中华传染病杂志
中華傳染病雜誌
중화전염병잡지
CHINESE JOURNAL OF INFECTIOUS DISEASES
1987年
4期
193-197,后插1
,共6页
张维%罗玉芳%童舒平%闻玉梅%俞翠珠
張維%囉玉芳%童舒平%聞玉梅%俞翠珠
장유%라옥방%동서평%문옥매%유취주
本文建立了自少量血清中研究I-IBsAg多肽图谱的方法,患者血清经纯化、SD.S聚丙烯酰胺凝胶电泳及Western吸印后,HBgAg多肽用酶免疫染色或放射自显影进行分析,发现10例慢性乙肝患者血清HBsAg多肽组成有明显差别.同一来源的HBV毒株在不同个体或同一个体随病程不同多肽图谱亦不同.血清HBV DNA阳性与多肽P39/P42的关系较P31/P34为密切,提示Pre-S1抗原不仅在急性感染中与病毒复制有关,在慢性感染中亦有关,PHSA'受体与P31/P42的符合率为94.1%,反映这一多肽确带有PHSA受体.
本文建立瞭自少量血清中研究I-IBsAg多肽圖譜的方法,患者血清經純化、SD.S聚丙烯酰胺凝膠電泳及Western吸印後,HBgAg多肽用酶免疫染色或放射自顯影進行分析,髮現10例慢性乙肝患者血清HBsAg多肽組成有明顯差彆.同一來源的HBV毒株在不同箇體或同一箇體隨病程不同多肽圖譜亦不同.血清HBV DNA暘性與多肽P39/P42的關繫較P31/P34為密切,提示Pre-S1抗原不僅在急性感染中與病毒複製有關,在慢性感染中亦有關,PHSA'受體與P31/P42的符閤率為94.1%,反映這一多肽確帶有PHSA受體.
본문건립료자소량혈청중연구I-IBsAg다태도보적방법,환자혈청경순화、SD.S취병희선알응효전영급Western흡인후,HBgAg다태용매면역염색혹방사자현영진행분석,발현10례만성을간환자혈청HBsAg다태조성유명현차별.동일래원적HBV독주재불동개체혹동일개체수병정불동다태도보역불동.혈청HBV DNA양성여다태P39/P42적관계교P31/P34위밀절,제시Pre-S1항원불부재급성감염중여병독복제유관,재만성감염중역유관,PHSA'수체여P31/P42적부합솔위94.1%,반영저일다태학대유PHSA수체.
A method of isolating HBsAg from small aniot of serum for polypeptide pattern analysis was established.7-14 ug of HBsAg was urifed through anti-HBs affnity chromatography.Followed by SDS-PAGE and transferred to nitrocellulose filters by Western blot.Filters were further stained with guinea pig anti-HBs,biotinylated anti-guinea pig IgG and avidinbiotin complex;or by 125I-SPA and autoradiOgraphy.Distinct polypeptide bands coald be seen.Serum samples from 10 chronic hepatitis B patients showed different polypepti le patterns.P31/P34 bands were seen in 9,and 3 showed high molecular woight band(P1OO).In the follow-up study of the 5 chronic hepatitis B patients,4 showed significant changes in patterns,some migrated from high to low molecular weight bands, while some changed from low to high molecular weight ban&s.In the 2 paired serum samples obtained from accidental transmission.HBsAg polypeptide bands of the donors and their relative recipients were found different.The data indicated that among the serum HBV DNA positive carriers,59%sjpwed P39/P42,whereas none of the HBV DNA negative carriers had such bands.In contrast.P31/P34 appeared both the serum HBV DNA positive and negative carriers.It seems that in tIBsAg positive carriers,P39/P42 is more closely related to HBV replication.