Evidence map›Paper›PMID 10338503›Full record

ArticleInfection and immunity1999

Molecular characterization and human T-cell responses to a member of a novel Mycobacterium tuberculosis mtb39 gene family.

D C Dillon, M R Alderson, C H Day, D M Lewinsohn, R Coler, T Bement, A Campos-Neto, Y A Skeiky, I M Orme, A Roberts and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 2 syntheses or guidelines pooled it, 153 citations in OpenAlex.

  1. Pooled it
  2. Immunogenicity and Safety of the M72/AS01Frontiers in immunology · 2019
    Pooled it
  3. Trial
  4. Phase 2b Controlled Trial of M72/AS01The New England journal of medicine · 2018
    Trial
  5. Trial
  6. Trial
  7. Trial
  8. Article
  9. Gene conversion is a key driver of diversity hotspots inbioRxiv : the preprint server for biology · 2026
    Article
  10. Protease shaving ofMicrobiology spectrum · 2025
    Article
  11. Review
  12. The PE/PPE family proteins ofFrontiers in immunology · 2025
    Review
  13. Protease shaving ofbioRxiv : the preprint server for biology · 2024
    Article
  14. Review
  15. Review
  16. Vaccines · 2023
    Review
  17. Article
  18. AttenuatediScience · 2023
    Article
  19. Review
  20. Review

11 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

14 authors at 6 institutions in 2 countries.

D C DillonCorixa Corporation, Seattle, Washington 98104, USA. dillon@corixa.com
M R Alderson
C H Day
D M Lewinsohn
R Coler
T Bement
A Campos-Neto
Y A Skeiky
I M Orme
A Roberts
S Steen
W Dalemans
R Badaro
S G Reed
Corixa Corporation · USInfectious Disease Research Institute · USColorado State University · USNew Frontier · USUniversidade Federal da Bahia · BRUniversity of Washington · US

Funding

TUBERCULOSIS RESEARCH MATERIALS AND VACINE TESTINGN01AI075320 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · 1997 to 2004
$980k
NIAID NIH HHS AI-75320
6 · The paper itself

Abstract

We have used expression screening of a genomic Mycobacterium tuberculosis library with tuberculosis (TB) patient sera to identify novel genes that may be used diagnostically or in the development of a TB vaccine. Using this strategy, we have cloned a novel gene, termed mtb39a, that encodes a 39-kDa protein. Molecular characterization revealed that mtb39a is a member of a family of three highly related genes that are conserved among strains of M. tuberculosis and Mycobacterium bovis BCG but not in other mycobacterial species tested. Immunoblot analysis demonstrated the presence of Mtb39A in M. tuberculosis lysate but not in culture filtrate proteins (CFP), indicating that it is not a secreted antigen. This conclusion is strengthened by the observation that a human T-cell clone specific for purified recombinant Mtb39A protein recognized autologous dendritic cells infected with TB or pulsed with purified protein derivative (PPD) but did not respond to M. tuberculosis CFP. Purified recombinant Mtb39A elicited strong T-cell proliferative and gamma interferon responses in peripheral blood mononuclear cells from 9 of 12 PPD-positive individuals tested, and overlapping peptides were used to identify a minimum of 10 distinct T-cell epitopes. Additionally, mice immunized with mtb39a DNA have shown increased protection from M. tuberculosis challenge, as indicated by a reduction of bacterial load. The human T-cell responses and initial animal studies provide support for further evaluation of this antigen as a possible component of a subunit vaccine for M.tuberculosis.

Indexed as

Genes, BacterialAdolescentAmino Acid SequenceAnimalsAntigens, BacterialBCG VaccineDendritic CellsFemaleHumansLeukocytes, MononuclearMaleMiceMice, Inbred C57BLMiddle AgedMolecular Sequence DataMultigene FamilyAntigens, BacterialBCG VaccineVaccines, DNA

Identifiers

PMID10338503
PMCPMC96604
OpenAlexW2132657101

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.