Literature DB >> 33523454

Regulatory T Cells for the Induction of Transplantation Tolerance.

Weitao Que1, Xiao-Kang Li2.   

Abstract

Organ transplantation is the optimal treatment for terminal and irreversible organ failure. Achieving transplantation tolerance has long been the ultimate goal in the field of transplantation. Regulatory T cell (Treg)-based therapy is a promising novel approach for inducing donor organ-specific tolerance. Tregs play critical roles in the maintenance of immune homeostasis and self-tolerance, by promoting transplantation tolerance through a variety of mechanisms on different target cells, including anti-inflammatory cytokine production, induction of apoptosis, disruption of metabolic pathways, and mutual interaction with dendritic cells. The continued success of Treg-based therapy in the clinical setting is critically dependent on preclinical studies that support its translational potential. However, although some initial clinical trials of adoptive Treg therapy have successively demonstrated safety and efficacy for immunosuppressant minimization and transplantation tolerance induction, most Treg-based hematopoietic stem cell and solid organ clinical trials are still in their infancy. These clinical trials have not only focused on safety and efficacy but also included optimization and standardization protocols of good manufacturing practice regarding cell isolation, expansion, dosing, timing, specificity, quality control, concomitant immunosuppressants, and post-administration monitoring. We herein report a brief introduction of Tregs, including their phenotypic and functional characterization, and focus on the clinical translation of Treg-based therapeutic applications in the setting of transplantation.

Entities:  

Keywords:  Allograft; Tolerance; Transplantation; Tregs

Mesh:

Year:  2021        PMID: 33523454     DOI: 10.1007/978-981-15-6407-9_15

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  117 in total

1.  Transforming growth factor-beta and interleukin-10 subvert alloreactive delayed type hypersensitivity in cardiac allograft acceptor mice.

Authors:  A A Bickerstaff; A M VanBuskirk; E Wakely; C G Orosz
Journal:  Transplantation       Date:  2000-04-15       Impact factor: 4.939

2.  Achieving donor-specific hyporesponsiveness is associated with FOXP3+ regulatory T cell recruitment in human renal allograft infiltrates.

Authors:  Oriol Bestard; Josep M Cruzado; Mariona Mestre; Anna Caldés; Jordi Bas; Marta Carrera; Joan Torras; Inés Rama; Francesc Moreso; Daniel Serón; Josep M Grinyó
Journal:  J Immunol       Date:  2007-10-01       Impact factor: 5.422

3.  The effect of costimulatory and interleukin 2 receptor blockade on regulatory T cells in renal transplantation.

Authors:  J A Bluestone; W Liu; J M Yabu; Z G Laszik; A Putnam; M Belingheri; D M Gross; R M Townsend; F Vincenti
Journal:  Am J Transplant       Date:  2008-10       Impact factor: 8.086

4.  Standardization and cross validation of alloreactive IFNγ ELISPOT assays within the clinical trials in organ transplantation consortium.

Authors:  I Ashoor; N Najafian; Y Korin; E F Reed; T Mohanakumar; D Ikle; P S Heeger; M Lin
Journal:  Am J Transplant       Date:  2013-05-24       Impact factor: 8.086

Review 5.  CD39 and CD73 in immunity and inflammation.

Authors:  Luca Antonioli; Pál Pacher; E Sylvester Vizi; György Haskó
Journal:  Trends Mol Med       Date:  2013-04-17       Impact factor: 11.951

6.  Cross-validation of IFN-γ Elispot assay for measuring alloreactive memory/effector T cell responses in renal transplant recipients.

Authors:  O Bestard; E Crespo; M Stein; M Lúcia; D L Roelen; Y J de Vaal; M P Hernandez-Fuentes; L Chatenoud; K J Wood; F H Claas; J M Cruzado; J M Grinyó; H D Volk; P Reinke
Journal:  Am J Transplant       Date:  2013-06-13       Impact factor: 8.086

7.  CD4+ CD25+ FOXP3+ regulatory T cells increase de novo in kidney transplant patients after immunodepletion with Campath-1H.

Authors:  D D Bloom; Z Chang; J H Fechner; W Dar; S P Polster; J Pascual; L A Turka; S J Knechtle
Journal:  Am J Transplant       Date:  2008-02-05       Impact factor: 8.086

8.  Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells.

Authors:  Manuela Battaglia; Angela Stabilini; Maria-Grazia Roncarolo
Journal:  Blood       Date:  2005-03-03       Impact factor: 22.113

9.  Rapamycin promotes expansion of functional CD4+CD25+FOXP3+ regulatory T cells of both healthy subjects and type 1 diabetic patients.

Authors:  Manuela Battaglia; Angela Stabilini; Barbara Migliavacca; Jutta Horejs-Hoeck; Thomas Kaupper; Maria-Grazia Roncarolo
Journal:  J Immunol       Date:  2006-12-15       Impact factor: 5.422

10.  CD4+ FoxP3+ regulatory T cells confer infectious tolerance in a TGF-beta-dependent manner.

Authors:  John Andersson; Dat Q Tran; Marko Pesu; Todd S Davidson; Heather Ramsey; John J O'Shea; Ethan M Shevach
Journal:  J Exp Med       Date:  2008-08-18       Impact factor: 14.307

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  1 in total

1.  Process development and validation of expanded regulatory T cells for prospective applications: an example of manufacturing a personalized advanced therapy medicinal product.

Authors:  Rosaria Giordano; Tiziana Montemurro; Cristiana Lavazza; Silvia Budelli; Elisa Montelatici; Mariele Viganò; Francesca Ulbar; Lucia Catani; Marta Giulia Cannone; Sara Savelli; Elisa Groppelli; Lorenza Lazzari; Roberto M Lemoli; Matteo Cescon; Gaetano La Manna
Journal:  J Transl Med       Date:  2022-01-05       Impact factor: 5.531

  1 in total

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