Antiretroviral therapy in HIV-2-infected patients:: changes in plasma viral load, CD4+cell counts, and drug resistance profiles of patients treated in Abidjan, Cote d'Ivoire

被引:74
|
作者
Adjé-Touré, CA
Cheingsong, R
Garcìa-Lerma, JG
Eholié, S
Borget, MY
Bouchez, JM
Otten, RA
Maurice, C
Sassan-Morokro, M
Ekpini, RE
Nolan, M
Chorba, T
Heneine, W
Nkengasong, JN
机构
[1] Projet RETRO CI, Virol Lab, Abidjan, Cote Ivoire
[2] CDCP, Div HIV AIDS Prevent Surveillance & Epidemiol, Natl Ctr HIV STD & TB Prevent, Atlanta, GA USA
[3] Ctr Dis Control & Prevent, Div AIDS STD TB Lab Res, Natl Ctr Infect Dis, Atlanta, GA USA
[4] Univ Teaching Hosp, Infect Dis Clin, Abidjan, Cote Ivoire
[5] Ctr Dis Control & Prevent, Natl Ctr HIV STD & TB Prevent, Atlanta, GA USA
关键词
genotypic mutations; HIV-2; indivavir-based highly active antiretroviral therapy; nelfinavir-based highly active antiretroviral therapy; phenotypic resistance; viral load response;
D O I
10.1097/00002030-200317003-00007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To describe changes in plasma viral load, CD4+ cell counts, and drug resistance profiles of HIV-2-infected patients receiving antiretroviral (ARV) therapy in Abidjan, Cote d'Ivoire. Methods: Consecutive blood samples were collected from 18 HIV-2-infected ARV-naive patients who had received ARV therapy in the UNAIDS drug access initiative (UNAIDS-DAI) in Abidjan between August 1998 and July 2000. Changes in HIV-2 plasma viral load, CD4+ cell counts, and genotypic and phenotypic drug resistance testing were determined. Results: At baseline, 11 (61%) of the 18 patients initiated highly active antiretroviral therapy (HAART) and seven (39%) received dual therapy. No significant change in median viral load was observed at 2 months (P = 0.09), at 6 months (P = 0.06), and at 12 months of therapy (P = 0.26). No significant increase in CD4+ cell counts was observed at 12 months (P = 0.10). All four patients on indinavir-containing HAART had undetectable viral loads at 2-4 months of therapy. However, none of seven patients on nelfinavir-containing HAART had a substantial decrease in viral load. Viruses from 14 patients were analyzed, 12 of which (86%) had at least one primary resistance mutation that is known to confer resistance to HIV-1 virus. Three patients had the multi-drug-resistant mutation, Q151M, two of whom showed reduced susceptibility to zidovudine, didanosine, stavudine and zalcitabine. Conclusion: Our limited findings show that nelfinavir-containing regimens may have limited virologic benefit to HIV-2-infected patients. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:S49 / S54
页数:6
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