中国寄生虫学与寄生虫病杂志 ›› 2009, Vol. 27 ›› Issue (1): 7-34.

• 论著 • 上一篇    下一篇

日本血吸虫副肌球蛋白合成肽的免疫学鉴定

陶方方1,2,王慧1,孙新娟1,刘丰1,王勇1,苏川1,吴海玮1,张兆松1 *   

  1. 1 南京医科大学病原生物学系,南京 210029;2 浙江中医药大学病原生物学教研室,杭州 310053
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2009-02-28 发布日期:2009-02-28
  • 通讯作者: 张兆松

Immunological Identification of a Synthetic Peptide from the Paramyosin of Schistosoma japonicum

TAO Fang-Fang1,2,WANG Hui1,SUN Xin-Juan1,LIU Feng1,WANG Yong1,SU Chuan1,WU Hai-Wei1,ZHANG Zhao-Song1 *   

  1. 1 Department of Pathogen Biology, Nanjing Medical University, Nanjing 210029, China; 2 Department of Pathogen Biology, Zhejiang Chinese Medical University, Hangzhou 310053, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-02-28 Published:2009-02-28
  • Contact: ZHANG Zhao-Song

摘要: 目的 鉴定日本血吸虫副肌球蛋白合成肽Sj97-P22。 方法 27只雌性C57BL/6小鼠随机均分为合成肽Sj97-P22免疫组、无关肽免疫组和PBS免疫组,分别于尾基部皮下注射与完全福氏佐剂等体积充分混匀的合成肽Sj97-P22(100 μg)乳化物、无关肽(100 μg)乳化物和PBS乳化物,抗原免疫剂量为100 μg/(只·次),共免疫2次,间隔1周。于免疫后7~10 d分离各组小鼠脾单个核细胞,运用流式细胞技术三色标记法检测其CD4 T细胞胞内因子干扰素γ(IFN-γ)和白介素4(IL-4)。将Sj97-P22免疫小鼠或PBS免疫小鼠的脾单个核细胞分别与Sj97-P22、无关肽或PBS共培养,采用3H-TdR掺入法观察细胞增殖效果,并用ELISA法检测细胞培养上清中IL-2、IFN-γ和IL-4的浓度。 结果 Sj97-P22免疫组小鼠脾脏CD4+ T细胞中胞内分泌IFN-γ的细胞百分率为(8.05±0.54)%,显著高于无关肽免疫组[(4.74±1.04)%]和PBS免疫组[(6.51±0.49)%] (P<0.05);而分泌IL-4的细胞百分率[(0.60±0.11)%]显著低于PBS免疫组[(1.31±0.27)%](P<0.05),与无关肽免疫组[(0.84±0.08)%]间的差异则无统计学意义(P>0.05)。Sj97-P22可明显刺激Sj97-P22免疫小鼠脾单个核细胞增殖,增殖指数达到3.12±1.59,细胞培养上清中IL-2和IFN-γ浓度分别为(9.13±1.54)和(39.75±9.69)pg/ml,与无关肽和PBS刺激相比显著升高(P<0.05),而IL-4浓度在3个刺激物间的差异无统计学意义(P>0.05)。Sj97-P22不能刺激PBS免疫鼠脾单个核细胞增殖及培养上清中IL-2、IFN-γ及IL-4浓度变化。 结论 Sj97-P22可能是C57BL/6小鼠特异的Th1型表位。

关键词: 日本血吸虫, 副肌球蛋白, Th1型表位, 免疫学鉴定

Abstract:

Objective To identify the immunologic property of a synthetic peptide Sj97-P22 from paramyosin of Schistosoma japonicum (Sj97). Methods Twenty-seven female C57BL/6 mice were divided into 3 groups each with 9 mice, Sj97-P22, control peptide and PBS groups, and each mouse was respectively immunized twice (seven days interval) with 100 μg of Sj97-P22, control peptide or PBS, emulsified with equal value of complete Freund′s adjuvant. Seven to ten days after the second immunization, the mouse spleen mononuclear cells were isolated for three-color flow cytometery to detect intracellular cytokines IFN-gamma and IL-4. Then the spleen mononuclear cells were co-cultured with Sj97-P22, control peptide or PBS respectively, and the incorporation rate of 3H-thymidine, as well as the levels of IL-2, IFN-gamma and IL-4 in the cultured cell supernatant, were measured. Results In CD4+ T cells, the percentage of IFN-gamma-producing cells in Sj97-P22 group [(8.05±0.54)%] was significantly higher than that of the control peptide group [(4.74±1.04)%] or PBS group [(6.51±0.49)%] (P<0.05), while the proportion of IL-4-producing cells was signifi-cantly lower in Sj97-P22 group [(0.60±0.11)%] than that in PBS group [(1.31±0.27)%] (P<0.05). Also, compared with control peptide or PBS stimulation, Sj97-P22 was able to effectively stimulate the proliferation with the stimulation index (3.12±1.59) and a higher secretion of IL-2 [(9.13±1.54) pg/ml] and IFN-gamma [(39.75±9.69) pg/ml] of spleen mono-nuclear cells in Sj97-P22-immunized mice (P<0.05). Both Sj97-P22 and control peptide were not effective stimulators to the spleen mononuclear cells from mice of PBS group. Conclusion It is highly possible that Sj97-P22 is a Th1-type epitope specific for C57BL/6 mice.

Key words: Schistosoma japonicum, Paramyosin, Th1-type epitope, Immunological identification