Evolution of the serologic response to Borrelia burgdorferi in treated patients with culture-confirmed erythema migrans
- PMID: 8748261
- PMCID: PMC228718
- DOI: 10.1128/jcm.34.1.1-9.1996
Evolution of the serologic response to Borrelia burgdorferi in treated patients with culture-confirmed erythema migrans
Abstract
We investigated the appearance and evolution of immunoglobulin M (IgM) and IgG antibodies to Borrelia burgdorferi in 46 patients with culture-proven erythema migrans (EM). All patients received antimicrobial treatment and were prospectively evaluated for up to 1 year. A total of 257 serially collected serum samples were tested by commercial IgG-IgM enzyme-linked immunosorbent assay and separate IgM and IgG immunoblots (IBs). At the baseline, 33% of the patients had a positive ELISA result and 43% of the patients had a positive IgM IB result by using the criteria of the Centers for Disease Control and Prevention-Association of State and Territorial Public Health Laboratory Directors for the interpretation of IB results. Positive serology at the baseline and the rate of seroconversion correlated directly with disease duration and/or evidence of dissemination prior to treatment. At days 8 to 14 after the baseline, 91% of patients had a positive ELISA result and/or IgM IB result. Peak IgM antibody levels were seen at this time in patients with localized or disseminated disease. The most frequent IgM bands at the baseline and the peak were of 24 kDa (OspC), 41 kDa, and 37 kDa. Although 89% of the patients developed IgG antibodies as determined at a follow-up examination, only 22% were positive by the IgG IB criteria of the Centers for Disease Control and Prevention-Association of State and Territorial Public Health Laboratory Directors. The persistence of antibodies was directly related to disease duration and/or dissemination prior to treatment. Since IgM antibodies to the 24- and 41-kDa antigens remained detectable for long periods, 38% of IgM IBs were still positive at 1 year postbaseline. IgM to antigens of 39, 58, 60, 66, or 93 kDa, conversely, were most often seen in sera obtained within 1 month postbaseline. Their presence may be of assistance in confirming a recent infection with B. burgdorferi in individuals living in areas where Lyme disease is endemic.
Similar articles
-
Immunoblot interpretation criteria for serodiagnosis of early Lyme disease.J Clin Microbiol. 1995 Feb;33(2):419-27. doi: 10.1128/jcm.33.2.419-427.1995. J Clin Microbiol. 1995. PMID: 7714202 Free PMC article.
-
Serological follow-up after treatment of patients with erythema migrans and neuroborreliosis.J Clin Microbiol. 1994 Jun;32(6):1519-25. doi: 10.1128/jcm.32.6.1519-1525.1994. J Clin Microbiol. 1994. PMID: 8077398 Free PMC article.
-
Erythema migrans and serodiagnosis by enzyme immunoassay and immunoblot with three borrelia species.Wien Klin Wochenschr. 1999 Dec 10;111(22-23):951-6. Wien Klin Wochenschr. 1999. PMID: 10666807
-
Lyme borreliosis--problems of serological diagnosis.Infection. 1996 Nov-Dec;24(6):470-2. doi: 10.1007/BF01713052. Infection. 1996. PMID: 9007597 Review.
-
Cutaneous manifestations of Lyme borreliosis.Rheum Dis Clin North Am. 1989 Nov;15(4):627-34. Rheum Dis Clin North Am. 1989. PMID: 2685922 Review.
Cited by
-
Cerebrospinal fluid-infiltrating CD4+ T cells recognize Borrelia burgdorferi lysine-enriched protein domains and central nervous system autoantigens in early lyme encephalitis.Infect Immun. 2007 Jan;75(1):243-51. doi: 10.1128/IAI.01110-06. Epub 2006 Oct 23. Infect Immun. 2007. PMID: 17060473 Free PMC article.
-
Temporal changes in outer surface proteins A and C of the lyme disease-associated spirochete, Borrelia burgdorferi, during the chain of infection in ticks and mice.J Clin Microbiol. 2000 Jan;38(1):382-8. doi: 10.1128/JCM.38.1.382-388.2000. J Clin Microbiol. 2000. PMID: 10618120 Free PMC article.
-
Borrelia miyamotoi: A Comprehensive Review.Pathogens. 2023 Feb 7;12(2):267. doi: 10.3390/pathogens12020267. Pathogens. 2023. PMID: 36839539 Free PMC article. Review.
-
Borrelia burgdorferi VlsE antigen for the serological diagnosis of Lyme borreliosis.Eur J Clin Microbiol Infect Dis. 2008 May;27(5):349-54. doi: 10.1007/s10096-007-0445-7. Epub 2008 Jan 16. Eur J Clin Microbiol Infect Dis. 2008. PMID: 18197445
-
Detection of a Low Level and Heterogeneous B Cell Immune Response in Peripheral Blood of Acute Borreliosis Patients With High Throughput Sequencing.Front Immunol. 2019 May 16;10:1105. doi: 10.3389/fimmu.2019.01105. eCollection 2019. Front Immunol. 2019. PMID: 31156648 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources