Evidence map›Paper›PMID 27393665›Full record

ReviewImmunogenetics2016

Immunotherapeutic strategies targeting natural killer T cell responses in cancer.

Susannah C Shissler, Dominique R Bollino, Irina V Tiper, Joshua P Bates, Roshanak Derakhshandeh, Tonya J Webb

Open access · greenAbstract readReview
In one paragraph

Review in Immunogenetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Immunopathogenesis of Sarcoidosis.Seminars in respiratory and critical care medicine · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Invariant Natural Killer T-cell Dynamics in Human Immunodeficiency Virus-associated Tuberculosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  11. Article
  12. Review
  13. Immune evasion of the CD1d/NKT cell axis.Current opinion in immunology · 2018
    Review
  14. Article
  15. Article
  16. Review
  17. Targeting TDO in cancer immunotherapy.Medical oncology (Northwood, London, England) · 2017
    Review
  18. Article
  19. Review
  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.

Susannah C ShisslerDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA.
Dominique R BollinoDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA.
Irina V TiperDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA.
Joshua P BatesDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA.
Roshanak DerakhshandehDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA.
Tonya J WebbDepartment of Microbiology and Immunology, University of Maryland School of Medicine and the Marlene and Stewart Greenebaum Cancer Center, 685 West Baltimore St; HSF I-Room 380, Baltimore, MD, 21201, USA. twebb@som.umaryland.edu.
HJF Medical Research International · USUniversity of Maryland, Baltimore · US

Funding

Signaling Pathways in Innate ImmunityT32AI095190 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Stefanie N. Vogel · 2012 to 2026
$4.7M
Generation of NKT cells from adult stem cells for adoptive immunotherapyR21CA184469 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI WEBB, TONYA J. · 2015 to 2016
$367k
NKT cells with chimeric antigen receptorsR21CA199544 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI WEBB, TONYA J. · 2015 to 2016
$367k
NCI NIH HHS R21 CA184469NCI NIH HHS R21 CA199544NIAID NIH HHS T32 AI095190
6 · The paper itself

Abstract

Natural killer T (NKT) cells are a unique subset of lymphocytes that bridge the innate and adaptive immune system. NKT cells possess a classic αβ T cell receptor (TCR) that is able to recognize self and foreign glycolipid antigens presented by the nonclassical class I major histocompatibility complex (MHC) molecule, CD1d. Type I NKT cells (referred to as invariant NKT cells) express a semi-invariant Vα14Jα18 TCR in mice and Vα24Jα18 TCR in humans. Type II NKT cells are CD1d-restricted T cells that express a more diverse set of TCR α chains. The two types of NKT cells often exert opposing effects especially in tumor immunity, where type II cells generally suppress tumor immunity while type I NKT cells can enhance anti-tumor immune responses. In this review, we focus on the role of NKT cells in cancer. We discuss their effector and suppressive functions, as well as describe preclinical and clinical studies utilizing therapeutic strategies focused on harnessing their potent anti-tumor effector functions, and conclude with a discussion on potential next steps for the utilization of NKT cell-targeted therapies for the treatment of cancer.

Indexed as

AnimalsHumansMiceNatural Killer T-CellsNeoplasmsReceptors, Antigen, T-CellT-Lymphocyte SubsetsReceptors, Antigen, T-CellCancer immunotherapyCD1dNKT cellsα-Galactosylceramide

Identifiers

PMID27393665
PMCPMC5580089
OpenAlexW2470318030

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.