Li Guang-Fu, Zhang Zhao-Song, Wang Yong, Zhu Xiang, Ji Min-Jun, Wu Guan-Ling
Department of Pathogenic Biology, Nanjing Medical University, Nanjing 210029, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2004 May;20(3):352-5.
To predict T-cell epitopes of recombinant schistosoma japonicum 28 kDa glutathione-S-transferase(GST) with software and identify the Th1 type T-cell epitopes by experiments.
T-cell epitopes of recombinant schistosoma japonicum 28kDa GST were predicted with software and several epitopic candidates were screened from them according to their scores. Some of the epitopic candidates were synthesized and the other epitope peptides fused with thioredoxin(Trx) were expressed in E.coli BL21(DE3) and purified by Ni(+) column affinity chromatography. C57BL/6 (H-2(b)) mice's were immunized via peritoneal infection with ultraviolet ray irradiated-cercariae and then boosted with recombinant schistosoma japonicum 28 kDa GST. The immunized mice splenocytes were prepared, cultured and stimulated with synthesized epitope peptides and epitope peptide fusion proteins, respectively. Stimulation activity of synthesized epitope peptides and epitope peptides fusion proteins were assayed by lymphocyte proliferation assay. Levels of IFN-gamma and IL-2 were measured by ELISA. CD4(+) T cells and T cells secreting IFN-gamma and IL-4 were detected by flow cytometry.
Epitope P6(73-86aa) among 9 epitopic candidates could generate the strongest stimulation effect on splenocytes, stimulate secretion of higher levels of IFN-gamma and IL-2, and induce more IFN-gamma(+) and IL-4 (+) T cells.
The recombinant 28 kDa GST possesses functional Th1 type T-cell epitope.
运用软件预测日本血吸虫重组28 kDa谷胱甘肽-S-转移酶(GST)的T细胞表位,并通过实验鉴定Th1型T细胞表位。
运用软件预测日本血吸虫重组28 kDa GST的T细胞表位,根据得分从中筛选出多个表位候选序列。合成部分候选表位肽,其余与硫氧还蛋白(Trx)融合的表位肽在大肠杆菌BL21(DE3)中表达,并用镍离子柱亲和层析法纯化。C57BL/6(H-2(b))小鼠经紫外线照射尾蚴腹腔感染免疫,然后用日本血吸虫重组28 kDa GST加强免疫。制备免疫小鼠脾细胞,分别用合成的表位肽和表位肽融合蛋白培养并刺激。通过淋巴细胞增殖试验检测合成表位肽和表位肽融合蛋白的刺激活性。用酶联免疫吸附测定法检测干扰素-γ和白细胞介素-2水平。通过流式细胞术检测CD4(+) T细胞以及分泌干扰素-γ和白细胞介素-4的T细胞。
9个表位候选序列中的表位P6(73-86aa)对脾细胞产生的刺激作用最强,刺激产生更高水平的干扰素-γ和白细胞介素-2,并诱导产生更多的干扰素-γ(+)和白细胞介素-4(+) T细胞。
重组28 kDa GST具有功能性Th1型T细胞表位。