Résumé
Officiellement découverte par Sir Alexander Fleming le 3 septembre 1928, la pénicilline est utilisée de façon très large à partir de 1941. Cette première molécule antibiotique a ouvert la porte au développement d’une multitude de familles qui a abouti à ce que l’on pourrait décrire comme un âge d’or de l’antibiothérapie. La résistance bactérienne était certes déjé une préoccupation, mais le nombre et la variété des composés introduits permettaient de garder une confiance absolue dans cette classe médicamenteuse. Les années 2000 ont sonné le glas de cette insouciance où le bon usage pouvait paraître une futilité, la multirésistance voire la panrésistance sont apparues aussi vite que le pipeline de nouvelles molécules s’est épuisé. Face à cette menace qui est maintenant bien installée dans nos institutions hospitalières, la réponse ne peut être monomorphe. Nous avons ainsi appris à respecter les molécules disponibles, à économiser les nouvelles, à faire du bon usage une priorité nationale et internationale. En parallèle, la place laissée par l’absence de nouvelles molécules a été rapidement comblée par l’apparition de thérapeutiques alternatives, des traitements anti-infectieux non antibiotiques. Les approches sont multiples, mais la plupart d’entre elles sont issues d’une recherche fondamentale qui s’est employée à préciser les déterminants majeurs de la relation hôtepathogène.
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Kipnis, E., Dessein, R., Faure, K., Guery, B. (2013). Les thérapeutiques infectieuses non antibiotiques. In: Infectiologie en réanimation. Références en réanimation. Collection de la SRLF. Springer, Paris. https://doi.org/10.1007/978-2-8178-0389-0_8
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