Jankelevich S, Mueller B U, Mackall C L, Smith S, Zwerski S, Wood L V, Zeichner S L, Serchuck L, Steinberg S M, Nelson R P, Sleasman J W, Nguyen B Y, Pizzo P A, Yarchoan R
HIV and AIDS Malignancy Branch, Division of Clinical Sciences, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
J Infect Dis. 2001 Apr 1;183(7):1116-20. doi: 10.1086/319274. Epub 2001 Mar 1.
Virologic and immunologic responses were examined for 33 human immunodeficiency virus (HIV)-infected children who participated for > or = 96 weeks in a phase 1/2 protocol of 16 weeks of indinavir monotherapy, followed by the addition of zidovudine and lamivudine. At week 96, a median increase of 199 CD4+ T cells/microL and a median decrease of 0.74 log(10) HIV RNA copies/mL were observed. The relationship between control of viral replication and CD4) T cell count was examined. Patients were categorized into 3 response groups on the basis of duration and extent of control of viral replication. Of 21 children with a transient decrease in virus load of > or = 0.7 log(10) HIV RNA copies/mL from baseline, 7 experienced sustained increases in CD4+, CD4+ CD45RA+, and CD4+ CD45RO+ T cell counts. CD4+ CD45RA+ (naive) T cells were the major contributor to CD4+ T cell expansion. Continued long-term immunologic benefit may be experienced by a subset of children, despite only transient virologic suppression.
对33名感染人类免疫缺陷病毒(HIV)的儿童进行了病毒学和免疫学反应检测,这些儿童参与了一项1/2期试验方案,该方案包括16周的茚地那韦单药治疗,随后添加齐多夫定和拉米夫定,参与时间≥96周。在第96周时,观察到CD4+ T细胞数量中位数增加199个/微升,HIV RNA拷贝数/毫升中位数下降0.74 log(10)。研究了病毒复制控制与CD4) T细胞计数之间的关系。根据病毒复制控制的持续时间和程度,将患者分为3个反应组。在21名病毒载量从基线水平短暂下降≥0.7 log(10) HIV RNA拷贝数/毫升的儿童中,7名儿童的CD4+、CD4+ CD45RA+和CD4+ CD45RO+ T细胞计数持续增加。CD4+ CD45RA+(初始)T细胞是CD4+ T细胞扩增的主要贡献者。尽管只有短暂的病毒学抑制,但一部分儿童可能会持续获得长期的免疫学益处。