Evidence map›Paper›PMID 17671656›Full record

ArticleThe Journal of clinical investigation2007

Enhanced priming of adaptive immunity by a proapoptotic mutant of Mycobacterium tuberculosis.

Joseph Hinchey, Sunhee Lee, Bo Y Jeon, Randall J Basaraba, Manjunatha M Venkataswamy, Bing Chen, John Chan, Miriam Braunstein, Ian M Orme, Steven C Derrick and 3 more

Abstract readComparative Study
In one paragraph

Article in The Journal of clinical investigation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers.

0numbers the graph read from it
0cells of the map it votes in
156citing 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

156 citing papers in PubMed.

  1. Review
  2. Article
  3. Construction and characterization of novelInfection and immunity · 2026
    Article
  4. Cell death pathways in response toInfection and immunity · 2025
    Review
  5. Review
  6. Pathogens (Basel, Switzerland) · 2023
    Article
  7. Virulence Factors ofPathogens (Basel, Switzerland) · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Pathological and protective roles of dendritic cells inFrontiers in cellular and infection microbiology · 2022
    Review
  14. The Role of NRF2 in Mycobacterial Infection.Antioxidants (Basel, Switzerland) · 2021
    Review
  15. Review
  16. Frontiers in immunology · 2021
    Article
  17. Review
  18. Towards new TB vaccines.Seminars in immunopathology · 2020
    Review
  19. eLife · 2020
    Article
  20. Review

96 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Joseph HincheyDepartment of Microbiology and Immunology and Howard Hughes Medical Institute, Albert Einstein College of Medicine, New York, New York 10461, USA.
Sunhee Lee
Bo Y Jeon
Randall J Basaraba
Manjunatha M Venkataswamy
Bing Chen
John Chan
Miriam Braunstein
Ian M Orme
Steven C Derrick
Sheldon L Morris
William R Jacobs
Steven A Porcelli

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Immunology/Pathology CoreP30AI051519 · NIAID · YESHIVA UNIVERSITY · PI GOLDSTEIN, HARRIS · 2003 to 2013
$18.6M
"The Tuberculous Granuloma"P01AI063537 · NIAID · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI CHAN, JOHN R. · 2005 to 2015
$15.7M
Guinea pig model for TB vaccine evaluationsR01AI054697 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI ORME, IAN M · 2003 to 2007
$3.0M
Protein Secretion Pathways of Mycobacterium tuberculosisR01AI054540 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BRAUNSTEIN, MIRIAM S. · 2004 to 2013
$2.7M
NCI NIH HHS CA 13330NCI NIH HHS P30 CA013330NIAID NIH HHS AI 051519NIAID NIH HHS AI054697NIAID NIH HHS AI063537NIAID NIH HHS AI54540NIAID NIH HHS HHSN266200400091CNIAID NIH HHS P01 AI063537NIAID NIH HHS P30 AI051519NIAID NIH HHS R01 AI054540NIAID NIH HHS R01 AI054697PHS HHS HHSN266200400091C
6 · The paper itself

Abstract

The inhibition of apoptosis of infected host cells is a well-known but poorly understood function of pathogenic mycobacteria. We show that inactivation of the secA2 gene in Mycobacterium tuberculosis, which encodes a component of a virulence-associated protein secretion system, enhanced the apoptosis of infected macrophages by diminishing secretion of mycobacterial superoxide dismutase. Deletion of secA2 markedly increased priming of antigen-specific CD8(+) T cells in vivo, and vaccination of mice and guinea pigs with a secA2 mutant significantly increased resistance to M. tuberculosis challenge compared with standard M. bovis bacille Calmette-Guérin vaccination. Our results define a mechanism for a key immune evasion strategy of M. tuberculosis and provide what we believe to be a novel approach for improving mycobacterial vaccines.

Indexed as

Adenosine TriphosphatasesBacterial ProteinsGene DeletionMembrane Transport ProteinsAnimalsCell LineGuinea PigsHumansMacrophagesMiceMice, Inbred BALB CMycobacterium bovisMycobacterium tuberculosisSuperoxide DismutaseTuberculosisTuberculosis VaccinesAdenosine TriphosphatasesBacterial ProteinsMembrane Transport ProteinsSecA2 protein, MycobacteriumSuperoxide DismutaseTuberculosis Vaccines

Identifiers

PMID17671656
PMCPMC1934588

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.