Immunobiology of pseudorabies (Aujeszky's disease)

被引:101
作者
Mettenleiter, TC
机构
关键词
pseudorabies virus; Aujeszky's disease; immunobiology; vaccines; immune response;
D O I
10.1016/S0165-2427(96)05695-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aujeszky's Disease (AD), a serious illness of pigs causing significant economic losses in the pig industry, is caused by Pseudorabies Virus (PrV). PrV belongs to the alphaherpesvirus subfamiliy of the herpesviruses with a double-stranded DNA genome in an enveloped capsid capable of encoding approximately 70 proteins. For disease control, vaccination with live and killed vaccines is performed. Recently, 'marked' vaccines have become available for use in eradication programs based on the differentiation between infected and vaccinated animals. PrV is also used as a viral vector for the development of multivalent vaccines. Despite the effectiveness of PrV vaccines, relatively little is known about the immune response against PrV infection. Several viral envelope glycoproteins have been shown to represent targets for antibody responses, and a number of isolated glycoproteins as well as genetically engineered proteins were able to elicit protective immunity. The nature of the cellular immune response is even less defined. Using viral mutants genetically engineered to lack specific antigens, it has been shown that glycoprotein C (gC) acts as a target for cytotoxic T-lymphocytes, and gB, gC, go, and gH appear to be involved in stimulation of in vitro proliferation of PBMC from immune animals. In addition, gB and gC have been implicated in recognition of infected cells by lymphokine-activated killer (LAK) cells. In summary, the data indicate a prominent role for viral envelope glycoproteins in eliciting humoral and cellular immune responses in the animal host. A complicating factor is the ability of PrV to productively infect cells of the hematopoietic system, which may impair immune responses and might also play a role in persistent or latent infection.
引用
收藏
页码:221 / 229
页数:9
相关论文
共 46 条
[41]   LIVE ATTENUATED PSEUDORABIES VIRUS EXPRESSING ENVELOPE GLYCOPROTEIN-E1 OF HOG-CHOLERA VIRUS PROTECTS SWINE AGAINST BOTH PSEUDORABIES AND HOG-CHOLERA [J].
VANZIJL, M ;
WENSVOORT, G ;
DEKLUYVER, E ;
HULST, M ;
VANDERGULDEN, H ;
GIELKENS, A ;
BERNS, A ;
MOORMANN, R .
JOURNAL OF VIROLOGY, 1991, 65 (05) :2761-2765
[42]   ISOLATION, CHARACTERIZATION, AND PHYSICAL MAPPING OF A PSEUDORABIES VIRUS MUTANT CONTAINING ANTIGENICALLY ALTERED GP50 [J].
WATHEN, MW ;
WATHEN, LMK .
JOURNAL OF VIROLOGY, 1984, 51 (01) :57-62
[43]   LATENT EQUID HERPESVIRUSES-1 AND 4 - DETECTION AND DISTINCTION USING THE POLYMERASE CHAIN-REACTION AND COCULTIVATION FROM LYMPHOID-TISSUES [J].
WELCH, HM ;
BRIDGES, CG ;
LYON, AM ;
GRIFFITHS, L ;
EDINGTON, N .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :261-268
[44]   THE EXPORT PATHWAY OF THE PSEUDORABIES VIRUS-GB HOMOLOG-GII INVOLVES OLIGOMER FORMATION IN THE ENDOPLASMIC-RETICULUM AND PROTEASE PROCESSING IN THE GOLGI-APPARATUS [J].
WHEALY, ME ;
ROBBINS, AK ;
ENQUIST, LW .
JOURNAL OF VIROLOGY, 1990, 64 (05) :1946-1955
[45]   COMPLEX BETWEEN GLYCOPROTEINS-GI AND GLYCOPROTEINS-GP63 OF PSEUDORABIES VIRUS - ITS EFFECT ON VIRUS-REPLICATION [J].
ZUCKERMANN, FA ;
METTENLEITER, TC ;
SCHREURS, C ;
SUGG, N ;
BENPORAT, T .
JOURNAL OF VIROLOGY, 1988, 62 (12) :4622-4626
[46]   PSEUDORABIES VIRUS GLYCOPROTEIN-GIII IS A MAJOR TARGET ANTIGEN FOR MURINE AND SWINE VIRUS-SPECIFIC CYTOTOXIC LYMPHOCYTES-T [J].
ZUCKERMANN, FA ;
ZSAK, L ;
METTENLEITER, TC ;
BENPORAT, T .
JOURNAL OF VIROLOGY, 1990, 64 (02) :802-812