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1型人类免疫缺陷病毒对修饰硫酸环糊精(mCDS71)的体外抗性特征

Characterization of human immunodeficiency virus type 1 resistant to modified cyclodextrin sulphate (mCDS71) in vitro.

作者信息

Mori H, Otake T, Oishi I, Kurimura T

机构信息

Osaka Prefectural Institute of Public Health, Japan.

出版信息

Antivir Chem Chemother. 1999 Jan;10(1):15-21. doi: 10.1177/095632029901000102.

Abstract

Drug resistance of human immunodeficiency virus type 1 (HIV) to modified cyclodextrin sulphate (mCDS71) has been analysed with respect to both the in vitro appearance of resistance to the compound and the mechanism of the acquisition of resistance. Resistant strains could be obtained in all three strains (NL432, KK-1 and A018) tested after serial passages in MT-4 cells with a gradual increase of the concentration of mCDS71. Cross-resistance both to mCDS71 and dextran sulphate 8000 was observed. As a result of sequencing analysis of the gp120 V3-C5 region of resistant strains, the mechanism of resistance can be explained in several ways: (i) substitution of sugar chain-binding amino acids, N and S; (ii) three to five amino acid deletion in V4 loop; and (iii) several mutations in V3 and V4 regions. The real cause of the resistance may be a combination of these three mechanisms. The results suggest that the target of mCDS71 is relatively widely distributed on the viral surface glycoprotein.

摘要

就1型人类免疫缺陷病毒(HIV)对硫酸化修饰环糊精(mCDS71)的耐药性而言,已对该化合物耐药性的体外表现以及耐药性的获得机制进行了分析。在MT - 4细胞中连续传代并逐渐增加mCDS71的浓度后,在所测试的所有三株病毒(NL432、KK - 1和A018)中均能获得耐药株。观察到对mCDS71和硫酸葡聚糖8000的交叉耐药性。通过对耐药株gp120 V3 - C5区域的测序分析,耐药机制可以从以下几个方面解释:(i)糖链结合氨基酸N和S的取代;(ii)V4环中三到五个氨基酸的缺失;以及(iii)V3和V4区域的若干突变。耐药的真正原因可能是这三种机制的组合。结果表明,mCDS71的靶点在病毒表面糖蛋白上分布相对广泛。

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