Special considerations in the initiation and management of antiretroviral therapy in individuals coinfected with HIV and hepatitis C

被引:27
作者
Braitstein, P
Palepu, A
Dieterich, D
Benhamou, Y
Montaner, JSG
机构
[1] Univ British Columbia, BC Ctr Excellence HIV AIDS, Vancouver, BC V6Z 1Y6, Canada
[2] Univ British Columbia, Dept Hlth Care & Epidemiol, Vancouver, BC V6T 1W5, Canada
[3] Univ British Columbia, Ctr Hlth Outcomes & Evaluat Sci, Vancouver, BC, Canada
[4] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[5] Mt Sinai Med Ctr, Dept Med, New York, NY 10029 USA
[6] Hosp Pitie Salpetriere, Serv Hepatogastroenterol, Paris, France
关键词
HIV; hepatitis c; coinfection; antiretroviral drugs; toxicity; immune restoration;
D O I
10.1097/00002030-200411190-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Although hepatitis C (HCV) treatment efficacy has improved in recent years, the majority of HIV/HCV-coinfected individuals may not enjoy the full benefits of these treatments and appropriate HIV management is crucial. Evidence is accumulating regarding the impact of HIV/HCV coinfection on the response to, and safety and tolerability of, antiretroviral therapy (ART) in this population. Methods: Computerized, English-language literature searches of MEDLINE and PubMed databases (January 1985 to May 2004) for studies of HIV and HCV infection in humans to examine critically (a) the impact of HCV on the HIV virologic and immunologic response to ART, (b) the safety and tolerability of ART in coinfected individuals; and (c) the relationship between immune suppression and immune restoration on hepatic injury. Results: Three key messages emerged regarding the use of ART in HIV/HCV-coinfected individuals: (a) although HCV appeared to have no impact on HIV virologic response, the data are equivocal regarding immunologic response; (b) morbidities associated with HCV infection such as insulin resistance, diabetes, mitochondrial dysfunction, and liver inflammation, are also associated toxicities of ART, and (c) both immune suppression and restoration can contribute to the onset and acceleration of HCV-related liver disease. Conclusions: The CD4 cell count threshold for initiating ART ill HIV/HCV-coinfected patients may be higher because of the impact of immune suppression and restoration on the onset of HCV-associated liver disease and the possibility of a blunted immune response to ART at lower CD4 cell counts. Further, overlapping morbidity between HCV-related mitochondrial and metabolic disease manifestations and ART toxicities warrant careful attention by clinicians. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:2221 / 2234
页数:14
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