Evidence map›Paper›PMID 37922270›Full record

Observational studyPloS one2023

Circulating antibody-secreting cells are a biomarker for early diagnosis in patients with Lyme disease.

Natalie S Haddad, Sophia Nozick, Shant Ohanian, Robert Smith, Susan Elias, Paul G Auwaerter, F Eun-Hyung Lee, John L Daiss

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Borrelia surface proteins: new horizons in Lyme disease diagnosis.Applied microbiology and biotechnology · 2025
    Review
  2. Article
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Natalie S HaddadMicroB-plex, Inc., Atlanta, GA, United States of America.ORCID 0000-0002-1348-3094
Sophia NozickMicroB-plex, Inc., Atlanta, GA, United States of America.
Shant OhanianMicroB-plex, Inc., Atlanta, GA, United States of America.
Robert SmithDivision of Infectious Diseases, Maine Medical Center, MaineHealth Institute for Research, Portland, ME, United States of America.
Susan EliasDivision of Infectious Diseases, Maine Medical Center, MaineHealth Institute for Research, Portland, ME, United States of America.
Paul G AuwaerterSherrilyn and Ken Fisher Center for Environmental Infectious Diseases, The Johns Hopkins School of Medicine, Baltimore, MD, United States of America.
F Eun-Hyung LeeMicroB-plex, Inc., Atlanta, GA, United States of America.
John L DaissMicroB-plex, Inc., Atlanta, GA, United States of America.ORCID 0000-0002-9690-7701
MaineHealth · USEmory University · USJohns Hopkins University · US

Funding

Novel Diagnostics for Early Lyme DiseaseR43AI134543 · NIAID · MICROBPLEX, INC. · PI DAISS, JOHN LINFORTH · 2018 to 2019
$596k
NIAID NIH HHS R43 AI134543
6 · The paper itself

Abstract

backgroundDiagnostic immunoassays for Lyme disease have several limitations including: 1) not all patients seroconvert; 2) seroconversion occurs later than symptom onset; and 3) serum antibody levels remain elevated long after resolution of the infection.

introductionMENSA (Medium Enriched for Newly Synthesized Antibodies) is a novel diagnostic fluid that contains antibodies produced in vitro by circulating antibody-secreting cells (ASC). It enables measurement of the active humoral immune response.

methodsIn this observational, case-control study, we developed the MicroB-plex Anti-C6/Anti-pepC10 Immunoassay to measure antibodies specific for the Borrelia burgdorferi peptide antigens C6 and pepC10 and validated it using a CDC serum sample collection. Then we examined serum and MENSA samples from 36 uninfected Control subjects and 12 Newly Diagnosed Lyme Disease Patients.

resultsAmong the CDC samples, antibodies against C6 and/or pepC10 were detected in all seropositive Lyme patients (8/8), but not in sera from seronegative patients or healthy controls (0/24). Serum antibodies against C6 and pepC10 were detected in one of 36 uninfected control subjects (1/36); none were detected in the corresponding MENSA samples (0/36). In samples from newly diagnosed patients, serum antibodies identified 8/12 patients; MENSA antibodies also detected 8/12 patients. The two measures agreed on six positive individuals and differed on four others. In combination, the serum and MENSA tests identified 10/12 early Lyme patients. Typically, serum antibodies persisted 80 days or longer while MENSA antibodies declined to baseline within 40 days of successful treatment. DISCUSSION: MENSA-based immunoassays present a promising complement to serum immunoassays for diagnosis and tracking therapeutic success in Lyme infections.

Indexed as

Borrelia burgdorferiLyme DiseaseAntibodies, BacterialAntibody-Producing CellsAntigens, BacterialBiomarkersCase-Control StudiesEarly DiagnosisHumansImmunoglobulin GAntibodies, BacterialAntigens, BacterialBiomarkersImmunoglobulin G

Identifiers

PMID37922270
PMCPMC10624293
OpenAlexW4388286214

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.