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Vol 273 No 7324 p674
6 November 2004

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No long-term benefit from HIV treatment interruption

“Structured treatment interruption” in which highly active antiretroviral therapy (HAART) is intermittently stopped is a practice which does not appear to provide long-term benefit to patients infected with HIV.

Researchers hypothesised that this approach might boost immune responses to control HIV infection better. Evidence from earlier research, published in Nature in 2000, suggested that treatment interruptions worked for patients during the earliest stages of acute infection. Viral loads in newly infected patients remained suppressed for a median of six months after therapy had been stopped. However, the same research group, led by Bruce Walker of Massachusetts General Hospital, Boston, has now shown that for most patients this effect was transient — viral load rebounded in eight of 14 patients by one year.

The patients underwent successive treatment interruptions after an initial treatment period of at least eight months. Treatment was restarted if viral load exceeded 50,000 RNA copies/ml plasma on a single occasion or 5,000 copies/ml for three consecutive weeks. Of the 14 patients in the study, 11 achieved virologic control for at least 90 days. However, for most patients there was a subsequent rise in viral load. Only three patients maintained control for more than two years.

“ We … now have about five years of follow-up on some of the patients,” says Dr Walker. “Although we were able to use early treatment and structured treatment interruption to boost immunity and have 11 of 14 patients control their virus, most of the persons ultimately ‘broke through’, meaning that they had a recurrence of viraemia.”

The researchers conclude that treatment interruptions should probably be avoided outside the setting of controlled clinical trials. They suggest that data from the study could be used to inform current efforts to develop a therapeutic AIDS vaccine (PLoS Medicine 2004;1:e36).

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