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接种疱疹病毒疫苗,是虚构还是现实?

Vaccination against herpesvirus, fiction or reality?

作者信息

Morein B, Merza M

机构信息

Department of Virology, National Veterinary Institute, Uppsala, Sweden.

出版信息

Scand J Infect Dis Suppl. 1991;80:110-8.

PMID:1666442
Abstract

Against Herpes simplex type 1 (HSV-1) there are commercially available vaccines which may induce protection against symptoms of primary infections, but not against establishment of latency. Effective animal vaccines have been developed against herpes simplex-like viruses, for example pseudorabies vaccine for pigs, and an experimental vaccine can protect cattle against infection with infectious bovine rhinotracheitis (IBR) virus. There are also commercially available effective live vaccines against Marek's disease virus which belongs to the lymphoproliferative group of herpesviruses and causes lymphoma in chicken. An experimental immunostimulating complex (iscom) vaccine against Equine herpesvirus 2, an equine cytomegalovirus, has been tested in horse and protective immunity was induced. In man vaccines against Cytomegalovirus are used in immunosuppressed patients. Several laboratory animal models have been created for HSV-1 and HSV-2 mostly using mice but also guinea pigs. In these models many different HSV-1 or HSV-2 vaccines have been tested and induced protective immunity. The antigens in the vaccines have been envelope proteins extracted from native virus or envelope glycoproteins gB or gD in single or combined use. Glycoprotein C seems to be a less interesting as antigen for a HSV-1 vaccine. The cottontop tamarin monkey has been studied as a model for Epstein-Barr virus (EBV) induced lymphoma. An iscom vaccine containing the envelop protein gp340 of EBV induced full protection in the cottontop tamarins against a challenge infection. The iscom vaccine concept is discussed and the formation of an iscom particle with "tailor made" antigens and immunomodulators is presented.

摘要

针对单纯疱疹病毒1型(HSV-1),有市售疫苗,这些疫苗可能诱导针对原发性感染症状的保护作用,但不能防止潜伏感染的建立。已经开发出针对单纯疱疹样病毒的有效动物疫苗,例如猪的伪狂犬病疫苗,并且一种实验性疫苗可以保护牛免受传染性牛鼻气管炎(IBR)病毒的感染。也有针对马立克氏病病毒的市售有效活疫苗,该病毒属于疱疹病毒的淋巴增生性组,可导致鸡发生淋巴瘤。一种针对马疱疹病毒2型(一种马巨细胞病毒)的实验性免疫刺激复合物(iscom)疫苗已在马身上进行了测试,并诱导了保护性免疫。在人类中,针对巨细胞病毒的疫苗用于免疫抑制患者。已经为HSV-1和HSV-2创建了几种实验动物模型,大多使用小鼠,但也使用豚鼠。在这些模型中,已经测试了许多不同的HSV-1或HSV-2疫苗,并诱导了保护性免疫。疫苗中的抗原是从天然病毒中提取的包膜蛋白或单独或联合使用的包膜糖蛋白gB或gD。糖蛋白C似乎作为HSV-1疫苗的抗原不太受关注。棉顶狨猴已被研究作为爱泼斯坦-巴尔病毒(EBV)诱导淋巴瘤的模型。一种含有EBV包膜蛋白gp340的iscom疫苗在棉顶狨猴中诱导了完全保护,使其免受攻击感染。讨论了iscom疫苗的概念,并介绍了具有“量身定制”抗原和免疫调节剂的iscom颗粒的形成。

相似文献

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Vaccination against herpesvirus, fiction or reality?接种疱疹病毒疫苗,是虚构还是现实?
Scand J Infect Dis Suppl. 1991;80:110-8.
2
Comparison of different forms of herpes simplex replication-defective mutant viruses as vaccines in a mouse model of HSV-2 genital infection.在单纯疱疹病毒2型生殖器感染小鼠模型中,不同形式的单纯疱疹复制缺陷型突变病毒作为疫苗的比较。
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[Prevention and therapy of herpesvirus infections].[疱疹病毒感染的预防与治疗]
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Protection, systemic IFNgamma, and antibody responses induced by an ISCOM-based vaccine against a recent equine influenza virus in its natural host.基于免疫刺激复合物(ISCOM)的疫苗在天然宿主中诱导的针对近期马流感病毒的保护、全身γ干扰素及抗体反应。
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Marek's disease in turkeys: lack of protection by vaccination.火鸡马立克氏病:疫苗接种无保护作用。
Am J Vet Res. 1982 Apr;43(4):740-2.
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Serum antibody responses to equine herpesvirus 1 glycoprotein D in horses, pregnant mares and young foals.马、怀孕母马和幼驹对马疱疹病毒1糖蛋白D的血清抗体反应。
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Efficacy and duration of immunity of a combined equine influenza and equine herpesvirus vaccine against challenge with an American-like equine influenza virus (A/equi-2/Kentucky/95).一种马流感和马疱疹病毒联合疫苗针对类似美国马流感病毒(A/equi-2/Kentucky/95)攻毒的免疫效力和免疫持续时间。
Vet J. 2004 Mar;167(2):150-7. doi: 10.1016/S1090-0233(03)00028-5.
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Use of DNA and recombinant canarypox viral (ALVAC) vectors for equine herpes virus vaccination.DNA和重组金丝雀痘病毒(ALVAC)载体在马疱疹病毒疫苗接种中的应用。
Vet Immunol Immunopathol. 2006 May 15;111(1-2):47-57. doi: 10.1016/j.vetimm.2006.01.008. Epub 2006 Mar 31.
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DNA vaccination against pseudorabies virus and bovine respiratory syncytial virus infections of young animals in the face of maternally derived immunity.在存在母源免疫的情况下,针对幼龄动物伪狂犬病病毒和牛呼吸道合胞体病毒感染的DNA疫苗接种
J Comp Pathol. 2007 Jul;137 Suppl 1:S35-41. doi: 10.1016/j.jcpa.2007.04.010. Epub 2007 Jun 5.

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