Artificial Intelligence Identification and Recruitment of Undiagnosed IEI Patients

Introduction Inborn errors of immunity (IEIs) often remain undiagnosed due to many factors including the fragmentation of care across subspecialties. The increasing complexity of these disorders poses a diagnostic challenge, even for immunologists. Artificial intelligence (AI) algorithms trained on electronic health records (EHRs) and expert knowledge can identify a broad range of IEI phenotypes. Clinical validation of these tools is needed to identify undiagnosed patients and impact care. Objectives We sought to describe patients with putative IEIs identified by an algorithm trained on EHR signatures. Methods We published an algorithm PheNet trained on EHR data of patients with IEIs [1]. PheNet identified suspected IEI patients across the University of California (UC) medical database. Algorithmically identified high-risk individuals were reviewed by clinicians and bioinformaticians; those of interest following chart review were recruited, consented, and underwent genetic and immune phenotyping. Results The top 500 cases identified via PheNet were subsequently reviewed by an immunologist. Each center found ∼15 subjects that were considered suspicious for IEIs. Currently, there are 25 subjects who consented who have undergone sequencing and full immune workup. Immune phenotyping revealed T and B cell defects, while genetic testing has identified several actionable variants. Conclusion AI algorithms are useful in the identification of patients with IEI phenotypes, with meaningful clinical implications. By combining AI to identify subjects with concerning clinical phenotypes with in-person clinical examination and sequencing, we identified ∼20 subjects who had remained undiagnosed despite receiving specialty care. One outcome of this effort will be to expand surveillance beyond simple “warning signs” to more sophisticated EHR signatures of IEIs.

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Publication Details

Journal
Journal of Human Immunity
Published
2025-12-22
DOI
https://doi.org/10.70962/lasid2025abstract.2
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
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article

Artificial Intelligence Identification and Recruitment of Undiagnosed IEI Patients

Aaron Chin, Rachel Mester, Alexis V. Stephens, Manish J. Butte et al.
Journal of Human Immunity
Immunodeficiency and Autoimmune Disorders
article

Artificial Intelligence Identification and Recruitment of Undiagnosed IEI Patients

Aaron Chin, Rachel Mester, Alexis V. Stephens, Manish J. Butte, Bogdan Pasanuic
article en

Abstract

Introduction Inborn errors of immunity (IEIs) often remain undiagnosed due to many factors including the fragmentation of care across subspecialties. The increasing complexity of these disorders poses a diagnostic challenge, even for immunologists. Artificial intelligence (AI) algorithms trained on electronic health records (EHRs) and expert knowledge can identify a broad range of IEI phenotypes. Clinical validation of these tools is needed to identify undiagnosed patients and impact care. Objectives We sought to describe patients with putative IEIs identified by an algorithm trained on EHR signatures. Methods We published an algorithm PheNet trained on EHR data of patients with IEIs [1]. PheNet identified suspected IEI patients across the University of California (UC) medical database. Algorithmically identified high-risk individuals were reviewed by clinicians and bioinformaticians; those of interest following chart review were recruited, consented, and underwent genetic and immune phenotyping. Results The top 500 cases identified via PheNet were subsequently reviewed by an immunologist. Each center found ∼15 subjects that were considered suspicious for IEIs. Currently, there are 25 subjects who consented who have undergone sequencing and full immune workup. Immune phenotyping revealed T and B cell defects, while genetic testing has identified several actionable variants. Conclusion AI algorithms are useful in the identification of patients with IEI phenotypes, with meaningful clinical implications. By combining AI to identify subjects with concerning clinical phenotypes with in-person clinical examination and sequencing, we identified ∼20 subjects who had remained undiagnosed despite receiving specialty care. One outcome of this effort will be to expand surveillance beyond simple “warning signs” to more sophisticated EHR signatures of IEIs.

Journal of Human ImmunityVol. 1(LASID2025)
University of California, Los Angeles (US), Institute of Human Genetics (PL), University of Pennsylvania (US)
Openalex Percentile: Top 37%
Immunodeficiency and Autoimmune Disorders
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