Sanchez R, Portilla J, Gimeno A, Boix V, et al. Immunovirologic consequences and safety of short, non-structured interruptions of successful antiretroviral treatment. J Infect 2006 May 8; [Epub ahead of print].
Sanchez et al evaluated the safety of short ART interruptions and their virologic and immunologic consequences in HIV-infected adults in Spain on HAART with suppressed viral replication. They prospectively followed 20 patients with undetectable viral load while on HAART to detect any treatment interruption, and analysed viral and cellular kinetics, incidence of resistance mutations, clinical outcome and results after therapy resumption. The mean time since HIV diagnosis was 95 months and time with undetectable viral load 16 months. Treatment was interrupted because of adverse effects, cancer, tuberculosis or patient will, and reintroduced after 4 weeks using, if possible, the same combination. HIV viral load was detectable on day 28 after interruption in 18 (90%) patients. There was a non-significant decrease in median CD4 count from 478/mm3 to 257/mm3. Resistance mutations were found in 9 (45%) patients after interruptions, and treatment was reintroduced in 14 patients; all of whom achieved viral suppression. The authors conclude that in patients on HAART who have undetectable viral load, an interruption no longer than 4 weeks due to any intercurrent problem seems to be safe. However, due to the frequent development of resistance, a genotypic test during interruption might be helpful.
Etard JF, Ndiaye I, Thierry-Mieg M, et al. Mortality and causes of death in adults receiving highly active antiretroviral therapy in Senegal: a 7-year cohort study. AIDS 2006;20: 1181-89
The authors evaluated survival and ascertained causes of death among the first HIV-1 infected adults patients of the Senegalese Antiretroviral Drug Access Initiative (enrolled between 08/1998 and 04/2002). The first-line regimen for these patients consisted of two NRTI and either a NNRTI or PI. Cause of death was ascertained through medical records or verbal autopsy. A total of 404 patients (54.7% women; median age 37 years, CD4 128 cells/μl, viral load 5.2 log cp/ml) were enrolled and followed for a median of 46 months after initiating HAART. At baseline, 5% were ART-experienced, and 39% and 55% were respectively at CDC stage B and C. 93 patients died during follow-up giving an overall death rate of 6.3/100 person-years. The death rate, which was highest during the first year after HAART initiation, decreased with time yielding a cumulative probability of dying of 17.4% at 2 years and 24.6% 5 years. The most frequent causes of death were mycobacterial infections, neurotropic infections and septicaemia.
Crabb C. Testing a CCR5 drug? Avoid mosquito bites. AIDS 2006; 28:N3-N4.
‘Sleep under netting, wear long sleeves and pants, and use mosquito repellent’, may be sage advice for HIV patients taking experimental CCR5-blocking drugs. Researchers at theNational Institutes of Allergy and Infectious Diseases in Bethesda, Maryland, have discovered that the genetic mutation of the CCR5 surface protein that makes individuals highly resistant to HIV infection also leaves them more susceptible to potentially fatal infection of the mosquito-borne West Nile virus.