Evidence map›Paper›PMID 38275935›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2024

Multiple Isomers of Photolumazine V Bind MR1 and Differentially Activate MAIT Cells.

Jason R Krawic, Nicole A Ladd, Meghan Cansler, Curtis McMurtrey, Jordan Devereaux, Aneta Worley, Tania Ahmed, Cara Froyd, Corinna A Kulicke, Gwendolyn Swarbrick and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

14 authors at 5 institutions in 1 country.

Jason R KrawicDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK.ORCID 0000-0003-0103-0212
Nicole A LaddDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL.
Meghan CanslerDepartment of Pediatrics, Oregon Health and Sciences University, Portland, OR.
Curtis McMurtreyPure MHC, Oklahoma City, OK.ORCID 0000-0003-4540-4140
Jordan DevereauxOregon Health and Sciences University Medicinal Chemistry Core, Portland, OR.ORCID 0000-0002-8542-7411
Aneta WorleyResearch and Development, VA Portland Health Care System, Portland, OR.ORCID 0009-0009-9772-8658
Tania AhmedDepartment of Pediatrics, Oregon Health and Sciences University, Portland, OR.
Cara FroydDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL.
Corinna A KulickeDivision of Pulmonary, Allergy, and Critical Care Medicine, Oregon Health & Science University, Por.ORCID 0000-0002-4217-3095
Gwendolyn SwarbrickDepartment of Pediatrics, Oregon Health and Sciences University, Portland, OR.ORCID 0000-0001-5786-1256
Aaron NilsenOregon Health and Sciences University Medicinal Chemistry Core, Portland, OR.ORCID 0000-0002-3827-8222
David M LewinsohnResearch and Development, VA Portland Health Care System, Portland, OR.
Erin J AdamsDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL.
William HildebrandDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Oregon Health & Science University · USUniversity of Illinois Chicago · USUniversity of Oklahoma Health Sciences Center · USPure Protein (United States) · USVA Portland Health Care System · US

Funding

T cell recognition of the MR1 presented microbial metabolomeR01AI147954 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE, HILDEBRAND, WILLIAM · 2019 to 2023
$7.3M
Lung Resident, MR1-Restricted T Cells: Association with Differential Outcomes Following Exposure to M. TuberculosisR01AI134790 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DAVID M., WALZL, GERHARD · 2018 to 2022
$3.3M
NIAID NIH HHS R01 AI134790NIAID NIH HHS R01 AI147954
6 · The paper itself

Abstract

In response to microbial infection, the nonclassical Ag-presenting molecule MHC class I-related protein 1 (MR1) presents secondary microbial metabolites to mucosal-associated invariant T (MAIT) cells. In this study, we further characterize the repertoire of ligands captured by MR1 produced in Hi5 (Trichoplusia ni) cells from Mycobacterium smegmatis via mass spectrometry. We describe the (to our knowledge) novel MR1 ligand photolumazine (PL)V, a hydroxyindolyl-ribityllumazine with four isomers differing in the positioning of a hydroxyl group. We show that all four isomers are produced by M. smegmatis in culture and that at least three can induce MR1 surface translocation. Furthermore, human MAIT cell clones expressing distinct TCR β-chains differentially responded to the PLV isomers, demonstrating that the subtle positioning of a single hydroxyl group modulates TCR recognition. This study emphasizes structural microheterogeneity within the MR1 Ag repertoire and the remarkable selectivity of MAIT cell TCRs.

Indexed as

Mucosal-Associated Invariant T CellsHistocompatibility Antigens Class IHumansMinor Histocompatibility AntigensReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaHistocompatibility Antigens Class IMinor Histocompatibility AntigensMR1 protein, humanReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID38275935
PMCPMC10909690
OpenAlexW4391255793

What OpenQuestion holds

Textmetadata
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.