The novel Lyme borreliosis vaccine VLA15 shows broad protection against Borrelia species expressing six different OspA serotypes

Autor: Andreas Meinke, Wolfgang Schüler, Pär Comstedt, Urban Lundberg
Rok vydání: 2017
Předmět:
0301 basic medicine
Serotype
Bacterial Diseases
Physiology
lcsh:Medicine
Booster dose
Pathology and Laboratory Medicine
Biochemistry
Mice
Lyme disease
Immune Physiology
Medicine and Health Sciences
Enzyme-Linked Immunoassays
lcsh:Science
Lyme Disease
Mice
Inbred C3H

Vaccines
Multidisciplinary
Immune System Proteins
Spirochetes
Antibody titer
Animal Models
Antibodies
Bacterial

Bacterial Pathogens
Body Fluids
Infectious Diseases
Blood
Experimental Organism Systems
Medical Microbiology
Antigens
Surface

Bacterial Vaccines
Antibody
Pathogens
Anatomy
Bacterial Outer Membrane Proteins
Research Article
Borrelia Burgdorferi
Infectious Disease Control
Lipoproteins
030106 microbiology
Immunology
Mouse Models
Biology
Serogroup
Research and Analysis Methods
complex mixtures
Microbiology
Antibodies
03 medical and health sciences
Model Organisms
Antigen
Borrelia burgdorferi Group
Immunity
medicine
Animals
Borrelia burgdorferi
Immunoassays
Microbial Pathogens
Bacteria
Borrelia
lcsh:R
Organisms
Lyme Disease Vaccines
Biology and Life Sciences
Proteins
Blood Serum
medicine.disease
biology.organism_classification
bacterial infections and mycoses
Virology
Borrelia Infection
030104 developmental biology
biology.protein
Immunologic Techniques
bacteria
lcsh:Q
Immune Serum
Zdroj: PLoS ONE
PLoS ONE, Vol 12, Iss 9, p e0184357 (2017)
ISSN: 1932-6203
Popis: We have previously shown that the Outer surface protein A (OspA) based Lyme borreliosis vaccine VLA15 induces protective immunity in mice. Herein, we report the induction of protective immunity by VLA15 with mouse models using ticks infected with B. burgdorferi (OspA serotype 1), B. afzelii (OspA serotype 2) and B. bavariensis (OspA serotype 4) or with in vitro grown B. garinii (OspA serotype 5 and 6) for challenge. For B. garinii (OspA serotype 3), we have developed a growth inhibition assay using chicken complement and functional antibodies targeting B. garinii (OspA serotype 3) could be demonstrated after immunization with VLA15. Furthermore, following three priming immunizations, a booster dose was administered five months later and the induction of immunological memory could be confirmed. Thus, the antibody titers after the booster dose were increased considerably compared to those after primary immunization. In addition, the half-lives of anti-OspA serotype specific antibodies after administration of the booster immunization were longer than after primary immunization. Taken together, we could show that VLA15 induced protection in mice against challenge with four different clinically relevant Borrelia species (B. burgdorferi, B. afzelii, B. garinii and B. bavariensis) expressing five of the six OspA serotypes included in the vaccine. The protection data is supported by functional assays showing efficacy against spirochetes expressing any of the six OspA serotypes (1 to 6). To our knowledge, this is the first time a Lyme borreliosis vaccine has been able to demonstrate such broad protection in preclinical studies. These new data provide further promise for the clinical development of VLA15 and supports our efforts to provide a new Lyme borreliosis vaccine available for global use.
Databáze: OpenAIRE