Liu J, Tasaka K, Yang J, Itoh T, Yamada M, Yoshikawa H, Nakajima Y
Department of Parasitology and Immunology, Yamanashi Medical University, Yamanashi 409-3898, Japan.
Infect Immun. 2001 Jun;69(6):4154-8. doi: 10.1128/IAI.69.6.4154-4158.2001.
Identification of T-cell epitopes harbored in soluble egg antigen (SEA) of Schistosoma japonicum and study of the immunological properties are essential for understanding the immunopathology and the control of schistosomiasis. As a follow-up to our previous work, the 66- to 80-kDa fragment from SEA was partially digested with protease, fractionated by reverse-phase high-pressure liquid chromatography, and found to be carrying a peptide which stimulated proliferation and gamma interferon (IFN-gamma) production of Th1 clones specific to SEA. Sequence analysis showed that the peptide was composed of 12 amino acids lined up as DLAVELAYLGNL. A synthetic homologue induced proliferation and IFN-gamma and interleukin-2 (IL-2) production, but not IL-4 or IL-6 production, by the Th1 clones as well as by the spleen cells from SEA-immunized mice, thus indicating that the peptide carries a Th1 epitope of SEA.
鉴定日本血吸虫可溶性虫卵抗原(SEA)中含有的T细胞表位并研究其免疫特性,对于理解血吸虫病的免疫病理学及控制该病至关重要。作为我们先前工作的后续研究,SEA的66至80 kDa片段用蛋白酶进行部分消化,通过反相高压液相色谱进行分离,发现其携带一种能刺激SEA特异性Th1克隆增殖及产生γ干扰素(IFN-γ)的肽段。序列分析表明,该肽段由12个氨基酸组成,排列为DLAVELAYLGNL。一种合成的同源物可诱导SEA免疫小鼠的Th1克隆以及脾细胞增殖并产生IFN-γ和白细胞介素-2(IL-2),但不产生IL-4或IL-6,这表明该肽段携带SEA的一个Th1表位。