Evidence map›Paper›PMID 21098224›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Nonconventional CD8+ T cell responses to Listeria infection in mice lacking MHC class Ia and H2-M3.

Hoonsik Cho, Hak-Jong Choi, Honglin Xu, Kyrie Felio, Chyung-Ru Wang

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. 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
1.0field-weighted citation impact, top 25% 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, 17 citations in OpenAlex.

  1. Article
  2. Innate and Adaptive Immune Responses duringMicrobiology spectrum · 2019
    Article
  3. Article
  4. Review
  5. CXCR3 expression defines a novel subset of innate CD8+ T cells that enhance immunity against bacterial infection and cancer upon stimulation with IL-15.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  6. Article
  7. Article
  8. Distinct populations of innate CD8+ T cells revealed in a CXCR3 reporter mouse.Journal of immunology (Baltimore, Md. : 1950) · 2013
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Positive selecting cell type determines the phenotype of MHC class Ib-restricted CD8+ T cells.Proceedings of the National Academy of Sciences of the United States of America · 2011
    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

5 authors at 3 institutions in 2 countries.

Hoonsik ChoDepartment of Microbiology and Immunology, Northwestern University, Chicago, IL 60611, USA.
Hak-Jong Choi
Honglin Xu
Kyrie Felio
Chyung-Ru Wang
Northwestern University · PHNorthwestern Medicine · USNorthwestern University · US

Funding

The Role of Group 1 CD1-restricted T Cells in Infectious DiseaseR01AI057460 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 2004 to 2020
$5.7M
The role of MHC class Lb in T cell development and infectious diseaseR01AI040310 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 2001 to 2016
$5.0M
The Role of Group 1 CD1-restricted T Cells in Infectious DiseaseR56AI057460 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WANG, CHYUNG-RU · 2015 to 2015
$449k
H2-M3 AND T CELL DEVELOPMENT AND IMMUNITYR29AI040310 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 1996 to 2000
$84k
NIAID NIH HHS AI40310NIAID NIH HHS AI57460NIAID NIH HHS R01 AI040310NIAID NIH HHS R01 AI057460NIAID NIH HHS R29 AI040310NIAID NIH HHS R56 AI057460
6 · The paper itself

Abstract

CD8(+) T cells restricted to MHC class Ib molecules other than H2-M3 have been shown to recognize bacterial Ags. However, the contribution of these T cells to immune responses against bacterial infection is not well defined. To investigate the immune potential of MHC class Ib-restricted CD8(+) T cells, we have generated mice that lack both MHC class Ia and H2-M3 molecules (K(b-/-)D (b-/-)M3(-/-)). The CD8(+) T cells present in K(b-/-)D (b-/-)M3(-/-) mice display an activated surface phenotype and are able to secrete IFN-γ rapidly upon anti-CD3 and anti-CD28 stimulation. Although the CD8(+) T cell population is reduced in K(b-/-)D (b-/-)M3(-/-) mice compared with that in K(b-/-)D (b-/-) mice, this population retains the capacity to expand significantly in response to primary infection with the bacteria Listeria monocytogenes. However, K(b-/-)D (b-/-)M3(-/-) CD8(+) T cells do not expand upon secondary infection, similar to what has been observed for H2-M3-restricted T cells. CD8(+) T cells isolated from Listeria-infected K(b-/-)D (b-/-)M3(-/-) mice exhibit cytotoxicity and secrete proinflammatory cytokines in response to Listeria-infected APCs. These T cells are protective against primary Listeria infection, as Listeria-infected K(b-/-)D (b-/-)M3(-/-) mice exhibit reduced bacterial burden compared with that of infected β(2)-microglobulin-deficient mice that lack MHC class Ib-restricted CD8(+) T cells altogether. In addition, adoptive transfer of Listeria-experienced K(b-/-)D (b-/-)M3(-/-) splenocytes protects recipient mice against subsequent Listeria infection in a CD8(+) T cell-dependent manner. These data demonstrate that other MHC class Ib-restricted CD8(+) T cells, in addition to H2-M3-restricted T cells, contribute to antilisterial immunity and may contribute to immune responses against other intracellular bacteria.

Indexed as

Animalsbeta 2-MicroglobulinCD8-Positive T-LymphocytesCell LineCell Line, TumorCell ProliferationCells, CulturedCytotoxicity, ImmunologicDisease Models, AnimalFemaleH-2 AntigensHistocompatibility Antigen H-2DHistocompatibility Antigens Class IListeria monocytogenesListeriosisLymphocyte Activationbeta 2-MicroglobulinH-2 AntigensH-2Kb protein, mouseH2-M3 antigenHistocompatibility Antigen H-2DHistocompatibility Antigens Class I

Identifiers

PMID21098224
PMCPMC3068915
OpenAlexW1585997769

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.