Development in lipid drugs.
Identifieur interne : 002752 ( PubMed/Checkpoint ); précédent : 002751; suivant : 002753Development in lipid drugs.
Auteurs : J. Raulin [France]Source :
- Mini reviews in medicinal chemistry [ 1389-5575 ] ; 2005.
Descripteurs français
- KwdFr :
- Acide glycyrrhizique (pharmacologie), Agents antiVIH (pharmacologie), Agents antiVIH (synthèse chimique), Animaux, Cellules dendritiques (), Cellules dendritiques (métabolisme), Complexe majeur d'histocompatibilité, Cytosine (analogues et dérivés), Cytosine (pharmacologie), Humains, Lipides (), Lipides (immunologie), Lipides (pharmacologie), Lymphocytes T (), Lymphocytes T (métabolisme), Mélanome (), Mélanome (immunologie), Orthopoxvirus (), Orthopoxvirus (croissance et développement), Peptides (), Peptides (immunologie), Peptides (pharmacologie), Phosphonates (pharmacologie), Thérapie antirétrovirale hautement active, VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (), VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (croissance et développement), Virus de la variole bovine (), Virus de la variole bovine (croissance et développement), Virus du SRAS (), Virus du SRAS (croissance et développement).
- MESH :
- analogues et dérivés : Cytosine.
- croissance et développement : Orthopoxvirus, VIH-1 (Virus de l'Immunodéficience Humaine de type 1), Virus de la variole bovine, Virus du SRAS.
- immunologie : Lipides, Mélanome, Peptides.
- métabolisme : Cellules dendritiques, Lymphocytes T.
- pharmacologie : Acide glycyrrhizique, Agents antiVIH, Cytosine, Lipides, Peptides, Phosphonates.
- synthèse chimique : Agents antiVIH.
- Animaux, Cellules dendritiques, Complexe majeur d'histocompatibilité, Humains, Lipides, Lymphocytes T, Mélanome, Orthopoxvirus, Peptides, Thérapie antirétrovirale hautement active, VIH-1 (Virus de l'Immunodéficience Humaine de type 1), Virus de la variole bovine, Virus du SRAS.
English descriptors
- KwdEn :
- Animals, Anti-HIV Agents (chemical synthesis), Anti-HIV Agents (pharmacology), Antiretroviral Therapy, Highly Active, Cidofovir, Cowpox virus (drug effects), Cowpox virus (growth & development), Cytosine (analogs & derivatives), Cytosine (pharmacology), Dendritic Cells (drug effects), Dendritic Cells (metabolism), Glycyrrhizic Acid (pharmacology), HIV-1 (drug effects), HIV-1 (growth & development), Humans, Lipids (chemistry), Lipids (immunology), Lipids (pharmacology), Major Histocompatibility Complex, Melanoma (immunology), Melanoma (prevention & control), Organophosphonates (pharmacology), Orthopoxvirus (drug effects), Orthopoxvirus (growth & development), Peptides (chemistry), Peptides (immunology), Peptides (pharmacology), SARS Virus (drug effects), SARS Virus (growth & development), T-Lymphocytes (drug effects), T-Lymphocytes (metabolism).
- MESH :
- chemical , analogs & derivatives : Cytosine.
- chemical , chemical synthesis : Anti-HIV Agents.
- chemical , chemistry : Lipids, Peptides.
- chemical , immunology : Lipids, Peptides.
- chemical , pharmacology : Anti-HIV Agents, Cytosine, Glycyrrhizic Acid, Lipids, Organophosphonates, Peptides.
- drug effects : Cowpox virus, Dendritic Cells, HIV-1, Orthopoxvirus, SARS Virus, T-Lymphocytes.
- growth & development : Cowpox virus, HIV-1, Orthopoxvirus, SARS Virus.
- immunology : Melanoma.
- metabolism : Dendritic Cells, T-Lymphocytes.
- prevention & control : Melanoma.
