Antibody responses to the SARS-CoV-2 vaccine in individuals with various inborn errors of immunity

J Allergy Clin Immunol. 2021 Nov;148(5):1192-1197. doi: 10.1016/j.jaci.2021.08.016. Epub 2021 Sep 4.

Abstract

Background: SARS-CoV-2 vaccination is recommended in patients with inborn errors of immunity (IEIs); however, little is known about immunogenicity and safety in these patients.

Objective: We sought to evaluate the impact of genetic diagnosis, age, and treatment on antibody response to COVID-19 vaccine and related adverse events in a cohort of patients with IEIs.

Methods: Plasma was collected from 22 health care worker controls, 81 patients with IEIs, and 2 patients with thymoma; the plasma was collected before immunization, 1 to 6 days before the second dose of mRNA vaccine, and at a median of 30 days after completion of the immunization schedule with either mRNA vaccine or a single dose of Johnson & Johnson's Janssen vaccine. Anti-spike (anti-S) and anti-nucleocapsid antibody titers were measured by using a luciferase immunoprecipitation systems method. Information on T- and B-cell counts and use of immunosuppressive drugs was extracted from medical records, and information on vaccine-associated adverse events was collected after each dose.

Results: Anti-S antibodies were detected in 27 of 46 patients (58.7%) after 1 dose of mRNA vaccine and in 63 of 74 fully immunized patients (85.1%). A lower rate of seroconversion (7 of 11 [63.6%]) was observed in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. Previous use of rituximab and baseline counts of less than 1000 CD3+ T cells/mL and less than 100 CD19+ B cells/mL were associated with lower anti-S IgG levels. No significant adverse events were reported.

Conclusion: Vaccinating patients with IEIs is safe, but immunogenicity is affected by certain therapies and gene defects. These data may guide the counseling of patients with IEIs regarding prevention of SARS-CoV-2 infection and the need for subsequent boosts.

Keywords: COVID-19; JAK inhibitors; SARS-CoV-2; adverse events; antibody response; immune suppressants; immunomodulators; inborn errors of immunity.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adolescent
  • Adult
  • Age Factors*
  • Aged
  • Antibodies, Viral / blood
  • Antibody Formation
  • B-Lymphocytes / immunology*
  • COVID-19 / genetics
  • COVID-19 / immunology*
  • COVID-19 Drug Treatment
  • COVID-19 Vaccines / immunology*
  • Cohort Studies
  • Coronavirus Nucleocapsid Proteins / immunology
  • Female
  • Humans
  • Immunization, Secondary
  • Immunogenicity, Vaccine
  • Immunoglobulin G / blood
  • Immunosuppressive Agents / therapeutic use
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Phosphoproteins / immunology
  • Polyendocrinopathies, Autoimmune / drug therapy
  • Polyendocrinopathies, Autoimmune / genetics
  • Polyendocrinopathies, Autoimmune / immunology*
  • Rituximab / therapeutic use
  • SARS-CoV-2 / physiology*
  • Seroconversion
  • Spike Glycoprotein, Coronavirus / immunology
  • T-Lymphocytes / immunology*
  • Young Adult

Substances

  • Antibodies, Viral
  • COVID-19 Vaccines
  • Coronavirus Nucleocapsid Proteins
  • Immunoglobulin G
  • Immunosuppressive Agents
  • Phosphoproteins
  • Spike Glycoprotein, Coronavirus
  • nucleocapsid phosphoprotein, SARS-CoV-2
  • Rituximab