›› 2009, Vol. 27 ›› Issue (1): 7-34.

• 论著 • Previous Articles     Next Articles

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

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