Bonneau R H, Salvucci L A, Johnson D C, Tevethia S S
Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey 17033.
Virology. 1993 Jul;195(1):62-70. doi: 10.1006/viro.1993.1346.
HSV-1-specific and HSV-1/HSV-2-cross-reactive H-2Kb-restricted cytotoxic T lymphocyte (CTL) clones were derived from a pool of splenic memory CTL (CTLm) obtained from HSV-1-infected C57BL/6 mice. Two of the HSV-1/HSV-2-cross-reactive CTL clones recognized HSV gB since H-2b cells infected with a recombinant adenovirus vector expressing HSV glycoprotein B (gB) provided a target for these CTL clones. The CTL recognition epitope was precisely defined as HSV-1 gB residues 498-505 using synthetic peptides and conforms to a predicted H-2Kb-binding motif. Immunization of C57BL/6 mice with the free synthetic peptide corresponding to this predicted minimal epitope (HSV-1 gB498-505) resulted in the generation of HSV-gB epitope-specific CD8+ CTL in the popliteal lymph nodes. The peptide-induced CTL recognize and lyse HSV-1 infected H-2b cells or cells pulsed with the synthetic peptide, gB498-505. The availability of CTL clones directed to this predicted minimal HSV CTL epitope should be helpful in understanding processing of HSV glycoprotein B and presentation of this CTL recognition epitope.
单纯疱疹病毒1型特异性及单纯疱疹病毒1型/2型交叉反应性H-2Kb限制性细胞毒性T淋巴细胞(CTL)克隆源自从感染单纯疱疹病毒1型的C57BL/6小鼠获得的脾记忆CTL(CTLm)库。两个单纯疱疹病毒1型/2型交叉反应性CTL克隆识别单纯疱疹病毒糖蛋白B(gB),因为用表达单纯疱疹病毒糖蛋白B(gB)的重组腺病毒载体感染的H-2b细胞为这些CTL克隆提供了靶标。使用合成肽将CTL识别表位精确界定为单纯疱疹病毒1型gB的498 - 505位残基,且符合预测的H-2Kb结合基序。用对应于该预测最小表位(单纯疱疹病毒1型gB498 - 505)的游离合成肽免疫C57BL/6小鼠,导致在腘淋巴结中产生单纯疱疹病毒gB表位特异性CD8 + CTL。肽诱导的CTL识别并裂解感染单纯疱疹病毒1型的H-2b细胞或用合成肽gB498 - 505脉冲处理的细胞。针对该预测的最小单纯疱疹病毒CTL表位的CTL克隆的可用性应有助于理解单纯疱疹病毒糖蛋白B的加工及该CTL识别表位的呈递。