# Proposition for a New Classification of Hypersensitivity Reactions – an Expanded Nomenclature

**Authors:** Andrea Szegedi, Werner J. Pichler, Anikó Kapitány, Zsuzsanna Bata-Csörgő, Gábor Koncz, Attila Bácsi

PMC · DOI: 10.1007/s12016-026-09143-9 · Clinical Reviews in Allergy & Immunology · 2026-02-26

## TL;DR

This paper proposes a new classification system for hypersensitivity reactions that includes all stages of the immune process and drug-induced reactions.

## Contribution

The paper introduces a revised classification system that integrates initiation, central, and effector phases of hypersensitivity reactions.

## Key findings

- The new classification considers initiation, central, and effector phases as interconnected processes.
- The classification incorporates small-molecule drug-induced reactions, including both immunological and non-immunological processes.

## Abstract

Diseases associated with hypersensitivity reactions (HRs) are extremely common and can affect the quality of life of millions of people, sometimes with life-threatening severity. In order to diagnose, treat, cure, or potentially prevent these diseases, clinicians and scientists need a better understanding of the entire immune process, from its initiation through the central mechanism to the effector phase. A new classification is needed, primarily because earlier classifications defined HRs almost exclusively by their effector mechanisms. However, outstanding achievements in immunological science over the past decades have revealed the critical, decision-making roles of initiation and central mechanisms in shaping the well-known effector phases. In addition, a crucially important group of HRs consists of small-molecule drug-induced reactions, which include both immunological and non-immunological pharmacological processes; therefore, the incorporation of these entities represents a key aspect of the revised classification. This review article provides a historical overview of the evolution of the main HR classifications, and proposes a new, expanded classification that (a) considers the initiation, central, and effector phases of HRs as interconnected, equally important processes; (b) highlights the role of peripheral barrier tissues in the breakdown of tolerance, thereby contributing to the development of HRs, and (c) distinguishes between classic and non-classic HRs (e.g., pharmacological interaction with immune receptors [p-i] reactions and pseudoallergies). Adoption of this new classification may expand the possibilities for developing preventive and causal therapies and help physicians appropriately interpret and thus effectively treat the heterogeneous phenotypes of hypersensitivity diseases.

## Full-text entities

- **Genes:** IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}, BTK (Bruton tyrosine kinase) [NCBI Gene 695] {aka AGMX1, AT, ATK, BPK, IGHD3, IMD1}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, TNFRSF4 (TNF receptor superfamily member 4) [NCBI Gene 7293] {aka ACT35, CD134, IMD16, OX40, TXGP1L}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, KNG1 (kininogen 1) [NCBI Gene 3827] {aka BDK, BK, HAE6, HK, HMWK, KNG}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, TTN (titin) [NCBI Gene 7273] {aka CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, TNFSF4 (TNF superfamily member 4) [NCBI Gene 7292] {aka CD134L, CD252, GP34, OX-40L, OX4OL, TNLG2B}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL31 (interleukin 31) [NCBI Gene 386653] {aka IL-31}, IL25 (interleukin 25) [NCBI Gene 64806] {aka IL17E}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, MRGPRX2 (MAS related GPR family member X2) [NCBI Gene 117194] {aka MGRG3, MRGX2}, MINDY3 (MINDY lysine 48 deubiquitinase 3) [NCBI Gene 80013] {aka C10orf97, CARP, DERP5, FAM188A, MST126, MSTP126}, Toll-like receptor 4 [NCBI Gene 724187], HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, GNLY (granulysin) [NCBI Gene 10578] {aka D2S69E, LAG-2, LAG2, NKG5, TLA519}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, FASLG (Fas ligand) [NCBI Gene 356] {aka ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}
- **Diseases:** tissue damage (MESH:D017695), Type III reaction (MESH:D007105), chronic rhinosinusitis (MESH:D000092562), immune dysregulation (OMIM:614878), AD (MESH:D003876), NSAID-exacerbated cutaneous disease (MESH:D018450), contact dermatitis (MESH:D003877), HDM (MESH:D000092542), Type IVc reactions (MESH:C567679), muscle cell necrosis (MESH:D009135), , type 2, and type 3 (MESH:C536044), Hypersensitivity (MESH:D004342), SLOs (MESH:D000092124), ARC (OMIM:613207), cytotoxic (MESH:D064420), AR (MESH:D013734), venom allergy (MESH:D000092422), allergic bronchopulmonary aspergillosis (MESH:D001229), HRs (MESH:D006967), infection (MESH:D007239), maculopapular drug eruptions (MESH:D003875), AGEP (MESH:D056150), allergic rhinitis (MESH:D065631), ADCC (MESH:D007153), II, III, (MESH:D017099), viral infection (MESH:D014777), neutrophilia (MESH:C563010), angioedema (MESH:D000799), induced enterocolitis syndrome (MESH:D004760), pruritus (MESH:D011537), anaphylaxis (MESH:D000707), CRS (MESH:D003398), Stevens-Johnson syndrome (MESH:D013262), hypoxia (MESH:D000860), autoinflammatory diseases (MESH:D056660), metabolic (MESH:D008659), genetic defects (MESH:D030342), IVa, IVb (MESH:C536467), immediate hypersensitivity (MESH:D006969), ACD (MESH:C535474), lung inflammation (MESH:D011014), tumor necrosis factor (MESH:C536657), exanthema (MESH:D005076), autoimmune diseases (MESH:D001327), urticaria (MESH:D014581), Obesity (MESH:D009765), Type VII hypersensitivity (MESH:C565200), VI pseudoallergy (MESH:D028243), allergic contact dermatitis (MESH:D017449), eosinophilic oesophagitis (MESH:D000077277), asthma (MESH:D001249), swelling (MESH:D004487), eosinophilia (MESH:D004802), DReSS (MESH:D063926), SJS (MESH:D010009), dysbiosis (MESH:D064806), respiratory disease (MESH:D012140), skin reactions (MESH:D012871), inflammation (MESH:D007249)
- **Chemicals:** DAMP (MESH:C116255), oleic acid (MESH:D019301), ATP (MESH:D000255), cobalt (MESH:D003035), steroids (MESH:D013256), saturated fatty acids (MESH:D005227), leukotrienes (MESH:D015289), phenytoin (MESH:D010672), AERD (-), abacavir (MESH:C106538), flucloxacillin (MESH:D005436), nitric oxide (MESH:D009569), free fatty acids (MESH:D005230), aspirin (MESH:D001241), palladium (MESH:D010165), triglycerides (MESH:D014280), nickel (MESH:D009532), uric acid (MESH:D014527), allopurinol (MESH:D000493), metal (MESH:D008670), histamine (MESH:D006632)
- **Species:** Apis mellifera (bee, species) [taxon 7460], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Arachis hypogaea (goober, species) [taxon 3818], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946285/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946285/full.md

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Source: https://tomesphere.com/paper/PMC12946285