Literature DB >> 30074507

Novel targeted drug delivery systems to minimize systemic immunosuppression in vascularized composite allotransplantation.

Adriano Taddeo1,2, Catherine Tsai1,2, Esther Vögelin2, Robert Rieben1.   

Abstract

PURPOSE OF REVIEW: The long-term adverse effects of immunosuppressive treatment, the high rate of acute rejection and the development of chronic rejection are the main factors preventing a wider clinical application of vascularized composite allotransplantation (VCA). Targeted immunosuppression using innovative drug delivery systems (DDS) may help to overcome these hurdles, increasing therapeutic efficacy while reducing systemic toxicity. This review provides a summary of the recently developed strategies for targeted delivery of immunosuppressive drugs in VCA. RECENT
FINDINGS: Currently, several innovative strategies for targeted immunosuppression have been designed based on the anatomy and function of the target organ. Site-specific DDS have been developed both for directly accessible organs (i.e. skin, eye and lung) and internal organs (i.e. lymph nodes, liver, nervous system, etc.). In preclinical models, DDS designed for sustained, 'on demand,' or 'on cue' drug release has been shown to promote VCA survival while reducing systemic toxicity. These findings suggest that targeted delivery could increase patient compliance and potentially decrease toxicity in VCA recipients.
SUMMARY: Targeted immunosuppression in VCA represents a promising approach for improving patient compliance and graft survival while reducing off-target toxicity, intensity and frequency of acute rejection episodes and risk of chronic rejection. VIDEO ABSTRACT.

Entities:  

Mesh:

Year:  2018        PMID: 30074507     DOI: 10.1097/MOT.0000000000000564

Source DB:  PubMed          Journal:  Curr Opin Organ Transplant        ISSN: 1087-2418            Impact factor:   2.640


  4 in total

1.  Delivery of Rapamycin Using In Situ Forming Implants Promotes Immunoregulation and Vascularized Composite Allograft Survival.

Authors:  Damian Sutter; Dzhuliya V Dzhonova; Jean-Christophe Prost; Cedric Bovet; Yara Banz; Lisa Rahnfeld; Jean-Christophe Leroux; Robert Rieben; Esther Vögelin; Jan A Plock; Paola Luciani; Adriano Taddeo; Jonas T Schnider
Journal:  Sci Rep       Date:  2019-06-25       Impact factor: 4.379

2.  Local FK506 implants in non-human primates to prevent early acute rejection in vascularized composite allografts.

Authors:  Alexandre G Lellouch; Corentin B Taveau; Alec R Andrews; Joseph Molde; Zhi Yang Ng; Philipp Tratnig-Frankl; Ivy A Rosales; Marion Goutard; Elise Lupon; Laurent A Lantieri; Robert B Colvin; Mark A Randolph; Joachim Kohn; Curtis L Cetrulo
Journal:  Ann Transl Med       Date:  2021-07

Review 3.  Implantable Immunosuppressant Delivery to Prevent Rejection in Transplantation.

Authors:  Madonna Rica Anggelia; Ren-Wen Huang; Hui-Yun Cheng; Chih-Hung Lin; Cheng-Hung Lin
Journal:  Int J Mol Sci       Date:  2022-01-29       Impact factor: 5.923

4.  Local release of tacrolimus from hydrogel-based drug delivery system is controlled by inflammatory enzymes in vivo and can be monitored non-invasively using in vivo imaging.

Authors:  Dzhuliya Dzhonova; Radu Olariu; Jonathan Leckenby; Ashish Dhayani; Praveen Kumar Vemula; Jean-Christophe Prost; Yara Banz; Adriano Taddeo; Robert Rieben
Journal:  PLoS One       Date:  2018-08-30       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.