Evidence map›Paper›PMID 22832272›Full record

ArticleCell reports2012

CD8(+) T cells from mice transnuclear for a TCR that recognizes a single H-2K(b)-restricted MHV68 epitope derived from gB-ORF8 help control infection.

Sharvan Sehrawat, Oktay Kirak, Paul-Albert Koenig, Marisa K Isaacson, Sofia Marques, Gunes Bozkurt, J Pedro Simas, Rudolph Jaenisch, Hidde L Ploegh

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cell reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. A CombinatorialBio-protocol · 2021
    Article
  3. Article
  4. ModelingOncoimmunology · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Herpesviruses: Harmonious Pathogens but Relevant Cofactors in Other Diseases?Frontiers in cellular and infection microbiology · 2018
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

9 authors at 4 institutions in 2 countries.

Sharvan SehrawatWhitehead Institute for Biomedical Research, Massachusetts Institute of Technology, 9 Cambridge Center, Cambridge, MA 02142, USA.
Oktay Kirak
Paul-Albert Koenig
Marisa K Isaacson
Sofia Marques
Gunes Bozkurt
J Pedro Simas
Rudolph Jaenisch
Hidde L Ploegh
Massachusetts Institute of Technology · USWhitehead Institute for Biomedical Research · USInstituto Gulbenkian de Ciência · PTScripps Research Institute · US

Funding

In Vitro Reprogramming of Somatic Cells into Pluripotent ES-like CellsR37HD045022 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2009 to 2017
$7.5M
Nuclear Cloning and the Reprogramming of the GenomeR01HD045022 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2003 to 2008
$4.7M
ASSEMBLY OF MHC CLASS I MOLECULES IN VITRO AND IN VIVOR01AI033456 · NIAID · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PLOEGH, HIDDE L. · 1993 to 2012
$4.0M
NIAID NIH HHS R01 AI033456NICHD NIH HHS R01 HD045022NICHD NIH HHS R37 HD045022
6 · The paper itself

Abstract

To study the CD8(+) T cell response against a mouse γ-herpes virus, we generated K(b)-MHV-68-ORF8(604-612)RAG(-/-) CD8(+) T cell receptor transnuclear (TN) mice as a source of virus-specific CD8(+) T cells. K(b)-ORF8-Tet(+) CD8(+) T cells, expanded in the course of a resolving MHV-68 infection, served as a source of nucleus donors. Various in vivo and ex vivo assay criteria demonstrated the fine specificity and functionality of TN cells. TN cells proliferated extensively in response to viral infection, helped control viral burden, and exhibited a phenotype similar to that of endogenous K(b)-ORF8-Tet(+) cells. When compared to OT-1 cells, TN cells displayed distinct properties in response to lymphopenia and cognate antigen stimulation, which may be attributable to the affinity of the TCR expressed by the TN cells. The availability of MHV-68-specific CD8(+) TCR TN mice provides a new tool for investigating aspects of host-pathogen interactions unique to γ-herpes viruses.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell NucleusCell ProliferationEpitopesGlycoproteinsH-2 AntigensHerpesviridae InfectionsHomeodomain ProteinsMiceMice, Inbred StrainsMice, KnockoutMice, TransgenicMolecular Sequence DataPhenotypeReceptors, Antigen, T-CellEpitopesGlycoproteinsH-2 AntigensH-2Kb protein, mouseHomeodomain ProteinsK8.1 protein, Human herpesvirus 8RAG-1 proteinReceptors, Antigen, T-CellViral Proteins

Identifiers

PMID22832272
PMCPMC3406328
OpenAlexW2165886054

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.