Evidence map›Paper›PMID 23315077›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

T cells home to the thymus and control infection.

Claudia Nobrega, Cláudio Nunes-Alves, Bruno Cerqueira-Rodrigues, Susana Roque, Palmira Barreira-Silva, Samuel M Behar, Margarida Correia-Neves

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Features of Peripheral T Cell Remigration into the Thymus.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Chronic virus infection drives CD8 T cell-mediated thymic destruction and impaired negative selection.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Thymic Microenvironment Is Modified by Malnutrition andFrontiers in cellular and infection microbiology · 2019
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Claudia NobregaLife and Health Sciences Research Institute, School of Health Sciences, University of Minho, 4710-057 Braga, Portugal.
Cláudio Nunes-Alves
Bruno Cerqueira-Rodrigues
Susana Roque
Palmira Barreira-Silva
Samuel M Behar
Margarida Correia-Neves
United Nations University · PTUniversity of Minho · PTHarvard University · US

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROBERT A. PARKER · 2004 to 2026
$94.4M
Regulation of CD8+ T cell immunity to tuberculosis (pending title)R01AI106725 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BEHAR, SAMUEL M · 2013 to 2022
$6.1M
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
NIAID NIH HHS P30 AI 060354NIAID NIH HHS P30 AI060354NIAID NIH HHS R01 AI067731NIAID NIH HHS R01 AI106725NIAID NIH HHS R56 AI067731
6 · The paper itself

Abstract

The thymus is a target of multiple pathogens. How the immune system responds to thymic infection is largely unknown. Despite being considered an immune-privileged organ, we detect a mycobacteria-specific T cell response in the thymus following dissemination of Mycobacterium avium or Mycobacterium tuberculosis. This response includes proinflammatory cytokine production by mycobacteria-specific CD4(+) and CD8(+) T cells, which stimulates infected cells and controls bacterial growth in the thymus. Importantly, the responding T cells are mature peripheral T cells that recirculate back to the thymus. The recruitment of these cells is associated with an increased expression of Th1 chemokines and an enrichment of CXCR3(+) mycobacteria-specific T cells in the thymus. Finally, we demonstrate it is the mature T cells that home to the thymus that most efficiently control mycobacterial infection. Although the presence of mature T cells in the thymus has been recognized for some time, to our knowledge, these data are the first to show that T cell recirculation from the periphery to the thymus is a mechanism that allows the immune system to respond to thymic infection. Maintaining a functional thymic environment is essential to maintain T cell differentiation and prevent the emergence of central tolerance to the invading pathogens.

Indexed as

AnimalsCell MovementChemokine CXCL10Chemokine CXCL9Immunity, InnateMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutMice, TransgenicMycobacterium aviumMycobacterium tuberculosisReceptors, CXCR3Thymus GlandT-Lymphocyte SubsetsTuberculosisChemokine CXCL10Chemokine CXCL9Cxcl10 protein, mouseCxcl9 protein, mouseCxcr3 protein, mouseReceptors, CXCR3

Identifiers

PMID23315077
PMCPMC3563877
OpenAlexW2139885236

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.