Evidence map›Paper›PMID 39560666›Full record

ArticleThe Journal of experimental medicine2024

Immunomolecular and reactivity landscapes of gut IgA subclasses in homeostasis and inflammatory bowel disease.

Sonia Tejedor Vaquero, Hadas Neuman, Laura Comerma, Xavi Marcos-Fa, Celia Corral-Vazquez, Mathieu Uzzan, Marc Pybus, Daniel Segura-Garzón, Joana Guerra, Lisa Perruzza and 23 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  5. B cell-driven immune remodeling in inflammatory bowel disease: links to pathogenesis and therapeutic failure.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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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

33 authors.

Sonia Tejedor Vaquero *Translational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0003-2873-4981
Hadas Neuman *Computational Immunology Laboratory, The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.ORCID 0000-0003-4098-7041
Laura ComermaTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-0249-4636
Xavi Marcos-FaTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-4216-1123
Celia Corral-VazquezTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-0621-4590
Mathieu UzzanDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Immunology Institute, New York, NY, USA.ORCID 0000-0002-7761-2879
Marc PybusTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-6195-5738
Daniel Segura-GarzónTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0003-0210-9571
Joana GuerraTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0001-7185-9283
Lisa PerruzzaInstitute for Research in Biomedicine, Faculty of Biomedical Sciences, Università della Svizzera Italiana , Bellinzona, Switzerland.ORCID 0009-0005-1692-5491
Roser Tachó-PiñotTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-4641-1134
Jordi SintesTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-1836-7076
Adam RosensteinDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Immunology Institute, New York, NY, USA.ORCID 0009-0000-4259-7165
Emilie K GrassetDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Immunology Institute, New York, NY, USA.ORCID 0000-0002-9592-1640
Mar IglesiasPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0000-0002-2274-4671
Monica Gonzalez FarréPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0000-0002-0653-0980
Joan LopPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0000-0002-9442-5688
Maria Evangelina Patriaca-AmianoPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0000-0003-1001-1910
Monica Larrubia-LoringPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0009-0002-9054-9269
Pablo Santiago-DiazPathology Department, Hospital del Mar, Barcelona, Spain.ORCID 0000-0003-2219-7687
Júlia Perera-BelTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-6809-132X
Pau Berenguer-MolinsTranslational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-0170-2931
Monica Martinez GalloImmunology Division, Vall d'Hebron University Hospital and Translational Immunology Research Group, Vall d'Hebron Research Institute (VHIR), Department of Cell Biology, Physiology and Immunology, Autonomous University of Barcelona (UAB), Barcelona, Spain.ORCID 0000-0002-7340-2161
Andrea Martin-NaldaPediatric Infectious Diseases and Immunodeficiencies Unit, Vall d'Hebron University Hospital, Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Barcelona, Spain.ORCID 0000-0002-3590-0186
Encarna VarelaDepartment of Gastroenterology, Vall d'Hebron Research Institute, Barcelona, Spain.ORCID 0000-0001-6334-9320
Marta Garrido-PontnouPathology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.ORCID 0000-0002-7762-7085
Fabio GrassiInstitute for Research in Biomedicine, Faculty of Biomedical Sciences, Università della Svizzera Italiana , Bellinzona, Switzerland.ORCID 0000-0003-3348-1712
Francisco GuarnerDepartment of Gastroenterology, Vall d'Hebron Research Institute, Barcelona, Spain.ORCID 0000-0002-4051-0836
Saurabh MehandruDepartment of Medicine, Icahn School of Medicine at Mount Sinai, Immunology Institute, New York, NY, USA.ORCID 0000-0001-9781-2969
Lucia Márquez-MosqueraDepartment of Gastroenterology, Hospital del Mar Medical Research Institute Barcelona, Barcelona, Spain.ORCID 0000-0002-3182-9570
Ramit Mehr *Computational Immunology Laboratory, The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.ORCID 0000-0002-4303-6834
Andrea Cerutti *Translational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0003-3026-4704
Giuliana Magri *Translational Clinical Research Program, Hospital del Mar Research Institute , Barcelona, Spain.ORCID 0000-0002-0163-3542

Funding

Regulation of IgA class switching in the intestinal mucosaP01AI061093 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CUNNINGHAM-RUNDLES, CHARLOTTE · 2004 to 2021
$29.8M
The impact of HIV-1 infection and its treatment on gastrointestinal B cellsR01DK112296 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MEHANDRU, SAURABH · 2017 to 2021
$2.0M
Crohn's & Colitis Foundation of America 877970European Fund for Regional DevelopmentGrant Miguel Servet MS19/0002Instituto de Salud Carlos III FIS PI21/00037Ministry of Economy and Competitiveness RTI2018-093894-B-I00NIAID NIH HHS P01 AI061093NIDDK NIH HHS R01 DK112296Spanish Ministry of Science and innovation RYC2021-031642-IUS-Israel Binational Science Foundation 2013432US National Institutes of Health P01 AI61093
6 · The paper itself

Abstract

The human gut includes plasma cells (PCs) expressing immunoglobulin A1 (IgA1) or IgA2, two structurally distinct IgA subclasses with elusive regulation, function, and reactivity. We show here that intestinal IgA1+ and IgA2+ PCs co-emerged early in life, comparably accumulated somatic mutations, and were enriched within short-lived CD19+ and long-lived CD19- PC subsets, respectively. IgA2+ PCs were extensively clonally related to IgA1+ PCs and a subset of them presumably emerged from IgA1+ precursors. Of note, secretory IgA1 (SIgA1) and SIgA2 dually coated a large fraction of mucus-embedded bacteria, including Akkermansia muciniphila. Disruption of homeostasis by inflammatory bowel disease (IBD) was associated with an increase in actively proliferating IgA1+ plasmablasts, a depletion in long-lived IgA2+ PCs, and increased SIgA1+SIgA2+ gut microbiota. Such increase featured enhanced IgA1 reactivity to pathobionts, including Escherichia coli, combined with depletion of beneficial A. muciniphila. Thus, gut IgA1 and IgA2 emerge from clonally related PCs and show unique changes in both frequency and reactivity in IBD.

Indexed as

Gastrointestinal MicrobiomeHomeostasisImmunoglobulin AInflammatory Bowel DiseasesAdultAkkermansiaFemaleHumansImmunoglobulin A, SecretoryIntestinal MucosaMalePlasma CellsImmunoglobulin AImmunoglobulin A, Secretory

Identifiers

PMID39560666
PMCPMC11577441

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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.