Response to Severe Acute Respiratory Syndrome Coronavirus 2 Initial Series and Additional Dose Vaccine in Patients With Predominant Antibody Deficiency

Copyright © 2022 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved..

BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in patients with predominant antibody deficiency (PAD) is associated with high morbidity, yet data regarding the response to SARS-CoV-2 immunization in PAD patients, including additional dose vaccine, are limited.

OBJECTIVE: To characterize antibody response to SARS-CoV-2 vaccine in PAD patients and define correlates of vaccine response.

METHODS: We assessed the levels and function of anti-SARS-CoV-2 antibodies in 62 PAD patients compared with matched healthy controls at baseline, at 4 to 6 weeks after the initial series of immunization (a single dose of Ad26.COV2.S [Janssen] or two doses of BNT162b2 [Pfizer-BioNTech] or mRNA-1273 [Moderna]), and at 4 to 6 weeks after an additional dose immunization, if received.

RESULTS: After the initial series of SARS-CoV-2 vaccination, PAD patients had lower mean anti-spike antibody levels compared with matched healthy controls (140.1 vs 547.3 U/mL; P = .02). Patients with secondary PAD (eg, B-cell depletion therapy was used) and those with severe primary PAD (eg, common variable immunodeficiency with autoinflammatory complications) had the lowest mean anti-spike antibody levels. Immune correlates of a low anti-spike antibody response included low CD4+ T helper cells, low CD19+ total B cells, and low class-switched memory (CD27+IgD/M-) B cells. In addition, a low (<100 U/mL) anti-spike antibody response was associated with prior exposure to B-cell depletion therapy, both at any time in the past (odds ratio = 5.5; confidence interval, 1.5-20.4; P = .01) and proximal to vaccination (odds ratio = 36.4; confidence interval, 1.7-791.9; P = .02). Additional dose immunization with an mRNA vaccine in a subset of 31 PAD patients increased mean anti-spike antibody levels (76.3 U/mL before to 1065 U/mL after the additional dose; P < .0001).

CONCLUSIONS: Patients with secondary and severe primary PAD, characterized by low T helper cells, low B cells, and/or low class-switched memory B cells, were at risk for low antibody response to SARS-CoV-2 immunization, which improved after an additional dose vaccination in most patients.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:10

Enthalten in:

The journal of allergy and clinical immunology. In practice - 10(2022), 6 vom: 01. Juni, Seite 1622-1634.e4

Sprache:

Englisch

Beteiligte Personen:

Barmettler, Sara [VerfasserIn]
DiGiacomo, Daniel V [VerfasserIn]
Yang, Nancy J [VerfasserIn]
Lam, Tiffany [VerfasserIn]
Naranbhai, Vivek [VerfasserIn]
Dighe, Anand S [VerfasserIn]
Burke, Kristin E [VerfasserIn]
Blumenthal, Kimberly G [VerfasserIn]
Ling, Morris [VerfasserIn]
Hesterberg, Paul E [VerfasserIn]
Saff, Rebecca R [VerfasserIn]
MacLean, James [VerfasserIn]
Ofoman, Onosereme [VerfasserIn]
Berrios, Cristhian [VerfasserIn]
St Denis, Kerri J [VerfasserIn]
Lam, Evan C [VerfasserIn]
Gregory, David [VerfasserIn]
Iafrate, Anthony John [VerfasserIn]
Poznansky, Mark [VerfasserIn]
Lee, Hang [VerfasserIn]
Balazs, Alejandro [VerfasserIn]
Pillai, Shiv [VerfasserIn]
Farmer, Jocelyn R [VerfasserIn]

Links:

Volltext

Themen:

Ad26COVS1
Additional dose
Anti-nucleocapsid antibody
Anti-spike antibody
BNT162 Vaccine
COVID-19
COVID-19 Vaccines
CVID
Common variable immunodeficiency
Humoral immunodeficiency
Hypogammaglobulinemia
IgG subclass deficiency
JT2NS6183B
Journal Article
MRNA Vaccines
N38TVC63NU
Neutralization assay
Predominant antibody deficiency
Research Support, N.I.H., Extramural
SARS-CoV-2
Specific antibody deficiency
Vaccine response
Vaccines, Synthetic
Viral Vaccines

Anmerkungen:

Date Completed 14.06.2022

Date Revised 14.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.jaip.2022.03.017

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM33911200X