中华传染病杂志
中華傳染病雜誌
중화전염병잡지
CHINESE JOURNAL OF INFECTIOUS DISEASES
1987年
1期
28-30
,共3页
倪贤珍%刘逢举%陈青锋%陈虹%王华信%肖萍
倪賢珍%劉逢舉%陳青鋒%陳虹%王華信%肖萍
예현진%류봉거%진청봉%진홍%왕화신%초평
本文用斑点杂交试验直接检测149例不同类型的乙型肝炎血清中HBV DNA,其阳性率为65.8%(98/149),各型间无差异.其中116例检测了DNAP,阳性率为62%(72/116),HBV DNA阳性率为72.4%(841/116).在116例中HBsAg、HBeAg和抗-HBc均阳性者54例,其DNAP和HBVDNA阳性率分别为79.6%(43/54)和92.6%(50/54); HBsAg、抗-HBe和抗-I-IBc均阳性者35例,DNAP和HBV DNA阳性率分别为37.1%(13/35)和60%(21/35);HBsAg和抗-HBc阳性者27例,DNAP和HBV DNA阳性率分别为59.2%(16/27)和 48.1%(13/27).同时有6份供血员血清阴性.结果表明,本法高度特异、敏感、简便,可作为判断病毒复制的手段.
本文用斑點雜交試驗直接檢測149例不同類型的乙型肝炎血清中HBV DNA,其暘性率為65.8%(98/149),各型間無差異.其中116例檢測瞭DNAP,暘性率為62%(72/116),HBV DNA暘性率為72.4%(841/116).在116例中HBsAg、HBeAg和抗-HBc均暘性者54例,其DNAP和HBVDNA暘性率分彆為79.6%(43/54)和92.6%(50/54); HBsAg、抗-HBe和抗-I-IBc均暘性者35例,DNAP和HBV DNA暘性率分彆為37.1%(13/35)和60%(21/35);HBsAg和抗-HBc暘性者27例,DNAP和HBV DNA暘性率分彆為59.2%(16/27)和 48.1%(13/27).同時有6份供血員血清陰性.結果錶明,本法高度特異、敏感、簡便,可作為判斷病毒複製的手段.
본문용반점잡교시험직접검측149례불동류형적을형간염혈청중HBV DNA,기양성솔위65.8%(98/149),각형간무차이.기중116례검측료DNAP,양성솔위62%(72/116),HBV DNA양성솔위72.4%(841/116).재116례중HBsAg、HBeAg화항-HBc균양성자54례,기DNAP화HBVDNA양성솔분별위79.6%(43/54)화92.6%(50/54); HBsAg、항-HBe화항-I-IBc균양성자35례,DNAP화HBV DNA양성솔분별위37.1%(13/35)화60%(21/35);HBsAg화항-HBc양성자27례,DNAP화HBV DNA양성솔분별위59.2%(16/27)화 48.1%(13/27).동시유6빈공혈원혈청음성.결과표명,본법고도특이、민감、간편,가작위판단병독복제적수단.
One hundred forty-nine patients with different types of hepatitis B were assayed for HBV DNA With direct spot hybridization.HBV DNA positive tale was 65.8%(98/149).There was no signflcant difference among various types.DNAP was tested in 116 of the 149 cases.the Positive rate Was 62%(72/116).and HBV DNA positive rate was 72.4%(s4/116).Of them.DNAP and HBV DNA positive rates were 79.6 %(43/54)and 92.6 %(50/54)respeotively in 54 cases with positive HBsAg,HBeAg and anti-HBc.DNAP and HBV DNA Positive rates were 37.1%(13/35)and 60%(21/35)respectively in 35 cases with posilive HBSAg,anti-HBe and anit-HBc.DNAP and HBV DNA positive rates were 59.2%(16/27) and 4S.1%(13/27)respectively in 27 cases with positive HBsAg and anti-HBc.In addition, these markers Were negative in 6 healthy blood donors. The results indicate that the new method for detecting serum HBV DNA is highly specific,sensitive and simple,and could be used as a more direct technique to re3ognize active viral replication.