Evidence map›Paper›PMID 42511814›Full record

ReviewInternational journal of molecular sciences2026

Research Advances and Biological Features of IgA for Immune-Related Diseases.

Han Guo, Xinying Li, Fenghao Peng, Jijun Yu, Jing Wang, Longlong Luo, He Xiao, Guojiang Chen, Chenghua Liu, Jiannan Feng and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

11 authors.

Han GuoState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Xinying LiState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Fenghao PengState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Jijun YuState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Jing WangState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.ORCID 0000-0001-9413-2378
Longlong LuoState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.ORCID 0000-0002-8307-6478
He XiaoState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Guojiang ChenState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Chenghua LiuState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Jiannan FengState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.
Chunxia QiaoState Key Laboratory of National Security Specially Needed Medicines, Beijing 100039, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the predominant antibody isotype at human mucosal surfaces, immunoglobulin A (IgA) exerts critical functions in mucosal defense and systemic immune homeostasis. The two IgA subclasses, IgA1 and IgA2, possess distinct structural and functional features and assemble into dimeric IgA (dIgA) and secretory IgA (sIgA) under physiological conditions. With advances in cryo-electron microscopy, the molecular architecture and assembly of sIgA have been clearly characterized. While IgA protects hosts from pathogenic infection and sustains immune balance, aberrantly altered IgA contributes to the pathogenesis of IgA nephropathy and autoimmune encephalitis. To date, IgA-based therapeutics have displayed promising therapeutic efficacy against respiratory disorders, inflammatory bowel diseases and oral fungal infections. Through standardized retrieval and categorical sorting of the published literature covering IgA structure, physiological functions, disease pathogenic mechanisms and therapeutic research, this review systematically organizes relevant research advances, analyzes the bottlenecks and translational prospects of IgA-targeted therapeutics, and provides objective references to accelerate the clinical translation of IgA antibody agents.

Indexed as

Immunoglobulin AAnimalsEncephalitisGlomerulonephritis, IGAHashimoto DiseaseHumansImmunoglobulin A, SecretoryImmunoglobulin AImmunoglobulin A, Secretoryautoimmune encephalitisIgAinfectious diseaseinflammatory diseasetherapeutic antibody

Identifiers

PMID42511814
PMCPMC13411176

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Registered trials

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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.