Antibody and IFN-γ responses induced by a recombinant canarypox vaccine and challenge infection with equine influenza virus

被引:60
作者
Paillot, R.
Kydd, J. H.
Sindle, T.
Hannant, D.
Toulemonde, C. Edlund
Audonnet, J. C.
Minke, J. M.
Daly, J. M.
机构
[1] Anim Hlth Trust, Ctr Prevent Med, Newmarket CB8 7UU, Suffolk, England
[2] Merial SAS, R&D, F-69007 Lyon, France
关键词
equine influenza virus; vaccine; immunity;
D O I
10.1016/j.vetimm.2006.02.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In horses, equine influenza virus (EIV) is a leading cause of respiratory disease. Conventional inactivated vaccines induce a short-lived immune response. By comparison, natural infection confers a long-term immunity to re-infection. An aim of new equine influenza vaccines is to more closely mimic natural infection in order to achieve a better quality of immunity. A new live recombinant vaccine derived from the canarypox virus vector and expressing haemagglutinin genes of EIV (subtype H3N8) has been developed. Stimulation of the immune system was studied after immunisation with this canarypox-based vaccine and challenue infection by exposure to a nebulised aerosol of EIV. The humoral immune response was evaluated by measuring serum antibody levels using the single radial haemolysis (SRH) assay. The cellular immune response was assessed by the measurement of interferon gamma (IFN-gamma) synthesis in peripheral blood mononuclear cells (PBMC). Clinical signs of the disease (temperature, coughing, nasal discharge, dyspnoea, depression and anorexia) and virus excretion were monitored after challenge infection. Clinical signs and virus shedding were significantly reduced in vaccinates compared with unvaccinated controls. EIV-specific immunity was stimulated by vaccination with a recombinant vaccine as serological responses were detected after immunisation. This study also provided the first evidence for increased IFN-gamma protein synthesis in vaccinated ponies following challenge infection with EIV compared with control ponies. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 233
页数:9
相关论文
共 22 条
[1]   Equine herpesvirus-1 infection induces IFN-γ production by equine T lymphocyte subsets [J].
Breathnach, CC ;
Soboll, G ;
Suresh, M ;
Lunn, DP .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2005, 103 (3-4) :207-215
[2]   Use of recombinant modified vaccinia Ankara viral vectors for equine influenza vaccination [J].
Breathnach, CC ;
Rudersdorf, R ;
Lunn, DP .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2004, 98 (3-4) :127-136
[3]   IDENTIFICATION OF VIRAL MOLECULES RECOGNIZED BY INFLUENZA-SPECIFIC HUMAN CYTOTOXIC LYMPHOCYTES-T [J].
GOTCH, F ;
MCMICHAEL, A ;
SMITH, G ;
MOSS, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (02) :408-416
[4]   DURATION OF CIRCULATING ANTIBODY AND IMMUNITY FOLLOWING INFECTION WITH EQUINE INFLUENZA-VIRUS [J].
HANNANT, D ;
MUMFORD, JA ;
JESSETT, DM .
VETERINARY RECORD, 1988, 122 (06) :125-128
[5]  
HANNANT D, 1987, EQUINE INFECT DIS, V5, P66
[6]   THE OUTBREAK OF EQUINE INFLUENZA (H3N8) IN THE UNITED-KINGDOM IN 1989 - DIAGNOSTIC USE OF AN ANTIGEN CAPTURE ELISA [J].
LIVESAY, GJ ;
ONEILL, T ;
HANNANT, D ;
YADAV, MP ;
MUMFORD, JA .
VETERINARY RECORD, 1993, 133 (21) :515-519
[7]   Use of DNA and recombinant canarypox viral (ALVAC) vectors for equine herpes virus vaccination [J].
Minke, JM ;
Fischer, L ;
Baudu, P ;
Guigal, PM ;
Sindle, T ;
Mumford, JA ;
Audonnet, JC .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2006, 111 (1-2) :47-57
[8]  
Minke JM, 2004, ARCH VIROL, P221
[9]   Genetically engineered poxviruses for recombinant gene expression, vaccination, and safety [J].
Moss, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) :11341-11348
[10]   DURATION OF PROTECTIVE EFFICACY OF EQUINE INFLUENZA IMMUNOSTIMULATING COMPLEX TETANUS VACCINES [J].
MUMFORD, JA ;
JESSETT, DM ;
ROLLINSON, EA ;
HANNANT, D ;
DRAPER, ME .
VETERINARY RECORD, 1994, 134 (07) :158-162