Cytomegalovirus Seropositivity in Older Adults Changes the T Cell Repertoire but Does Not Prevent Antibody or Cellular Responses to SARS-CoV-2 Vaccination

Author:

Breznik Jessica A.1234ORCID,Huynh Angela3,Zhang Ali125,Bilaver Lucas123ORCID,Bhakta Hina3,Stacey Hannah D.125,Ang Jann C.125,Bramson Jonathan L.1235,Nazy Ishac36ORCID,Miller Matthew S.125ORCID,Denburg Judah3ORCID,Costa Andrew P.378ORCID,Bowdish Dawn M. E.1239ORCID,

Affiliation:

1. *McMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada;

2. †Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada;

3. ‡Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada;

4. §McMaster Institute for Research on Aging, McMaster University, Hamilton, Ontario, Canada;

5. ¶Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada;

6. ‖McMaster Centre for Transfusion Research, McMaster University, Hamilton, Ontario, Canada;

7. #Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada;

8. **Centre for Integrated Care, St. Joseph’s Health System, Hamilton, Ontario, Canada; and

9. ††Firestone Institute for Respiratory Health, St. Joseph’s Healthcare, Hamilton, Ontario, Canada

Abstract

Abstract Chronic infection with human CMV may contribute to poor vaccine efficacy in older adults. We assessed the effects of CMV serostatus on Ab quantity and quality, as well as cellular memory recall responses, after two and three SARS-CoV-2 mRNA vaccine doses, in older adults in assisted living facilities. CMV serostatus did not affect anti-Spike and anti–receptor-binding domain IgG Ab levels, nor neutralization capacity against wild-type or β variants of SARS-CoV-2 several months after vaccination. CMV seropositivity altered T cell expression of senescence-associated markers and increased effector memory re-expressing CD45RA T cell numbers, as has been previously reported; however, this did not impact Spike-specific CD4+ T cell memory recall responses. CMV-seropositive individuals did not have a higher incidence of COVID-19, although prior infection influenced humoral immunity. Therefore, CMV seropositivity may alter T cell composition but does not impede the durability of humoral protection or cellular memory responses after SARS-CoV-2 mRNA vaccination in older adults.

Funder

Gouvernement du Canada | Canadian Institutes of Health Research

Canada Research Chairs

Ontario Research Foundation

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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