中国病毒学
中國病毒學
중국병독학
VIROLOGICA SINICA
2001年
2期
119-123
,共5页
徐焕宾%贲昆龙%曾涛%李劲光
徐煥賓%賁昆龍%曾濤%李勁光
서환빈%분곤룡%증도%리경광
HIV-1%实时定量PCR%外参照%前病毒载量%病毒载量%合胞体形成抑制试验
HIV-1%實時定量PCR%外參照%前病毒載量%病毒載量%閤胞體形成抑製試驗
HIV-1%실시정량PCR%외삼조%전병독재량%병독재량%합포체형성억제시험
准确测定HIV-1的前病毒载量和病毒载量的技术,在感染者预后和艾滋病患者药物治疗效果的评价以及艾滋病的其它研究方面,都具有十分重要的应用价值。以定量的HIV-1 DNA和RNA为标准外参照,利用SYBR Green荧光染料和GeneAmp5700 Sequence Detection System (5700系统),建立了测定HIV-1的前病毒载量和病毒载量的荧光实时定量PCR技术。以病毒感染细胞和培养上清为材料,测定了三种化合物(AZT,GL和WT)对细胞内的前病毒载量和培养上清中的病毒载量的抑制活性,并与合胞体形成抑制方法测定化合物抗病毒活性的结果进行了比较。根据病毒载量、前病毒载量和合胞体形成计算出的三种化合物的治疗指数均依次变小,提出以荧光实时定量PCR技术测定前病毒载量,会在评价药物在体内外根除或减少存在于CD4休止或记忆T淋巴细胞中的HIV-1前病毒方面有特别的价值。
準確測定HIV-1的前病毒載量和病毒載量的技術,在感染者預後和艾滋病患者藥物治療效果的評價以及艾滋病的其它研究方麵,都具有十分重要的應用價值。以定量的HIV-1 DNA和RNA為標準外參照,利用SYBR Green熒光染料和GeneAmp5700 Sequence Detection System (5700繫統),建立瞭測定HIV-1的前病毒載量和病毒載量的熒光實時定量PCR技術。以病毒感染細胞和培養上清為材料,測定瞭三種化閤物(AZT,GL和WT)對細胞內的前病毒載量和培養上清中的病毒載量的抑製活性,併與閤胞體形成抑製方法測定化閤物抗病毒活性的結果進行瞭比較。根據病毒載量、前病毒載量和閤胞體形成計算齣的三種化閤物的治療指數均依次變小,提齣以熒光實時定量PCR技術測定前病毒載量,會在評價藥物在體內外根除或減少存在于CD4休止或記憶T淋巴細胞中的HIV-1前病毒方麵有特彆的價值。
준학측정HIV-1적전병독재량화병독재량적기술,재감염자예후화애자병환자약물치료효과적평개이급애자병적기타연구방면,도구유십분중요적응용개치。이정량적HIV-1 DNA화RNA위표준외삼조,이용SYBR Green형광염료화GeneAmp5700 Sequence Detection System (5700계통),건립료측정HIV-1적전병독재량화병독재량적형광실시정량PCR기술。이병독감염세포화배양상청위재료,측정료삼충화합물(AZT,GL화WT)대세포내적전병독재량화배양상청중적병독재량적억제활성,병여합포체형성억제방법측정화합물항병독활성적결과진행료비교。근거병독재량、전병독재량화합포체형성계산출적삼충화합물적치료지수균의차변소,제출이형광실시정량PCR기술측정전병독재량,회재평개약물재체내외근제혹감소존재우CD4휴지혹기억T림파세포중적HIV-1전병독방면유특별적개치。
Accurate determination of HIV-1 proviral burden and viral load is very useful in prognosis of HIV-1 infected patients and in assessment of drug for therapy of AIDS patients. In order to establish a quantitative method in detecting HIV-1 proviral burden and viral load, 8E5 cell line and a recombinant RNA constructs were used as the HIV-1 proviral DNA and viral RNA external references, respectively. The PCR products were labeled with the fluorescent DNA dye SYBR green. The amount of burden or load was measured by GeneAmp 5700 Sequence Detection System. Using this method, the HIV-1 proviral burdens in PBMC of patient and in cell suspension treated with the compounds AZT, GL and WT were measured. HIV-1 viral loads in supernatant of the cell culture treated with the above compounds were also determined. The therapeutic indices (TIs) of the compounds calculated based on the inhibition of virus induced syncytial formation, and inhibitionn of proviral burdens and viral loads were compared, and their TIs successively increased. The fluorescent real time quantitative PCR possesses very good specificity, sensitivity and duplication. TI value of a drug based on inhibition of proviral burden in cell culture, and the proviral burden in PBMC of patient may be useful in evaluating a drug on eradicating provirus from resting and memory CD4 T cells.