Evidence map›Paper›PMID 42409455›Full record

ReviewThe journal of allergy and clinical immunology. In practice2026

Clinical Spectrum and Therapeutic Options in Monogenic CTLA-4-, LRBA-, or SOCS1-Related Primary Immune Regulatory Disorders.

Chen Wang, Jessica Durkee-Shock, Chi Adrian Ma, Katherine R Calvo, David E Kleiner, Stefania Pittaluga, Gulbu Uzel

Abstract readReviewCase Reports
In one paragraph

Review in The journal of allergy and clinical immunology. In practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Chen WangImmunopathogenesis Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
Jessica Durkee-ShockMedical Virology Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md. Electronic address: jessica.durkee-shock@nih.gov.
Chi Adrian MaImmunopathogenesis Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
Katherine R CalvoHematology Section, Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, Md.
David E KleinerLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Md.
Stefania PittalugaLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Md.
Gulbu UzelImmunopathogenesis Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md. Electronic address: guzel@niaid.nih.gov.

Funding

Intramural NIH HHS Z99 AI999999NIH HHS
6 · The paper itself

Abstract

Primary immune regulatory disorders (PIRDs) are defined by a loss of immune homeostasis and are clinically characterized by autoimmunity, autoinflammation, lymphoproliferation, infection susceptibility, and cancer predisposition. An increasing number of genetic defects have been described that result in impaired regulation of immune responses. Evolving clinical manifestations and variable disease spectrum lead to significant diagnostic challenges and treatment conundrum. In this review, we present 3 clinical vignettes of PIRDs, including cytotoxic T-lymphocyte-associated protein 4 haploinsufficiency, lipopolysaccharide-responsive beige-like anchor protein deficiency, and suppressor of cytokine signaling 1 deficiency, to illustrate step-by-step approaches to diagnostic evaluation, disease assessment, and therapeutic management. We describe tailored treatment strategies, including immunomodulatory agents and hematopoietic stem cell transplantation, that address each patient's clinical manifestations, treatment response, and adverse effects. We also explain the clinical decision-making process, incorporating immunologic insights from the specific underlying genetic defects, relevant literature, and pearls from our clinical experience. Through these cases, we aim to offer a practical framework for clinicians managing patients with PIRDs.

Indexed as

Adaptor Proteins, Signal TransducingCTLA-4 AntigenImmune System DiseasesSuppressor of Cytokine Signaling 1 ProteinAdultFemaleHematopoietic Stem Cell TransplantationHumansMaleAdaptor Proteins, Signal TransducingCTLA-4 AntigenCTLA4 protein, humanLRBA protein, humanSOCS1 protein, humanSuppressor of Cytokine Signaling 1 ProteinAbataceptCTLA-4LRBAPrimary immune regulatory disordersSOCS1

Identifiers

PMID42409455
PMCPMC13344167

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.