The combination of attenuated Newcastle disease (ND) vaccine with rHVT-ND vaccine at 1 day old is more protective against ND virus challenge than when combined with inactivated ND vaccine

被引:15
作者
Rauw, F. [1 ]
Gardin, Y. [2 ]
Palya, V. [3 ]
van den Berg, T. [1 ]
Lambrecht, B. [1 ]
机构
[1] Vet & Agrochem Res Ctr VAR, Avian Virol & Immunol Unit, Brussels, Belgium
[2] CEVA Sante Anim, Libourne, France
[3] CEVA Phylaxia, Budapest, Hungary
关键词
CELL-MEDIATED-IMMUNITY; CHICKENS; LIVE; EMULSION; EFFICACY; ANTIGEN; HERPESVIRUS; POULTRY;
D O I
10.1080/03079457.2013.859655
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The recurrent outbreaks of fatal Newcastle disease (ND) in commercial poultry flocks throughout the world indicate that routine vaccinations are failing to sufficiently induce the high levels of immunity necessary to control ND. There is a need for vaccination programmes that could be initiated at 1-day-old for mass application and which would induce a long-lasting immunity, with no need for a booster vaccination at a later age. In this context, the duration of immunity delivered by a vaccination programme including a recombinant herpesvirus of turkeys expressing the F gene of ND virus (rHVT-ND) and live ND vaccine at 1-day-old was compared with a classical programme that included a conventional live and an inactivated ND vaccine at the same age in commercial layer chickens. The humoral, cell-mediated and local immunity were followed weekly and birds were challenged with a viscerotropic velogenic ND virus strain at 6 and 10 weeks of age. We determined that immunity induced by the vaccination programme involving the rHVT-ND vaccine was more protective than that provided by the conventional vaccine-based regime. This might be related to a T-helper type 1 (Th1) cellular-driven immunological response, in contrast to the T-helper type 2 (Th2) humoral-oriented immune response provided by the current conventional vaccine-based vaccination programmes.
引用
收藏
页码:26 / 36
页数:11
相关论文
共 34 条
[1]  
Alexander D.J., 2008, DIS POULTRY, V12th, P75
[2]   Adjuvants designed for veterinary and human vaccines [J].
Aucouturier, J ;
Dupuis, L ;
Ganne, V .
VACCINE, 2001, 19 (17-19) :2666-2672
[3]   VACCINATION OF ONE-DAY-OLD CHICKS AGAINST NEWCASTLE-DISEASE USING INACTIVATED OIL ADJUVANT VACCINE AND-OR LIVE VACCINE [J].
BENNEJEAN, G ;
GUITTET, M ;
PICAULT, JP ;
BOUQUET, JF ;
DEVAUX, B ;
GAUDRY, D ;
MOREAU, Y .
AVIAN PATHOLOGY, 1978, 7 (01) :15-27
[4]   Thrombocytopenia in Newcastle disease:: Haematological evaluation and histological study of bone marrow [J].
Calderbón, NL ;
Galindo-Muñiz, F ;
Ortiz, M ;
Lomniczi, B ;
Fehervari, T ;
Paasch, LH .
ACTA VETERINARIA HUNGARICA, 2005, 53 (04) :507-513
[5]   SECONDARY INVITRO STIMULATION OF SPECIFIC CYTOTOXIC-CELLS TO NEWCASTLE-DISEASE VIRUS IN CHICKENS [J].
CANNON, MJ ;
RUSSELL, PH .
AVIAN PATHOLOGY, 1986, 15 (04) :731-740
[6]   Efficacy of live B1 or Ulster 2C Newcastle disease vaccines simultaneously vaccinated with inactivated oil adjuvant vaccine for protection of Newcastle disease virus in broiler chickens [J].
Chansiripornchai, N. ;
Sasipreeyajan, J. .
ACTA VETERINARIA SCANDINAVICA, 2006, 48 (1)
[7]   Third genome size category of avian paramyxovirus serotype 1 (Newcastle disease virus) and evolutionary implications [J].
Czegledi, Aliz ;
Ujvari, Dorina ;
Somogyi, Eszter ;
Wehmann, Eniko ;
Werner, Ortrud ;
Lomniczi, Bela .
VIRUS RESEARCH, 2006, 120 (1-2) :36-48
[8]  
Degen Winfried G J, 2003, Expert Rev Vaccines, V2, P327, DOI 10.1586/14760584.2.2.327
[9]   Efficacy of combined killed-in-oil emulsion and live Newcastle disease vaccines in chickens [J].
Folitse, R ;
Halvorson, DA ;
Sivanandan, V .
AVIAN DISEASES, 1998, 42 (01) :173-178
[10]   VACCINATION OF DAY-OLD BROILER CHICKS AGAINST NEWCASTLE-DISEASE AND INFECTIOUS BURSAL DISEASE USING COMMERCIAL LIVE AND OR INACTIVATED VACCINES [J].
GIAMBRONE, JJ ;
CLAY, RP .
AVIAN DISEASES, 1986, 30 (03) :557-561