Evidence map›Paper›PMID 27377534›Full record

ArticleClinical immunology (Orlando, Fla.)2017

Adoptive transfer of natural killer cells promotes the anti-tumor efficacy of T cells.

Stephen R Goding, Shaohong Yu, Lisa M Bailey, Michael T Lotze, Per H Basse

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Stephen R GodingDepartment of Immunology, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA. Electronic address: sgoding@som.umaryland.edu.
Shaohong YuDepartment of Immunology, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA.
Lisa M BaileyDepartment of Immunology, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA.
Michael T LotzeDepartment of Immunology, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA; Department of Surgery, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA.
Per H BasseDepartment of Immunology, University of Pittsburgh Schools of the Health Sciences, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA; UPCI Cell and Tissue Imaging facility at HCC, University of Pittsburgh Cancer Institute, The Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213-1863, USA. Electronic address: basse@pitt.edu.
UPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
Pancreatic Ductal Adenocarcinoma is a disease of constitutive autophagyR01CA181450 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LOTZE, MICHAEL T, ZEH, HERBERT J · 2014 to 2018
$1.6M
A New Strategy for Targeted Chemoimmunotherapy of CancerR01CA087672 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BASSE, PER H. · 2002 to 2004
$732k
Cytokine Delivery By Tumor-Seeking LymphocytesR01CA104560 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BASSE, PER H. · 2004 to 2006
$672k
NCI NIH HHS P30 CA047904NCI NIH HHS R01 CA087672NCI NIH HHS R01 CA104560NCI NIH HHS R01 CA181450
6 · The paper itself

Abstract

The density of NK cells in tumors correlates positively with prognosis in many types of cancers. The average number of infiltrating NK cells is, however, quite modest (approximately 30 NK cells/sq.mm), even in tumors deemed to have a "high" density of infiltrating NK cells. It is unclear how such low numbers of tumor-infiltrating NK cells can influence outcome. Here, we used ovalbumin-expressing tumor cell lines and TCR transgenic, OVA-specific cytotoxic T lymphocytes (OT-I-CTLs) to determine whether the simultaneous attack by anti-tumor CTLs and IL-2-activated NK (A-NK) cells synergistically increases the overall tumor cell kill and whether upregulation of tumor MHC class-I by NK cell-derived interferon-gamma (IFNγ) improves tumor-recognition and kill by anti-tumor CTLs. At equal E:T ratios, A-NK cells killed OVA-expressing tumor cells better than OT-I-CTLs. The cytotoxicity against OVA-expressing tumor cells increased by combining OT-I-CTLs and A-NK cells, but the increase was additive rather than synergistic. A-NK cells adenovirally-transduced to produce IL-12 (A-NK

Indexed as

Adoptive TransferAnimalsCell Line, TumorCytokinesFemaleGenes, MHC Class IKiller Cells, NaturalLung NeoplasmsMaleMice, Inbred C57BLMice, TransgenicOvalbuminT-Lymphocytes, CytotoxicCytokinesOvalbuminAdoptive cell transferCancer immunotherapyCell trafficCytotoxicityCytotoxic T lymphocytes (CTL)Natural killer cells (NK cells)

Identifiers

PMID27377534
PMCPMC5203973
OpenAlexW2465971942

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.