Evidence map›Paper›PMID 11095745›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Recombinant bacillus calmette-guerin (BCG) vaccines expressing the Mycobacterium tuberculosis 30-kDa major secretory protein induce greater protective immunity against tuberculosis than conventional BCG vaccines in a highly susceptible animal model.

M A Horwitz, G Harth, B J Dillon, S Maslesa-Galic'

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 158 papers.

0numbers the graph read from it
0cells of the map it votes in
158citing papers in PubMed
15.3field-weighted citation impact, top 1% 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

158 citing papers in PubMed, 434 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Antigen 85B ofVaccines · 2026
    Review
  5. Article
  6. Construction and characterization of novelInfection and immunity · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. RecombinantVaccines · 2025
    Review
  11. Article
  12. Novel Targets for the Development of Tuberculosis Vaccine.Current drug discovery technologies · 2025
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Serosal membrane tuberculosis in Iran: A comprehensive review of evidences.Journal of clinical tuberculosis and other mycobacterial diseases · 2023
    Review
  19. Article
  20. The Induction of Antigen 85B-Specific CD8International journal of molecular sciences · 2023
    Article

98 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

4 authors at 2 institutions in 1 country.

M A HorwitzDepartment of Medicine, School of Medicine, University of California, 10833 Le Conte Avenue, Los Angeles, CA 90095, USA.
G Harth
B J Dillon
S Maslesa-Galic'
University of California, Los Angeles · USRockefeller University · US

Funding

IMMUNOPROTECTIVE DETERMINANTS OF M TUBERCULOSIS IN AIDSR01AI031338 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HORWITZ, MARCUS AARON · 1991 to 2010
$6.3M
NIAID NIH HHS AI31338NIAID NIH HHS R01 AI031338
6 · The paper itself

Abstract

Tuberculosis (TB) continues to ravage humanity, causing 2 million deaths per year. A vaccine against TB more potent than the current live vaccine, bacillus Calmette-Guérin (BCG), is desperately needed. Using two commercially available strains of BCG as host strains, BCG Connaught and Tice, we have constructed two recombinant BCG vaccines stably expressing and secreting the 30-kDa major secretory protein of Mycobacterium tuberculosis (M. tb.), the primary causative agent of TB. We have tested the efficacy of the two strains in the highly susceptible guinea pig model of pulmonary TB, a model noteworthy for its close resemblance to human TB. Animals immunized with the recombinant BCG vaccines and challenged by aerosol with a highly virulent strain of M. tb. had 0.5 logs fewer M. tb. bacilli in their lungs and 1 log fewer bacilli in their spleens on average than animals immunized with their parental conventional BCG vaccine counterparts. Statistically, these differences were highly significant. Paralleling these results, at necropsy, animals immunized with the recombinant BCG vaccines had fewer and smaller lesions in the lung, spleen, and liver and significantly less lung pathology than animals immunized with the parental BCG vaccines. The recombinant vaccines are the first vaccines against TB more potent than the current commercially available BCG vaccines, which were developed nearly a century ago.

Indexed as

AnimalsBCG VaccineDisease Models, AnimalGuinea PigsHypersensitivity, DelayedMaleMycobacterium tuberculosisSkinTuberculosisVaccines, SyntheticBCG VaccineVaccines, Synthetic

Identifiers

PMID11095745
PMCPMC17665
OpenAlexW2049675690

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.