Intramuscular vaccination with Strangvac is safe and induces protection against equine strangles caused by Streptococcus equi.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
26 06 2020
Historique:
received: 13 03 2020
revised: 13 05 2020
accepted: 15 05 2020
pubmed: 9 6 2020
medline: 28 4 2021
entrez: 9 6 2020
Statut: ppublish

Résumé

The equine disease strangles, caused by Streptococcus equi, remains a major cause of welfare and economic cost to the global horse industry. Here we report the safety, immunogenicity and efficacy of a novel multi-component chimeric fusion protein vaccine, called Strangvac, when administered to ponies via the intramuscular route. Across the four studies, Strangvac was safe and induced robust antibody responses towards the vaccine components in blood serum and the nasopharynx, which were boosted by revaccination up to 12 months after a primary course of 2 vaccinations 4 weeks apart. The vaccine response did not cross-react with a commercial strangles iELISA, which identifies horses that have been exposed to S. equi, demonstrating that it was possible to differentiate infected from vaccinated animals (DIVA). Following challenge with S. equi strain 4047 (Se4047), all 36 control ponies that had received an adjuvant-only placebo vaccine developed clinical signs of strangles. In contrast, intramuscular vaccination with Strangvac protected ponies significantly from challenge with Se4047 at two weeks (5 of 16 ponies protected (31%), P = 0.04) and two months (7 of 12 ponies protected (58%), P = 0.0046 (including pooled control data) after second vaccination. Optimal protection (15 of 16 ponies protected (94%), P < 0.0001) was observed following challenge at two weeks post-third vaccination. Our data demonstrate that Strangvac is safe, has DIVA capability and provides a rapid onset of protective immunity against strangles. We conclude that Strangvac is a valuable tool with which to protect horses from strangles, particularly during high-risk periods, whilst maintaining the mobility of horse populations as required by the global equine industry.

Identifiants

pubmed: 32507408
pii: S0264-410X(20)30691-5
doi: 10.1016/j.vaccine.2020.05.046
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4861-4868

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: This work was sponsored by Intervacc AB and clinical trials were conducted at Animal Health Trust. J-IF has a current employment at Intervacc and OZ a previous employment. The following authors are stakeholders of Intervacc AB: J-IF, MF, OZ, BG and LF.

Auteurs

Carl Robinson (C)

Department of Bacteriology, Animal Health Trust, Lanwades Park, Kentford, Newmarket, CB8 7UU, United Kingdom.

Andrew S Waller (AS)

Department of Bacteriology, Animal Health Trust, Lanwades Park, Kentford, Newmarket, CB8 7UU, United Kingdom.

Lars Frykberg (L)

Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, P.O. Box 7036, SE-750 07 Uppsala, Sweden.

Margareta Flock (M)

Department of Microbiology, Tumour and Cellbiology, Karolinska Institutet, P.O. Box 280, SE-171 77 Stockholm, Sweden.

Olof Zachrisson (O)

Intervacc AB, P.O. Box 112, SE-129 22 Hӓgersten, Sweden.

Bengt Guss (B)

Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, P.O. Box 7036, SE-750 07 Uppsala, Sweden.

Jan-Ingmar Flock (JI)

Department of Microbiology, Tumour and Cellbiology, Karolinska Institutet, P.O. Box 280, SE-171 77 Stockholm, Sweden; Intervacc AB, P.O. Box 112, SE-129 22 Hӓgersten, Sweden. Electronic address: jan-ingmar.flock@intervacc.com.

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