Evidence map›Paper›PMID 42618697›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Dynamics of IgM and IgG responses in Lyme neuroborreliosis - a Norwegian longitudinal study.

Ingerid Skarstein, Anne Marit Solheim, Åslaug Rudjord Lorentzen, Unn Ljøstad, Åse Mygland, Randi Eikeland, Harald Reiso, Christian Alexander Vedeler, Karl Brokstad, Steffan Daniel Bos and 1 more

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors.

Ingerid SkarsteinDepartment of Microbiology, Helse Bergen, Haukeland University Hospital, 1400, 5021, Bergen, Norway. Ingerid.skarstein@helse-bergen.no.ORCID https://orcid.org/0009-0006-3221-3643
Anne Marit SolheimDepartment of Neurology, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0001-7357-6287
Åslaug Rudjord LorentzenDepartment of Neurology, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0002-6918-4157
Unn LjøstadDepartment of Neurology, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0002-7666-1396
Åse MyglandDepartment of Neurology, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0001-9160-2805
Randi EikelandNorwegian National Advisory Unit on Tick-Borne Diseases, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0003-0104-9626
Harald ReisoNorwegian National Advisory Unit on Tick-Borne Diseases, Sørlandet Hospital Trust, Kristiansand, Norway.ORCID http://orcid.org/0000-0003-4874-8707
Christian Alexander VedelerDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Karl BrokstadDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0003-0593-2731
Steffan Daniel BosDepartment of Microbiology, Helse Bergen, Haukeland University Hospital, 1400, 5021, Bergen, Norway.ORCID http://orcid.org/0000-0002-2975-7520
Elling UlvestadDepartment of Microbiology, Helse Bergen, Haukeland University Hospital, 1400, 5021, Bergen, Norway.ORCID http://orcid.org/0000-0001-5901-8422

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe investigated longitudinal antibody responses against 13 different Borrelia burgdorferi (Bb) antigens in patients with Lyme neuroborreliosis (LNB) and explored whether antibody profiles were linked to length of symptoms and burden of symptoms prior to and after initiation of treatment.

methodsA well-characterized cohort of 106 patients of whom 85% had definite LNB were followed for twelve months, with serum and cerebrospinal fluid (CSF) sampled at baseline, six- and twelve-months follow-up. Antibodies were measured by the recomBead Borrelia IgG and IgM assay, with a subgroup examined for oligoclonal IgG production restricted to CSF.

resultsAntibody levels in both serum and CSF declined gradually after antibiotic treatment, with most of the reduction occurring within the first six months after treatment. Higher baseline IgM reactivity against p18 in both serum and CSF was associated with higher symptom burden prior to treatment. We found no differences in CSF antibody reactivity between patients with short (< 42 days) and long (≥ 42 days) symptom duration prior to treatment. In serum, patients with short symptom duration prior to treatment had higher IgM reactivity against p58 and higher IgG reactivity against OspC and p18. At baseline, 68% exhibited oligoclonal IgG production, falling to 41% six months after treatment. There was no correlation between oligoclonal IgG production and symptom burden.

conclusionBoth specific antibody production against a variety of antigens and intrathecal oligoclonal IgG production decreased after treatment for LNB, reflecting reduced antigenic load and thus reduced neuroinflammation. IgM and IgG reactivity against p18 were indicative of a shorter symptom duration and higher symptom burden prior to treatment.

Indexed as

AntibodiesCentral nervous system infectionsLyme neuroborreliosisTick-borne diseases

Identifiers

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Registered trials

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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 Socratic graph.