Evidence map›Paper›PMID 21646050›Full record

ReviewClinical immunology (Orlando, Fla.)2011

Developing understanding of the roles of CD1d-restricted T cell subsets in cancer: reversing tumor-induced defects.

Mark A Exley, Lydia Lynch, Bindu Varghese, Michael Nowak, Nadia Alatrakchi, Steven P Balk

Open access · greenAbstract readReview
In one paragraph

Review in Clinical immunology (Orlando, Fla.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

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  17. Advances in NKT cell Immunotherapy for Glioblastoma.Journal of cancer science & therapy · 2018
    Article
  18. Review
  19. Adoptive Transfer of Invariant NKT Cells as Immunotherapy for Advanced Melanoma: A Phase I Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  20. 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

6 authors at 2 institutions in 1 country.

Mark A ExleyDepartment of Medicine, Division of Hematology/Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. mexley@bidmc.harvard.edu
Lydia Lynch
Bindu Varghese
Michael Nowak
Nadia Alatrakchi
Steven P Balk
Beth Israel Deaconess Medical Center · USHarvard University · US

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI GARRAWAY, LEVI A. · 2002 to 2017
$36.2M
Viral, T Cell, &Cytokine Determinants of Stellate CellU19AI066313 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KOZIEL, MARGARET J · 2005 to 2009
$2.6M
CTRIP: Treatment of Sickle Cell Crisis with inhibitors of NKT cell activationRC2HL101367 · NHLBI · DANA-FARBER CANCER INST · PI LINDEN, JOEL M., NATHAN, DAVID G. · 2009 to 2010
$1.8M
Innate-like hepatic CD1d-reative NKT cells:Liver DiseaseR01DK066917 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI EXLEY, MARK A · 2004 to 2008
$1.1M
Regulation of hepatic NKT cells by CDld+ liver cellsR21CA143748 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI EXLEY, MARK A · 2010 to 2011
$410k
NCI NIH HHS P50 CA090381NCI NIH HHS R21 CA143748NHLBI NIH HHS RC2 HL101367NIAID NIH HHS U19 AI066313NIAID NIH HHS U19 AI082630NIDDK NIH HHS R01 DK066917
6 · The paper itself

Abstract

Invariant natural killer T-cells ('iNKT') are the best-known CD1d-restricted T-cells, with recently-defined roles in controlling adaptive immunity. CD1d-restricted T-cells can rapidly produce large amounts of Th1 and/or Th2//Treg/Th17-type cytokines, thereby regulating immunity. iNKT can stimulate potent anti-tumor immune responses via production of Th1 cytokines, direct cytotoxicity, and activation of effectors. However, Th2//Treg-type iNKT can inhibit anti-tumor activity. Furthermore, iNKT are decreased and/or reversibly functionally impaired in many advanced cancers. In some cases, CD1d-restricted T-cell cancer defects can be traced to CD1d(+) tumor interactions, since hematopoietic, prostate, and some other tumors can express CD1d. Ligand and IL-12 can reverse iNKT defects and therapeutic opportunities exist in correcting such defects alone and in combination. Early stage clinical trials have shown potential for reconstitution of iNKT IFN-gamma responses and evidence of activity in a subset of patients, with rational new approaches to capitalize on this progress ongoing, as will be discussed here.

Indexed as

Antigen-Presenting CellsAntigens, CD1dCytokinesGalactosylceramidesHumansLymphocyte ActivationModels, ImmunologicalNatural Killer T-CellsNeoplasmsT-Lymphocyte SubsetsAntigens, CD1dCytokinesGalactosylceramides

Identifiers

PMID21646050
PMCPMC3143311
OpenAlexW2081254732

What OpenQuestion holds

Textmetadata
LicenceTDM
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.