Evidence map›Paper›PMID 11773115›Full record

ArticleJournal of clinical microbiology2002

Recombinant assay for serodiagnosis of Lyme disease regardless of OspA vaccination status.

Maria J C Gomes-Solecki, Gary P Wormser, Martin Schriefer, Glenn Neuman, Laura Hannafey, John D Glass, Raymond J Dattwyler

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Journal of clinical microbiology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.7field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Detection ofVeterinary sciences · 2022
    Article
  3. Article
  4. Laboratory Diagnosis of Lyme Borreliosis.Clinical microbiology reviews · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Laboratory diagnosis of Lyme disease: advances and challenges.Infectious disease clinics of North America · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. 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

7 authors at 5 institutions in 1 country.

Maria J C Gomes-SoleckiBrook Biotechnologies, Inc., Stony Brook, New York 11790-3350, USA.
Gary P Wormser
Martin Schriefer
Glenn Neuman
Laura Hannafey
John D Glass
Raymond J Dattwyler
Stony Brook University · USBostwick Laboratories · USCenters for Disease Control and Prevention · USNew York Medical College · USState University of New York · US

Funding

B BURGDORFERI IMMUNODIAGNOSTICS FOR THE VACCINE ERAR44AI044572 · NIAID · BROOK BIOTECHNOLOGIES, INC. · PI GLASS, JOHN D · 1999 to 2001
$855k
NIAID NIH HHS 5 R44 AI44572
6 · The paper itself

Abstract

All current seroassays using cultured Borrelia burgdorferi as their antigen source have been rendered obsolete by the recombinant OspA Lyme disease vaccine. OspA is the major outer surface protein expressed in cultured B. burgdorferi, and any seroassay that uses whole organisms as its antigen source cannot differentiate between subjects who received the vaccine and those who were naturally infected. We developed a new sensitive and specific enzyme-linked immunosorbent assay (ELISA) utilizing recombinant chimeric borrelia proteins devoid of OspA (rNon-OspA) that can be used to detect antibodies to diagnostically important B. burgdorferi antigens in both OspA-vaccinated and nonvaccinated individuals. We tested sera from patients with Lyme disease and with conditions associated with false-positive serologies, OspA-vaccinated individuals, and healthy high-risk workers from an area of endemicity and normal sera from individuals from areas of nonendemicity. The rNon-OspA test was compared with two commercially available whole-cell immunoassays. The rNon-OspA assay is as sensitive and specific as the whole-cell assay (P > 0.05) for detection of anti-B. burgdorferi antibodies. However, the rNon-OspA assay can differentiate between populations comprised of naturally infected and OspA-vaccinated individuals (P < 0.05). Our data demonstrate that this new sensitive rNon-OspA ELISA can be used for the laboratory detection of B. burgdorferi antibodies regardless of vaccination status and could replace existing serologic assays for Lyme disease.

Indexed as

LipoproteinsAntibodies, BacterialAntigens, SurfaceBacterial Outer Membrane ProteinsBacterial ProteinsBacterial VaccinesBorrelia burgdorferiEnzyme-Linked Immunosorbent AssayHumansLyme DiseaseLyme Disease VaccinesRecombinant Fusion ProteinsSensitivity and SpecificityVaccinationVaccines, DNAAntibodies, BacterialAntigens, SurfaceBacterial Outer Membrane ProteinsBacterial ProteinsBacterial VaccinesLipoproteinsLyme Disease VaccinesOspA proteinRecombinant Fusion ProteinsVaccines, DNA

Identifiers

PMID11773115
PMCPMC120112
OpenAlexW2082117707

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.