Evidence map›Paper›PMID 30789961›Full record

ReviewPLoS pathogens2019

Casting a wider net: Immunosurveillance by nonclassical MHC molecules.

M Patricia D'Souza, Erin Adams, John D Altman, Michael E Birnbaum, Cesar Boggiano, Giulia Casorati, Yueh-Hsiu Chien, Anthony Conley, Sidonia Barbara Guiomar Eckle, Klaus Früh and 15 more

Abstract readReview
In one paragraph

Review in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Review
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  11. Review
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  14. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  15. Intracellular trafficking of HLA-E and its regulation.The Journal of experimental medicine · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. 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

25 authors.

M Patricia D'SouzaDivision of AIDS, NIAID, Bethesda, Maryland, United States of America.
Erin AdamsUniversity of Chicago, Chicago, Illinois, United States of America.
John D AltmanEmory University, Atlanta, Georgia, United States of America.
Michael E BirnbaumMassachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Cesar BoggianoDivision of AIDS, NIAID, Bethesda, Maryland, United States of America.ORCID 0000-0002-5503-8335
Giulia CasoratiSan Raffaele Scientific Institute, Milano, Italy.ORCID 0000-0002-5102-4112
Yueh-Hsiu ChienStanford University, Stanford, California, United States of America.
Anthony ConleyDivision of AIDS, NIAID, Bethesda, Maryland, United States of America.
Sidonia Barbara Guiomar EcklePeter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia.ORCID 0000-0003-0766-171X
Klaus FrühOregon Health & Science University, Portland, Oregon, United States of America.
Timothy Gondré-LewisDivision of Allergy, Immunology and Transplantation, NIAID, Bethesda, Maryland, United States of America.ORCID 0000-0003-2327-7734
Namir HassanImmunocore Limited, Abingdon, United Kingdom.
Huang HuangStanford University, Stanford, California, United States of America.
Lakshmi JayashankarColumbus Technologies, Contractor to NIAID, Bethesda, Maryland, United States of America.
Anne G KasmarBill & Melinda Gates Foundation, Seattle, Washington, United States of America.ORCID 0000-0001-6292-1612
Nina KunwarDivision of AIDS, NIAID, Bethesda, Maryland, United States of America.
Judith LavelleOfficer of the Director, NIAID, Bethesda, Maryland, United States of America.
David M LewinsohnOregon Health & Science University, Portland, Oregon, United States of America.
Branch MoodyBrigham and Women's Hospital, Boston, Massachusetts, United States of America.
Louis PickerOregon Health & Science University, Portland, Oregon, United States of America.
Lakshmi RamachandraDivision of Allergy, Immunology and Transplantation, NIAID, Bethesda, Maryland, United States of America.
Nilabh ShastriUniversity of California, Berkeley, California, United States of America.
Peter ParhamStanford University, Stanford, California, United States of America.
Andrew J McMichaelUniversity of Oxford, Oxford, United Kingdom.
Jonathan W YewdellLaboratory of Viral Diseases, NIAID, Bethesda, Maryland, United States of America.

Funding

Translation in ImmunityZIAAI001210 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI YEWDELL, JONATHAN W · 2016 to 2025
$12.5M
Immunobiology and Virology of Influenza A VirusZIAAI001211 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI YEWDELL, JONATHAN W · 2016 to 2025
$10.4M
Viral Testing CoreU42OD010426 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Andrew Haertel, Lauren Drew Martin · 2013 to 2026
$6.0M
NIH HHS U42 OD010426
6 · The paper itself

Abstract

Most studies of T lymphocytes focus on recognition of classical major histocompatibility complex (MHC) class I or II molecules presenting oligopeptides, yet there are numerous variations and exceptions of biological significance based on recognition of a wide variety of nonclassical MHC molecules. These include αβ and γδ T cells that recognize different class Ib molecules (CD1, MR-1, HLA-E, G, F, et al.) that are nearly monomorphic within a given species. Collectively, these T cells can be considered "unconventional," in part because they recognize lipids, metabolites, and modified peptides. Unlike classical MHC-specific cells, unconventional T cells generally exhibit limited T-cell antigen receptor (TCR) repertoires and often produce innate immune cell-like rapid effector responses. Exploiting this system in new generation vaccines for human immunodeficiency virus (HIV), tuberculosis (TB), other infectious agents, and cancer was the focus of a recent workshop, "Immune Surveillance by Non-classical MHC Molecules: Improving Diversity for Antigens," sponsored by the National Institute of Allergy and Infectious Diseases. Here, we summarize salient points presented regarding the basic immunobiology of unconventional T cells, recent advances in methodologies to measure unconventional T-cell activity in diseases, and approaches to harness their considerable clinical potential.

Indexed as

AnimalsAntigensHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHLA AntigensHumansImmunologic SurveillanceMajor Histocompatibility ComplexReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesAntigensHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHLA AntigensReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID30789961
PMCPMC6383864

What OpenQuestion holds

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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.