Evidence map›Paper›PMID 12857778›Full record

ReviewClinical microbiology reviews2003

Mycobacterium tuberculosis pathogenesis and molecular determinants of virulence.

Issar Smith

Abstract readReview
In one paragraph

Review in Clinical microbiology reviews, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 418 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
418citing papers in PubMed, 1 pooled it
–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

418 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Bacterialized tumor cells as vaccine.EMBO molecular medicine · 2026
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358 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

1 author.

Issar SmithTB Center, Public Health Research Institute, International Center for Public Health, Newark, New Jersey 07103-3535, USA. smitty@phri.org

Funding

Regulated expression of B. burgdorferi virulence genesR01AI048856 · NIAID · NEW YORK MEDICAL COLLEGE · PI CABELLO, FELIPE CARDENAS · 2001 to 2010
$2.6M
M. tuberculosis &host gene expression during infectionR01HL068513 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI SMITH, ISSAR · 2001 to 2005
$2.6M
STUDIES OF M TUBERCULOSIS SURVIVAL IN ANIMAL MODELSR01HL064544 · NHLBI · PUBLIC HEALTH RESEARCH INSTITUTE · PI SMITH, ISSAR · 1999 to 2003
$1.7M
NHLBI NIH HHS R01 HL064544NHLBI NIH HHS R01 HL068513NHLBI NIH HHS R01 HL 64544NHLBI NIH HHS R01 HL 68513NIAID NIH HHS R01 AI48856
6 · The paper itself

Abstract

Tuberculosis (TB), one of the oldest known human diseases. is still is one of the major causes of mortality, since two million people die each year from this malady. TB has many manifestations, affecting bone, the central nervous system, and many other organ systems, but it is primarily a pulmonary disease that is initiated by the deposition of Mycobacterium tuberculosis, contained in aerosol droplets, onto lung alveolar surfaces. From this point, the progression of the disease can have several outcomes, determined largely by the response of the host immune system. The efficacy of this response is affected by intrinsic factors such as the genetics of the immune system as well as extrinsic factors, e.g., insults to the immune system and the nutritional and physiological state of the host. In addition, the pathogen may play a role in disease progression since some M. tuberculosis strains are reportedly more virulent than others, as defined by increased transmissibility as well as being associated with higher morbidity and mortality in infected individuals. Despite the widespread use of an attenuated live vaccine and several antibiotics, there is more TB than ever before, requiring new vaccines and drugs and more specific and rapid diagnostics. Researchers are utilizing information obtained from the complete sequence of the M. tuberculosis genome and from new genetic and physiological methods to identify targets in M. tuberculosis that will aid in the development of these sorely needed antitubercular agents.

Indexed as

AnimalsAntitubercular AgentsDisease Models, AnimalGenome, BacterialHumansMacrophagesMycobacterium tuberculosisProteomicsTranscription, GeneticTuberculosisVirulenceAntitubercular Agents

Identifiers

PMID12857778
PMCPMC164219

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.