Hraba T, Dolezal J
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Praha.
Folia Biol (Praha). 1994;40(3):103-11.
A mathematical model of CD4+ lymphocyte depletion in HIV infection is used to simulate and analyse the effect of AZT treatment. In most cases, permanent administration of AZT is observed to stop the CD4+ lymphocyte count decline and to stimulate their increase up to a new steady-state level, which depends on the intensity of AZT treatment, i.e. AZT dose. Temporary administration of AZT leads only to a temporary increase in CD4+ lymphocyte count. After the treatment is terminated, the count starts to decline again. However, the resulting prolongation of patient's survival exceeds the time interval of AZT administration. Interestingly, the survival prolongation is greater, if the treatment is started at five than at two years after the infection and there is no striking increase in survival time if a dose of AZT inhibiting 75% of HIV proliferation is used instead of a lower one inducing 25% inhibition only.
一个用于模拟和分析齐多夫定(AZT)治疗效果的HIV感染中CD4 +淋巴细胞耗竭的数学模型。在大多数情况下,观察到持续给予AZT可阻止CD4 +淋巴细胞计数下降,并刺激其增加至新的稳态水平,这取决于AZT治疗的强度,即AZT剂量。临时给予AZT仅导致CD4 +淋巴细胞计数暂时增加。治疗终止后,计数又开始下降。然而,患者生存时间的延长超过了AZT给药的时间间隔。有趣的是,如果在感染后五年开始治疗,生存延长比在两年开始治疗更大,并且如果使用抑制75%HIV增殖的AZT剂量而不是仅诱导25%抑制的较低剂量,生存时间没有显著增加。