Issue |
Vet. Res.
Volume 39, Number 3, May-June 2008
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Number of page(s) | 14 | |
DOI | https://doi.org/10.1051/vetres:2007062 | |
Published online | 07 February 2008 | |
How to cite this article | Vet. Res. (2008) 39:21 |
DOI: 10.1051/vetres:2007062
Protection, systemic IFN
, and antibody responses induced by an ISCOM-based vaccine against a recent equine influenza virus in its natural host
Romain Paillot1, Humphrey Grimmett2, Debra Elton1 and Janet M. Daly1, 3 1 Animal Health Trust, Centre for Preventive Medicine, Lanwades Park, Newmarket, Suffolk, CB8 7UU, UK
2 Schering Plough, Animal Health, Breakspear Rd, South Harefield, Uxbridge, Middlesex, UB9 6LS, UK
3 Present address: Viral Brain Infections Group, University of Liverpool, Daulby Street, Liverpool L69 3GA, UK
(Received 31 August 2007; accepted 9 November 2007; published online 7 February 2008)
Abstract - In the horse, conventional inactivated or subunit
vaccines against equine influenza virus (EIV)
induce a short-lived antibody-based immunity to infection. Alternative
strategies of vaccination have been
subsequently developed to mimic the long-term protection induced by natural
infection with the virus. One
of these approaches is the use of immune-stimulating complex (ISCOM)-based
vaccines. ISCOM vaccines
induce a strong antibody response and protection against influenza in
horses, humans, and a mouse model.
Cell-mediated immunity (CMI) has been demonstrated in humans and mice after
ISCOM vaccination, but
rarely investigated in the horse. The aim of this study was to evaluate
EIV-specific immune responses after
intra-muscular vaccination with an ISCOM-EIV vaccine (EQUIP F) containing
both equine influenza H7N7
(A/eq/Newmarket/77) and H3N8 (A/eq/Borlänge/91 and A/eq/Kentucky/98)
strains. The antibody response
was measured by single radial haemolysis (SRH) assay using different H3N8
EIV strains. Stimulation
of type-1 immunity was evaluated with a recently developed method that
measures EIV-specific IFN
synthesis by peripheral blood lymphocytes (PBL). The protective efficacy of
this ISCOM-based vaccine
against challenge infection with a recent equine influenza (H3N8; A/eq/South
Africa/4/03) strain was
also evaluated. Vaccinated ponies developed elevated levels of EIV-specific
SRH antibody and increased
percentage of EIV-specific IFN
PBL, whereas these responses were only
detected after challenge infection
in unvaccinated control ponies. Vaccinates showed minimal signs of disease
and did not shed virus when
challenged shortly after the second immunisation. In conclusion, evidence of
type-1 immunity induced by
an ISCOM-based vaccine is described for the first time in horses.
Key words: equine influenza virus / vaccine / ISCOM / equine IFN gamma / immunity
Corresponding author: romain.paillot@aht.org.uk
© INRA, EDP Sciences 2008