Frontiers in Immunology (May 2023)

Detection of specific RBD+ IgG+ memory B cells by flow cytometry in healthcare workers and patients with inborn errors of immunity after BNT162b2 m RNA COVID-19 vaccination

  • Lucía del Pino Molina,
  • Lucía del Pino Molina,
  • Luz Yadira Bravo Gallego,
  • Luz Yadira Bravo Gallego,
  • Pilar Nozal,
  • Pilar Nozal,
  • Pilar Nozal,
  • Yolanda Soto-Serrano,
  • Ana Martínez-Feito,
  • Ana Martínez-Feito,
  • Keren Reche-Yebra,
  • Andrea González-Torbay,
  • Ricardo Cuesta-Martín de la Cámara,
  • Carla Gianelli,
  • Carla Gianelli,
  • Carmen Cámara,
  • Carmen Cámara,
  • J. González-García,
  • Miguel González-Muñoz,
  • Rebeca Rodríguez-Pena,
  • Rebeca Rodríguez-Pena,
  • Rebeca Rodríguez-Pena,
  • Eduardo López Granados,
  • Eduardo López Granados,
  • Eduardo López Granados

DOI
https://doi.org/10.3389/fimmu.2023.1136308
Journal volume & issue
Vol. 14

Abstract

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IntroductionInborn errors of immunity (IEI) are a heterogeneous group of diseases caused by intrinsic defects of the immune system. Estimating the immune competence of immunocompromised patients for an infection risk assessment or after SARS-CoV-2 vaccination constituted a challenge.MethodsThe aim of this study was to determine the humoral responses of patients with IEI through a comprehensive analysis of specific receptor-binding domain-positive (RBD+) IgG+ memory B cells (MBCs) by flow cytometry, together with routine S-specific IgG antibodies and QuantiFERON SARS-CoV-2 (T-cell response), before the vaccine and 3 weeks after a second dose.Results and discussionWe first analyzed the percentage of specific RBD+ IgG+ MBCs in healthy healthcare workers. Within the control group, there was an increase in the percentage of specific IgG+ RBD+ MBCs 21 days after the second dose, which was consistent with S-specific IgG antibodies.Thirty-one patients with IEI were included for the pre- and post-vaccination study; IgG+ RBD+ MBCs were not evaluated in 6 patients due to an absence of B cells in peripheral blood. We detected various patterns among the patients with IEI with circulating B cells (25, 81%): an adequate humoral response was observed in 12/25, consider by the detection of positive S-specific IgG antibodies and the presence of specific IgG+ RBD+ MBCs, presenting a positive T-cell response; in 4/25, very low S-specific IgG antibody counts correlated with undetectable events in the IgG+ RBD+ MBC compartment but with positive cellular response. Despite the presence of S-specific IgG antibodies, we were unable to detect a relevant percentage of IgG+ RBD+ MBCs in 5/25; however, all presented positive T-cell response. Lastly, we observed a profound failure of B and T-cell response in 3 (10%) patients with IEI, with no assessment of S-specific IgG antibodies, IgG+ RBD+ MBCs, and negative cellular response. The identification of specific IgG+ RBD+ MBCs by flow cytometry provides information on different humoral immune response outcomes in patients with IEI and aids the assessment of immune competence status after SARS-CoV-2 mRNA vaccine (BNT162b2), together with S-specific IgG antibodies and T-cell responses.

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