Literature DB >> 30385419

Inhalable poly(lactic-co-glycolic acid) (PLGA) microparticles encapsulating all-trans-Retinoic acid (ATRA) as a host-directed, adjunctive treatment for Mycobacterium tuberculosis infection.

Gemma O'Connor1, Nitya Krishnan2, Aidan Fagan-Murphy3, Joseph Cassidy4, Seonadh O'Leary5, Brian D Robertson6, Joseph Keane7, Mary P O'Sullivan8, Sally-Ann Cryan9.   

Abstract

Ending the tuberculosis (TB) epidemic by 2030 was recently listed in the United Nations (UN) Sustainable Development Goals alongside HIV/AIDS and malaria as it continues to be a major cause of death worldwide. With a significant proportion of TB cases caused by resistant strains of Mycobacterium tuberculosis (Mtb), there is an urgent need to develop new and innovative approaches to treatment. Since 1989, researchers have been assessing the anti-bacterial effects of the active metabolite of vitamin A, all trans-Retinoic acid (ATRA) solution, in Mtb models. More recently the antibacterial effect of ATRA has been shown to regulate the immune response to infection via critical gene expression, monocyte activation and the induction of autophagy leading to its application as a host-directed therapy (HDT). Inhalation is an attractive route for targeted treatment of TB, and therefore we have developed ATRA-loaded microparticles (ATRA-MP) within the inhalable size range (2.07 ± 0.5 µm) offering targeted delivery of the encapsulated cargo (70.5 ± 2.3%) to the site of action within the alveolar macrophage, which was confirmed by confocal microscopy. Efficient cellular delivery of ATRA was followed by a reduction in Mtb growth (H37Ra) in THP-1 derived macrophages evaluated by both the BACT/ALERT® system and enumeration of colony forming units (CFU). The antibacterial effect of ATRA-MP treatment was further assessed in BALB/c mice infected with the virulent strain of Mtb (H37Rv). ATRA-MP treatments significantly decreased the bacterial burden in the lungs alongside a reduction in pulmonary pathology following just three doses administered intratracheally. The immunomodulatory effects of targeted ATRA treatment in the lungs indicate a distinct yet effective mechanism of action amongst the formulations. This is the first study to-date of a controlled release ATRA treatment for TB suitable for inhalation that offers improved targeting of a HDT, retains antibacterial efficacy and improves pulmonary pathology compared to ATRA solution.
Copyright © 2018. Published by Elsevier B.V.

Entities:  

Keywords:  All trans-Retinoic acid; Intratracheal; Microparticles; Mouse model; THP-1 cells; Tuberculosis

Mesh:

Substances:

Year:  2018        PMID: 30385419     DOI: 10.1016/j.ejpb.2018.10.020

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  13 in total

1.  Chitosan Microparticles Loaded with New Non-Cytotoxic Isoniazid Derivatives for the Treatment of Tuberculosis: In Vitro and In Vivo Studies.

Authors:  Ionut Dragostin; Oana-Maria Dragostin; Andreea Teodora Iacob; Maria Dragan; Carmen Lidia Chitescu; Luminita Confederat; Alexandra-Simona Zamfir; Rodica Tatia; Catalina Daniela Stan; Carmen Lacramioara Zamfir
Journal:  Polymers (Basel)       Date:  2022-06-07       Impact factor: 4.967

Review 2.  Recent Advances in Host-Directed Therapies for Tuberculosis and Malaria.

Authors:  Kely C Matteucci; André A S Correa; Diego L Costa
Journal:  Front Cell Infect Microbiol       Date:  2022-05-20       Impact factor: 6.073

3.  Mycobacterium tuberculosis-Induced Bronchoalveolar Lavage Gene Expression Signature in Latent Tuberculosis Infection Is Dominated by Pleiotropic Effects of CD4+ T Cell-Dependent IFN-γ Production despite the Presence of Polyfunctional T Cells within the Airways.

Authors:  Jessica Jarvela; Michelle Moyer; Patrick Leahy; Tracey Bonfield; David Fletcher; Wambura N Mkono; Htin Aung; David H Canaday; Jean-Eudes Dazard; Richard F Silver
Journal:  J Immunol       Date:  2019-09-20       Impact factor: 5.422

4.  CRISPR Interference Reveals That All-Trans-Retinoic Acid Promotes Macrophage Control of Mycobacterium tuberculosis by Limiting Bacterial Access to Cholesterol and Propionyl Coenzyme A.

Authors:  Gregory H Babunovic; Michael A DeJesus; Barbara Bosch; Michael R Chase; Thibault Barbier; Amy K Dickey; Bryan D Bryson; Jeremy M Rock; Sarah M Fortune
Journal:  mBio       Date:  2022-01-18       Impact factor: 7.867

Review 5.  Emerging vaccine nanotechnology: From defense against infection to sniping cancer.

Authors:  Chan Feng; Yongjiang Li; Bijan Emiliano Ferdows; Dylan Neal Patel; Jiang Ouyang; Zhongmin Tang; Na Kong; Enguo Chen; Wei Tao
Journal:  Acta Pharm Sin B       Date:  2022-01-04       Impact factor: 14.903

Review 6.  Targeting Molecular Inflammatory Pathways in Granuloma as Host-Directed Therapies for Tuberculosis.

Authors:  Reto Guler; Mumin Ozturk; Solima Sabeel; Bongani Motaung; Suraj P Parihar; Friedrich Thienemann; Frank Brombacher
Journal:  Front Immunol       Date:  2021-10-20       Impact factor: 7.561

Review 7.  All trans retinoic acid as a host-directed immunotherapy for tuberculosis.

Authors:  Ahmad Z Bahlool; Conor Grant; Sally-Ann Cryan; Joseph Keane; Mary P O'Sullivan
Journal:  Curr Res Immunol       Date:  2022-03-30

Review 8.  Recent advances in PLGA micro/nanoparticle delivery systems as novel therapeutic approach for drug-resistant tuberculosis.

Authors:  Liqun Shao; Shu Shen; Huan Liu
Journal:  Front Bioeng Biotechnol       Date:  2022-07-22

9.  Tuberculosis lymph node granulomas: using transcriptomics to discover immunopathology paradigms and guide host-directed therapy.

Authors:  James J Phelan; Seónadh O'Leary; Joseph Keane
Journal:  J Clin Invest       Date:  2021-08-02       Impact factor: 19.456

10.  Inhibiting Histone Deacetylases in Human Macrophages Promotes Glycolysis, IL-1β, and T Helper Cell Responses to Mycobacterium tuberculosis.

Authors:  Donal J Cox; Amy M Coleman; Karl M Gogan; James J Phelan; Cilian Ó Maoldomhnaigh; Pádraic J Dunne; Sharee A Basdeo; Joseph Keane
Journal:  Front Immunol       Date:  2020-07-23       Impact factor: 7.561

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.