# The significance of component-resolved diagnostics in atopic dermatitis

**Authors:** Małgorzata Błażowska, Julia Nowowiejska-Purpurowicz, Maria Tomasiak-Łozowska, Łukasz Błażowski, Iwona Flisiak

PMC · DOI: 10.3389/fimmu.2026.1711854 · Frontiers in Immunology · 2026-03-02

## TL;DR

This paper reviews how component-resolved diagnostics can improve personalized treatment and understanding of atopic dermatitis by analyzing specific allergen molecules.

## Contribution

The paper comprehensively summarizes the potential of CRD in managing atopic dermatitis and identifying disease endotypes.

## Key findings

- CRD can detect genuine and cross-sensitization in atopic dermatitis patients.
- Molecular profiling using CRD helps identify biomarkers for disease severity and treatment response.
- CRD improves understanding of AD endotypes and enables personalized management.

## Abstract

Atopic dermatitis (AD) is a common and chronic inflammatory skin disease characterized by an abnormal skin barrier, resulting in skin dryness, pruritus, and an increased risk of allergies and secondary infections. AD patients often show hypersensitivity to both food and airborne allergens. Component-resolved diagnostics (CRD) offers sIgE testing of individual allergen molecules and provides additional insights, especially in polysensitized patients, in case of sensitization to allergens with low abundance, low stability, or associated with risks of anaphylaxis. It enables the detection of genuine and cross-sensitization or the composition of an allergen immunotherapy vaccine. So far, the utility of CRD in AD has never been thoroughly analyzed. This review provides basic information about CRD and comprehensively summarizes its potential application in the personalized management of patients with AD. Molecular profiling of allergen components moves closer to explaining the mechanisms of development of different molecular endotypes and clinical phenotypes of AD and provides biomarkers of disease severity, autoimmune IgE responses, and therapeutic response, improving understanding of atopic dermatitis endotypes and treatment outcomes.

## Linked entities

- **Diseases:** atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** skin dryness (MESH:D014987), pruritus (MESH:D011537), infections (MESH:D007239), AD (MESH:D003876), skin disease (MESH:D012871), allergies (MESH:D004342), anaphylaxis (MESH:D000707), inflammatory (MESH:D007249)
- **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/PMC12989354/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12989354/full.md

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Source: https://tomesphere.com/paper/PMC12989354