# Building alliances for early detection of immunodeficiencies: from primary care to hematology

**Authors:** Jacques G. Rivière, Marlène Pasquet, Eleonora Gambineri

PMC · DOI: 10.3389/fimmu.2025.1701384 · Frontiers in Immunology · 2026-01-02

## TL;DR

This paper discusses strategies to improve early detection of primary immunodeficiencies by integrating primary care, hematology, and AI technologies.

## Contribution

The paper introduces a multidisciplinary approach combining clinical tools, AI, and structured models like PIDCAP for early IEI detection.

## Key findings

- Tools like newborn screening and the JMF warning signs help identify at-risk patients for IEI.
- AI can detect diagnostic patterns in electronic health records but faces challenges with data quality and interoperability.
- Hematologic conditions like autoimmune cytopenias often precede IEI and should prompt immunological evaluation.

## Abstract

Inborn errors of immunity (IEI), also known as primary immunodeficiencies, are a heterogeneous group of rare disorders characterized by increased susceptibility to infections, immune dysregulation, and malignancy. Early detection remains a major challenge due to the complexity of clinical presentations, limited awareness among non-specialists, and delayed diagnostic pathways. This review explores current strategies to enhance early detection of IEI, highlighting both technological innovations and clinical insights. Tools such as newborn screening, the Jeffrey Modell Foundation (JMF) warning signs, software like SPIRIT, and the PIDCAP project—a structured model designed for primary care implementation using ICD-coded clinical data— have shown promise in identifying at-risk patients. Artificial intelligence (AI) offers additional potential by detecting diagnostic patterns in electronic health records, although challenges related to data quality, heterogeneity, and system interoperability persist. Importantly, hematologic manifestations such as autoimmune cytopenias, lymphoproliferative disorders, and myelodysplastic syndromes often precede or accompany IEI and should prompt immunological evaluation. These conditions, frequently encountered in hematology, may serve as early clinical clues and justify genetic and immunophenotypic assessment. A multidisciplinary approach combining primary care, immunology, hematology, and AI technologies is essential to advance the early detection of IEI. Projects like PIDCAP, and their potential extension to secondary immunodeficiencies, exemplify scalable, patient-centered strategies that may significantly improve diagnostic timeliness and clinical outcomes.

## Linked entities

- **Diseases:** inborn errors of immunity (MONDO:0003778), myelodysplastic syndromes (MONDO:0018881)

## Full-text entities

- **Diseases:** immunodeficiencies (MESH:D007153), secondary immunodeficiencies (MESH:D000068376), IEI (MESH:D007154), myelodysplastic syndromes (MESH:D009190), primary immunodeficiencies (MESH:D000081207), malignancy (MESH:D009369), infections (MESH:D007239), autoimmune cytopenias (MESH:D001327), lymphoproliferative disorders (MESH:D008232), immune dysregulation (OMIM:614878)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12808396/full.md

## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC12808396/full.md

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Source: https://tomesphere.com/paper/PMC12808396