Evidence map›Paper›PMID 18337581›Full record

ArticleJournal of virology2008

Generation of antiviral major histocompatibility complex class I-restricted T cells in the absence of CD8 coreceptors.

Nicolas P Andrews, Christopher D Pack, Aron E Lukacher

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Memory T cell-mediated rejection is mitigated by FcγRIIB expression on CD8American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  3. Article
  4. Pathogen Stimulation History Impacts Donor-Specific CD8(+) T Cell Susceptibility to Costimulation/Integrin Blockade-Based Therapy.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2015
    Article
  5. Article
  6. Duality of the murine CD8 compartment.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  7. CD8 T cells recruited early in mouse polyomavirus infection undergo exhaustion.Journal of immunology (Baltimore, Md. : 1950) · 2012
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Minor antigens on transfused RBCs crossprime CD8 T cells but do not induce full effector function.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2011
    Article
  13. Review
  14. Article
  15. Article
  16. 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

3 authors at 1 institution in 1 country.

Nicolas P AndrewsDepartment of Pathology, Emory University School of Medicine, Woodruff Memorial Research Building, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Christopher D Pack
Aron E Lukacher
Emory University · US

Funding

T CELL IMMUNITY TO POLYOMA VIRUS INDUCED TUMORSR01CA071971 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LUKACHER, ARON ELIOT · 2001 to 2011
$3.0M
Regulation of Polyoma Virus-Specific CD8+ T CellsR01CA100644 · NCI · EMORY UNIVERSITY · PI LUKACHER, ARON · 2003 to 2007
$1.4M
NCI NIH HHS R01 CA071971NCI NIH HHS R01 CA100644NCI NIH HHS R01CA100644NCI NIH HHS R01CA71971
6 · The paper itself

Abstract

The CD8 coreceptor is important for positive selection of major histocompatibility complex I (MHC-I)-restricted thymocytes and in the generation of pathogen-specific T cells. However, the requirement for CD8 in these processes may not be essential. We previously showed that mice lacking beta(2)-microglobulin are highly susceptible to tumors induced by mouse polyoma virus (PyV), but CD8-deficient mice are resistant to these tumors. In this study, we show that CD8-deficient mice also control persistent PyV infection as efficiently as wild-type mice and generate a substantial virus-specific, MHC-I-restricted, T-cell response. Infection with vesicular stomatitis virus (VSV), which is acutely cleared, also recruited antigen-specific, MHC-I-restricted T cells in CD8-deficient mice. Yet, unlike in VSV infection, the antiviral MHC-I-restricted T-cell response to PyV has a prolonged expansion phase, indicating a requirement for persistent infection in driving T-cell inflation in CD8-deficient mice. Finally, we show that the PyV-specific, MHC-I-restricted T cells in CD8-deficient mice, while maintained long term at near-wild-type levels, are short lived in vivo and have extremely narrow T-cell receptor repertoires. These findings provide a possible explanation for the resistance of CD8-deficient mice to PyV-induced tumors and have implications for the maintenance of virus-specific MHC-I-restricted T cells during persistent infection.

Indexed as

Adoptive TransferAnimalsCD3 ComplexCD4 AntigensCD8-Positive T-LymphocytesCytotoxicity, ImmunologicFlow CytometryHistocompatibility Antigens Class IInterferon-gammaMiceMice, Inbred C57BLMice, KnockoutPolyomavirusPolyomavirus InfectionsReceptors, Antigen, T-CellRhabdoviridae InfectionsCD3 ComplexCD4 AntigensHistocompatibility Antigens Class IInterferon-gammaReceptors, Antigen, T-Cell

Identifiers

PMID18337581
PMCPMC2346753
OpenAlexW2117897933

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.