Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jul;80(7):1831-1847.
doi: 10.1111/all.16576. Epub 2025 May 7.

Endotypes in Immune Mediated Drug Reactions: Present and Future of Relevant Biomarkers. An EAACI Task Force Report

Affiliations
Review

Endotypes in Immune Mediated Drug Reactions: Present and Future of Relevant Biomarkers. An EAACI Task Force Report

C Mayorga et al. Allergy. 2025 Jul.

Abstract

Drug-induced immune reactions are an important burden for patients and health systems. They can be classified into immediate-drug hypersensitivity reactions (IDHRs) and delayed-DHRs (DDHRs) based on their phenotype. Drugs do not always behave as allergens and need to bind to proteins, forming adducts. Therefore, IDHRs can be classified as antigenic (IgE, and IgG mediated) and nonantigenic immune responses (complement activation-[CARPA], mas-related G-protein coupled receptor member X2 [MRGPRX2], cyclooxygenase [COX]-1 and cytokine release reactions [CRRs]). DDHRs are even more complex due to the different cell subsets and mechanisms involved, showing both antigenic and nonantigenic immune responses too. Since different endotypes result in similar phenotypes, the establishment of specific biomarkers is essential for an accurate diagnosis, with important relevance for the management of patients, as well as for risk stratification. The biomarkers of clinical utility are skin tests, specific IgE (sIgE), tryptase, and some HLA-DR genotyping. The diagnostic performance depends on the responsible drug. This review highlights that, unfortunately, most biomarkers have not gone beyond analytic or clinical validity. It is therefore important to set up multicentre translational studies to advance the validation process towards reaching a clinical utility phase.

Keywords: biomarkers; drug reactions; endotypes; mechanisms; phenotypes.

PubMed Disclaimer

References

    1. C. Mayorga, T. D. Fernandez, M. I. Montañez, E. Moreno, and M. J. Torres, “Recent Developments and Highlights in Drug Hypersensitivity,” Allergy 74, no. 12 (2019): 2368–2381.
    1. M. Jutel, I. Agache, M. Zemelka‐Wiacek, et al., “Nomenclature of Allergic Diseases and Hypersensitivity Reactions: Adapted to Modern Needs: An EAACI Position Paper,” Allergy 78, no. 11 (2023): 2851–2874.
    1. B. D. Jakubovic, L. L. Vecillas, T. W. Jimenez‐Rodriguez, S. Sanchez‐Sanchez, and M. Castells, “Drug Hypersensitivity in the Fast Lane: What Clinicians Should Know About Phenotypes, Endotypes, and Biomarkers,” Annals of Allergy, Asthma & Immunology 124, no. 6 (2020): 566–572, https://doi.org/10.1016/j.anai.2020.04.005.
    1. I. Dona, M. J. Torres, G. Celik, E. Phillips, L. K. Tanno, and M. Castells, “Changing Patterns in the Epidemiology of Drug Allergy,” Allergy 79, no. 3 (2024): 613–628.
    1. W. J. Pichler, “Immune Pathomechanism and Classification of Drug Hypersensitivity,” Allergy 74, no. 8 (2019): 1457–1471.