4.6 Article

Inhibition of DC-SIGN-Mediated HIV Infection by a Linear Trimannoside Mimic in a Tetravalent Presentation

Journal

ACS CHEMICAL BIOLOGY
Volume 5, Issue 3, Pages 301-312

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cb900216e

Keywords

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Funding

  1. EU [LSHP-CT-2004-50-3487]
  2. Azioni Integrate Italia-Spagna [IT074ABCCM, 12005-0212]
  3. Ministry of Science and Innovation (MICINN) [CTQ2008-01694]
  4. FIRB [RBPR05NWWC]
  5. Marie Curie ITN FP7 project CARMUSYS [PITN-GA-2008-213592]
  6. AVIP EC WP6
  7. Japan Health Science Foundation
  8. Italian Ministry of Health
  9. MEC
  10. Doctorate School of Molecular Medicine, University of Milan
  11. Siclaction-Ensemble contre le Sida

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HIV infection is pandemic in humans and is responsible for millions of deaths every year. The discovery of new cellular targets that can be used to prevent the infection process represents a new opportunity for developing more effective antiviral drugs. In this context, dendritic cell-specific ICAM-3 grabbing nonintegrin (DC-SIGN), a lectin expressed at the surface of immature dendritic cells and involved in the initial stages of HIV infection, is a promising therapeutic target. Herein we show the ability of a new tetravalent dendron containing four copies of a linear trimannoside mimic to inhibit the trans HIV infection process of CD4+ T lymphocytes at low micromolar range. This compound presents a high solubility in physiological media, a neglectable cytotoxicity, and a long-lasting effect and is based on carbohydrate-mimic units. Notably, the HIV antiviral activity is independent of viral tropism (X4 or R5). The formulation of this compound as a gel could allow its use as topical microbicide.

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