Evidence map›Paper›PMID 24810599›Full record

ArticlePLoS neglected tropical diseases2014

Field-evaluation of a new lateral flow assay for detection of cellular and humoral immunity against Mycobacterium leprae.

Kidist Bobosha, Elisa M Tjon Kon Fat, Susan J F van den Eeden, Yonas Bekele, Jolien J van der Ploeg-van Schip, Claudia J de Dood, Karin Dijkman, Kees L M C Franken, Louis Wilson, Abraham Aseffa and 4 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Synthetic Phenolic Glycolipids for Application in Diagnostic Tests for Leprosy.Chembiochem : a European journal of chemical biology · 2021
    Article
  10. Article
  11. Insights intoProteomes · 2021
    Review
  12. Detection and Monitoring ofFrontiers in microbiology · 2021
    Article
  13. Review
  14. Transcriptomic Analysis ofFrontiers in cellular and infection microbiology · 2021
    Article
  15. Article
  16. Review
  17. Article
  18. [Research advance of lateral flow assay labels].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2018
    Review
  19. Article
  20. Article
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.

Kidist BoboshaDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Elisa M Tjon Kon FatDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Susan J F van den EedenDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Yonas BekeleArmauer Hansen Research Institute, Addis Ababa, Ethiopia.
Jolien J van der Ploeg-van SchipDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Claudia J de DoodDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Karin DijkmanDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Kees L M C FrankenDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Louis WilsonDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Abraham AseffaArmauer Hansen Research Institute, Addis Ababa, Ethiopia.
John S SpencerDepartment of Microbiology, Immunology & Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Tom H M OttenhoffDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Paul L A M CorstjensDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Annemieke GelukDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundField-applicable tests detecting asymptomatic Mycobacterium leprae (M. leprae) infection or predicting progression to leprosy, are urgently required. Since the outcome of M. leprae infection is determined by cellular- and humoral immunity, we aim to develop diagnostic tests detecting pro-/anti-inflammatory and regulatory cytokines as well as antibodies against M. leprae. Previously, we developed lateral flow assays (LFA) for detection of cytokines and anti-PGL-I antibodies. Here we evaluate progress of newly developed LFAs for applications in resource-poor settings.

methodsThe combined diagnostic value of IP-10, IL-10 and anti-PGL-I antibodies was tested using M. leprae-stimulated blood of leprosy patients and endemic controls (EC). For reduction of the overall test-to-result time the minimal whole blood assay time required to detect distinctive responses was investigated. To accommodate LFAs for field settings, dry-format LFAs for IP-10 and anti-PGL-I antibodies were developed allowing storage and shipment at ambient temperatures. Additionally, a multiplex LFA-format was applied for simultaneous detection of anti-PGL-I antibodies and IP-10. For improved sensitivity and quantitation upconverting phosphor (UCP) reporter technology was applied in all LFAs.

resultsSingle and multiplex UCP-LFAs correlated well with ELISAs. The performance of dry reagent assays and portable, lightweight UCP-LF strip readers indicated excellent field-robustness. Notably, detection of IP-10 levels in stimulated samples allowed a reduction of the whole blood assay time from 24 h to 6 h. Moreover, IP-10/IL-10 ratios in unstimulated plasma differed significantly between patients and EC, indicating the feasibility to identify M. leprae infection in endemic areas.

conclusionsDry-format UCP-LFAs are low-tech, robust assays allowing detection of relevant cytokines and antibodies in response to M. leprae in the field. The high levels of IP-10 and the required shorter whole blood assay time, render this cytokine useful to discriminate between leprosy patients and EC.

Indexed as

Antibodies, BacterialAntigens, BacterialCytokinesHumansImmunologic TestsKineticsLeprosyMycobacterium lepraeAntibodies, BacterialAntigens, BacterialCytokines

Identifiers

PMID24810599
PMCPMC4014418

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.