Kelley Colleen F, Barbour Jason D, Hecht Frederick M
Department of Medicine, San Francisco General Hospital, University of California at San Francisco, 995 Potrero Avenue, San Francisco, CA 94110, USA.
J Acquir Immune Defic Syndr. 2007 Aug 1;45(4):445-8. doi: 10.1097/QAI.0b013e318074ef6e.
To examine the relation between symptoms, initial viral load, and viral load set point in primary HIV infection (PHI).
Prospective cohort of patients with preseroconversion or recent seroconversion HIV infection (typically <60 days) in San Francisco.
Subjects were questioned about 21 potential PHI symptoms at enrollment and were subsequently followed with viral load measures.
The analysis included 57 subjects with preseroconversion HIV infection and 120 with recent seroconversion. In univariate analysis, most symptoms and the total number of symptoms were each associated with a significantly higher initial viral load. In stepwise multiple linear regression, however, only the number of symptoms was independently associated with a higher initial viral load, with an increase in the initial viral load of 0.08 log10 per additional symptom (P < 0.001). In univariate analysis, more PHI symptoms were associated with a higher viral load set point, but in a multivariable mixed-effects model, this association was accounted for by the initial viral load, which was strongly correlated with viral load set point (R = 0.44, P < 0.001).
A high initial viral load was associated with more symptoms during PHI. The strong correlation between initial HIV-1 RNA viral load levels and viral load set point suggests that early interactions between the HIV-1 virus and a new host, even before fully developed adaptive immune responses, are important in establishing viral load set point.
研究原发性HIV感染(PHI)中症状、初始病毒载量与病毒载量设定点之间的关系。
对旧金山处于血清转化前或近期血清转化的HIV感染患者(通常<60天)进行前瞻性队列研究。
在入组时询问受试者21种潜在的PHI症状,随后对其进行病毒载量检测。
分析纳入了57例血清转化前HIV感染患者和120例近期血清转化患者。在单变量分析中,大多数症状及症状总数均与显著更高的初始病毒载量相关。然而,在逐步多元线性回归中,只有症状数量与更高的初始病毒载量独立相关,每增加一个症状,初始病毒载量增加0.08 log10(P<0.001)。在单变量分析中,更多的PHI症状与更高的病毒载量设定点相关,但在多变量混合效应模型中,这种关联由初始病毒载量解释,初始病毒载量与病毒载量设定点密切相关(R = 0.44,P<0.001)。
在PHI期间,高初始病毒载量与更多症状相关。HIV-1 RNA病毒载量初始水平与病毒载量设定点之间的强相关性表明,即使在适应性免疫反应完全发展之前,HIV-1病毒与新宿主之间的早期相互作用对于建立病毒载量设定点也很重要。