Regression of AIDS-related Kaposi's sarcoma following antiretroviral therapy with protease inhibitors: Biological correlates of clinical outcome

被引:79
作者
Cattelan, AM
Calabro, ML
Aversa, SML
Zanchetta, M
Meneghetti, F
De Rossi, A
Chieco-Bianchi, L
机构
[1] Univ Padua, AIDS Reference Ctr, Oncol Sect, Dept Oncol & Surg Sci, I-35128 Padua, Italy
[2] Gen Hosp Padova, Dept Infect Dis, Padua, Italy
[3] Gen Hosp Padova, Dept Med Oncol, Padua, Italy
关键词
Kaposi's sarcoma; HIV-1; HHV-8; antibodies; protease inhibitors; HAART;
D O I
10.1016/S0959-8049(99)00161-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical response of AIDS-related Kaposi's sarcoma (KS) to highly active antiretroviral therapy (HAART), a combination of human immunodeficiency virus type 1 (HIV-1) protease and reverse transcriptase inhibitors, was studied in 11 patients, all but one with progressive KS. CD4 + cell counts, plasma HIV-1 RNA levels, and antibody titres to lytic ORF65 and latency-associated human herpes virus type 8 (HHV-8) proteins were determined in sequential samples. Six complete and three partial clinical responses were achieved in a median time of 6 and 3 months, respectively, and confirmed after a median time of 16 months on HAART. 2 patients showed disease progression. A consistent decrease in HIV-1 RNA levels, paralleled by an increase in CD4 + cell counts, was observed in all patients who showed complete or partial clinical response; HIV-1 RNA levels remained persistently high in the two patients who progressed, despite a change in HAART. HHV-8 antibody titres were generally higher in patients with mucosal/visceral involvement compared with patients with limited disease; a decrease in ORF65 antibody titre was significantly associated with a clinical response. These results indicate that HAART is effective for AIDS-related KS; the clinical response correlates with a decrease in plasma HIV-1 RNA levels, an increase in CD4 + lymphocytes, and a decrease in antibodies to ORF65 HHV-8 protein. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1809 / 1815
页数:7
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