A brief history of OspA vaccines including their impact on diagnostic testing for Lyme disease

Diagn Microbiol Infect Dis. 2022 Jan;102(1):115572. doi: 10.1016/j.diagmicrobio.2021.115572. Epub 2021 Oct 10.

Abstract

The only United States Food and Drug Administration approved vaccine preparation to prevent Lyme disease consisted of a single recombinant outer surface protein A (OspA), which was marketed for use from late 1998 until early 2002, with no vaccine currently available for humans for nearly 20 years. OspA vaccines generate an antibody-mediated, transmission blocking immunity, that prevents Borrelia burgdorferi from being transmitted during a tick bite. Although this OspA vaccine was safe and effective, it likely would have required booster doses to maintain immunity, and vaccination regularly caused false positive results on first-tier serologic testing for Lyme disease, when a whole cell-based enzyme immunoassay was used. Clinical trials are in progress to test a new multivalent OspA vaccine designed to prevent Lyme disease in both the United States and Europe.

Keywords: Borrelia burgdorferi; Lyme disease; Prevention; Tick-borne infection; Vaccine.

Publication types

  • Review

MeSH terms

  • Antigens, Surface / immunology*
  • Bacterial Outer Membrane Proteins / immunology*
  • Bacterial Vaccines / immunology*
  • Humans
  • Lipoproteins / immunology*
  • Lyme Disease / prevention & control*
  • Lyme Disease Vaccines / adverse effects
  • Lyme Disease Vaccines / immunology*

Substances

  • Antigens, Surface
  • Bacterial Outer Membrane Proteins
  • Bacterial Vaccines
  • Lipoproteins
  • Lyme Disease Vaccines
  • OspA protein