Evidence map›Paper›PMID 26320061›Full record

ReviewSeminars in oncology2015

Enhancing Cancer Immunotherapy Via Activation of Innate Immunity.

Jacob L Goldberg, Paul M Sondel

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  10. Circadian clock: a regulator of the immunity in cancer.Cell communication and signaling : CCS · 2021
    Review
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  12. Article
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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

2 authors at 1 institution in 1 country.

Jacob L GoldbergDepartment of Pediatrics, The University of Wisconsin, Madison WI.
Paul M SondelDepartment of Pediatrics, The University of Wisconsin, Madison WI; Department of Human Oncology, The University of Wisconsin, Madison WI; Department of Genetics, The University of Wisconsin, Madison WI. Electronic address: pmsondel@humonc.wisc.edu.
University of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
Enhancing Antibody-directed Innate Immunity to Improve Cancer OutcomeR35CA197078 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SONDEL, PAUL M · 2015 to 2021
$6.4M
THE IMMUNOBIOLOGY OF HUMAN ANTILEUKEMIC LYMPHOCYTESR01CA032685 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SONDEL, PAUL M · 1985 to 2014
$4.3M
T-Cell Independent Antitumor Mechanisms of CD40 LigationR01CA087025 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SONDEL, PAUL M · 2002 to 2012
$2.4M
Institutional Clinical and Translational Science Award (UW-Madison)(TL1)TL1RR025013 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$1.1M
The Role of KIR and FcR Genotype in the Efficacy of mAb and IL2 ImmunotherapyR01CA166105 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SONDEL, PAUL M · 2012 to 2014
$987k
Falgellar gene homologues in Brucella melitensisF31GM067386 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI SOTO-BONILLA, BRENDA L · 2002 to 2009
$193k
Howard Hughes Medical InstituteNCI NIH HHS CA032685NCI NIH HHS CA14520NCI NIH HHS CA166105NCI NIH HHS CA87025NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA032685NCI NIH HHS R01 CA087025NCI NIH HHS R01 CA166105NCI NIH HHS R35 CA197078NCRR NIH HHS 1TL1RR025013-01NCRR NIH HHS TL1 RR025013NIGMS NIH HHS F31 GM067386NIGMS NIH HHS GM067386
6 · The paper itself

Abstract

Given recent technological advances and advances in our understanding of cancer, immunotherapy of cancer is being used with clear clinical benefit. The immunosuppression accompanying cancer itself, as well as with current cancer treatment with radiation or chemotherapy, impairs adaptive immune effectors to a greater extent than innate effector cells. In addition to being less suppressed, innate immune cells are capable of being enhanced via immune-stimulatory regimens. Most strategies being investigated to promote innate immune responses against cancer do not require complex, patient-specific, ex vivo cellular or molecular creation of therapeutic agents; thus they can, generally, be used as "off the shelf" therapeutics that could be administered by most cancer clinics. Successful applications of innate immunotherapy in the clinic have effectively targeted components of the innate immune response. Preclinical data demonstrate how initiation of innate immune responses can lead to subsequent adaptive long-term cancer immunity. We hypothesize that integration of innate immune activation strategies into combination therapies for cancer treatment will lead to more effective and long-term clinical benefit.

Indexed as

Adaptive ImmunityAnimalsCancer VaccinesHumansImmunity, InnateImmunosuppression TherapyImmunotherapyNeoplasmsCancer Vaccines

Identifiers

PMID26320061
PMCPMC4555881
OpenAlexW2159648765

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.