Pandemic and seasonal influenza: therapeutic challenges.
Identifieur interne : 001C95 ( Main/Exploration ); précédent : 001C94; suivant : 001C96Pandemic and seasonal influenza: therapeutic challenges.
Auteurs : Matthew J. Memoli [États-Unis] ; David M. Morens ; Jeffery K. TaubenbergerSource :
- Drug discovery today [ 1359-6446 ] ; 2008.
Descripteurs français
- KwdFr :
- MESH :
- traitement médicamenteux : Infection croisée.
- usage thérapeutique : Antiviraux.
- épidémiologie : Grippe humaine, Infection croisée.
- Flambées de maladies, Grippe humaine, Humains, Infection croisée, Pharmacologie clinique, Saisons.
English descriptors
- KwdEn :
- MESH :
- chemical , therapeutic use : Antiviral Agents.
- complications : Cross Infection, Influenza, Human.
- drug therapy : Cross Infection.
- epidemiology : Cross Infection, Influenza, Human.
- therapy : Influenza, Human.
- Disease Outbreaks, Humans, Pharmacology, Clinical, Seasons.
Abstract
Influenza A viruses cause significant morbidity and mortality annually, and the threat of a pandemic underscores the need for new therapeutic strategies. Here, we briefly discuss novel antiviral agents under investigation, the limitations of current antiviral therapy and stress the importance of secondary bacterial infections in seasonal and pandemic influenza. Additionally, the lack of new antibiotics available to treat increasingly drug resistant organisms such as methicillin-resistant Staphylococcus aureus, pneumococci, Acinetobacter, extended spectrum beta-lactamase producing gram negative bacteria and Clostridium difficile is highlighted as an important component of influenza treatment and pandemic preparedness. Addressing these problems will require a multidisciplinary approach, which includes the development of novel antivirals and new antibiotics, as well as a better understanding of the role secondary infections play on the morbidity and mortality of influenza infection.
DOI: 10.1016/j.drudis.2008.03.024
PubMed: 18598914
Affiliations:
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Le document en format XML
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<term>Cross Infection (epidemiology)</term>
<term>Disease Outbreaks</term>
<term>Humans</term>
<term>Influenza, Human (complications)</term>
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<term>Pharmacology, Clinical</term>
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<term>Flambées de maladies</term>
<term>Grippe humaine ()</term>
<term>Grippe humaine (épidémiologie)</term>
<term>Humains</term>
<term>Infection croisée ()</term>
<term>Infection croisée (traitement médicamenteux)</term>
<term>Infection croisée (épidémiologie)</term>
<term>Pharmacologie clinique</term>
<term>Saisons</term>
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<term>Influenza, Human</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Cross Infection</term>
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<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Cross Infection</term>
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<term>Grippe humaine</term>
<term>Humains</term>
<term>Infection croisée</term>
<term>Pharmacologie clinique</term>
<term>Saisons</term>
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<front><div type="abstract" xml:lang="en">Influenza A viruses cause significant morbidity and mortality annually, and the threat of a pandemic underscores the need for new therapeutic strategies. Here, we briefly discuss novel antiviral agents under investigation, the limitations of current antiviral therapy and stress the importance of secondary bacterial infections in seasonal and pandemic influenza. Additionally, the lack of new antibiotics available to treat increasingly drug resistant organisms such as methicillin-resistant Staphylococcus aureus, pneumococci, Acinetobacter, extended spectrum beta-lactamase producing gram negative bacteria and Clostridium difficile is highlighted as an important component of influenza treatment and pandemic preparedness. Addressing these problems will require a multidisciplinary approach, which includes the development of novel antivirals and new antibiotics, as well as a better understanding of the role secondary infections play on the morbidity and mortality of influenza infection.</div>
</front>
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<country name="États-Unis"><region name="Maryland"><name sortKey="Memoli, Matthew J" sort="Memoli, Matthew J" uniqKey="Memoli M" first="Matthew J" last="Memoli">Matthew J. Memoli</name>
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