Zhang Hai-ping, Yan Hui-ping, Zhang Yong-hong, Feng Xia, Zhao Yan, Liao Hui-yu, Liu Yan-min, Chen Yu, Tan Yu-fen, Liu Yan
Infection and Immune Research Center, Beijing Youan Hospital, Capital Medical University, Beijing 100069, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2009 Aug;43(8):690-4.
To investigate the ability of secreting interferon-gamma (IFN-gamma) of the peripheral blood monocular cells (PBMC) stimulated by hepatitis B virus (HBV)-specific cytotoxic T lymphocyte (CTL) epitopes peptides and to analyze the difference of CTL immune response in patients with HBV infection.
Four HLA-A2-restricted HBV cytotoxic T lymphocyte epitopes [Tp: HBV polymerase 575-583 (FLLSLGIHL), Te1: envelope 28-39 (IPQSLDSWWTSL), Te2: envelope 183-191 (FLLTRILTI) and Tc: core 18-27 (FLPSDFFPSV)] were synthesized. Human leucocyte antigen (HLA)-A2 typing was detected by Flow cytometry. PBMCs which were isolated from patients with chronic hepatitis B(CHB), patients with chronic severe hepatitis B(CSH), subjects with past HBV infection(N1) and healthy blood donors (N2) were stimulated by the four HLA-A2-restricted HBV CTLs epitopes. Enzyme linked immunospot (ELISPOT) assay was used to detect the frequency of secreting IFN-gamma CTL in each group.
(1) HLA-A2 typing: 20 of 44 patients with CHB (45.5%) were HLA-A2 positive, 10/18 (55.6%) in CSH and 6/10 (60%) in group N1 were HLA-A2 positive.10 healthy blood donors' HLA-typing was detected in the early study.(2) ELISPOT results: (1) The total responses to the four epitopes in CHB, CSH, N1 and N2 groups were 50% (10/20), 10% (1/10), 83.3% (5/6) and 10% (1/10), respectively. The response in N1 group was significantly higher than that in CSH group (chi(2) = 9.000, P = 0.008) and N2 group (chi(2) = 9.000, P = 0.008). (2) The CTL average magnitude response to Tp epitope, Te1 epitope, Te2 epitope and Tc epitope was also significantly higher in past HBV infection group (77 SFC/10(6) PBMC, 59 SFC/10(6) PBMC, 100 SFC/10(6) PBMC and 57 SFC/10(6) PBMC, respectively) than that of CSH group (10 SFC/10(6) PBMC, 0 SFC/10(6) PBMC, 0 SFC/10(6) PBMC and 20 SFC/10(6) PBMC respectively, all P < 0.01) and N2 group (15 SFC/10(6) PBMC, 0 SFC/10(6) PBMC, 22 SFC/10(6) PBMC and 30 SFC/10(6) PBMC respectively, all P < 0.01).
This study indicates that the T cell immune response to HBV-specific epitopes might be detected either in patient with chronic HBV infection or with previous HBV infection. This response should be much higher in patients with past HBV infection, even the virus had been cleared for long time. These results demonstrate that HBV-specific CTL might play an important role in the clearance of the virus.
探讨乙型肝炎病毒(HBV)特异性细胞毒性T淋巴细胞(CTL)表位肽刺激外周血单个核细胞(PBMC)分泌γ干扰素(IFN-γ)的能力,并分析HBV感染患者CTL免疫反应的差异。
合成4个HLA-A2限制性HBV细胞毒性T淋巴细胞表位 [Tp:HBV聚合酶575 - 583(FLLSLGIHL),Te1:包膜28 - 39(IPQSLDSWWTSL),Te2:包膜183 - 191(FLLTRILTI)和Tc:核心18 - 27(FLPSDFFPSV)]。采用流式细胞术检测人类白细胞抗原(HLA)-A2分型。用4个HLA-A2限制性HBV CTL表位刺激从慢性乙型肝炎(CHB)患者、慢性重型乙型肝炎(CSH)患者、既往HBV感染受试者(N1)和健康献血者(N2)中分离的PBMC。采用酶联免疫斑点(ELISPOT)试验检测各组分泌IFN-γ CTL的频率。
(1)HLA-A2分型:44例CHB患者中20例(45.5%)HLA-A2阳性,CSH组10/18(55.6%)阳性,N1组6/10(60%)阳性。早期研究检测了10名健康献血者的HLA分型。(2)ELISPOT结果:(1)CHB组、CSH组、N1组和N2组对4个表位的总反应率分别为50%(10/20)、10%(1/10)、83.3%(5/6)和10%(1/10)。N1组的反应明显高于CSH组(χ(2)=9.000,P = 0.008)和N2组(χ(2)=9.000,P = 0.008)。(2)既往HBV感染组对Tp表位、Te1表位、Te2表位和Tc表位的CTL平均反应强度也明显高于CSH组(分别为77 SFC/10(6) PBMC、59 SFC/10(6) PBMC、100 SFC/10(6) PBMC和57 SFC/10(6) PBMC)(CSH组分别为10 SFC/10(6) PBMC、0 SFC/10(6) PBMC、0 SFC/10(6) PBMC和20 SFC/10(6) PBMC,均P < 0.01)和N2组(分别为15 SFC/10(6) PBMC、0 SFC/10(6) PBMC、22 SFC/10(6) PBMC和30 SFC/10(6) PBMC,均P < 0.01)。
本研究表明,慢性HBV感染患者或既往有HBV感染的患者均可检测到对HBV特异性表位的T细胞免疫反应。既往有HBV感染的患者,即使病毒已清除很长时间,这种反应也应更高。这些结果表明,HBV特异性CTL可能在病毒清除中起重要作用。