| Literature DB >> 33717141 |
Jingming Zhuang1, Jiangang Hou1.
Abstract
Kidney transplantation is a primary therapy for end-stage renal disease (ESRD) all the time. But it does not mean that we have fully unraveling the mystery of kidney transplantation and confer every patient favorable prognosis. Immune rejection has always been a stumbling block when we try to increase the success rate of kidney transplantation and improve long-term outcomes. Even if the immune rejection is effectively controlled in acute phase, there is a high possibility that the immune response mediated by chronically activated antibodies will trigger chronic rejection and ultimately lead to graft failure. At present, immunosuppressive agent prepared chemically is mainly used to prevent acute or chronic rejection, but it failed to increase the long-term survival rate of allografts or reduce the incidence of chronic rejection after acute rejection, and is accompanied by many adverse reactions. Therefore, many studies have begun to use immune cells to regulate the immune response in order to control allograft rejection. This article will focus on the latest study and prospects of more popular regulatory myeloid cells in the direction of renal transplantation immunotherapy and introduce their respective progress from experimental research to clinical research.Entities:
Keywords: allograft rejection; end-stage renal disease; immunosuppression; kidney transplant; prevention; regulatory myeloid cell
Year: 2021 PMID: 33717141 PMCID: PMC7943475 DOI: 10.3389/fimmu.2021.625998
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561