NK cells, macrophages, and humoral immune responses are dominant in primary nonfunction of islet grafts in the dog-to-rat xenotransplant model
Author:
Publisher
Elsevier BV
Subject
Transplantation,Surgery
Reference5 articles.
1. Beyond Hyperacute Rejection
2. THE MAIN INFILTRATING CELL IN XENOGRAFT REJECTION IS A CD4+ MACROPHAGE AND NOT A T LYMPHOCYTE
3. MARKED PROLONGATION OF HUMAN ISLET XENOGRAFT SURVIVAL (HUMAN-TO-MOUSE) BY LOW-TEMPERATURE CULTURE AND TEMPORARY IMMUNOSUPPRESSION WITH HUMAN AND MOUSE ANTI-LYMPHOCYTE SERA
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1. G-CSF and Exenatide Might Be Associated with Increased Long-Term Survival of Allogeneic Pancreatic Islet Grafts;PLOS ONE;2016-06-10
2. Cellular Immune Responses to Xenografts;Xenotransplantation;2014-04-08
3. Pancreatic Islet Xenograft Survival in Mice Is Extended by a Combination of Alpha-1-Antitrypsin and Single-Dose Anti-CD4/CD8 Therapy;PLoS ONE;2013-05-22
4. Oleanolic Acid, a Plant Triterpenoid, Significantly Improves Survival and Function of Islet Allograft;Transplantation;2009-10-27
5. Attenuation of Primary Nonfunction for Syngeneic Islet Graft Using Sodium 4-Phenylbutyrate;Transplantation Proceedings;2005-05
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