Evidence map›Paper›PMID 37140910›Full record

ArticleThe Journal of experimental medicine2023

Intracellular trafficking of HLA-E and its regulation.

Wanlin He, Ester Gea-Mallorquí, Huw Colin-York, Marco Fritzsche, Geraldine M Gillespie, Simon Brackenridge, Persephone Borrow, Andrew J McMichael

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

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  15. A cytoplasmic motif in HLA-E that drives clathrin-mediated endocytosis and VCP-associated postendocytic trafficking.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

8 authors.

Wanlin HeNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-8117-9692
Ester Gea-MallorquíNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-6915-074X
Huw Colin-YorkKennedy Institute of Rheumatology, University of Oxford , Oxford, UK.ORCID 0000-0002-6585-3237
Marco FritzscheKennedy Institute of Rheumatology, University of Oxford , Oxford, UK.ORCID 0000-0002-8712-7471
Geraldine M GillespieNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-1075-870X
Simon BrackenridgeNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-0587-7560
Persephone BorrowNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-3877-9780
Andrew J McMichaelNuffield Department of Medicine, Center for Immuno-Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-9101-7478

Funding

Collaboratory of AIDS Researchers for Eradication (CARE)UM1AI164567 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2021 to 2026
$31.6M
Collaboratory of AIDS Researchers for Eradication (CARE)UM1AI126619 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARGOLIS, DAVID M. · 2016 to 2020
$23.2M
NIAID NIH HHS UM1 AI126619NIAID NIH HHS UM1 AI164567
6 · The paper itself

Abstract

Interest in MHC-E-restricted CD8+ T cell responses has been aroused by the discovery of their efficacy in controlling simian immunodeficiency virus (SIV) infection in a vaccine model. The development of vaccines and immunotherapies utilizing human MHC-E (HLA-E)-restricted CD8+ T cell response requires an understanding of the pathway(s) of HLA-E transport and antigen presentation, which have not been clearly defined previously. We show here that, unlike classical HLA class I, which rapidly exits the endoplasmic reticulum (ER) after synthesis, HLA-E is largely retained because of a limited supply of high-affinity peptides, with further fine-tuning by its cytoplasmic tail. Once at the cell surface, HLA-E is unstable and is rapidly internalized. The cytoplasmic tail plays a crucial role in facilitating HLA-E internalization, which results in its enrichment in late and recycling endosomes. Our data reveal distinctive transport patterns and delicate regulatory mechanisms of HLA-E, which help to explain its unusual immunological functions.

Indexed as

Histocompatibility Antigens Class IVaccinesAnimalsAntigen PresentationCD8-Positive T-LymphocytesHLA-E AntigensHumansHistocompatibility Antigens Class IHLA-E AntigensVaccines

Identifiers

PMID37140910
PMCPMC10165540

What OpenQuestion holds

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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.