Evidence map›Paper›PMID 42125312›Full record

ReviewJournal of human immunity2026

Primary atopic disorders: Monogenic insights into immunity.

Bhavi P Modi, Cassandra McDonald, Liam Golding, Leandro B R Da Silva, Catherine M Biggs, Julia Körholz, Elliot L James, Stuart E Turvey

Abstract readReview
In one paragraph

Review in Journal of human immunity, 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

8 authors.

Bhavi P ModiDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0003-1510-5916
Cassandra McDonaldDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0001-5559-2494
Liam GoldingDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0002-8851-8052
Leandro B R Da SilvaDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0001-6545-5725
Catherine M BiggsDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0002-4363-2660
Julia KörholzDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.ORCID https://orcid.org/0000-0001-6313-4434
Elliot L JamesDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0009-0009-5249-857X
Stuart E TurveyDepartment of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0003-1599-1065

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary atopic disorders (PADs), a subset of inborn errors of immunity, are a growing group of more than 50 monogenic diseases characterized by severe, early-onset allergic inflammation, often coexisting with immune deficiency or dysregulation. Once considered clinical curiosities, PADs have emerged as powerful human models for understanding immune homeostasis. Advances in next-generation sequencing have accelerated gene discovery, revealing that allergic disease can arise from disruption of interconnected regulatory systems rather than immune hyperactivity alone. Here, we synthesize insights from genetically defined PADs to illustrate how defects across epithelial barrier function, immune signaling, cytoskeletal organization, antigen receptor pathways, lymphocyte repertoire, and regulatory networks converge on impaired tolerance and persistent type 2 inflammation. Beyond mechanistic insights, PADs provide a framework for precision therapy enabling targeted use of cytokine inhibitors, JAK inhibitors, biologics, hematopoietic stem cell transplantation, and emerging gene therapies. These insights bridge rare and common disease, informing the pathophysiology and treatment of polygenic atopy.

Identifiers

PMID42125312
PMCPMC13159798

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.