Journal Article

Immune response after pig-to-human kidney xenotransplantation: a multimodal phenotyping study

Giraud, Sébastien, Tissier, Renaud, Mehta, Sapna, Morgand, Erwan, Tatapudi, Vasishta, Narula, Navneet, Sannier, Aurélie, Giarraputo, Alessia, Hauet, Thierry, Ayares, David, Mangiola, Massimo, Stern, Jeffrey, Wu, Ming, Keating, Brendan, Loupy, Alexandre, Pass, Harvey I, Mezine, Fariza, Bruneval, Patrick, Robin, Blaise, Goutaudier, Valentin, Dandro, Amy, Certain, Anaïs, Lefaucheur, Carmen, Montgomery, Robert A, Tharaux, Pierre-Louis, Khalil, Karen, Griesemer, Adam

2023

Overview

Cross-species immunological incompatibilities have hampered pig-to-human xenotransplantation, but porcine genome engineering recently enabled the first successful experiments. However, little is known about the immune response after the transplantation of pig kidneys to human recipients. We aimed to precisely characterise the early immune responses to the xenotransplantation using a multimodal deep phenotyping approach. We did a complete phenotyping of two pig kidney xenografts transplanted to decedent humans. We used a multimodal strategy combining morphological evaluation, immunophenotyping (IgM, IgG, C4d, CD68, CD15, NKp46, CD3, CD20, and von Willebrand factor), gene expression profiling, and whole-transcriptome digital spatial profiling and cell deconvolution. Xenografts before implantation, wild-type pig kidney autografts, as well as wild-type, non-transplanted pig kidneys with and without ischaemia-reperfusion were used as controls. The data collected from xenografts suggested early signs of antibody-mediated rejection, characterised by microvascular inflammation with immune deposits, endothelial cell activation, and positive xenoreactive crossmatches. Capillary inflammation was mainly composed of intravascular CD68+ and CD15+ innate immune cells, as well as NKp46+ cells. Both xenografts showed increased expression of genes biologically related to a humoral response, including monocyte and macrophage activation, natural killer cell burden, endothelial activation, complement activation, and T-cell development. Whole-transcriptome digital spatial profiling showed that antibody-mediated injury was mainly located in the glomeruli of the xenografts, with significant enrichment of transcripts associated with monocytes, macrophages, neutrophils, and natural killer cells. This phenotype was not observed in control pig kidney autografts or in ischaemia-reperfusion models. Despite favourable short-term outcomes and absence of hyperacute injuries, our findings suggest that antibody-mediated rejection in pig-to-human kidney xenografts might be occurring. Our results suggest specific therapeutic targets towards the humoral arm of rejection to improve xenotransplantation results. OrganX and MSD Avenir.

• Publisher: Elsevier Ltd,Elsevier Limited,Elsevier
• Subject: Animals / Antibodies / Autografts / Biopsy / Brain death / Brain research / CD20 antigen / CD3 antigen / Cell activation / Complement activation / Cytotoxicity / Endothelial cells / Gene expression / Genes / Genome editing / Genomes / Graft Rejection / Human health and pathology / Humans / Immune response / Immune response (humoral) / Immune system / Immunity / Immunoglobulin G / Immunoglobulin M / Immunology / Inflammation / Injuries / Ischemia / Kidney / Kidney transplantation / Kidneys / Leukocytes (neutrophilic) / Life Sciences / Lymphocytes T / Macrophages / Monocytes / Natural killer cells / Neutrophils / Pathogenesis / Phenotypes / Phenotyping / Rejection / Reperfusion / Software / Swine / Transplantation, Heterologous / Transplants & implants / Urine / Xenografts / Xenotransplantation