Evidence map›Paper›PMID 21670315›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Activated NKT cells and NK cells render T cells resistant to myeloid-derived suppressor cells and result in an effective adoptive cellular therapy against breast cancer in the FVBN202 transgenic mouse.

Maciej Kmieciak, Debasmita Basu, Kyle K Payne, Amir Toor, Adly Yacoub, Xiang-Yang Wang, Lisa Smith, Harry D Bear, Masoud H Manjili

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Trial
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  10. Gr1Journal of leukocyte biology · 2018
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  17. Tumour Microenvironment: Overview with an Emphasis on the Colorectal Liver Metastasis Pathway.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2015
    Article
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  19. 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

9 authors.

Maciej KmieciakDepartment of Microbiology and Immunology, Virginia Commonwealth University, Massey Cancer Center, Richmond, VA 23298, USA.
Debasmita Basu
Kyle K Payne
Amir Toor
Adly Yacoub
Xiang-Yang Wang
Lisa Smith
Harry D Bear
Masoud H Manjili

Funding

Large Stress Proteins in Biology and MedicineR01CA154708 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2011 to 2015
$1.5M
Enhancement of HER-2/neu-based therapy using HSP110R01CA104757 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI MANJILI, MASOUD H. · 2005 to 2008
$912k
NCI NIH HHS R01 CA104757NCI NIH HHS R01 CA154708
6 · The paper itself

Abstract

Attempts to cure breast cancer by adoptive cellular therapy (ACT) have not been successful. This is primarily due to the presence of tumor-induced immune-suppressive mechanisms as well as the failure of tumor-reactive T cells to provide long-term memory responses in vivo. To address these clinically important challenges, we developed an ex vivo protocol for the expansion of tumor-reactive immune cells obtained from tumor-bearing animals prior to or after local radiation therapy. We used an Ag-free protocol that included bryostatin 1/ionomycin and sequential common γ-chain cytokines (IL-7/IL-15 + IL-2). The proposed protocol expanded tumor-reactive T cells as well as activated non-T cells, including NKT cells, NK cells, and IFN-γ-producing killer dendritic cells. Antitumor efficacy of T cells depended on the presence of non-T cells. The effector non-T cells also rendered T cells resistant to myeloid-derived suppressor cells. Radiation therapy altered phenotypic distribution and differentiation of T cells as well as their ability to generate central memory T cells. ACT by means of the expanded cells protected animals from tumor challenge and generated long-term memory responses against the tumor, provided that leukocytes were derived from tumor-bearing animals prior to radiation therapy. The ex vivo protocol was also able to expand HER-2/neu-specific T cells derived from the PBMC of a single patient with breast carcinoma. These data suggest that the proposed ACT protocol should be studied further in breast cancer patients.

Indexed as

AnimalsCell Line, TumorCells, CulturedCoculture TechniquesCytotoxicity Tests, ImmunologicErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunity, InnateImmunologic MemoryImmunotherapy, AdoptiveKiller Cells, NaturalLymphocyte ActivationMammary Neoplasms, ExperimentalMiceMice, TransgenicErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID21670315
PMCPMC3131490

What OpenQuestion holds

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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.