Coordinated IgG2 and IgE responses as a marker of allergen immunotherapy efficacy

Allergy. 2022 Apr;77(4):1263-1273. doi: 10.1111/all.15107. Epub 2021 Oct 6.

Abstract

Background: IgG2 responses are associated with repeated antigen exposure and display highly mutated variable domains. A recent study highlighted a role of IgG2+ memory B cells and allergen-specific IgG2 levels after a 3rd consecutive pre-seasonal sublingual allergen immunotherapy (AIT) with grass pollen tablet. Herein, we aim to explore changes in allergen-specific IgG2 in individuals undergoing house dust mite immunotherapy (HDM-AIT) and explore whether the interrelationship with other humoral responses (i.e., IgG4 and IgE) may discriminate between high and low responders.

Methods: Levels of serum Dermatophagoides pteronyssinus and Dermatophagoides farinae-specific IgG2, IgG4, and IgE antibodies were measured by ELISA or ImmunoCap in a sub-group of individuals enrolled in a randomized, double-blind, placebo-controlled, sublingual AIT study evaluating the safety and efficacy of a 300 IR HDM tablet.

Results: After 1-year sublingual AIT, HDM-specific serum IgG2 responses increase mostly in high versus low responders and are distinctive according to the clinical benefit. Higher correlation between HDM-specific IgG2, IgE, and/or IgG4 responses is seen in subjects benefiting the most from HDM-AIT as indicated by changes in Average Total Combined Scores. More strikingly, statistically significant correlation between HDM-specific IgG2 and IgE responses is only observed in individuals stratified as high responders.

Conclusions: We provide evidence for coordinated serum immune responses upon AIT in HDM-allergic subjects exhibiting high clinical benefit when compared with low responders. Assessing HDM-specific IgE, IgG2, and IgG4 in serum could be used as follow-up combined markers to support decision as to AIT continuation and/or adaptation.

Keywords: IgG2; allergen immunotherapy efficacy; house dust mite; humoral responses; sublingual immunotherapy.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens
  • Animals
  • Antigens, Dermatophagoides
  • Biomarkers
  • Desensitization, Immunologic
  • Humans
  • Immunoglobulin E
  • Immunoglobulin G*
  • Pyroglyphidae
  • Sublingual Immunotherapy*
  • Tablets
  • Treatment Outcome

Substances

  • Allergens
  • Antigens, Dermatophagoides
  • Biomarkers
  • Immunoglobulin G
  • Tablets
  • Immunoglobulin E