Evidence map›Paper›PMID 25662997›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Functional heterogeneity in the CD4+ T cell response to murine γ-herpesvirus 68.

Zhuting Hu, Marcia A Blackman, Kenneth M Kaye, Edward J Usherwood

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  10. CD4Cold Spring Harbor perspectives in biology · 2021
    Review
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  18. Many Th Cell Subsets Have Fas Ligand-Dependent Cytotoxic Potential.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  19. Cytokine- and TCR-Mediated Regulation of T Cell Expression of Ly6C and Sca-1.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  20. Article
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

4 authors at 3 institutions in 1 country.

Zhuting HuDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756;
Marcia A BlackmanTrudeau Institute, Saranac Lake, NY 12983; and.
Kenneth M KayeDepartment of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Edward J UsherwoodDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756; Edward.J.Usherwood@Dartmouth.EDU.
Dartmouth College · USBrigham and Women's Hospital · USTrudeau Institute · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
GENETIC AND BIOCHEMICAL STUDIES OF THE KSHV LANA GENER01CA082036 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI KAYE, KENNETH M · 1999 to 2019
$7.6M
T cell function in murine gammaherpesvirus infectionR01AI069943 · NIAID · DARTMOUTH COLLEGE · PI USHERWOOD, EDWARD J · 2007 to 2016
$3.3M
Immune surveillance in murine gammaherpesvirus infectionR01CA103642 · NCI · DARTMOUTH COLLEGE · PI USHERWOOD, EDWARD J · 2004 to 2013
$3.1M
T CELL IMMUNITY TO MHV 68, A MURINE GAMMA HERPEVIRUSR01AI042927 · NIAID · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A · 1998 to 2008
$2.5M
NCI NIH HHS P30 CA023108NCI NIH HHS R01 CA082036NCI NIH HHS R01CA082036NCI NIH HHS R01 CA103642NCI NIH HHS R01CA103642NIAID NIH HHS AI42927NIAID NIH HHS R01 AI042927NIAID NIH HHS R01 AI069943NIAID NIH HHS R01AI069943
6 · The paper itself

Abstract

CD4(+) T cells are critical for the control of virus infections, T cell memory, and immune surveillance. We studied the differentiation and function of murine γ-herpesvirus 68 (MHV-68)-specific CD4(+) T cells using gp150-specific TCR-transgenic mice. This allowed a more detailed study of the characteristics of the CD4(+) T cell response than did previously available approaches for this virus. Most gp150-specific CD4(+) T cells expressed T-bet and produced IFN-γ, indicating that MHV-68 infection triggered differentiation of CD4(+) T cells largely into the Th1 subset, whereas some became follicular Th cells and Foxp3(+) regulatory T cells. These CD4(+) T cells were protective against MHV-68 infection in the absence of CD8(+) T cells and B cells, and protection depended on IFN-γ secretion. Marked heterogeneity was observed in the CD4(+) T cells, based on lymphocyte Ag 6C (Ly6C) expression. Ly6C expression positively correlated with IFN-γ, TNF-α, and granzyme B production; T-bet and KLRG1 expression; proliferation; and CD4(+) T cell-mediated cytotoxicity. Ly6C expression inversely correlated with survival, CCR7 expression, and secondary expansion potential. Ly6C(+) and Ly6C(-) gp150-specific CD4(+) T cells were able to interconvert in a bidirectional manner upon secondary Ag exposure in vivo. These results indicate that Ly6C expression is closely associated with antiviral activity in effector CD4(+) T cells but is inversely correlated with memory potential. Interconversion between Ly6C(+) and Ly6C(-) cells may maintain a balance between the two Ag-specific CD4(+) T cell populations during MHV-68 infection. These findings have significant implications for Ly6C as a surface marker to distinguish functionally distinct CD4(+) T cells during persistent virus infection.

Indexed as

AnimalsAntigens, LyApoptosisB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationCell SurvivalFlow CytometryHerpesviridae InfectionsHost-Pathogen InteractionsInterferon-gammaMice, Inbred C57BLMice, KnockoutMice, TransgenicRhadinovirusAntigens, LyInterferon-gammaLy-6C antigen, mouseTumor Necrosis Factor-alpha

Identifiers

PMID25662997
PMCPMC4355211
OpenAlexW1957802948

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.