Literature DB >> 31680428

RNA interference therapeutics in organ transplantation: The dawn of a new era.

Isabel M A Brüggenwirth1, Paulo N Martins2.   

Abstract

RNA interference (RNAi) is a natural process through which double-stranded RNA molecules can silence the gene carrying the same code as the particular RNA of interest. In 2006, the discovery of RNAi was awarded the Nobel Prize in Medicine and its success has accumulated since. Gene silencing through RNAi has been used successfully in a broad range of diseases, and, more recently, this technique has gained interest in the field of organ transplantation. Here, genes related to ischemia-reperfusion injury (IRI) or graft rejection may be silenced to improve organ quality after transplantation. Several strategies have been used to deliver siRNA, and pretransplant machine perfusion presents a unique opportunity to deliver siRNA to the target organ during ex situ preservation. In this review, the potential of RNAi in the field of organ transplantation will be discussed. A brief overview on the discovery of RNAi, its mechanism, and limitations are included. In addition, studies using RNAi to target genes related to IRI in liver, kidney, lung, and heart transplantation are discussed.
© 2019 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  RNA interference; RNA therapeutics; ex situ machine perfusion; ex vivo perfusion; gene editing; gene silencing; gene therapy; graft modulation; graft pretreatment; graft treatment; ischemia-reperfusion injury (IRI); miRNA; organ preservation; organ transplantation; regenerative medicine; rejection; shRNA; siRNA; small interfering RNA (siRNA); translational research/science; transplant

Mesh:

Substances:

Year:  2019        PMID: 31680428     DOI: 10.1111/ajt.15689

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  7 in total

Review 1.  Implication of microRNAs in Carcinogenesis with Emphasis on Hematological Malignancies and Clinical Translation.

Authors:  Zsuzsanna Gaál
Journal:  Int J Mol Sci       Date:  2022-05-23       Impact factor: 6.208

2.  Virus-Derived Chemokine Modulating Protein Pre-Treatment Blocks Chemokine-Glycosaminoglycan Interactions and Significantly Reduces Transplant Immune Damage.

Authors:  Isabela R Zanetti; Michelle Burgin; Liqiang Zhang; Steve T Yeh; Sriram Ambadapadi; Jacquelyn Kilbourne; Jordan R Yaron; Kenneth M Lowe; Juliane Daggett-Vondras; David Fonseca; Ryan Boyd; Dara Wakefield; William Clapp; Efrem Lim; Hao Chen; Alexandra Lucas
Journal:  Pathogens       Date:  2022-05-16

3.  Impact of Graft-Resident Leucocytes on Treg Mediated Skin Graft Survival.

Authors:  Romy Steiner; Anna M Weijler; Thomas Wekerle; Jonathan Sprent; Nina Pilat
Journal:  Front Immunol       Date:  2021-11-29       Impact factor: 7.561

Review 4.  Ex Vivo Lung Perfusion: A Review of Current and Future Application in Lung Transplantation.

Authors:  Kareem Ahmad; Jennifer L Pluhacek; A Whitney Brown
Journal:  Pulm Ther       Date:  2022-03-22

Review 5.  Impact of Machine Perfusion on the Immune Response After Liver Transplantation - A Primary Treatment or Just a Delivery Tool.

Authors:  Rebecca Panconesi; Mauricio Flores Carvalho; Daniele Dondossola; Paolo Muiesan; Philipp Dutkowski; Andrea Schlegel
Journal:  Front Immunol       Date:  2022-07-08       Impact factor: 8.786

Review 6.  Recent Advances in Stimulus-Responsive Nanocarriers for Gene Therapy.

Authors:  Cheng Yu; Long Li; Pei Hu; Yan Yang; Wei Wei; Xin Deng; Lu Wang; Franklin R Tay; Jingzhi Ma
Journal:  Adv Sci (Weinh)       Date:  2021-05-16       Impact factor: 16.806

7.  Mineralizing Gelatin Microparticles as Cell Carrier and Drug Delivery System for siRNA for Bone Tissue Engineering.

Authors:  Sandra Hinkelmann; Alexandra H Springwald; Sabine Schulze; Ute Hempel; Franziska Mitrach; Christian Wölk; Michael C Hacker; Michaela Schulz-Siegmund
Journal:  Pharmaceutics       Date:  2022-02-28       Impact factor: 6.321

  7 in total

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