Evidence map›Paper›PMID 20693851›Full record

ReviewCancer journal (Sudbury, Mass.)

Toll-like receptor agonists: are they good adjuvants?

Sacha Gnjatic, Nikhil B Sawhney, Nina Bhardwaj

Abstract readReview
In one paragraph

Review in Cancer journal (Sudbury, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 10% 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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 163 citations in OpenAlex.

  1. Pooled it
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  17. Therapeutic applications of toll-like receptors (TLRs) agonists in AML.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  18. Review
  19. Article
  20. Article

21 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Sacha GnjaticLudwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York City, NY, USA.
Nikhil B Sawhney
Nina Bhardwaj
Memorial Sloan Kettering Cancer Center · USNewark Academy · US

Funding

Thymic output, lymphocyte activation and turnoverP01AI057127 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI VALENTINE, FRED T · 2004 to 2009
$9.0M
Induction of Immunity by Non-Replicating HIV-1R37AI044628 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHARDWAJ, NINA · 2004 to 2014
$4.2M
Dendritic Cell mediated induction of Anti-HCV immunityR01AI061684 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHARDWAJ, NINA · 2004 to 2008
$2.9M
Modulating Immunity through Dendritic Cell Phagocytic ReceptorsR01AI071078 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHARDWAJ, NINA · 2008 to 2011
$1.7M
Immunosuppressive pathways in acute HIV infectionRC1AI087097 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BHARDWAJ, NINA · 2009 to 2010
$959k
NIAID NIH HHS 1RC1AI087097NIAID NIH HHS 3R37AI044628-11S1NIAID NIH HHS 4R37AI044628NIAID NIH HHS 5P01AI057127NIAID NIH HHS 5R01AI06684NIAID NIH HHS 5R01AI071078NIAID NIH HHS P01 AI057127NIAID NIH HHS R01 AI061684NIAID NIH HHS R01 AI071078NIAID NIH HHS R37 AI044628NIAID NIH HHS RC1 AI087097
6 · The paper itself

Abstract

Therapeutic immunization leading to cancer regression remains a significant challenge. Successful immunization requires activation of adaptive immunity, including tumor specific CD4 T cells and CD8 T cells. Generally, the activation of T cells is compromised in patients with cancer because of immune suppression, loss of tumor antigen expression, and dysfunction of antigen-presenting cells. Antigen-presenting cells such as dendritic cells (DCs) are key for the induction of adaptive antitumor immune responses. Recently, attention has focused on novel adjuvants that enhance dendritic cell function and their ability to prime T cells. Agonists that target toll-like receptors are being used clinically either alone or in combination with tumor antigens and showing initial success both in terms of enhancing immune responses and eliciting antitumor activity. This review summarizes the application of these adjuvants to treat cancer and the potential for boosting responses in vivo.

Indexed as

Adjuvants, ImmunologicHumansNeoplasmsToll-Like ReceptorsAdjuvants, ImmunologicToll-Like Receptors

Identifiers

PMID20693851
PMCPMC2922045
OpenAlexW2041747503

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.