Anti-Borrelia burgdorferi antibody response over the course of Lyme neuroborreliosis

Author:

Baig S1,Olsson T1,Hansen K1,Link H1

Affiliation:

1. Department of Neurology, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden.

Abstract

Characteristic findings on examination of cerebrospinal fluid (CSF) in Lyme neuroborreliosis include mononuclear pleocytosis, oligoclonal immunoglobulin G (IgG) bands, and evidence for local production of specific antibodies. We utilized an immunospot assay to detect cells secreting anti-Borrelia burgdorferi antibodies of different isotypes over the course of disease. Such cells were detected in CSF from 13 consecutive patients with neuroborreliosis examined before treatment. IgG antibody-secreting cells were present in high numbers (mean, 32 cells per 10(4) CSF cells), whereas IgA and IgM antibody-secreting cells were found less frequently and at lower numbers (mean, 5 and 6 cells per 10(4) CSF cells, respectively). Clinical improvement after penicillin treatment was paralleled by a rapid decline of antibody-secreting cells in CSF, but they were still detected, although at lower numbers, in 5 of 10 patients examined more than 6 months after treatment. This specific B-cell response persisted despite clinical improvement. Whether it reflects persistence of antigen is unsettled.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference38 articles.

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2. Baig S. T. Olsson and H. Link. 1989. Predominance of Borrelia burgdorferi specific B cells in cerebrospinal fluid in neuroborreliosis. Lancet ii:71-74.

3. The neurological complications of Borrelia burgdorferi in New Forest area of Hampshire;Bateman D. E.;J. Neurol. Neurosurg. Psych.,1988

4. Brouwer 0. F. 1987. Neuroborreliosis: Bannwarth syndrome and Lyme disease p. 199-213. In W. B. Matthews (ed.) Handbook of clinical neurology vol. 7. Elsevier Science Publishers Amsterdam.

5. Antigens of Borrelia burgdorferi recognized during Lyme disease, appearance of new immunoglobulin M response and expansion of the immunoglobulin G response late in illness;Craft J. E.;J. Clin. Invest.,1986

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