Evidence map›Paper›PMID 19250549›Full record

Trial reportBMC infectious diseases2009

T-SPOT.TB responses during treatment of pulmonary tuberculosis.

Samantha Ribeiro, Kelly Dooley, Judith Hackman, Carla Loredo, Anne Efron, Richard E Chaisson, Marcus B Conde, Neio Boechat, Susan E Dorman

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in BMC infectious diseases, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Interferon-gamma response to the treatment of active pulmonary and extra-pulmonary tuberculosis.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2017
    Observational
  14. Article
  15. Diagnostic Significance ofChinese medical journal · 2017
    Article
  16. Article
  17. Article
  18. Diagnostic value of T-SPOT.Experimental and therapeutic medicine · 2015
    Article
  19. Article
  20. Review
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

9 authors.

Samantha RibeiroInstituto de Doenças do Torax/Hospital Clementino Fraga Filho/Universidade Federal do Rio de Janeiro, Brazil. sbrmicroimuno@yahoo.com.br
Kelly Dooley
Judith Hackman
Carla Loredo
Anne Efron
Richard E Chaisson
Marcus B Conde
Neio Boechat
Susan E Dorman

Funding

Rapid Detection of Mycobacterium tuberculosisK23AI051528 · NIAID · JOHNS HOPKINS UNIVERSITY · PI DORMAN, SUSAN E · 2003 to 2007
$657k
NIAID NIH HHS AI51528
6 · The paper itself

Abstract

backgroundImmune responses to Mycobacterium tuberculosis antigens could serve as surrogate markers of treatment response.

methodsUsing the T-SPOT.TB assay and frozen peripheral blood mononuclear cells, we enumerated ESAT-6- and CFP-10-specific IFN-gamma-producing T cells over time in pulmonary TB patients receiving directly observed treatment. T cell responses (measured as "spot forming cells" or "SFCs") were assessed prior to treatment and at 16 and 24 weeks of treatment.

results58 patients were evaluated, of whom 57 were HIV seronegative. Mean (SD) ESAT-6, CFP-10, and summed RD1 specific SFCs declined from 42.7 (72.7), 41.2 (66.4), and 83.8 (105.7) at baseline to 23.3 (39.4, p = 0.01), 23.2 (29.4, p = 0.18), and 46.5 (59.5, p = 0.02) at completion of 24 weeks of treatment, respectively. Only 10% of individuals with a baseline reactive test reverted to negative at treatment week 24. For the group that was culture positive at completion of 8 weeks of treatment compared to the culture negative group, the incidence rate ratio (IRR) of ESAT-6, CFP-10, and summed RD1 specific SFC counts were, respectively, 2.23 (p = 0.048), 1.51 (p = 0.20), and 1.83 (p = 0.047). Patients with cavitary disease had mean ESAT-6 specific SFC counts that were higher than those without cavitary disease (IRR 2.08, p = 0.034).

conclusionIFN-gamma-producing RD1-specific T cells, as measured in the T-SPOT.TB assay, may be directly related to bacterial load in patients undergoing treatment for pulmonary TB. However, high inter-subject variability in quantitative results coupled with failure of reversion to negative of qualitative results in most subjects at treatment completion may limit the utility of this assay as a surrogate marker for treatment efficacy.

Indexed as

AdultAntigens, BacterialBacterial ProteinsCell CountDouble-Blind MethodEnzyme-Linked Immunosorbent AssayFemaleHumansInterferon-gammaLongitudinal StudiesMaleMycobacterium tuberculosisPredictive Value of TestsT-LymphocytesTreatment OutcomeTuberculosis, PulmonaryAntigens, BacterialBacterial ProteinsESAT-6 protein, Mycobacterium tuberculosisInterferon-gamma

Identifiers

PMID19250549
PMCPMC2651889

What OpenQuestion holds

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Registered trials

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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.