Evidence map›Paper›PMID 39024572›Full record

ArticleJCI insight2024

Mucosal signatures of pathogenic T cells in HLA-B*27+ anterior uveitis and axial spondyloarthritis.

Michael A Paley, Xinbo Yang, Lynn M Hassman, Frank Penkava, Lee I Garner, Grace L Paley, Nicole Linskey, Ryan Agnew, Paulo Henrique Arantes de Faria, Annie Feng and 13 more

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Exhaustion-Resistant CD8Immunology · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
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

23 authors.

Michael A PaleyDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Xinbo YangDepartments of Molecular and Cellular Physiology and Structural Biology, Stanford University School of Medicine, Stanford, California, USA.
Lynn M HassmanDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.
Frank PenkavaNuffield Department of Orthopaedics Rheumatology and Musculoskeletal Science, Botnar Research Center.
Lee I GarnerNDM Research Building, Nuffield Department of Medicine, and.
Grace L PaleyDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.
Nicole LinskeyDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Ryan AgnewDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Paulo Henrique Arantes de FariaDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Annie FengDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Sophia Y LiDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Davide SimoneNuffield Department of Orthopaedics Rheumatology and Musculoskeletal Science, Botnar Research Center.
Elisha DO RobersonDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Philip A RuzyckiDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.
Ekaterina EsaulovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Jennifer LaurentDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Lacey Feigl-LenzenDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Luke E SpringerDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Chang LiuDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Geraldine M GillespieNDM Research Building, Nuffield Department of Medicine, and.
Paul BownessNuffield Department of Orthopaedics Rheumatology and Musculoskeletal Science, Botnar Research Center.
K Christopher GarciaDepartments of Molecular and Cellular Physiology and Structural Biology, Stanford University School of Medicine, Stanford, California, USA.
Wayne M YokoyamaDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Christine T. Pham · 2018 to 2026
$7.6M
Structural correlates of T cell receptor signalingR01AI103867 · NIAID · STANFORD UNIVERSITY · PI Kenan Christopher GARCIA · 2014 to 2026
$5.3M
Resolution of ocular inflammation: the role of type 1 conventional dendritic cellsK08EY033045 · NEI · WASHINGTON UNIVERSITY · PI Lynn M Hassman · 2022 to 2026
$1.1M
Identification of Pathogenic T cells in Axial SpondyloarthritisK08AR079593 · NIAMS · WASHINGTON UNIVERSITY · PI Michael Alexander Paley · 2022 to 2026
$774k
NEI NIH HHS K08 EY033045NIAID NIH HHS R01 AI103867NIAID NIH HHS U19 AI057229NIAMS NIH HHS K08 AR079593NIAMS NIH HHS P30 AR073752UK Medical Research Council MR/M019837/1Wellcome Centre for Human Genetics (Wellcome Trust 203141/Z/16/ZWellcome Trust
6 · The paper itself

Abstract

HLA-B*27 was one of the first HLA alleles associated with an autoimmune disease, i.e., axial spondyloarthritis (axSpA) and acute anterior uveitis (B27AAU), which cause joint and eye inflammation, respectively. Gastrointestinal inflammation has been suggested as a trigger of axSpA. We recently identified a bacterial peptide (YeiH) that can be presented by HLA-B*27 to expanded public T cell receptors in the joint in axSpA and the eye in B27AAU. While YeiH is present in enteric microbiota and pathogens, additional evidence that pathogenic T cells in HLA-B*27-associated autoimmunity may have had a prior antigenic encounter within the gastrointestinal tract remains lacking. Here, we analyzed ocular, synovial, and blood T cells in B27AAU and axSpA, showing that YeiH-specific CD8+ T cells express a mucosal gene set and surface proteins consistent with intestinal differentiation, including CD161, integrin α4β7, and CCR6. In addition, we found an expansion of YeiH-specific CD8+ T cells in axSpA and B27AAU blood compared with that from individuals acting as healthy controls, whereas influenza-specific CD8+ T cells were equivalent across groups. Finally, we demonstrated the dispensability of TRBV9 for antigen recognition. Collectively, our data suggest that, in HLA-B27-associated autoimmunity, early antigen exposure and differentiation of pathogenic CD8+ T cells may occur in enteric organs.

Indexed as

Axial SpondyloarthritisHLA-B27 AntigenReceptors, CCR6Uveitis, AnteriorAdultCD8-Positive T-LymphocytesFemaleHumansIntegrinsMaleMiddle AgedCCR6 protein, humanHLA-B27 Antigenintegrin alpha4beta7IntegrinsReceptors, CCR6AutoimmunityRheumatologyT cell receptorT cells

Identifiers

PMID39024572
PMCPMC11343591

What OpenQuestion holds

Textmetadata
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.