# Endotype-driven decisions in choosing a biologic for airway diseases

**Authors:** Carmen Panaitescu, Laura Haidar, Maria-Roxana Buzan, Răzvan-Ionuț Zimbru, Valentin-Cristian Iovin, Elena-Larisa Zimbru, Alexandru Lăculiceanu, Ioana Agache

PMC · DOI: 10.3389/falgy.2025.1754173 · Frontiers in Allergy · 2026-01-12

## TL;DR

This paper discusses how using endotypes to guide biologic therapy choices can improve treatment outcomes for allergic airway diseases.

## Contribution

The paper introduces decision algorithms for endotype-guided biologic therapy selection in allergic diseases.

## Key findings

- Endotype-driven strategies improve patient outcomes in asthma and chronic rhinosinusitis with nasal polyps.
- Biologics targeting IgE, IL-5, IL-4/IL-13, or TSLP pathways should be selected based on specific endotypes.
- Incorporating endotype classification into care pathways enhances personalized treatment decisions.

## Abstract

The increasing availability of biologic therapies for allergic diseases has highlighted the need for more precise, mechanism-based patient selection. Traditional approaches based on disease phenotypes often fall short in predicting therapeutic response. Escalating healthcare costs together with questions about the efficacy of the current management of allergic diseases prompt to a shift toward endotype-driven and biomarker-guided strategies. This review explores the role of endotypes, defined by distinct immunologic, molecular, or cellular mechanisms, in guiding the use of targeted biologics in asthma and in chronic rhinosinusitis with nasal polyps. Endotype classification based on the type 1, type 2 and type 3 immune response is critical for selecting biologics targeting the IgE, IL-5, IL-4/IL-13, or TSLP pathways. The endotype-driven approach in allergic diseases has tremendous potential if incorporated into comprehensive care pathways, with endotype identification playing a key role in the management decision tree, with improved outcomes and greater patient satisfaction. To this purpose this review provides decision algorithms for the endotype-guided approach at the point of care and discusses the unmet needs with potential practical solutions to support a personalized precision approach.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon), IL5 (interleukin 5), IL4 (interleukin 4), IL13 (interleukin 13), TSLP (thymic stromal lymphopoietin)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}
- **Diseases:** rhinosinusitis (MESH:D000092562), airway diseases (MESH:D029424), allergic diseases (MESH:D004342), asthma (MESH:D001249), nasal polyps (MESH:D009298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832300/full.md

## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832300/full.md

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Source: https://tomesphere.com/paper/PMC12832300