Evidence map›Paper›PMID 18460016›Full record

ArticleClinical and experimental immunology2008

Identification and characterization of Mycobacterium tuberculosis antigens in urine of patients with active pulmonary tuberculosis: an innovative and alternative approach of antigen discovery of useful microbial molecules.

S S Kashino, N Pollock, D R Napolitano, V Rodrigues, A Campos-Neto

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
1.5field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Proteomic Analysis of Urine from Patients withTropical medicine and infectious disease · 2022
    Article
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  14. Advances in Diagnostic Assays for Tuberculosis.Cold Spring Harbor perspectives in medicine · 2015
    Review
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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

5 authors at 3 institutions in 3 countries.

S S KashinoThe Forsyth Institute, Boston, MA, USA.
N Pollock
D R Napolitano
V Rodrigues
A Campos-Neto
Hadassah Medical Center · ILUniversidade Federal do Triângulo Mineiro · BRUniversity of Massachusetts Chan Medical School · US

Funding

TB Vaccine Candidates Found in Patients' Bodily Fluids and Murine MHC-1 MoleculeR01AI076425 · NIAID · ADA FORSYTH INSTITUTE, INC. · PI CAMPOS-NETO, ANTONIO · 2008 to 2012
$2.9M
Development and Evaluation of a Novel Diagnostic Test for Active TuberculosisK23AI074638 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI POLLOCK, NIRA · 2008 to 2012
$633k
Antigen Detection Assay for TuberculosisR41AI068291 · NIAID · INBIOS INTERNATIONAL, INC. · PI CAMPOS-NETO, ANTONIO · 2006 to 2006
$387k
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR011244 · NCRR · FORSYTH INSTITUTE · PI STASHENKO, PHILIP · 1996 to 1996
–
NCRR NIH HHS C06RR11244NIAID NIH HHS AI068291NIAID NIH HHS K23 AI074638NIAID NIH HHS R01 AI076425NIAID NIH HHS R41 AI068291NIAID NIH HHS R41AI068291
6 · The paper itself

Abstract

Despite the clear need to control tuberculosis, the diagnosis and prevention of this serious disease are poorly developed and have remained fundamentally unchanged for more than 50 years. Here, we introduce an innovative approach to directly identify Mycobacterium tuberculosis antigens produced in vivo in humans with tuberculosis. We combined reversed phase high performance liquid chromatography and mass spectrometry and categorize four distinct M. tuberculosis proteins produced presumably in lung lesions and excreted in the urine of patients with pulmonary tuberculosis. The genes (MT_1721, MT_1694, MT_2462 and MT_3444) coding for these proteins were cloned and the recombinant molecules were produced in Escherichia coli. The proteins were recognized by immunoglobulin G antibodies from tuberculosis patients but not from non-diseased subjects. In addition, the recombinant proteins were recognized strongly by peripheral blood mononuclear cells from healthy purified protein derivative of tuberculin-positive individuals and to a lesser extent from patients with tuberculosis. These molecules are the only proteins reported to date that are derived directly from bodily fluids of tuberculosis patients, therefore are interesting candidate antigens for the development of vaccine and/or antigen detection assay for accurate diagnosis of active tuberculosis.

Indexed as

Acute DiseaseAntigens, BacterialBlotting, WesternCase-Control StudiesCell ProliferationGenes, BacterialHumansImmunoglobulin GInterferon-gammaMass SpectrometryMolecular WeightMycobacterium tuberculosisOpen Reading FramesRecombinant ProteinsT-LymphocytesTuberculosis, PulmonaryAntigens, BacterialImmunoglobulin GInterferon-gammaMycobacterium tuberculosis antigensRecombinant ProteinsTuberculosis Vaccines

Identifiers

PMID18460016
PMCPMC2432097
OpenAlexW2100739881

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.