Bridging the gap: identifying factors impacting mRNA severe acute respiratory syndrome coronavirus 2 vaccine booster response in people with HIV-1

Author:

Chammartin Frédérique1,Griessbach Alexandra1,Kusejko Katharina23,Audigé Annette3,Epp Selina3,Stoeckle Marcel P.4,Eichenberger Anna L.5,Amstutz Alain1,Schoenenberger Christof M.1,Hasse Barbara2,Braun Dominique L.23,Rauch Andri5,Trkola Alexandra3,Briel Matthias1,Bucher Heiner C.1,Günthard Huldrych F.23,Speich Benjamin1,Abela Irene A.23

Affiliation:

1. Division of Clinical Epidemiology, Department of Clinical Research, University Hospital of Basel and University of Basel, Basel, Switzerland

2. Department of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland

3. Institute of Medical Virology, University of Zurich, Zurich, Switzerland

4. Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, University of Basel, Basel, Switzerland

5. Department of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Abstract

Objectives: This study aimed to investigate the association of demographic and clinical characteristics, including HIV-specific parameters with the antibody response to a third dose of a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA vaccine in people with HIV-1 (PWH). Design: Post hoc analysis of data collected during the observational extension of the COrona VaccinE tRiAL pLatform trial (COVERALL-2) nested into the Swiss HIV Cohort Study (SHCS). Methods: Serological measurements were conducted on a total of 439 PWH who had received a third dose of either mRNA-1273 (Moderna) or BNT162b2 (Pfizer-BioNTech) SARS-CoV-2 vaccine. Antibody reactivity was assessed using the multifactorial ABCORA immunoassay that defines SARS-CoV-2 seroconversion and predicts neutralization activity. The association between log transformed antibody reactivity and various baseline factors, including vaccine type, demographics, immune and viral status, smoking status, comorbidities, infection history, and co-medication with chemotherapy and immunosuppressive drugs, was investigated using a multivariable linear regression model. Results: Antibody response to third SARS-CoV-2 vaccination was significantly lower among PWH with CD4+ cell count less than 350 cells/μl [ratio of means 0.79; 95% confidence interval (CI) 0.65–0.95]. Having a detectable HIV-1 viral load at least 50 copies/ml and being on concurrent chemotherapy was associated with an overall lower humoral immune response (ratio of means 0.75; 95% CI 0.57–1.00 and 0.34; 95% CI 0.22–0.52, respectively). Conclusion: The study highlights the importance of optimal antiretroviral treatment for PWH, emphasizing the need for timely intervention to enhance the vaccine immunogenicity in this population. Moreover, it underscores the significance of sequential mRNA vaccination and provides important evidence for informing vaccine guidelines.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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