Summary
May 2007, Vol. 8, No. 7, Pages 923-933 , DOI 10.1517/14656566.8.7.923

Access denied? The status of co-receptor inhibition to counter HIV entry

Priscilla Biswas1, Giuseppe Tambussi2 & Adriano Lazzarin3
1Consultant (Senior Researcher), San Raffaele Scientific Institute, Lab. of Clinical Immunology, Via Stamira d’ Ancona n. 20, 20127 Milan, Italy.
2Head of Experimental Therapies Unit, San Raffaele Scientific Institute, Clinic of Infectious Diseases, Milan, Italy
3Head of the Clinic of Infectious Diseases and Professor, Università Vita-Salute San Raffaele, Milano, Italia
Author for correspondence



As resistance and long-term metabolic abnormalities hamper the efficacy of previous drugs against HIV-1, targeting of HIV co-receptors represents an exciting new frontier for antiretroviral therapeutics. CCR5 inhibitors are most likely to be the new available drugs within the class of entry inhibitors. This paper reviews the most recent clinical data available on the small-molecule compounds vicriviroc and maraviroc and on the antibodies PRO 140 and CCR5mAb004, as well as some novel genetic approaches. A thorough overview of the many challenges, past, present and future, that CCR5 inhibitors encounter during their development pathway is then presented. Possible immunologic consequences are also discussed. It could be foreseen that the benefit for HIV-infected individuals derived by the use of these potential novel drugs will outweigh the costs/risks intrinsically present in every new therapeutic approach.

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Authors:
Priscilla Biswas
Giuseppe Tambussi
Adriano Lazzarin
Keywords:
antiretroviral
entry inhibitor
CCL3
CCL4
CCL5
CCR5 inhibitor
CCR5mAb004
CCR5-tropic
CXCR4-tropic
HIV infection
maraviroc
PRO 140
R5
R5X4
vicriviroc
viral tropism
X4