravenstein Stefan78,Canaday David H24ORCID

Affiliation:

1. Department of Pathology, Case Western Reserve University School of Medicine , Cleveland, Ohio , USA

2. Division of Infectious Disease, Case Western Reserve University School of Medicine , Cleveland, Ohio , USA

3. Department of Nutrition, Case Western Reserve University , Cleveland, Ohio , USA

4. Geriatric Research, Education, and Clinical Center, Louis Stokes Veterans Affairs Northeast Ohio Healthcare System , Cleveland, Ohio , USA

5. Division of Infectious Diseases and HIV Medicine, Case Western Reserve School of Medicine , Cleveland, Ohio , USA

6. Department of Population and Quantitative Health Sciences, Case Western Reserve University , Cleveland, Ohio , USA

7. Division of Geriatrics and Palliative Medicine, Warren Alpert Medical School, Brown University , Providence, Rhode Island , USA

8. Center on Innovation in Long-Term Services and Supports, Providence Veterans Administration Medical Center , Providence, Rhode Island , USA

Abstract

Abstract Background Vaccines and vaccine boosting have blunted excess morbidity and mortality from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in older nursing home residents (NHR). However, the impact of repeated vaccination on the T-cell response based on biological sex and prior infection of NHR remain understudied. Methods We examined T-cell responses to SARS-CoV-2 mRNA vaccines in a cohort of NHR and healthcare workers (HCW) over 2 years. We used interferon-γ ELIspot and flow cytometry to assess T-cell response before, 2 weeks, and 6 months after the initial series and each of 2 booster vaccines. We analyzed these data longitudinally with mixed-effect modeling and also examined subsets of our cohorts for additional changes in T-cell effector function. Results Prior SARS-CoV-2 infection and female sex contributed to higher T-cell response in NHR but not HCW. When looking across time points, NHR but not HCW with prior infection had significantly higher T-cell responses than infection-naive subjects. These patterns of response were maintained across multiple booster vaccinations. Conclusions These results suggest that the age, multimorbidity, and/or frailty of the NHR cohort may accentuate sex and infection status differences in T-cell response to mRNA vaccination.

Funder

National Institutes of Health

Centers for Disease Control and Prevention

Publisher

Oxford University Press (OUP)

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