Neurath A Robert, Strick Nathan, Li Yun-Yao
Biochemical Virology Laboratory, The Lindsley F, Kimball Research Institute of the New York Blood Center, New York, NY 10021, USA.
BMC Infect Dis. 2002 Nov 21;2:27. doi: 10.1186/1471-2334-2-27.
Cellulose acetate phthalate (CAP) in soluble form blocks coreceptor binding sites on the virus envelope glycoprotein gp120 and elicits gp41 six-helix bundle formation, processes involved in virus inactivation. CAP is not soluble at pH < 5.5, normal for microbicide target sites. Therefore, the interaction between insoluble micronized CAP and HIV-1 was studied. Carbomer 974P/BufferGel; carrageenan; cellulose sulfate; dextran/dextrin sulfate, poly(napthalene sulfonate) and poly(styrene-4-sulfonate) are also being considered as anti-HIV-1 microbicides, and their antiviral properties were compared with those of CAP.
Enzyme linked immunosorbent assays (ELISA) were used to (1) study HIV-1 IIIB and BaL binding to micronized CAP; (2) detect virus disintegration; and (3) measure gp41 six-helix bundle formation. Cells containing integrated HIV-1 LTR linked to the beta-gal gene and expressing CD4 and coreceptors CXCR4 or CCR5 were used to measure virus infectivity.
Micronized CAP is the only candidate topical microbicide with the capacity to remove rapidly by adsorption from physiological fluids HIV-1 of both the X4 and R5 biotypes and is likely to prevent virus contact with target cells. The interaction between micronized CAP and HIV-1 leads to rapid virus inactivation. Among other anionic polymers, cellulose sulfate, BufferGel and aryl sulfonates appear most effective in this respect.
可溶形式的邻苯二甲酸醋酸纤维素(CAP)会阻断病毒包膜糖蛋白gp120上的共受体结合位点,并引发gp41六螺旋束的形成,这些过程参与病毒的灭活。CAP在pH值低于5.5时不溶解,而这正是杀微生物剂作用靶点部位的正常pH值。因此,研究了不溶性微粉化CAP与HIV-1之间的相互作用。卡波姆974P/缓冲凝胶、角叉菜胶、硫酸纤维素、葡聚糖/硫酸糊精、聚萘磺酸盐和聚苯乙烯-4-磺酸盐也被视为抗HIV-1杀微生物剂,并将它们的抗病毒特性与CAP的进行了比较。
采用酶联免疫吸附测定(ELISA)来:(1)研究HIV-1 IIIB和BaL与微粉化CAP的结合;(2)检测病毒解体;(3)测定gp41六螺旋束的形成。含有与β-半乳糖苷基因相连的整合型HIV-1长末端重复序列并表达CD4和共受体CXCR4或CCR5的细胞用于测定病毒感染性。
1)HIV-1 IIIB和BaL分别有效地与微粉化CAP结合。2)HIV-1与微粉化CAP之间的相互作用导致:(a)gp41六螺旋束的形成;(b)病毒解体和包膜糖蛋白的脱落;(c)感染性迅速丧失。除卡波姆974P外,CAP以外的聚合物在HIV-1 IIIB中引发了gp41六螺旋束的形成,但除CAP外,只有聚萘磺酸盐对HIV-1 BaL有此作用。这些聚合物在杀病毒活性方面存在差异,对HIV-1 BaL的差异更为明显。
微粉化CAP是唯一一种能够通过吸附从生理流体中快速去除X4和R5两种生物型HIV-1的局部杀微生物剂候选物,并且可能会阻止病毒与靶细胞接触。微粉化CAP与HIV-1之间的相互作用导致病毒迅速失活。在其他阴离子聚合物中,硫酸纤维素、缓冲凝胶和芳基磺酸盐在这方面似乎最有效。