Evidence map›Paper›PMID 11381117›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Dual HLA class I and class II restricted recognition of alloreactive T lymphocytes mediated by a single T cell receptor complex.

M H Heemskerk, R A de Paus, E G Lurvink, F Koning, A Mulder, R Willemze, J J van Rood, J H Falkenburg

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Regulation of NK-Cell Function by HLA Class II.Frontiers in cellular and infection microbiology · 2020
    Article
  5. Targeting cancers through TCR-peptide/MHC interactions.Journal of hematology & oncology · 2019
    Review
  6. Article
  7. Review
  8. Review
  9. Cytotoxic CD8Nature medicine · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Antiviral CD8Immunity · 2016
    Article
  15. Article
  16. Article
  17. Programming CMV for vaccine vector design.Nature biotechnology · 2013
    Article
  18. The human leukocyte antigen-presented ligandome of B lymphocytes.Molecular & cellular proteomics : MCP · 2013
    Article
  19. Article
  20. Tumor vaccines and beyond.Cytotherapy · 2011
    Review
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.

M H HeemskerkDepartment of Hematology, Leiden University Medical Center, C2-R, P.O. Box 9600, 2300 RC Leiden, The Netherlands. m.h.m.heemskerk@lumc.nl
R A de Paus
E G Lurvink
F Koning
A Mulder
R Willemze
J J van Rood
J H Falkenburg

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The alloreactive human T cell clone MBM15 was found to exhibit dual specificity recognizing both an antigen in the context of the HLA class I A2 molecule and an antigen in the context of the HLA class II DR1. We demonstrated that the dual reactivity that was mediated via a single clonal T cell population depended on specific peptide binding. For complete recognition of the HLA-A2-restricted specificity the interaction of CD8 with HLA class I is essential. Interestingly, interaction of the CD8 molecule with HLA class I contributed to the HLA-DR1-restricted specificity. T cell clone MBM15 expressed two in-frame T cell receptor (TCR) Valpha transcripts (Valpha1 and Valpha2) and one TCR Vbeta transcript (Vbeta13). To elucidate whether two TCR complexes were responsible for the dual recognition or one complex, cytotoxic T cells were transduced with retroviral vectors encoding the different TCR chains. Only T cells transduced with the TCR Valpha1Vbeta13 combination specifically recognized both the HLA-A2(+) and HLA-DR1(+) target cells, whereas the Valpha2Vbeta13 combination did not result in a TCR on the cell surface. Thus a single TCRalphabeta complex can have dual specificity, recognizing both a peptide in the context of HLA class I as well as a peptide in the context of HLA class II. Transactivation of T cells by an unrelated antigen in the context of HLA class II may evoke an HLA class I-specific T cell response. We propose that this finding may have major implications for immunotherapeutic interventions and insight into the development of autoimmune diseases.

Indexed as

CD8 AntigensCross ReactionsHLA-A2 AntigenHLA-DR1 AntigenHumansReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesCD8 AntigensHLA-A2 AntigenHLA-DR1 AntigenReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID11381117
PMCPMC34434

What OpenQuestion holds

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Read underepoch 390

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.