MHC restriction in allergic bronchopulmonary aspergillosis

Bela Chauhan1, Patricia S Hutcheson, Raymond G Slavin

  • 1Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, USA. chauhamb@slu.edu

Insights

Genetic factors influence allergic bronchopulmonary aspergillosis (ABPA) development. Specific HLA-DR alleles increase ABPA risk, while HLA-DQ2 may offer protection against Aspergillus fumigatus sensitivity.

Area of Science:

  • Immunogenetics
  • Pulmonology
  • Allergy and Immunology

Background:

  • Allergic bronchopulmonary aspergillosis (ABPA) is a lung disease caused by Aspergillus fumigatus (Af).
  • While common in cystic fibrosis, ABPA is a rare asthma complication.
  • Immune responses involving CD4+ T cells, IL-4, IL-5, and specific antibodies are implicated in ABPA pathogenesis.

Purpose of the Study:

  • To investigate the role of Human Leukocyte Antigen (HLA) class II genes in the development of ABPA.
  • To identify specific HLA alleles associated with susceptibility or protection in ABPA patients.

Main Methods:

  • Analysis of HLA class II allele distribution in North American Caucasian patients with cystic fibrosis and/or asthma.
  • Comparison between patients diagnosed with ABPA and those sensitive to Af but without ABPA.

Main Results:

  • A predisposition to ABPA was associated with HLA-DR2 and HLA-DR5 alleles, with possible links to HLA-DR4 or HLA-DR7.
  • HLA-DR antigens may present disease-causing peptides in ABPA.
  • A significant association of HLA-DQ2 with Af-sensitive non-ABPA patients suggests a protective role.

Conclusions:

  • HLA class II alleles play a significant role in determining the outcome of ABPA.
  • Specific HLA-DR alleles are linked to ABPA susceptibility, while HLA-DQ2 may be protective.
  • Genetic factors, particularly HLA associations, are crucial in understanding ABPA in patients with cystic fibrosis and asthma.