Immunoblot reactivity at follow-up in treated patients with Lyme neuroborreliosis and healthy controls.


Journal

Ticks and tick-borne diseases
ISSN: 1877-9603
Titre abrégé: Ticks Tick Borne Dis
Pays: Netherlands
ID NLM: 101522599

Informations de publication

Date de publication:
01 2019
Historique:
received: 20 07 2018
revised: 19 09 2018
accepted: 24 09 2018
pubmed: 26 10 2018
medline: 12 2 2019
entrez: 25 10 2018
Statut: ppublish

Résumé

About 5-20% of the general population in endemic areas have seroprevalence for anti-borrelial antibodies. Previous studies have shown a high rate of 25-97% of persisting anti-borrelial antibodies in patients with treated Lyme neuroborreliosis (LNB) at follow-up. These studies used immunoblots with antigens from whole-cell sonicates, which could be less specific than modern recombinant antigens. We assessed the seroprevalence of anti-borrelial antibodies in serum from patients with definite LNB and healthy controls with a line immunoblot using highly specific recombinant antigens. We retrospectively identified patients with treated definite LNB who were treated at the Medical Center-University of Freiburg. Serum from LNB patients at a mean follow-up period of 4.9 years (SD: 3.3) and serum from healthy controls were assessed for anti-borrelial antibodies with a line immunoblot with recombinant antigens. A total of 45 patients with definite LNB and 40 healthy controls were included. Ten LNB patients (22.7%) had persisting antibodies (IgG and/or IgM) in serum at follow-up. Serum samples from six healthy controls (15%) were positive for anti-borrelial antibodies (IgG and or IgM). Prevalence of positive IgM or IgG antibodies showed no statistically significant difference between LNB patients at follow-up and healthy controls (IgM p = 0.32, IgG p = 0.54). Immunoblot reactivity patterns at follow-up in LNB patients did not have statistically significant differences from healthy controls. The discrepancy regarding earlier studies reporting higher amounts of LNB patients with persisting antibodies could be due to a higher specificity of the antigens used in recombinant immunoblots compared to other immunoblots (e.g., whole-cell sonicates). The results of our study should be replicated in a larger prospective multi-center study.

Identifiants

pubmed: 30352738
pii: S1877-959X(18)30317-0
doi: 10.1016/j.ttbdis.2018.09.011
pii:
doi:

Substances chimiques

Antibodies, Bacterial 0
Antigens, Bacterial 0
Immunoglobulin G 0
Immunoglobulin M 0
Recombinant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

166-169

Informations de copyright

Copyright © 2018. Published by Elsevier GmbH.

Auteurs

R Dersch (R)

Department of Neurology, Medical Center - University of Freiburg, Germany. Electronic address: rick.dersch@uniklinik-freiburg.de.

A Sarnes (A)

Department of Neurology, Medical Center - University of Freiburg, Germany.

M Maul (M)

Department of Neurology, Medical Center - University of Freiburg, Germany.

O Minakowski (O)

Department of Neurology, Medical Center - University of Freiburg, Germany.

T Hottenrott (T)

Department of Neurology, Medical Center - University of Freiburg, Germany.

O Stich (O)

MVZ Neurology, Constance, Germany.

S Rauer (S)

Department of Neurology, Medical Center - University of Freiburg, Germany.

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Classifications MeSH