Evidence map›Paper›PMID 25121778›Full record

ArticleClinical and vaccine immunology : CVI2014

Decorin binding proteins A and B in the serodiagnosis of Lyme disease in North America.

Paul M Arnaboldi, Mariya Sambir, Raymond J Dattwyler

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Laboratory Diagnosis of Lyme Borreliosis.Clinical microbiology reviews · 2021
    Review
  8. Detection of antibodies to decorin-binding protein A (DbpA) and DbpB after infection of dogs withJournal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2020
    Article
  9. Article
  10. Advances in Serodiagnostic Testing for Lyme Disease Are at Hand.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Cross-Reactive Epitopes in Borrelia burgdorferi p66.Clinical and vaccine immunology : CVI · 2015
    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

3 authors at 2 institutions in 1 country.

Paul M ArnaboldiBiopeptides Corp., East Setauket, New York, USA Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA.
Mariya SambirBiopeptides Corp., East Setauket, New York, USA Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA.
Raymond J DattwylerBiopeptides Corp., East Setauket, New York, USA Department of Microbiology and Immunology, New York Medical College, Valhalla, New York, USA Department of Medicine, New York Medical College, Valhalla, New York, USA raymond_dattwyler@nymc.edu.
New York Medical College · USBiopeptide (United States) · US

Funding

Multi-antigen peptide assay for the serodiagnosis of Lyme diseaseR44AI074092 · NIAID · BIOPEPTIDES, INC. · PI GOMES-SOLECKI, MARIA · 2009 to 2011
$2.0M
Development of a Cytokine Release Assay as a Diagnostic Test for Lyme DiseaseR43AI102435 · NIAID · BIOPEPTIDES, INC. · PI ARNABOLDI, PAUL MICHAEL · 2012 to 2013
$600k
NIAID NIH HHS R43 AI102435NIAID NIH HHS R44 AI074092
6 · The paper itself

Abstract

The laboratory diagnosis of Lyme disease is based upon the detection of antibodies generated against Borrelia burgdorferi using a two-tier assay, typically consisting of an enzyme-linked immunosorbent assay (ELISA), followed by a Western blot. This system, put into place to address the nonspecificity associated with standalone first-tier assays, is insensitive for diagnosing early infection, when most people seek care. The use of bacterial lysates or whole-protein antigens as first-tier assay targets contributes to nonspecificity due, in part, to the presence of cross-reactive epitopes that are also found in other bacteria. This precludes their use as sensitive standalone assays. The use of peptides containing linear epitopes that are highly specific for B. burgdorferi offers a method for reducing this cross-reactivity. In the present study, we mapped the linear epitopes of the prominently expressed Borrelia adhesins decorin binding protein A (DbpA) and DbpB. We identified several epitopes in each protein that were highly conserved among North American strains of B. burgdorferi, and we screened peptides containing specific epitopes using serum panels from early and late Lyme disease patients. The individual peptides primarily detected IgM but not IgG, while the proteins efficiently detected both IgM and IgG. While no individual peptide demonstrated better utility for antibody detection than its respective whole protein, an assay containing a combination of a DbpA and a DbpB peptide adequately detected both IgM and IgG, accurately identifying 87.5% (84/96) of the early Lyme disease patients and 80.0% (16/20) of the late Lyme disease patients.

Indexed as

Adhesins, BacterialAntigens, BacterialEpitopes, B-LymphocyteAntibodies, BacterialBorrelia burgdorferiEarly DiagnosisHumansImmunoglobulin GImmunoglobulin MLyme DiseaseNorth AmericaSensitivity and SpecificitySerologic TestsAdhesins, BacterialAntibodies, BacterialAntigens, BacterialDdpB protein, Borrelia burgdorferiEpitopes, B-LymphocyteImmunoglobulin GImmunoglobulin M

Identifiers

PMID25121778
PMCPMC4266351
OpenAlexW2154533825

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.