Evidence map›Paper›PMID 23225891›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Immune-mediated regression of established B16F10 melanoma by intratumoral injection of attenuated Toxoplasma gondii protects against rechallenge.

Jason R Baird, Katelyn T Byrne, Patrick H Lizotte, Seiko Toraya-Brown, Uciane K Scarlett, Matthew P Alexander, Mee Rie Sheen, Barbara A Fox, David J Bzik, Marcus Bosenberg and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Pooled it
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  16. Parasites revive hope for cancer therapy.European journal of medical research · 2024
    Review
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27 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

13 authors at 3 institutions in 1 country.

Jason R BairdDepartment of Microbiology and Immunology, Dartmouth Medical School, Hanover, NH 03755, USA.
Katelyn T Byrne
Patrick H Lizotte
Seiko Toraya-Brown
Uciane K Scarlett
Matthew P Alexander
Mee Rie Sheen
Barbara A Fox
David J Bzik
Marcus Bosenberg
David W Mullins
Mary Jo Turk
Steven Fiering
Dartmouth College · USUSC Norris Comprehensive Cancer Center · USYale University · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
Toxicology, Pathology and Biodistribution Core (TPB Core)U54CA151662 · NCI · DARTMOUTH COLLEGE · PI POGUE, BRIAN WILLIAM · 2010 to 2014
$11.6M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
T GONDII--PYRIMIDINE SYNTHESIS AS A CHEMOTHERAPY TARGETR01AI041930 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 1997 to 2013
$4.2M
Mechanisms of concomitant tumor immunity and autoimmunityR01CA120777 · NCI · DARTMOUTH COLLEGE · PI TURK, MARY JO · 2006 to 2016
$2.5M
Role of CXCR3 for CD8+ T cells in cancer immunotherapyR01CA134799 · NCI · UNIVERSITY OF VIRGINIA · PI MULLINS, DAVID W. · 2009 to 2013
$1.6M
CENTER FOR MOLECULAR, CELLULAR, AND TRANSLATIONAL IMMUNOLOGYP30RR032136 · NCRR · DARTMOUTH COLLEGE · PI GREEN, WILLIAM R · 2011 to 2011
$1.2M
Regulated virulence and cyst maturation in Toxoplasma gondiiR21AI075931 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 2008 to 2009
$440k
Enhanced homologous recombination in Toxoplasma gondiiR21AI073142 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 2007 to 2008
$435k
Genetic models for post-genome functional analysis of Toxoplasma gondiiR21AI084570 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 2009 to 2010
$435k
Genetic dissection of the Toxoplasma gondii rhoptry kinomeR21AI097018 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 2011 to 2012
$435k
Functional analysis of CD8 T cell immune control in Toxoplasma gondii infectionR21AI091461 · NIAID · DARTMOUTH COLLEGE · PI BZIK, DAVID J · 2010 to 2011
$432k
NCI NIH HHS 5P30CA023108NCI NIH HHS CA120777NCI NIH HHS CA134799NCI NIH HHS P30 CA023108NCI NIH HHS R01 CA120777NCI NIH HHS R01 CA134799NCI NIH HHS U54 CA151662NCI NIH HHS U54CA151662NCRR NIH HHS 1P30RR032136NCRR NIH HHS P30 RR032136NIAID NIH HHS AI041930NIAID NIH HHS R01 AI041930NIAID NIH HHS R21 AI073142NIAID NIH HHS R21 AI075931NIAID NIH HHS R21 AI084570NIAID NIH HHS R21 AI091461NIAID NIH HHS R21 AI097018NIAID NIH HHS T32 AI007363
6 · The paper itself

Abstract

Immune recognition of tumors can limit cancer development, but antitumor immune responses are often blocked by tumor-mediated immunosuppression. Because microbes or microbial constituents are powerful adjuvants to stimulate immune responses, we evaluated whether intratumoral administration of a highly immunogenic but attenuated parasite could induce rejection of an established poorly immunogenic tumor. We treated intradermal B16F10 murine melanoma by intratumoral injection of an attenuated strain of Toxoplasma gondii (cps) that cannot replicate in vivo and therefore is not infective. The cps treatment stimulated a strong CD8(+) T cell-mediated antitumor immune response in vivo that regressed established primary melanoma. The cps monotherapy rapidly modified the tumor microenvironment, halting tumor growth, and subsequently, as tumor-reactive T cells expanded, the tumors disappeared and rarely returned. The treatment required live cps that could invade cells and also required CD8(+) T cells and NK cells, but did not require CD4(+) T cells. Furthermore, we demonstrate that IL-12, IFN-γ, and the CXCR3-stimulating cytokines are required for full treatment efficacy. The treatment developed systemic antitumor immune activity as well as antitumor immune memory and therefore might have an impact against human metastatic disease. The approach is not specific for either B16F10 or melanoma. Direct intratumoral injection of cps has efficacy against an inducible genetic melanoma model and transplantable lung and ovarian tumors, demonstrating potential for broad clinical use. The combination of efficacy, systemic antitumor immune response, and complete attenuation with no observed host toxicity demonstrates the potential value of this novel cancer therapy.

Indexed as

Adjuvants, ImmunologicAnimalsCancer VaccinesCell Line, TumorInjections, IntradermalMelanoma, ExperimentalMiceMice, Inbred C57BLMice, Inbred NODMice, KnockoutMice, SCIDMice, TransgenicNeoplasm Recurrence, LocalSkin NeoplasmsToxoplasmaTumor EscapeAdjuvants, ImmunologicCancer VaccinesVaccines, Attenuated

Identifiers

PMID23225891
PMCPMC3529845
OpenAlexW2096288074

What OpenQuestion holds

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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.