- Animals, Antiretroviral Therapy, Highly Active, Cidofovir, Humans, Major Histocompatibility Complex.
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
Affiliations:
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pubmed:15892690Le document en format XML
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<term>Anti-HIV Agents (chemical synthesis)</term>
<term>Anti-HIV Agents (pharmacology)</term>
<term>Antiretroviral Therapy, Highly Active</term>
<term>Cidofovir</term>
<term>Cowpox virus (drug effects)</term>
<term>Cowpox virus (growth & development)</term>
<term>Cytosine (analogs & derivatives)</term>
<term>Cytosine (pharmacology)</term>
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<term>Glycyrrhizic Acid (pharmacology)</term>
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<term>HIV-1 (growth & development)</term>
<term>Humans</term>
<term>Lipids (chemistry)</term>
<term>Lipids (immunology)</term>
<term>Lipids (pharmacology)</term>
<term>Major Histocompatibility Complex</term>
<term>Melanoma (immunology)</term>
<term>Melanoma (prevention & control)</term>
<term>Organophosphonates (pharmacology)</term>
<term>Orthopoxvirus (drug effects)</term>
<term>Orthopoxvirus (growth & development)</term>
<term>Peptides (chemistry)</term>
<term>Peptides (immunology)</term>
<term>Peptides (pharmacology)</term>
<term>SARS Virus (drug effects)</term>
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<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>
<term>Cytosine (pharmacologie)</term>
<term>Humains</term>
<term>Lipides ()</term>
<term>Lipides (immunologie)</term>
<term>Lipides (pharmacologie)</term>
<term>Lymphocytes T ()</term>
<term>Lymphocytes T (métabolisme)</term>
<term>Mélanome ()</term>
<term>Mélanome (immunologie)</term>
<term>Orthopoxvirus ()</term>
<term>Orthopoxvirus (croissance et développement)</term>
<term>Peptides ()</term>
<term>Peptides (immunologie)</term>
<term>Peptides (pharmacologie)</term>
<term>Phosphonates (pharmacologie)</term>
<term>Thérapie antirétrovirale hautement active</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) ()</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (croissance et développement)</term>
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<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Cytosine</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en"><term>Anti-HIV Agents</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Lipids</term>
<term>Peptides</term>
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<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Lipids</term>
<term>Peptides</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-HIV Agents</term>
<term>Cytosine</term>
<term>Glycyrrhizic Acid</term>
<term>Lipids</term>
<term>Organophosphonates</term>
<term>Peptides</term>
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<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
<term>Virus de la variole bovine</term>
<term>Virus du SRAS</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><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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<keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Cowpox virus</term>
<term>HIV-1</term>
<term>Orthopoxvirus</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Lipides</term>
<term>Mélanome</term>
<term>Peptides</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Melanoma</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Dendritic Cells</term>
<term>T-Lymphocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Cellules dendritiques</term>
<term>Lymphocytes T</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Acide glycyrrhizique</term>
<term>Agents antiVIH</term>
<term>Cytosine</term>
<term>Lipides</term>
<term>Peptides</term>
<term>Phosphonates</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Melanoma</term>
</keywords>
<keywords scheme="MESH" qualifier="synthèse chimique" xml:lang="fr"><term>Agents antiVIH</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Antiretroviral Therapy, Highly Active</term>
<term>Cidofovir</term>
<term>Humans</term>
<term>Major Histocompatibility Complex</term>
</keywords>
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<term>Cellules dendritiques</term>
<term>Complexe majeur d'histocompatibilité</term>
<term>Humains</term>
<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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<front><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>
</front>
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<ArticleTitle>Development in lipid drugs.</ArticleTitle>
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<Abstract><AbstractText>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.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Raulin</LastName>
<ForeName>J</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Université Denis Diderot (Paris 7), 2 place Jussieu, 75005 Paris, France. jeanine.raulin@wanadoo.fr</Affiliation>
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<QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName>
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<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
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