MHC restriction in allergic bronchopulmonary aspergillosis
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Updated: Sep 28, 2026

Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
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
Abstract:
Allergic bronchopulmonary aspergillosis (ABPA) is a rare complication in patients with asthma but more common in patients with cystic fibrosis. In the presence of the fungus Aspergillus fumigatus (Af) in the lower respiratory tract, patients mount a heightened IgG and IgE humoral response specific for Af antigens. Studies on ABPA have suggested a pathogenic role for antigen specific CD4+ Th2 like T lymphocytes producing increased levels of IL-4 and IL-5. MHC class II genes coding for highly polymorphic HLA molecules have been shown to be the likely candidates for controlling immune responses to common allergens. However there has been a lack of information on the pathophysiological role of HLA genes in the development of ABPA. This review describes an association between HLA- class II alleles and the specific responses to Af antigen (Asp f 1) in ABPA. These studies focused on MHC restriction and distribution of HLA- class II alleles in two groups of unrelated North American Caucasian patients with cystic fibrosis and/or asthma. One group consisted of patients with a confirmed diagnosis of ABPA and a second group of patients with Af sensitivity but no ABPA. HLA association studies revealed that the predisposition to develop ABPA is associated with HLA-DR2 and DR5, and possibly DR4 or DR7. A strong association of HLA-DR antigens with ABPA reflects that HLA-DR molecules may present disease-causing peptides. On the other hand a significant association of HLA-DQ2 with Af sensitive nonABPA indicates the involvement of HLA-DQ molecules in protection. A combination of these genetic factors determines the outcome of ABPA in patients with cystic fibrosis and asthma.
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.
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