| Literature DB >> 29654214 |
Andrew D Hughes1,2, Fadi G Lakkis1,3,4, Martin H Oberbarnscheidt5,3,6.
Abstract
Kidney transplantation is the treatment of choice for ESRD but is complicated by the response of the recipient's immune system to nonself histocompatibility antigens on the graft, resulting in rejection. Multiphoton intravital microscopy, referred to as four-dimensional imaging because it records dynamic events in three-dimensional tissue volumes, has emerged as a powerful tool to study immunologic processes in living animals. Here, we will review advances in understanding the complex mechanisms of T cell-mediated rejection made possible by four-dimensional imaging of mouse renal allografts. We will summarize recent data showing that activated (effector) T cell migration to the graft is driven by cognate antigen presented by dendritic cells that surround and penetrate peritubular capillaries, and that T cell-dendritic cell interactions persist in the graft over time, maintaining the immune response in the tissue.Entities:
Keywords: dendritic cells; effector CD8 T cells; intravital multiphoton microscopy; lymphocytes; rejection; transplantation
Mesh:
Year: 2018 PMID: 29654214 PMCID: PMC6054351 DOI: 10.1681/ASN.2017070800
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121