结核杆菌热休克蛋白70作为表位肽载体体外诱导HBV特异性免疫应答  被引量:2

The study of heat shock protein 70 as a adjuvant carrier on HBV-specific immune response in vitro

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作  者:罗莉 何松[2] 罗娜[3] 彭明利[4] 

机构地区:[1]重庆市渝北区人民医院消化内科,401120 [2]重庆医科大学附属第二医院消化内科,400010 [3]重庆医科大学附属第一医院急诊科,400016 [4]重庆医科大学病毒性肝炎研究所,400016

出  处:《重庆医学》2014年第9期1025-1028,共4页Chongqing medicine

基  金:国家自然科学基金资助项目(30300297);重庆市自然科学基金资助项目(2008BB5402)

摘  要:目的在体外研究结核杆菌热休克蛋白70(TB.HSP70)作为乙型肝炎病毒(HBV)核心抗原(HBcAg)细胞毒性T淋巴细胞表位肽载体,诱导HBV特异性免疫应答。方法应用毕赤酵母分泌表达HSP70(P1)、HSP70-HBcAg(18-27)(P2)、HSP70-PreS2B(18-24)-PreS2Th(37-53)-HBcAg(18-27)(P3),用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白免疫印迹法鉴定各重组蛋白的表达。体外考察重组蛋白(P1、P2、P3)对慢性乙型肝炎外周血来源的树突状细胞和淋巴细胞的作用,流式细胞术评估树突状细胞的成熟,酶联免疫吸附测定法检测细胞因子白细胞介素(IL)-12p70、IL-1β、肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)分泌情况,TdR-3H掺入法检测淋巴细胞的增殖情况,应用经典51 Cr法检测重组蛋白诱导HBV特异性细胞毒活性。结果重组蛋白P1、P2、P3构建成功,P1、P2、P3能诱导树突状细胞成熟,上调CD1a、CD40、CD86表达,释放Th1型细胞因子IL-12p70、IL-1β和TNF-α,P3最能有效激活自体淋巴细胞成为细胞毒活性细胞,促进淋巴细胞增殖和IFN-γ的释放,而单独的HSP70无杀伤活性。结论 TB.HSP70可作为HBV HBcAg细胞毒性T淋巴细胞表位肽载体,提高T淋巴细胞表位肽的免疫原性,且含有B、Th表位的P3能更好地激活HBV特异性免疫应答。Objective To investigate the effect of mycobacterium tuberculosis heat shock protein 70(TB .HSP70) as an adjuvant carrier on stimulating hepatitis B virus (HBV) core antigen(HBcAg)specific immune response to an accompanying cytotoxic T lym-phocytes epitope peptide from HBV core antigen in vitro .Methods Recombinant proteins HSP70(P1)、HSP70-HBcAg(18-27) (P2)、HSP70-PreS2B (18-24)-PreS2Th(37-53)-HBcAg(18-27)(P3) were expressed in methylotropic yeast Pichia pastoris GS115 . The expression of recombinant proteins was identified by SDS-PAGE and Western blot .The effect of recombinant proteins on den-dritic cell and lymphocytes of chronic HBV infection volunteers was investigated in vitro .The maturation of dendritic cell was meas-ured by flow cytometry ;the secretion of Th1 cytokines such as IL-12p70 ,IL-1β,TNF-αand IFN-γ was measured by ELISA ;the proliferation of lymphocytes was measured by TdR-3H ;the HBV-spesific cytotoxic activity was measured by the classic 51 Cr .Re-sults The recombinant proteins (P1 ,P2 ,P3) were constructed successfully .P1 ,P2 ,P3 could activate dendritic cell from chronic HBV infection volunteers by upregulation CD1a ,CD40 ,CD86 and production Th1 cytokines such as IL-12p70 ,IL-1β and TNF-α. Especially P3 could better induce autologous T cells to generate HBV specific cytotoxic T lymphocytes response ,activate the prolif-eration of lymphocytes and release IFN-γeffectively .However ,the recombinant HSP70 showed no target cell killing and could not induce immune response effectively .Conclusion TB .HSP70 can be used as an adjuvant carrier to stimulate HBV specific immune response to an accompanying cytotoxic T lymphocytes epitope peptide from HBV core antigen ,and enhance immunogenicity of the cytotoxic T lymphocytes epitope peptide .The P3 with B-and T-epitope can activate the HBV specific immune response effectively .

关 键 词:HSP70热休克蛋白 T淋巴细胞 乙型肝炎病毒 树突细胞 

分 类 号:R392[医药卫生—免疫学]

 

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