Evidence map›Paper›PMID 27757307›Full record

ArticleOncoimmunology

CD1b-autoreactive T cells recognize phospholipid antigens and contribute to antitumor immunity against a CD1b

Sreya Bagchi, Sha Li, Chyung-Ru Wang

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Novel Molecular Insights into Human Lipid-Mediated T Cell Immunity.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Prognostic Value ofInternational journal of environmental research and public health · 2019
    Article
  12. Review
  13. Review
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  16. 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

3 authors at 1 institution in 1 country.

Sreya BagchiDepartment of Microbiology and Immunology, Northwestern University , Chicago, IL, USA.
Sha LiDepartment of Microbiology and Immunology, Northwestern University, Chicago, IL, USA; Department of Microbiology, Cornell University, Ithaca, NY, USA.
Chyung-Ru WangDepartment of Microbiology and Immunology, Northwestern University , Chicago, IL, USA.
Northwestern University · US

Funding

The Role of Group 1 CD1-restricted T Cells in Infectious DiseaseR01AI057460 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 2004 to 2020
$5.7M
Group 1 CD1-restricted Autoreactive T cells in Inflammatory DiseaseR21AI117238 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WANG, CHYUNG-RU · 2015 to 2016
$411k
NIAID NIH HHS R01 AI057460NIAID NIH HHS R21 AI117238
6 · The paper itself

Abstract

Adoptive immunotherapy for cancer treatment is an emerging field of study. Till now, several tumor-derived, peptide-specific T cell responses have been harnessed for treating cancers. However, the contribution of lipid-specific T cells in tumor immunity has been understudied. CD1 molecules, which present self- and foreign lipid antigens to T cells, are divided into group 1 (CD1a, CD1b, and CD1c) and group 2 (CD1d). Although the role of CD1d-restricted natural killer T cells (NKT) in several tumor models has been well established, the contribution of group 1 CD1-restricted T cells in tumor immunity remains obscure due to the lack of group 1 CD1 expression in mice. In this study, we used a double transgenic mouse model expressing human group 1 CD1 molecules (hCD1Tg) and a CD1b-restricted, self-lipid reactive T cell receptor (HJ1Tg) to study the potential role of group 1 CD1-restricted autoreactive T cells in antitumor response. We found that HJ1 T cells recognized phospholipids and responded more potently to lipid extracted from tumor cells than the equivalent amount of lipids extracted from normal cells. Additionally, the autoreactivity of HJ1 T cells was enhanced upon treatment with various intracellular toll-like receptor (TLR) agonists, including CpG oligodeoxynucleotides (ODN), R848, and poly (I:C). Interestingly, the adoptive transfer of HJ1 T cells conferred protection against the CD1b-transfected murine T cell lymphoma (RMA-S/CD1b) and CpG ODN enhanced the antitumor effect. Thus, this study, for the first time, demonstrates the antitumor potential of CD1b-autoreactive T cells and their potential use in adoptive immunotherapy.

Indexed as

Autoreactive T cellsCD1CpGself-lipidstumor immunity

Identifiers

PMID27757307
PMCPMC5048778
OpenAlexW2490440257

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.