| Literature DB >> 32515944 |
Federico Fenaroli1, James D Robertson2,3, Edoardo Scarpa4, Virginia M Gouveia4, Claudia Di Guglielmo5, Cesare De Pace4,6, Philip M Elks2,7, Alessandro Poma4,8, Dimitrios Evangelopoulos9, Julio Ortiz Canseco9, Tomasz K Prajsnar10,11, Helen M Marriott7,10, David H Dockrell7, Simon J Foster10,11, Timothy D McHugh9, Stephen A Renshaw3,7,10, Josep Samitier Martí5,12,13, Giuseppe Battaglia4,5,6,14,15, Loris Rizzello4,5,16.
Abstract
Mononuclear phagocytes such as monocytes, tissue-specific macrophages, and dendritic cells are primary actors in both innate and adaptive immunity. These professional phagocytes can be parasitized by intracellular bacteria, turning them from housekeepers to hiding places and favoring chronic and/or disseminated infection. One of the most infamous is the bacteria that cause tuberculosis (TB), which is the most pandemic and one of the deadliest diseases, with one-third of the world's population infected and an average of 1.8 million deaths/year worldwide. Here we demonstrate the effective targeting and intracellular delivery of antibiotics to infected macrophages both in vitro and in vivo, using pH-sensitive nanoscopic polymersomes made of PMPC-PDPA block copolymer. Polymersomes showed the ability to significantly enhance the efficacy of the antibiotics killing Mycobacterium bovis, Mycobacterium tuberculosis, and another established intracellular pathogen, Staphylococcus aureus. Moreover, they demonstrated to easily access TB-like granuloma tissues-one of the harshest environments to penetrate-in zebrafish models. We thus successfully exploited this targeting for the effective eradication of several intracellular bacteria, including M. tuberculosis, the etiological agent of human TB.Entities:
Keywords: drug delivery; intracellular pathogens; polymersomes; tuberculosis; zebrafish
Mesh:
Year: 2020 PMID: 32515944 DOI: 10.1021/acsnano.0c01870
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881