Evidence map›Paper›PMID 26652001›Full record

ArticleeLife2015

Mycolic acid-specific T cells protect against Mycobacterium tuberculosis infection in a humanized transgenic mouse model.

Jie Zhao, Sarah Siddiqui, Shaobin Shang, Yao Bian, Sreya Bagchi, Ying He, Chyung-Ru Wang

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Applications of humanized mice inMolecular medicine reports · 2026
    Review
  4. Review
  5. Article
  6. CD8+ lymphocytes in immunity against tuberculosis.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Invariant natural killer T cells in lung diseases.Experimental & molecular medicine · 2023
    Review
  12. Horizontal Gene Transfer and Drug Resistance InvolvingAntibiotics (Basel, Switzerland) · 2023
    Article
  13. Article
  14. Clinical manifestations and immune response to tuberculosis.World journal of microbiology & biotechnology · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Jie ZhaoDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Sarah SiddiquiDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Shaobin ShangDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Yao BianDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Sreya BagchiDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Ying HeDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Chyung-Ru WangDepartment of Microbiology and Immunology, Northwestern University, Chicago, United States.
Northwestern 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 AI040310NIAID NIH HHS AI057460NIAID NIH HHS R01 AI040310NIAID NIH HHS R01 AI057460NIAID NIH HHS R29 AI040310NIAID NIH HHS R56 AI057460
6 · The paper itself

Abstract

Group 1 CD1 molecules, CD1a, CD1b and CD1c, present lipid antigens from Mycobacterium tuberculosis (Mtb) to T cells. Mtb lipid-specific group 1 CD1-restricted T cells have been detected in Mtb-infected individuals. However, their role in protective immunity against Mtb remains unclear due to the absence of group 1 CD1 expression in mice. To overcome the challenge, we generated mice that expressed human group 1 CD1 molecules (hCD1Tg) and a CD1b-restricted, mycolic-acid specific TCR (DN1Tg). Using DN1Tg/hCD1Tg mice, we found that activation of DN1 T cells was initiated in the mediastinal lymph nodes and showed faster kinetics compared to Mtb Ag85B-specific CD4(+) T cells after aerosol infection with Mtb. Additionally, activated DN1 T cells exhibited polyfunctional characteristics, accumulated in lung granulomas, and protected against Mtb infection. Therefore, our findings highlight the vaccination potential of targeting group 1 CD1-restricted lipid-specific T cells against Mtb infection.

Indexed as

AnimalsAntigens, BacterialAntigens, CD1HumansLymphocyte ActivationMiceMice, SCIDMice, TransgenicMycobacterium tuberculosisMycolic AcidsReceptors, Antigen, T-CellT-Lymphocyte SubsetsTuberculosisAntigens, BacterialAntigens, CD1Mycolic AcidsReceptors, Antigen, T-CellCD1immunologymouseMycobaterium tuberculosisMycolic acidT lymphocytes

Identifiers

PMID26652001
PMCPMC4718816
OpenAlexW2275794920

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.