Otake T, Miyano K, Mori H, Morimoto M, Ueba N, Kunita N, Nakashima H, Kurimura T
Osaka Prefectural Institute of Public Health, Japan.
Antiviral Res. 1991 Oct;16(3):243-55. doi: 10.1016/0166-3542(91)90004-b.
To reduce the toxicity of amphotericin B methyl ester (AME), which shows some anti-HIV-1 activity, sulfated amphotericin B (SAB) was prepared from amphotericin B (AB), and its anti-HIV-1 activity was examined in vitro. SAB at concentration of 7.8 micrograms/ml completely suppressed the HIV-1-induced cytopathic effect in MT-4 cells, at 3.9 micrograms/ml inhibited the expression of HIV-1 antigen in peripheral blood mononuclear cells infected with freshly isolated HIV-1 and at 22 micrograms/ml completely suppressed formation of giant cells in cocultures of MOLT-4 with MOLT-4/HIV-1 cells. Reverse transcriptase activity was inhibited by SAB, but only at higher concentrations (0.2-1 mg/ml). Furthermore, the toxicity of SAB was lower than that of AME or AB, and SAB did not affect the proliferation of MT-4 cells at concentrations up to 0.5 mg/ml. The anti-coagulant effect of SAB was 10-fold less than that of dextran sulfate (MW = 8000). The anti-HIV-1 effect of SAB is attributed to inhibition of binding of virions to target cells.
为降低具有一定抗HIV-1活性的两性霉素B甲酯(AME)的毒性,由两性霉素B(AB)制备了硫酸化两性霉素B(SAB),并对其体外抗HIV-1活性进行了检测。浓度为7.8微克/毫升的SAB可完全抑制MT-4细胞中HIV-1诱导的细胞病变效应,3.9微克/毫升时可抑制新鲜分离的HIV-1感染的外周血单个核细胞中HIV-1抗原的表达,22微克/毫升时可完全抑制MOLT-4与MOLT-4/HIV-1细胞共培养体系中巨细胞的形成。SAB可抑制逆转录酶活性,但仅在较高浓度(0.2 - 1毫克/毫升)时有效。此外,SAB的毒性低于AME或AB,且在浓度高达0.5毫克/毫升时不影响MT-4细胞的增殖。SAB的抗凝血作用比硫酸葡聚糖(分子量 = 8000)小10倍。SAB的抗HIV-1作用归因于其对病毒体与靶细胞结合的抑制。