Rosenthal K S, Mao H, Horne W I, Wright C, Zimmerman D
N.E. Ohio Universities College of Medicine, Rootstown, 44272-0095, USA.
Vaccine. 1999 Feb 12;17(6):535-42. doi: 10.1016/s0264-410x(98)00231-x.
A ligand epitope antigen presentation system (LEAPS) heteroconjugate vaccine containing a CTL epitope (H1) from the HSV-1 immediate early protein ICP27 (322-332) and a peptide sequence (J) from beta-2-microglobulin (35-50) elicited protection from intraperitoneal viral challenge and promoted DTH responses. The H1 peptide and other H1 containing heteroconjugates did not elicit protection or DTH responses. Antibody to the H1 peptide could not be detected by ELISA following vaccination with peptide, heteroconjugate or natural infection. The LEAPS heteroconjugate appears to prime a Thl-like response which is subsequently boosted by infection. These studies show that attachment of the J peptide can make a CTL epitope into a vaccine which is immunogenic and promotes a protective Th1 type of response.
一种配体表位抗原呈递系统(LEAPS)异源缀合物疫苗,其包含来自单纯疱疹病毒1型(HSV-1)即刻早期蛋白ICP27(322-332)的细胞毒性T淋巴细胞(CTL)表位(H1)和来自β2-微球蛋白(35-50)的肽序列(J),该疫苗可诱导对腹腔内病毒攻击的保护作用并促进迟发型超敏反应(DTH)。H1肽和其他含H1的异源缀合物未诱导保护作用或DTH反应。在用肽、异源缀合物或自然感染进行疫苗接种后,通过酶联免疫吸附测定(ELISA)无法检测到针对H1肽的抗体。LEAPS异源缀合物似乎引发了类似Th1的反应,随后该反应会因感染而增强。这些研究表明,J肽的连接可使CTL表位成为具有免疫原性并促进保护性Th1型反应的疫苗。