摘要
用人EBV转化恒河猴的自体B淋巴细胞,再以表达SIV不同抗原成分的重组痘苗病毒VAC-SIVenv、VAC-SIVgag感染,制备51Cr释放试验的靶细胞。恒河猴于制备B淋巴细胞30d后,皮下接种BV-SIVenv亚单位疫苗,每只动物1mL于强化免疫后的30、60、90d,从动物四肢内侧静脉采血,分离淋巴细胞,采用51Cr释放试验检测动物体内的CD8+Tc的动态变化。结果:19只免疫恒河猴中,有3只于强化免疫后呈现明显的CD8+Tc特异性细胞免疫反应,对靶细胞的杀伤活性在16.7%~20.2%之间,井可在体内维持3个月之久;在靶细胞数量不变,渐次增加效应细胞时,免疫细胞的CD8+Tc的杀伤活性随数量增加而增强。从而证明该SIV亚单位疫苗可使部分(16%)免疫动物产生较好的特异性细胞免疫反应。
Autologous B-lymphocytes of Macaca rhesus
transformed with EBV wereinfected with VAC-SIVgag or VAC-SIVenv that makes each product of
SIV-gag or SIV-env,and prepared as targets for the 51Cr release assay。 The rhesus monkeys
were sub-cutaneously inoculated with BV-SIVenv subunit vaccine at a dose of l mL per animal
30 davs later after successful preparation of the B-lymphocytes。Peripherial blood was
col-lected from the veins of their limbs by 30,60 and 90 days after booster inoculation。
Lymphocytes were separated and used for evaluating the kinetic fluctuation of cytotoxic CD8+T
cells in inoculated animals by 51Cr release assay。What we observed from this study was
that 3 out of 19 animals inoculated with this vaccine showed apparent re-sponse of CD8+ T
cells specific for SIV after booster,The specific killing activity of cy-totoxic CD8+ T cells to
autologous targets ranged from 16.7%to 20.2%and retained about 3 months,The KIlling
activities of cytotoxic CD8+ T cells derived from inoculated animals were strengthened
according as the amount of targets were added,which sug-gesting that this SIV-subunit vaccine
is able to induce strong cellular immune responses specific for SIV in immunized
animals(16%)。
出处
《中国兽医学报》
CAS
CSCD
1994年第4期369-372,共4页
Chinese Journal of Veterinary Science
基金
WHO爱滋病研究和人员培训基金
关键词
疫苗接种
靶细胞
SIV
HIV
疫苗
恒河猴
CD8^+Tc
target
SIV
HIV
subunit vaccine
Macaca rhesus
CD8+Tc
cellular
immune responses
51Cr release assay