Abstract

Triple-knockout (TKO) pigs (with added protective human transgenes) are likely to be optimal sources of organs for clinical organ xenotransplantation because many humans have minimal or no natural antibody to TKO pig cells. However, Old World monkeys (OWMs) have naturally-existing antibodies directed to TKO cells. We measured anti-pig IgM/IgG binding, and complement-dependent cytotoxicity to wild-type (WT), α1,3-galactosyltransferase gene-knockout (GTKO), and TKO pig peripheral blood mononuclear cells (PBMCs) using sera from humans, several OWMs, and two New World monkeys (NWMs). Furthermore, we compared survival of GTKO (n = 5) and TKO (n = 3) pig kidneys in baboons. OWMs had significantly greater IgM binding and cytotoxicity to TKO PBMCs than humans or NWMs. Mean anti-TKO IgM was significantly higher in OWMs and significantly lower in NWMs than in humans. Cytotoxicity of OWM sera to TKO PBMCs was significantly greater than of human serum, but there was no significant difference between human and NWM sera. The median survival of TKO pig kidneys (4 days) in baboons was significantly shorter than that of GTKO kidneys (136 days) (p < 0.05). Even though considered ideal for clinical xenotransplantation, the presence of naturally-existing antibodies to TKO pig cells in OWMs complicates the transplantation of TKO pig kidneys in OWMs.

Highlights

  • Choosing the best nonhuman primate (NHP) model to perform pig-to-NHP xenotransplantation is crucial to determine the feasibility of pig organ transplantation in humans

  • peripheral blood mononuclear cells (PBMCs) of WT pigs expressed Gal, Neu5Gc, and Sda antigens, while PBMCs of GTKO pigs did not express the Gal antigen, and those of TKO pigs did not express any of the 3 carbohydrate xenoantigens, as previously described[10]

  • Serum cytotoxicity in Old World monkeys (OWMs) (74%) to TKO PBMCs was significantly higher than in humans (2.7%) (p < 0.01), but there was no significant difference between humans and New World monkeys (NWMs) (19%)

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Summary

Introduction

Choosing the best nonhuman primate (NHP) model to perform pig-to-NHP xenotransplantation is crucial to determine the feasibility of pig organ transplantation in humans. Old World monkeys (OWMs), such as baboons[1,2,3] or rhesus monkeys[4,5], have been used as the preferred species for preclinical studies of pig kidney xenotransplantation. The serum complement-dependent cytotoxicity (CDC) of rhesus monkeys (an OWM) is known to be higher against triple-knockout (TKO) pig cells than against double-knockout (GTKO/β4GalNT2KO) pig cells[4]. The aim of the present study was to investigate (i) anti-pig IgM/IgG binding, and (ii) serum CDC to wild-type (WT), GTKO, and TKO pig peripheral blood mononuclear cells (PBMCs) using sera from humans, four OWM species, and two NWM species, and (iii) to compare the survival of GTKO (with added human transgenes) pig kidneys with that of TKO (with added transgenes) pig kidneys in baboons using an anti-CD40mAb-based immunosuppressive regimen

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