Evidence map›Paper›PMID 21544695›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2011

Specific IgG antibody responses may be used to monitor leprosy treatment efficacy and as recurrence prognostic markers.

M S Duthie, M N Hay, E M Rada, J Convit, L Ito, L K M Oyafuso, M I P Manini, I M B Goulart, J Lobato, L R Goulart and 2 more

Abstract read
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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Leprosy surveillance study in a highly endemic Brazilian area using leprosy specific serologic tests and IFNγ whole blood assay.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Accuracy of Enzyme-Linked Immunosorbent Assays (ELISAs) in Detecting Antibodies againstThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2018
    Review
  13. Frontiers in immunology · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Leprosy in the 21st century.Clinical microbiology reviews · 2015
    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

12 authors.

M S DuthieInfectious Disease Research Institute, 1124 Columbia St., Suite 400, Seattle, WA 98104, USA. mduthie@idri.org
M N Hay
E M Rada
J Convit
L Ito
L K M Oyafuso
M I P Manini
I M B Goulart
J Lobato
L R Goulart
D Carter
S G Reed

Funding

Developing a new leprosy diagnostic testR44AI066613 · NIAID · PAI LIFE SCIENCES, INC. · PI CARTER, DARRICK ALBERT · 2008 to 2009
$720k
Developing a new leprosy diagnostic testR43AI066613 · NIAID · PAI LIFE SCIENCES, INC. · PI CARTER, DARRICK ALBERT · 2007 to 2007
$100k
NIAID NIH HHS 1R43AI066613-01A1NIAID NIH HHS 2R44AI066613-02
6 · The paper itself

Abstract

Although curable, leprosy requires better diagnostic and prognostic tools to accompany therapeutic strategies. We evaluated the serum samples of leprosy patients from Venezuela and Brazil for reactivity against the specific recombinant proteins, ML0405 and ML2331, and the LID-1 fusion protein that incorporates both of these antigens. Antigen-specific IgG was highest in lepromatous leprosy patients (LL) and decreased across the disease spectrum, such that only a small subset of true tuberculoid patients (TT) tested positive. The impact of multidrug therapy (MDT) on these antibody responses was also examined. Several years after treatment, the vast majority of Venezuelan patients did not possess circulating anti-LID-1, anti-ML0405, and anti-ML2331 IgG, and the seropositivity of the remaining cases could be attributed to irregular treatment. At discharge, the magnitude and proportion of positive responses of Brazilian patients against the proteins and phenolic glycolipid (PGL)-I were lower for most of the clinical forms. The monthly examination of IgG levels in LL patient sera after MDT initiation indicated that these responses are significantly reduced during treatment. Thus, responses against these antigens positively correlate with bacillary load, clinical forms, and operational classification at diagnosis. Our data indicate that these responses could be employed as an auxiliary tool for the assessment of treatment efficacy and disease relapse.

Indexed as

Anti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialBrazilDrug MonitoringHumansImmunoglobulin GLeprosyLongitudinal StudiesRecombinant ProteinsRecurrenceTime FactorsTreatment OutcomeVenezuelaAnti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialImmunoglobulin GRecombinant Proteins

Identifiers

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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.