Format

Send to

Choose Destination
Clin Vaccine Immunol. 2014 Nov;21(11):1490-9. doi: 10.1128/CVI.00406-14. Epub 2014 Sep 3.

A Novel multivalent OspA vaccine against Lyme borreliosis is safe and immunogenic in an adult population previously infected with Borrelia burgdorferi sensu lato.

Author information

1
Vaccine R&D, Baxter BioScience, Vienna, Austria nina_wressnigg@baxter.com.
2
Vaccine R&D, Baxter BioScience, Orth/Donau, Austria.
3
Vaccine R&D, Baxter BioScience, Vienna, Austria.
4
Global R&D, Baxter BioScience, Vienna, Austria.
5
Health Center Mainz, Mainz, Germany.
6
Medical University of Vienna, Vienna, Austria.
7
University of Tübingen Institute of Tropical Medicine, Tübingen, Germany.
8
Berlin Center for Travel and Tropical Medicine, Berlin, Germany.
9
Klinik und Polikinik für Dermatologie Universitätsklinikum Carl Gustav Carus an der TU Dresden, Dresden, Germany.
10
Hautarztpraxis Cutanis, Freiburg, Germany.
11
Private practice, Rodgau, Germany.

Abstract

Lyme borreliosis (LB) patients who recover, as well as previously infected asymptomatic individuals, remain vulnerable to reinfection with Borrelia burgdorferi sensu lato. There is limited information available about the use of OspA vaccines in this population. In this study, a randomized double-blind phase I/II trial was performed to investigate the safety and immunogenicity of a novel multivalent OspA vaccine in healthy adults who were either seronegative or seropositive for previous B. burgdorferi sensu lato infection. The participants received three monthly priming immunizations with either 30 μg or 60 μg alum-adjuvanted OspA antigen and a booster vaccination either 6 months or 9 to 12 months after the first immunization. The antibody responses to the six OspA serotypes included in the vaccine were evaluated. Adverse events were predominantly mild and transient and were similar in the seronegative and seropositive populations. Substantial enzyme-linked immunosorbent assay (ELISA) and surface-binding antibody responses against all six OspA antigens were induced after the primary immunization schedule in both populations, and they were substantially increased with both booster schedules. The antibody responses induced by the two doses were similar in the seronegative population, but there was a significant dose response in the seropositive population. These data indicate that the novel multivalent OspA vaccine is well tolerated and immunogenic in individuals previously infected with B. burgdorferi sensu lato. (This study is registered at ClinicalTrials.gov under registration no. NCT01504347.).

PMID:
25185574
PMCID:
PMC4248771
DOI:
10.1128/CVI.00406-14
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center