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Antibody-based inhibitors of HIV infection

  1. Author:
    Choudhry, V.
    Zhang, M. Y.
    Dimitrova, D.
    Prabakaran, P.
    Dimitrov, A. S.
    Fouts, T. R.
    Dimitrov, D. S.
  2. Author Address

    NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA. SAIC Frederick Inc, BRP, NCI Frederick, Frederick, MD 21702 USA. Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA. UMBC, Techctr, Profectus BioSci Inc, Baltimore, MD 21227 USA Choudhry, V, NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Bldg 320,Rm 8,POB B,Miller Dr, Frederick, MD 21702 USA
    1. Year: 2006
    2. Date: MAY
  1. Journal: Expert Opinion on Biological Therapy
    1. 6
    2. 5
    3. Pages: 523-531
  2. Type of Article: Review
  1. Abstract:

    The demand for new treatment options against HIV is becoming increasingly desperate as the side effects and the expansion and spread of drug-resistant virus within the infected population limit the clinical benefits provided by available anti-HIV drugs. Preparations of polyclonal antibodies have a long history of proven clinical utility against some viruses; however, they have enjoyed very limited success against HIV. Recent clinical trials and in vitro experiments suggest that monoclonal antibodies against HIV may have promise clinically. These antibodies and antibody-based reagents target either the viral envelope glycoprotein, the receptor (CD4) or coreceptor (CCR5) molecules, or transition-state structures that appear during viral entry. The challenge is whether an antibody-based therapy can be identified (with or without their small molecule brethren) that presents long-term clinical efficacy, low toxicity and minimal risk of clinical failure from viral resistance

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External Sources

  1. DOI: 10.1517/14712598.6.5.523
  2. No sources found.

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