Zhang L, Ramratnam B, Tenner-Racz K, He Y, Vesanen M, Lewin S, Talal A, Racz P, Perelson A S, Korber B T, Markowitz M, Ho D D
Aaron Diamond AIDS Research Center, Rockefeller University, New York, NY 10016, USA.
N Engl J Med. 1999 May 27;340(21):1605-13. doi: 10.1056/NEJM199905273402101.
In patients infected with human immunodeficiency virus type 1 (HIV-1), combination antiretroviral therapy can result in sustained suppression of plasma levels of the virus. However, replication-competent virus can still be recovered from latently infected resting memory CD4 lymphocytes; this finding raises serious doubts about whether antiviral treatment can eradicate HIV-1.
We looked for evidence of residual HIV-1 replication in eight patients who began treatment soon after infection and in whom plasma levels of HIV-1 RNA were undetectable after two to three years of antiretroviral therapy. We examined whether there had been changes over time in HIV-1 proviral sequences in peripheral-blood mononuclear cells, which would indicate residual viral replication. We also performed in situ hybridization studies on tissues from one patient to identify cells actively expressing HIV-1 RNA. We estimated the rate of decrease of latent, replication-competent HIV-1 in resting CD4 lymphocytes on the basis of the decrease in the numbers of proviral sequences identified during primary infection and direct sequential measurements of the size of the latent reservoir.
Six of the eight patients had no significant variations in proviral sequences during treatment. However, in two patients there was sequence evolution but no evidence of drug-resistant viral genotypes. In one patient, extensive in situ studies provided additional evidence of persistent viral replication in lymphoid tissues. Using two independent approaches, we estimated that the half-life of the latent, replication-competent virus in resting CD4 lymphocytes was approximately six months.
These findings suggest that combination antiretroviral regimens suppress HIV-1 replication in some but not all patients. Given the half-life of latently infected CD4 lymphocytes of about six months, it may require many years of effective antiretroviral treatment to eliminate this reservoir of HIV-1.
在感染1型人类免疫缺陷病毒(HIV-1)的患者中,联合抗逆转录病毒疗法可导致血浆病毒水平得到持续抑制。然而,仍可从潜伏感染的静息记忆CD4淋巴细胞中分离出具有复制能力的病毒;这一发现使人严重怀疑抗病毒治疗能否根除HIV-1。
我们在8例感染后不久即开始治疗且接受抗逆转录病毒治疗两到三年后血浆中检测不到HIV-1 RNA的患者中寻找残留HIV-1复制的证据。我们检查外周血单核细胞中HIV-1前病毒序列是否随时间发生变化,这可能表明存在残留病毒复制。我们还对1例患者的组织进行原位杂交研究,以识别活跃表达HIV-1 RNA的细胞。我们根据初次感染期间鉴定的前病毒序列数量的减少以及对潜伏病毒库大小的直接连续测量,估算静息CD4淋巴细胞中潜伏性、具有复制能力的HIV-1的减少速率。
8例患者中有6例在治疗期间前病毒序列无显著变化。然而,有2例患者存在序列演变,但没有耐药病毒基因型的证据。在1例患者中,广泛的原位研究提供了淋巴组织中持续病毒复制的额外证据。使用两种独立的方法,我们估计静息CD4淋巴细胞中潜伏性、具有复制能力的病毒的半衰期约为6个月。
这些发现表明,联合抗逆转录病毒方案可抑制部分但并非所有患者的HIV-1复制。鉴于潜伏感染的CD4淋巴细胞的半衰期约为6个月,可能需要多年有效的抗逆转录病毒治疗才能消除这个HIV-1病毒库。