Literature DB >> 22790071

Modulating T-cell costimulation as new immunosuppressive concept in organ transplantation.

Nina Pilat1, Christoph Schwarz, Thomas Wekerle.   

Abstract

PURPOSE OF REVIEW: Blockade of costimulatory signalling is a promising approach to inhibit T-cell responses and consequently allograft rejection. The last decade was marked by progress in understanding the details of various costimulatory pathways and by the development of biologicals targeting these pathways with the aim of selectively and efficiently modulating T-cell responses. RECENT
FINDINGS: Here we focus on the clinically relevant costimulatory pathways CD28:CD80/86, CD40:CD154 (CD40L), CD2:LFA-3 and ICAM:LFA-1. We will give a short overview of the physiologic function of these pathways and discuss results from preclinical and clinical studies of costimulation blockers targeting these pathways.
SUMMARY: The development of costimulation blockers for clinical application in the field of organ transplantation was delayed by several setbacks. However, belatacept has recently been approved as first in class for renal transplantation. Several additional costimulation blockers are under development with some having already entered into clinical trials. Costimulation blockers are a new class of rationally designed immunosuppressive drugs with considerable potential for improving outcome of organ transplantation.

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Year:  2012        PMID: 22790071     DOI: 10.1097/MOT.0b013e328355fc94

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


  3 in total

Review 1.  Regulatory myeloid cells in transplantation.

Authors:  Brian R Rosborough; Dàlia Raïch-Regué; Heth R Turnquist; Angus W Thomson
Journal:  Transplantation       Date:  2014-02-27       Impact factor: 4.939

2.  Effect of abatacept on immunogenicity of vaccines in individuals with type 1 diabetes.

Authors:  Adriana Weinberg; David Boulware; Bonnie Dighero; Tihamer Orban
Journal:  Vaccine       Date:  2013-08-17       Impact factor: 3.641

3.  Induction of macrophage-like immunosuppressive cells from mouse ES cells that contribute to prolong allogeneic graft survival.

Authors:  Hiroya Kudo; Haruka Wada; Hajime Sasaki; Hyuma Tsuji; Ryo Otsuka; Muhammad Baghdadi; Satoshi Kojo; Tatsuya Chikaraishi; Ken-ichiro Seino
Journal:  PLoS One       Date:  2014-10-30       Impact factor: 3.240

  3 in total

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