Induction of Functional Specific Antibodies, IgG-Secreting Plasmablasts and Memory B Cells Following BCG Vaccination

Tuberculosis (TB) is a major global health problem and the only currently-licensed vaccine, BCG, is inadequate. Many TB vaccine candidates are designed to be given as a boost to BCG; an understanding of the BCG-induced immune response is therefore critical, and the opportunity to relate this to circ...

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Published inFrontiers in immunology Vol. 12; p. 798207
Main Authors Bitencourt, Julia, Peralta-Álvarez, Marco Polo, Wilkie, Morven, Jacobs, Ashley, Wright, Daniel, Salman Almujri, Salem, Li, Shuailin, Harris, Stephanie A, Smith, Steven G, Elias, Sean C, White, Andrew D, Satti, Iman, Sharpe, Sally S, O'Shea, Matthew K, McShane, Helen, Tanner, Rachel
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 05.01.2022
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Summary:Tuberculosis (TB) is a major global health problem and the only currently-licensed vaccine, BCG, is inadequate. Many TB vaccine candidates are designed to be given as a boost to BCG; an understanding of the BCG-induced immune response is therefore critical, and the opportunity to relate this to circumstances where BCG does confer protection may direct the design of more efficacious vaccines. While the T cell response to BCG vaccination has been well-characterized, there is a paucity of literature on the humoral response. We demonstrate BCG vaccine-mediated induction of specific antibodies in different human populations and macaque species which represent important preclinical models for TB vaccine development. We observe a strong correlation between antibody titers in serum versus plasma with modestly higher titers in serum. We also report for the first time the rapid and transient induction of antibody-secreting plasmablasts following BCG vaccination, together with a robust and durable memory B cell response in humans. Finally, we demonstrate a functional role for BCG vaccine-induced specific antibodies in opsonizing mycobacteria and enhancing macrophage phagocytosis , which may contribute to the BCG vaccine-mediated control of mycobacterial growth observed. Taken together, our findings indicate that the humoral immune response in the context of BCG vaccination merits further attention to determine whether TB vaccine candidates could benefit from the induction of humoral as well as cellular immunity.
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Reviewed by: Sara Suliman, Brigham and Women’s Hospital and Harvard Medical School Boston, United States; Carmen Fernández, Stockholm University, Sweden; Taylor Foreman, National Institutes of Health (NIH), United States; Susanna Brighenti, Karolinska Institutet (KI), Sweden
This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology
Edited by: Deepak Kaushal, Southwest National Primate Research Center (S​NPRC), United States
These authors have contributed equally to this work
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.798207