Eisenberg R J, Cerini C P, Heilman C J, Joseph A D, Dietzschold B, Golub E, Long D, Ponce de Leon M, Cohen G H
J Virol. 1985 Dec;56(3):1014-7. doi: 10.1128/JVI.56.3.1014-1017.1985.
Glycoprotein D (gD) of herpes simplex virus (HSV) protects mice from a lethal challenge by either HSV type 1 (HSV-1; oral) or HSV-2 (genital). We evaluated whether synthetic peptides representing residues 1 through 23 of gD (mature protein) can be used as a potential synthetic herpesvirus vaccine. The immunogenicity of the peptides was demonstrated by the biological reactivity of antipeptide sera in immunoprecipitation and neutralization assays. All sera which immunoprecipitated gD had neutralizing against both HSV-1 and HSV-2. The highest titers were found in animals immunized with the longest peptides. The region of residues 1 through 23 was immunogenic regardless of whether the type 1 or type 2 sequence was presented to the animal. Immunization of mice with gD or synthetic peptides conferred solid protection against a footpad challenge with HSV-2. However, the peptides were not as effective as gD in protection against an intraperitoneal challenge. The results suggested that synthetic vaccines based on gD show promise and should be more rigorously tested in a variety of animal models.
单纯疱疹病毒(HSV)的糖蛋白D(gD)可保护小鼠免受1型单纯疱疹病毒(HSV-1;口腔型)或2型单纯疱疹病毒(HSV-2;生殖器型)的致死性攻击。我们评估了代表gD(成熟蛋白)第1至23位残基的合成肽是否可用作潜在的合成疱疹病毒疫苗。抗肽血清在免疫沉淀和中和试验中的生物学反应性证明了这些肽的免疫原性。所有能免疫沉淀gD的血清均对HSV-1和HSV-2具有中和作用。在用最长肽免疫的动物中发现了最高滴度。无论向动物呈现的是1型还是2型序列,第1至23位残基区域都具有免疫原性。用gD或合成肽免疫小鼠可对HSV-2的足垫攻击提供可靠的保护。然而,这些肽在抵抗腹腔内攻击方面不如gD有效。结果表明,基于gD的合成疫苗具有前景,应在多种动物模型中进行更严格的测试。