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Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia

PURPOSE OF REVIEW: Community-acquired bacterial pneumonia (CABP) continues to be a worldwide health concern since it is the major cause of mortality and hospitalisation worldwide. Increased macrolide resistance among Streptococcus pneumoniae and other infections has resulted in a significantly large...

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Autores principales: Adhikary, Shubham, Duggal, Meher Kaur, Nagendran, Saraswathy, Chintamaneni, Meena, Tuli, Hardeep Singh, Kaur, Ginpreet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257118/
https://www.ncbi.nlm.nih.gov/pubmed/35811574
http://dx.doi.org/10.1007/s40495-022-00297-6
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author Adhikary, Shubham
Duggal, Meher Kaur
Nagendran, Saraswathy
Chintamaneni, Meena
Tuli, Hardeep Singh
Kaur, Ginpreet
author_facet Adhikary, Shubham
Duggal, Meher Kaur
Nagendran, Saraswathy
Chintamaneni, Meena
Tuli, Hardeep Singh
Kaur, Ginpreet
author_sort Adhikary, Shubham
collection PubMed
description PURPOSE OF REVIEW: Community-acquired bacterial pneumonia (CABP) continues to be a worldwide health concern since it is the major cause of mortality and hospitalisation worldwide. Increased macrolide resistance among Streptococcus pneumoniae and other infections has resulted in a significantly larger illness burden, which has been exacerbated by evolving demography and a higher prevalence of comorbid disorders. Owing to such circumstances, the creation of new antibiotic classes is critical. RECENT FINDINGS: Lefamulin, also referred to as BC-3781, is the primary pleuromutilin antibiotic which has been permitted for both intravenous and oral use in humans for the remedy of bacterial infections. It has shown activity against gram-positive bacteria including methicillin-resistant strains as well as atypical organisms which as often implicated in CABP. It has a completely unique mechanism of action that inhibits protein synthesis via way of means of stopping the binding of tRNA for peptide transfer. The C(14) side chain is responsible for its pharmacodynamic and antimicrobial properties, together with supporting in overcoming bacterial ribosomal resistance and mutations improvement amplifying the number of hydrogen bonds to the target site. SUMMARY: This review aims to highlight the pre-existing treatment options and specific purposes to shed some light upon the development of a new drug lefamulin and its specifications and explore this novel drug’s superior efficacy to already existing treatment strategies.
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spelling pubmed-92571182022-07-06 Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia Adhikary, Shubham Duggal, Meher Kaur Nagendran, Saraswathy Chintamaneni, Meena Tuli, Hardeep Singh Kaur, Ginpreet Curr Pharmacol Rep Clinical Pharmacology (L Brunetti, Section Editor) PURPOSE OF REVIEW: Community-acquired bacterial pneumonia (CABP) continues to be a worldwide health concern since it is the major cause of mortality and hospitalisation worldwide. Increased macrolide resistance among Streptococcus pneumoniae and other infections has resulted in a significantly larger illness burden, which has been exacerbated by evolving demography and a higher prevalence of comorbid disorders. Owing to such circumstances, the creation of new antibiotic classes is critical. RECENT FINDINGS: Lefamulin, also referred to as BC-3781, is the primary pleuromutilin antibiotic which has been permitted for both intravenous and oral use in humans for the remedy of bacterial infections. It has shown activity against gram-positive bacteria including methicillin-resistant strains as well as atypical organisms which as often implicated in CABP. It has a completely unique mechanism of action that inhibits protein synthesis via way of means of stopping the binding of tRNA for peptide transfer. The C(14) side chain is responsible for its pharmacodynamic and antimicrobial properties, together with supporting in overcoming bacterial ribosomal resistance and mutations improvement amplifying the number of hydrogen bonds to the target site. SUMMARY: This review aims to highlight the pre-existing treatment options and specific purposes to shed some light upon the development of a new drug lefamulin and its specifications and explore this novel drug’s superior efficacy to already existing treatment strategies. Springer International Publishing 2022-07-06 2022 /pmc/articles/PMC9257118/ /pubmed/35811574 http://dx.doi.org/10.1007/s40495-022-00297-6 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Clinical Pharmacology (L Brunetti, Section Editor)
Adhikary, Shubham
Duggal, Meher Kaur
Nagendran, Saraswathy
Chintamaneni, Meena
Tuli, Hardeep Singh
Kaur, Ginpreet
Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title_full Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title_fullStr Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title_full_unstemmed Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title_short Lefamulin: a New Hope in the Field of Community-Acquired Bacterial Pneumonia
title_sort lefamulin: a new hope in the field of community-acquired bacterial pneumonia
topic Clinical Pharmacology (L Brunetti, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257118/
https://www.ncbi.nlm.nih.gov/pubmed/35811574
http://dx.doi.org/10.1007/s40495-022-00297-6
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