| Literature DB >> 28092486 |
Melissa Y Yeung1, Steven Gabardi1, Mohamed H Sayegh1,2.
Abstract
INTRODUCTION: For over thirty years, antibody (mAb)-based therapies have been a standard component of transplant immunosuppression, and yet much remains to be learned in order for us to truly harness their therapeutic capabilities. Current mAbs used in transplant directly target and destroy graft-destructive immune cells, interrupt cytokine and costimulation-dependent T and B cell activation, and prevent down-stream complement activation. Areas covered: This review summarizes our current approaches to using antibody-based therapies to prevent and treat allograft rejection. It also provides examples of promising novel mAb therapies, and discusses the potential for future mAb development in transplantation. Expert opinion: The broad capability of antibodies, in parallel with our growing ability to synthetically modulate them, offers exciting opportunities to develop better biologic therapeutics. In order to do so, we must further our understanding about the basic biology underlying allograft rejection, and gain better appreciation of how characteristics of therapeutic antibodies affect their efficacy.Keywords: Acute cellular rejection; TOL101; Thymoglobulin; alemtuzumab; antibody mediated rejection; antithymocyte globulin; basiliximab; belimumab; eculizumab; induction therapy; monoclonal antibodies; rATG; rituximab; tocilizumab; transplant rejection; transplantation
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Year: 2017 PMID: 28092486 DOI: 10.1080/14712598.2017.1283400
Source DB: PubMed Journal: Expert Opin Biol Ther ISSN: 1471-2598 Impact factor: 4.388