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Development in lipid drugs.

Identifieur interne : 000336 ( France/Analysis ); précédent : 000335; suivant : 000337

Development in lipid drugs.

Auteurs : J. Raulin [France]

Source :

RBID : pubmed:15892690

Descripteurs français

English descriptors

Abstract

Lipopeptide lipid moieties induce dendritic cell (DC) internalization and epitopes are recognized by MHC, the major histocompatibility complex. HIV-1 (human immunodeficiency virus type 1) lipopeptide vaccine candidate elicits immune responses, and sustains HIV control after highly active antiretroviral therapy (HAART). Mp- and Dp-MART (anti-melanoma lipopeptides) induce strong CTL (cytolytic T lymphocyte) response. New BGTC, BGDA, TGKC lipoplexes mediate gene delivery, e.g., into mouse pancreatic tumor nodules. Triterpene glycyrrhizic acid (GL) inhibits SARS-CoV (severe acute respiratory syndrome associated coronavirus) replication. Compared to CDV (cidofovir), CDV ether lipid esters have enhanced activity against vaccinia (VV) and cowpox (CV) viruses in vitro. Oral treatment of VV and CV infected mice with CDV ether lipid esters, as effective as i.p. CDV, may be useful against orthopoxvirus infections in humans.

DOI: 10.2174/1389557053765574
PubMed: 15892690


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pubmed:15892690

Le document en format XML

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<term>Cidofovir</term>
<term>Cowpox virus (drug effects)</term>
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<term>Glycyrrhizic Acid (pharmacology)</term>
<term>HIV-1 (drug effects)</term>
<term>HIV-1 (growth & development)</term>
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<term>Lipids (chemistry)</term>
<term>Lipids (immunology)</term>
<term>Lipids (pharmacology)</term>
<term>Major Histocompatibility Complex</term>
<term>Melanoma (immunology)</term>
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<term>Organophosphonates (pharmacology)</term>
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<term>Peptides (immunology)</term>
<term>Peptides (pharmacology)</term>
<term>SARS Virus (drug effects)</term>
<term>SARS Virus (growth & development)</term>
<term>T-Lymphocytes (drug effects)</term>
<term>T-Lymphocytes (metabolism)</term>
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<term>Acide glycyrrhizique (pharmacologie)</term>
<term>Agents antiVIH (pharmacologie)</term>
<term>Agents antiVIH (synthèse chimique)</term>
<term>Animaux</term>
<term>Cellules dendritiques ()</term>
<term>Cellules dendritiques (métabolisme)</term>
<term>Complexe majeur d'histocompatibilité</term>
<term>Cytosine (analogues et dérivés)</term>
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<term>Peptides (immunologie)</term>
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<term>Cowpox virus</term>
<term>Dendritic Cells</term>
<term>HIV-1</term>
<term>Orthopoxvirus</term>
<term>SARS Virus</term>
<term>T-Lymphocytes</term>
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<term>Animals</term>
<term>Antiretroviral Therapy, Highly Active</term>
<term>Cidofovir</term>
<term>Humans</term>
<term>Major Histocompatibility Complex</term>
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<term>Animaux</term>
<term>Cellules dendritiques</term>
<term>Complexe majeur d'histocompatibilité</term>
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<term>Lipides</term>
<term>Lymphocytes T</term>
<term>Mélanome</term>
<term>Orthopoxvirus</term>
<term>Peptides</term>
<term>Thérapie antirétrovirale hautement active</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
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<div type="abstract" xml:lang="en">Lipopeptide lipid moieties induce dendritic cell (DC) internalization and epitopes are recognized by MHC, the major histocompatibility complex. HIV-1 (human immunodeficiency virus type 1) lipopeptide vaccine candidate elicits immune responses, and sustains HIV control after highly active antiretroviral therapy (HAART). Mp- and Dp-MART (anti-melanoma lipopeptides) induce strong CTL (cytolytic T lymphocyte) response. New BGTC, BGDA, TGKC lipoplexes mediate gene delivery, e.g., into mouse pancreatic tumor nodules. Triterpene glycyrrhizic acid (GL) inhibits SARS-CoV (severe acute respiratory syndrome associated coronavirus) replication. Compared to CDV (cidofovir), CDV ether lipid esters have enhanced activity against vaccinia (VV) and cowpox (CV) viruses in vitro. Oral treatment of VV and CV infected mice with CDV ether lipid esters, as effective as i.p. CDV, may be useful against orthopoxvirus infections in humans.</div>
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