Rubio A, Leal M, Rey C, Pineda J A, Sanchez-Quijano A, Lissen E
Department of Biochemistry, Virgen del Rocío University Hospital, Seville, Spain.
AIDS. 1998 Mar 5;12(4):395-8. doi: 10.1097/00002030-199804000-00008.
To investigate the different responses to antiretroviral treatment including zidovudine, of patients harbouring HIV with primary resistance to zidovudine, serum viral load, and CD4+ cell counts, for 24 weeks in a group of antiretroviral-naive patients with the codon 215 mutation of the HIV pol gene and in a control group at the start of treatment.
A case-control retrospective study (1989-1996).
Nineteen out of 210 patients previously studied harboured the codon 215 mutation, had a self-reported compliance with treatment, a minimum follow-up of 24 weeks, and were treated with zidovudine alone or in combination with other nucleoside analogues. These patients were matched with 19 patients with wild-type strains at entry by initial CD4+ cell counts, clinical status, and antiretroviral treatment.
During the first 12 weeks, CD4+ cell counts increased (76+/-26 and 64+/-26 x 10(6)/l in wild-type and mutant virus-infected groups, respectively), decreasing slightly until week 24, although no significant differences were found between the two groups studied. Serum viral load decreased in both groups (change in serum viral load of 0.80+/-0.11 log10 and 0.87+/-0.26 log10 copies/ml, wild-type and mutant virus-infected, respectively), although no significant differences were found between groups.
No significant differences were found between patients with the primary mutation to zidovudine and control patients harbouring wild-type virus in terms of short-term response measured by serum viral load and CD4+ cell counts.
在一组初治的、携带HIV pol基因215密码子突变的患者及一个对照组中,于治疗开始时,研究携带对齐多夫定原发耐药的HIV患者对包括齐多夫定在内的抗逆转录病毒治疗的不同反应,以及血清病毒载量和CD4+细胞计数,为期24周。
一项病例对照回顾性研究(1989 - 1996年)。
先前研究的210名患者中有19名携带215密码子突变,自述治疗依从性良好,至少随访24周,接受单独齐多夫定治疗或与其他核苷类似物联合治疗。这些患者与19名初治时携带野生型毒株的患者按初始CD4+细胞计数、临床状态和抗逆转录病毒治疗情况进行匹配。
在最初12周内,CD4+细胞计数增加(野生型和突变病毒感染组分别为76±26和64±26×10⁶/l),至第24周时略有下降,不过在两组研究对象之间未发现显著差异。两组的血清病毒载量均下降(野生型和突变病毒感染组的血清病毒载量变化分别为0.80±0.11 log₁₀和0.87±0.26 log₁₀拷贝/ml),但组间未发现显著差异。
就通过血清病毒载量和CD4+细胞计数衡量的短期反应而言,对齐多夫定有原发突变的患者与携带野生型病毒的对照患者之间未发现显著差异。