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The effect of anti-SARS-CoV-2 monoclonal antibody, bamlanivimab, on endogenous immune response to COVID-19 vaccination
Robert J. Benschop; Jay L. Tuttle; Lin Zhang; Josh Poorbaugh; Nicole L. Kallewaard; Peter Vaillancourt; Melissa L. Crisp; Thi Ngoc Vy Trinh; Joshua J. Freitas; Stephanie Beasley; Montanea Daniels; Natalie Haustrup; Richard E. Higgs; Ajay Nirula; Myron S. Cohen; Mary Marovich.
Affiliation
  • Robert J. Benschop; Eli Lilly and Company
  • Jay L. Tuttle; Eli Lilly and Company
  • Lin Zhang; Eli Lilly and Company
  • Josh Poorbaugh; Eli Lilly and Company
  • Nicole L. Kallewaard; Eli Lilly and Company
  • Peter Vaillancourt; Eli Lilly and Company
  • Melissa L. Crisp; Eli Lilly and Company
  • Thi Ngoc Vy Trinh; Eli Lilly and Company
  • Joshua J. Freitas; Eli Lilly and Company
  • Stephanie Beasley; Eli Lilly and Company
  • Montanea Daniels; Eli Lilly and Company
  • Natalie Haustrup; Eli Lilly and Company
  • Richard E. Higgs; Eli Lilly and Company
  • Ajay Nirula; Eli Lilly and Company
  • Myron S. Cohen; Institute of Global Health and Infectious Diseases, University of North Carolina at Chapel Hill
  • Mary Marovich; Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health
Preprint in English | medRxiv | ID: ppmedrxiv-21267605
ABSTRACT
As the COVID-19 pandemic evolves, and vaccine rollout progresses, the availability and demand for monoclonal antibodies for the prevention and treatment of SARS-CoV-2 infection are also accelerating. This longitudinal serological study evaluated the magnitude and potency of the endogenous antibody response to COVID-19 vaccination in participants who first received a COVID-19 monoclonal antibody in a prevention study. Over the course of six months, serum samples were collected from the prevention population (nursing home residents and staff) enrolled in the BLAZE-2 clinical trial who had received either bamlanivimab (4200 mg) or placebo. In an unplanned component of this trial, a subset of these participants was subsequently fully vaccinated with two doses of either SpikeVax (Moderna) or Comirnaty (BioNTech/Pfizer) COVID-19 mRNA vaccines, as part of the US vaccination program. This post-hoc analysis assessed the immune response to vaccination for the subset of participants (N=135) without prior SARS-CoV-2 infection. Antibody titers and potency were assessed using three assays against SARS-CoV-2 proteins that bamlanivimab does not significantly bind to, thereby reflecting the endogenous antibody response. All bamlanivimab and placebo participants mounted a robust immune response to full COVID-19 vaccination, irrespective of age, risk-category and vaccine type, with any observed differences unlikely to be clinically meaningful. These findings are pertinent for informing public health policy with results that suggest a complementary role for COVID-19 monoclonal antibodies (mAbs) with COVID-19 vaccines and that the benefit of receiving COVID-19 vaccination at the earliest opportunity outweighs the minimal effect on the endogenous immune response due to prior prophylactic COVID-19 mAb infusion. One Sentence SummaryIndividuals infused with an anti-SARS-CoV-2 antibody demonstrated a robust immune response to subsequent full COVID-19 vaccination.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
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