天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2001年
4期
217-219
,共3页
杜德伟%吴学勤%李谨革%连建奇%冯志华%贾占生%周永兴%姚志强
杜德偉%吳學勤%李謹革%連建奇%馮誌華%賈佔生%週永興%姚誌彊
두덕위%오학근%리근혁%련건기%풍지화%가점생%주영흥%요지강
疫苗%DNA肝炎表面抗原%乙型肝炎疫苗%乙型免疫性
疫苗%DNA肝炎錶麵抗原%乙型肝炎疫苗%乙型免疫性
역묘%DNA간염표면항원%을형간염역묘%을형면역성
目的:观察乙型肝炎病毒(HBV)S区DNA疫苗pCR3.1-S诱导BALB/C小鼠(H-2d)的特异性免疫应答,及其对稳定表达HBsAg的小鼠肥大细胞瘤细胞P815(P815-HBV-S)成瘤性的影响。方法:肌肉注射DNA疫苗;背部皮下接种P815-HBV-S细胞,观察成瘤情况;ELISA法检测小鼠血清抗HBs;4h51Cr释放法检测小鼠脾细胞CTL活性。结果:pCR3.1-S体外可表达HBsAg;小鼠接种该疫苗后血清450nmrA值为0.38,强化免疫后达0.87;pCR3.1-S组CTL细胞杀伤活性为51.1%,对照组为20.5%(P<0.01)。接种P815-HBV-S细胞后对照组成瘤率1100%,pCR3.1-S小鼠成瘤率为16.70%6,对照组小鼠6周后全部死亡;pCR3.1-S组6周后存活率为87.5%。结论:HBV S区DNA疫苗具有良好的免疫原性,能够诱导小鼠产生特异性体液免疫和细胞免疫应答,对体内HBV感染具有预防及治疗作用。
目的:觀察乙型肝炎病毒(HBV)S區DNA疫苗pCR3.1-S誘導BALB/C小鼠(H-2d)的特異性免疫應答,及其對穩定錶達HBsAg的小鼠肥大細胞瘤細胞P815(P815-HBV-S)成瘤性的影響。方法:肌肉註射DNA疫苗;揹部皮下接種P815-HBV-S細胞,觀察成瘤情況;ELISA法檢測小鼠血清抗HBs;4h51Cr釋放法檢測小鼠脾細胞CTL活性。結果:pCR3.1-S體外可錶達HBsAg;小鼠接種該疫苗後血清450nmrA值為0.38,彊化免疫後達0.87;pCR3.1-S組CTL細胞殺傷活性為51.1%,對照組為20.5%(P<0.01)。接種P815-HBV-S細胞後對照組成瘤率1100%,pCR3.1-S小鼠成瘤率為16.70%6,對照組小鼠6週後全部死亡;pCR3.1-S組6週後存活率為87.5%。結論:HBV S區DNA疫苗具有良好的免疫原性,能夠誘導小鼠產生特異性體液免疫和細胞免疫應答,對體內HBV感染具有預防及治療作用。
목적:관찰을형간염병독(HBV)S구DNA역묘pCR3.1-S유도BALB/C소서(H-2d)적특이성면역응답,급기대은정표체HBsAg적소서비대세포류세포P815(P815-HBV-S)성류성적영향。방법:기육주사DNA역묘;배부피하접충P815-HBV-S세포,관찰성류정황;ELISA법검측소서혈청항HBs;4h51Cr석방법검측소서비세포CTL활성。결과:pCR3.1-S체외가표체HBsAg;소서접충해역묘후혈청450nmrA치위0.38,강화면역후체0.87;pCR3.1-S조CTL세포살상활성위51.1%,대조조위20.5%(P<0.01)。접충P815-HBV-S세포후대조조성류솔1100%,pCR3.1-S소서성류솔위16.70%6,대조조소서6주후전부사망;pCR3.1-S조6주후존활솔위87.5%。결론:HBV S구DNA역묘구유량호적면역원성,능구유도소서산생특이성체액면역화세포면역응답,대체내HBV감염구유예방급치료작용。
Objective:To observe the specific immune responses and the protection against P815 mastocytoma cells stable expressing HbsAg in H-2d mice after immunized by DNA vaccine of HBV S gene. Methods: The immunization was performed by intramuscular injection of DNA and subcutaneous injection of P815-HBV-S. Serum anti-HBs was detected by ELISA. HbsAg secific cytotoxic T lymphocyte(CTL) activity was measured by 51 Chromium release assay. Results:The expression of HBsAg was demonstrated by indirect immunofluorescent method. The 450nm A value of serum in immunized mice was 0.87.HBsAg specific CTL activity was 51.1%. HBV-SDNA vaccine could evidently inhibit the tumor growth, prolong the surviv
al period(>38.2 d), and improve the survival rate. Conclusion: pCR3.1-S DNA vaccine has a strong antigenicity and marked killing effect to HBV infected cells in vivo.