Evidence map›Paper›PMID 19539970›Full record

ArticleVirology2009

Defining the mechanism(s) of protection by cytolytic CD8 T cells against a cryptic epitope derived from a retroviral alternative reading frame.

Melanie R Rutkowski, On Ho, William R Green

Open access · greenAbstract read
In one paragraph

Article in Virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 12 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

3 authors at 2 institutions in 1 country.

Melanie R RutkowskiDepartment of Microbiology and Immunology, Dartmouth Medical School, Lebanon, NH, USA.
On Ho
William R Green
Dartmouth College · USUniversity of Washington · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
The Pathogenesis of MAIDS and Specific T Cell ResponsesR01CA050157 · NCI · DARTMOUTH COLLEGE · PI GREEN, WILLIAM R · 1990 to 2009
$2.6M
AUTOIMMUNITY &CONNECTIVE TISSUE BIOLOGY TRAININGT32AR007576 · NIAMS · DARTMOUTH COLLEGE · PI RIGBY, WILLIAM FREDERICK CARSON · 1994 to 2008
$1.7M
MOUSE RETROVIRUS CO-OPTING OF IMMUNE CELL INTERACTIONSR56AI059580 · NIAID · DARTMOUTH COLLEGE · PI GREEN, WILLIAM R · 2005 to 2005
$320k
NCI NIH HHS CA50257NCI NIH HHS P30 CA023108NCI NIH HHS R01 CA050157NIAID NIH HHS AI059580NIAID NIH HHS R56 AI059580NIAID NIH HHS T32 AI007363NIAID NIH HHS T32AI07363NIAMS NIH HHS T32 AR007576NIAMS NIH HHS T32AR007576
6 · The paper itself

Abstract

The biological significance of protective CD8 T-cell-mediated responses against non-traditional alternative reading frame epitopes remains relatively unknown. Cytolytic CD8 T cells (CTL) specific for a non-traditional cryptic MHC class I epitope, SYNTGRFPPL, are critically involved in the protection of mice during infection with the LP-BM5 murine retrovirus. The goal of this study was to determine the functional properties of the protective SYNTGRFPPL-specific CTL during LP-BM5 infection of susceptible BALB/c CD8(-/-) mice. Direct infection experiments and adoptive transfer of CD8 T cells derived from perforin (pfp)(-/-), IFN gamma(-/-), FasL(-/-) and, as a positive control, wild-type BALB/c mice, were utilized to assess the effector mechanisms responsible for protection. Our results indicate that SYNTGRFPPL-specific effector CTL preferentially utilize perforin-mediated cytolysis to provide protection against LP-BM5-induced pathogenesis, whereas CTL production of IFN gamma is not required. Our results also suggest a minimal contribution of FasL/Fas-mediated lysis during the effector response. Collectively, these results provide insight into effector mechanisms utilized by protective CTL directed against non-traditional cryptic epitopes during disease protection.

Indexed as

Reading FramesAdoptive TransferAnimalsAntigens, ViralCD8-Positive T-LymphocytesCytotoxicity Tests, ImmunologicEpitopesFemaleMiceMice, Inbred BALB CMice, KnockoutPerforinRetroviridaeT-Lymphocytes, CytotoxicAntigens, ViralEpitopesPerforin

Identifiers

PMID19539970
PMCPMC2760248
OpenAlexW1964096433

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.