Evidence map›Paper›PMID 10377193›Full record

ArticleThe Journal of experimental medicine1999

Susceptibility of mice deficient in CD1D or TAP1 to infection with Mycobacterium tuberculosis.

S M Behar, C C Dascher, M J Grusby, C R Wang, M B Brenner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

144 citing papers in PubMed, 369 citations in OpenAlex.

  1. Trial
  2. Review
  3. Therapeutic remodeling of the tuberculosis granuloma with 1-methyl-D-tryptophan enhances CD8Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. CD8+ lymphocytes in immunity against tuberculosis.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. CD226 identifies effector CD8Cell reports · 2025
    Article
  10. Review
  11. Article
  12. Article
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  14. Article
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  16. Article
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84 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

S M BeharDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA. sbehar@rics.bwh.harvard.edu
C C Dascher
M J Grusby
C R Wang
M B Brenner
Brigham and Women's Hospital · US

Funding

The Regulation and Function of Murine CD1 MoleculesR01AI043407 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 1998 to 2017
$5.2M
REGULATION OF THE DIFFERENTIATION AND FUNCTION OF TH2 CER01AI040171 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI GRUSBY, MICHAEL J · 1997 to 2006
$1.9M
SECOND COSTIMULATORY PATHWAY PREVENTS T CELL ANERGYK08AR001978 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 1996 to 2000
$129k
T-CELLS AND DISEASESR01AR039582 · NIAMS · DANA-FARBER CANCER INSTITUTE · PI BRENNER, MICHAEL B · 1988 to 1995
–
NIAID NIH HHS AI43407NIAID NIH HHS R01 AI040171NIAID NIH HHS R01 AI043407NIAMS NIH HHS AR01978NIAMS NIH HHS AR39582
6 · The paper itself

Abstract

Cellular immunity against Mycobacterium tuberculosis controls infection in the majority of infected humans. Studies in mice have delineated an important role for CD4(+) T cells and cytokines including interferon gamma and tumor necrosis factor alpha in the response to infection with mycobacteria. Recently, the identification of CD8(+) CD1-restricted T cells that kill M. tuberculosis organisms via granulysin and the rapid death after infection of beta2 microglobulin deficient mice in humans has drawn attention to a critical role for CD8(+) T cells. The nature of mycobacterial-specific CD8(+) T cells has been an enigma because few have been identified in any species. Here, we delineate the contribution of class I MHC-restricted T cells in the defense against tuberculosis as transporter associated with antigen processing (TAP)1-deficient mice died rapidly, bore a greater bacterial burden, and had more severe tissue pathology than control mice. In contrast, CD1D-/- mice were not significantly different in their susceptibility to infection than control mice. This data demonstrates a critical role for TAP-dependent peptide antigen presentation and provides further evidence that class I MHC-restricted CD8(+) T cells, the major T cell subset activated by this antigen processing pathway, play an essential role in immunity to tuberculosis.

Indexed as

AnimalsAntigens, CD1Antigens, CD1dATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2beta 2-MicroglobulinCD8-Positive T-LymphocytesHistocompatibility Antigens Class ILungMiceMice, Inbred StrainsMice, KnockoutMycobacterium tuberculosisStem CellsTuberculosisAntigens, CD1Antigens, CD1dATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2beta 2-MicroglobulinCD1D protein, humanHistocompatibility Antigens Class ITAP1 protein, humanTap1 protein, mouse

Identifiers

PMID10377193
PMCPMC2192974
OpenAlexW1982727887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.