Bagby Gregory J, Zhang Ping, Purcell Jeanette E, Didier Peter J, Nelson Steve
Department of Physiology, LSU Health Sciences Center, New Orleans, Louisiana 70112-1393, USA.
Alcohol Clin Exp Res. 2006 Oct;30(10):1781-90. doi: 10.1111/j.1530-0277.2006.00211.x.
While alcohol consumption is known to increase the incidence and severity of infections, the impact of alcohol consumption on human immunodeficiency virus (HIV) disease progression has been difficult to assess. Therefore, we examined the effect of ethanol on simian immunodeficiency virus (SIV) disease progression in a well-defined model utilizing rhesus macaques.
Alcohol was administered for 5 hours via an indwelling intragastric catheter to achieve an alcohol concentration of 50 to 60 mM for 4 consecutive days per week for the duration of the study. Control animals received isocaloric sucrose. After 3 months, animals were inoculated intravenously with 10,000 times the ID(50) of SIV(DeltaB670) and followed to end-stage disease.
Plasma SIV ribonucleic acid (RNA) was higher in alcohol-consuming animals compared with sucrose-treated animals during the early asymptomatic stage of disease but not at later time points. This increase in viral set point was associated with more rapid progression to end-stage disease in macaques administered alcohol (median=374 days) compared with sucrose (median=900 days). The decline in blood CD4+ cells was similar in both groups of animals.
This study indicates that frequent episodes of alcohol intoxication in SIV+ macaques increase viral set point in association with more rapid development of end-stage disease.
虽然已知饮酒会增加感染的发生率和严重程度,但饮酒对人类免疫缺陷病毒(HIV)疾病进展的影响一直难以评估。因此,我们在一个利用恒河猴的明确模型中研究了乙醇对猴免疫缺陷病毒(SIV)疾病进展的影响。
在研究期间,通过留置胃内导管给予酒精5小时,每周连续4天达到50至60 mM的酒精浓度。对照动物接受等热量的蔗糖。3个月后,给动物静脉注射10000倍SIV(DeltaB670)的半数感染剂量(ID50),并随访至疾病终末期。
在疾病早期无症状阶段,与蔗糖处理的动物相比,饮酒动物的血浆SIV核糖核酸(RNA)水平更高,但在后期时间点则不然。与蔗糖组(中位数=900天)相比,饮酒猕猴的病毒载量增加与疾病进展至终末期更快相关(中位数=374天)。两组动物血液中CD4 +细胞的下降情况相似。
本研究表明,SIV感染的猕猴频繁发生酒精中毒会增加病毒载量,并与终末期疾病的更快发展相关。