Evidence map›Paper›PMID 25711213›Full record

ArticleThe Journal of experimental medicine2015

CD160 is essential for NK-mediated IFN-γ production.

Tony C Tu, Nicholas K Brown, Tae-Jin Kim, Joanna Wroblewska, Xuanming Yang, Xiaohuan Guo, Seoyun Hyunji Lee, Vinay Kumar, Kyung-Mi Lee, Yang-Xin Fu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
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  6. MutantFrontiers in immunology · 2026
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  8. Review
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  13. Effect ofInternational journal of molecular sciences · 2024
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  19. Review
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13 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

10 authors at 3 institutions in 2 countries.

Tony C TuDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Nicholas K BrownDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Tae-Jin KimDepartment of Pathology, The University of Chicago, Chicago, IL 60637 Global Research Lab, Department of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul 136-705, South Korea.
Joanna WroblewskaDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Xuanming YangDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Xiaohuan GuoDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Seoyun Hyunji LeeDepartment of Pathology, The University of Chicago, Chicago, IL 60637 Global Research Lab, Department of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul 136-705, South Korea.
Vinay KumarDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Kyung-Mi LeeDepartment of Pathology, The University of Chicago, Chicago, IL 60637 Global Research Lab, Department of Biochemistry and Molecular Biology, Korea University College of Medicine, Seoul 136-705, South Korea Department of Melanoma Medical Oncology and Immunology, MD Anderson Cancer Center, Houston, TX 77054 kyunglee@korea.ac.kr yxfu@uchicago.edu.
Yang-Xin FuDepartment of Pathology, The University of Chicago, Chicago, IL 60637 kyunglee@korea.ac.kr yxfu@uchicago.edu.
University of Chicago · USKorea University · KRThe University of Texas MD Anderson Cancer Center · US

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
TNF family members for lymph angiogenesis and lymph node hypertrophyR01CA141975 · NCI · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2010 to 2014
$1.6M
The role of Id2 in gut innate lymphoid cellsR01DK100427 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI FU, YANG-XIN · 2014 to 2017
$1.4M
NCATS NIH HHS UL1 TR000430NCI NIH HHS CA141975NCI NIH HHS R01 CA141975NIAID NIH HHS T32 AI007090NIAID NIH HHS T32AI007090NIDDK NIH HHS DK100427NIDDK NIH HHS R01 DK100427NIGMS NIH HHS GM007281NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

NK-derived cytokines play important roles for natural killer (NK) function, but how the cytokines are regulated is poorly understood. CD160 is expressed on activated NK or T cells in humans but its function is unknown. We generated CD160-deficient mice to probe its function. Although CD160(-/-) mice showed no abnormalities in lymphocyte development, the control of NK-sensitive tumors was severely compromised in CD160(-/-) mice. Surprisingly, the cytotoxicity of NK cells was not impaired, but interferon-γ (IFN-γ) secretion by NK cells was markedly reduced in CD160(-/-) mice. Functionally targeting CD160 signaling with a soluble CD160-Ig also impaired tumor control and IFN-γ production, suggesting an active role of CD160 signaling. Using reciprocal bone marrow transfer and cell culture, we have identified the intrinsic role of CD160 on NK cells, as well as its receptor on non-NK cells, for regulating cytokine production. To demonstrate sufficiency of the CD160(+) NK cell subset in controlling NK-dependent tumor growth, intratumoral transfer of the CD160(+) NK fraction led to tumor regression in CD160(-/-) tumor-bearing mice, indicating demonstrable therapeutic potential for controlling early tumors. Therefore, CD160 is not only an important biomarker but also functionally controls cytokine production by NK cells.

Indexed as

AnimalsAntigens, CDFemaleGPI-Linked ProteinsInterferon-gammaKiller Cells, NaturalMaleMice, Inbred C57BLMice, Mutant StrainsReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14Antigens, CDCd160 protein, mouseGPI-Linked ProteinsInterferon-gammaReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14

Identifiers

PMID25711213
PMCPMC4354368
OpenAlexW2101148372

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.