Evidence map›Paper›PMID 18480435›Full record

ArticleJournal of virology2008

Qualitative and quantitative characteristics of rotavirus-specific CD8 T cells vary depending on the route of infection.

Janina Q Jiang, Xiao-Song He, Ningguo Feng, Harry B Greenberg

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  4. CXCR6 deficiency impairs cancer vaccine efficacy and CD8Journal for immunotherapy of cancer · 2021
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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

4 authors at 2 institutions in 1 country.

Janina Q JiangDepartment of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
Xiao-Song He
Ningguo Feng
Harry B Greenberg
Stanford University · USVA Palo Alto Health Care System · US

Funding

Proteomics/GenomicsP30DK056339 · NIDDK · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 2001 to 2010
$10.4M
VIRAL GASTROENTERITIS--BASIS OF PROTECTION AND VIRULENCER01AI021362 · NIAID · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 1989 to 2014
$5.4M
VIRAL GASTROENTERITIS--BASIS OF PROTECTION AND VIRULENCER37AI021362 · NIAID · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 1994 to 2003
$789k
Viral Gastroenteritis: Basis of Virulence and ProtectionR56AI021362 · NIAID · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI GREENBERG, HARRY BERNARD · 2015 to 2015
$506k
VIRAL GASTROENTERITIS: BASIS OF VIRULENCE AND PROTECTIONR22AI021362 · NIAID · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 1985 to 1991
–
NIAID NIH HHS AI021362-24NIAID NIH HHS R01 AI021362NIAID NIH HHS R37 AI021362NIAID NIH HHS R56 AI021362NIDDK NIH HHS P30 DK056339NIDDK NIH HHS P30DK56339
6 · The paper itself

Abstract

CD8 T-cell response provides an important defense against rotavirus, which infects a variety of systemic locations in addition to the gut. Here we investigated the distribution, phenotype, and function of rotavirus-specific CD8 T cells in multiple organs after rotavirus infection initiated via the intranasal, oral, or intramuscular route. The highest level of virus-specific CD8 T cells was observed in the Peyer's patches of orally infected mice and in the lungs of intranasally infected animals. Very low levels of virus-specific CD8 T cells were detected in peripheral blood or spleen irrespective of the route of infection. Rotavirus-specific CD8 T cells from Peyer's patches of orally infected mice expressed high levels of CCR9, while CXCR6 and LFA-1 expression was associated with virus-specific CD8 T cells in lungs of intranasally infected mice. Oral infection induced the highest proportion of gamma interferon(-) CD107a/b(+) CD8 T cells in Peyer's patches. When equal numbers of rotavirus-specific CD8 T cells were transferred into Rag-1 knockout mice chronically infected with rotavirus, the donor cells derived from Peyer's patches of orally infected mice were more efficient than those derived from lungs of intranasally infected animals in clearing intestinal infection. These results suggest that different routes of infection induce virus-specific CD8 T cells with distinct homing phenotypes and effector functions as well as variable abilities to clear infection.

Indexed as

Adoptive TransferAnimalsBloodBlood CellsCD8-Positive T-LymphocytesFecesFlow CytometryHomeodomain ProteinsInterferon-gammaLungLymphocyte Function-Associated Antigen-1Lysosomal-Associated Membrane Protein 1Lysosomal-Associated Membrane Protein 2MiceMice, Inbred C57BLMice, KnockoutCC chemokine receptor 9Cxcr6 protein, mouseHomeodomain ProteinsInterferon-gammaLymphocyte Function-Associated Antigen-1Lysosomal-Associated Membrane Protein 1Lysosomal-Associated Membrane Protein 2RAG-1 proteinReceptors, CCRReceptors, CXCRReceptors, CXCR6

Identifiers

PMID18480435
PMCPMC2446946
OpenAlexW2157470684

What OpenQuestion holds

Textmetadata
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.