Evidence map›Paper›PMID 17073557›Full record

ReviewCritical reviews in immunology2006

Mycobacterium tuberculosis-specific CD8+ T cells and their role in immunity.

Joshua S M Woodworth, Samuel M Behar

Abstract readReview
In one paragraph

Review in Critical reviews in immunology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
–field-weighted citation impact
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

96 citing papers in PubMed.

  1. Trial
  2. 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
  3. Construction of RecombinantPathogens (Basel, Switzerland) · 2026
    Article
  4. Lung Resident T Cells Across the Spectrum of TB Infection and Disease.bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
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  12. Article
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  14. Article
  15. Article
  16. Article
  17. Article
  18. Peptide-Based Vaccines for Tuberculosis.Frontiers in immunology · 2022
    Review
  19. Article
  20. Article

36 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

2 authors.

Joshua S M WoodworthDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Samuel M Behar

Funding

Antigen-specific CD8+ T cells and protective immunity to tuberculosisR01AI067731 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 2006 to 2010
$2.0M
Antigen-specific CD8+ T cells and protective immunity to tuberculosisR56AI067731 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 2012 to 2012
$507k
TREATMENT OF TUBERCULOSIS WITH IMMUNOMODULATORSR03AI049093 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 2001 to 2003
$212k
NIAID NIH HHS AI067731NIAID NIH HHS AI49093NIAID NIH HHS R01 AI067731NIAID NIH HHS R03 AI049093NIAID NIH HHS R56 AI067731
6 · The paper itself

Abstract

There are more cases of tuberculosis in the world today than at any other time in history. The global epidemic has generated intense interest into the immunological mechanisms that control infection. Although CD4+ T cells play a critical role in host immunity to Mycobacterium tuberculosis, there is considerable interest in understanding the role of other T cell subsets in preventing disease development following infection. CD8+ T cells are required for optimum host defense following M. tuberculosis infection, which has led to investigation into how this protective effect is mediated. A critical review of recent literature regarding the role of CD8+ T cells in protective immunity to M. tuberculosis infection is now required to address the strengths and weaknesses of these studies. In this article, we evaluate the evidence that CD8+ T cells are critical in immunity to M. tuberculosis infection. We discuss the specific mycobacterial proteins that are recognized by CD8+ T cells elicited during infection. Finally, we examine the effector mechanisms of CD8+ T cells generated during infection and synthesize recent studies to consider the protective roles that these T cells serve in vivo.

Indexed as

AnimalsAntigens, BacterialCD8-Positive T-LymphocytesHumansMiceMice, KnockoutMycobacterium tuberculosisTuberculosisAntigens, Bacterial

Identifiers

PMID17073557
PMCPMC3134450

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.