TY - JOUR
T1 - Factors affecting transplant outcomes in diabetic nude mice receiving human, porcine, and nonhuman primate islets
T2 - Analysis of 335 transplantations
AU - Loganathan, Gopalakrishnan
AU - Graham, Melanie L.
AU - Radosevich, David M.
AU - Soltani, Sajjad M.
AU - Tiwari, Mukesh
AU - Anazawa, Takayuki
AU - Papas, Klearchos K.
AU - Sutherland, David E R
AU - Hering, Bernhard J.
AU - Balamurugan, A. N.
PY - 2013/6/27
Y1 - 2013/6/27
N2 - Background. In the absence of a reliable islet potency assay, nude mice (NM) transplantation is the criterion standard to assess islet quality for clinical transplantation. There are factors other than islet quality that affect the transplant outcome. Methods. Here, we analyzed the transplant outcomes in 335 NM receiving islets from human (n=103), porcine (n=205), and nonhuman primate (NHP; n=27) donors. The islets (750, 1000, and 2000 islet equivalents [IEQ]) were transplanted under the kidney capsule of streptozotocin-induced diabetic NM. Results. The proportion of mice that achieved normoglycemia was significantly higher in the group implanted with 2000 IEQ of human, porcine, or NHP islets (75% normoglycemic) versus groups that were implanted with 750 IEQ (7% normoglycemic) and 1000 IEQ (30% normoglycemic). In this study, we observed that the purity of porcine islet preparations (Pe0.001), islet pellet size in porcine preparations (Pe 0.01), and mice recipient body weight for human islet preparations (P=0.013) were independently associated with successful transplant outcome. NHP islets of 1000 IEQ were sufficient to achieve normoglycemic condition (83%). An islet mass of 2000 IEQ, high islet purity, increased recipient body weight, and high islet pellet volume increased the likelihood of successful reversal of diabetes in transplanted mice. Also, higher insulin secretory status of islets at basal stimulus was associated with a reduced mouse cure rate. The cumulative incidence of graft failure was significantly greater in human islets (56.12%) compared with porcine islets (35.57%; Pe0.001). Conclusion. Factors affecting NM bioassay were identified (islet mass, islet purity, pellet size, in vitro insulin secretory capability, and mouse recipient body weight) and should be considered when evaluating islet function.
AB - Background. In the absence of a reliable islet potency assay, nude mice (NM) transplantation is the criterion standard to assess islet quality for clinical transplantation. There are factors other than islet quality that affect the transplant outcome. Methods. Here, we analyzed the transplant outcomes in 335 NM receiving islets from human (n=103), porcine (n=205), and nonhuman primate (NHP; n=27) donors. The islets (750, 1000, and 2000 islet equivalents [IEQ]) were transplanted under the kidney capsule of streptozotocin-induced diabetic NM. Results. The proportion of mice that achieved normoglycemia was significantly higher in the group implanted with 2000 IEQ of human, porcine, or NHP islets (75% normoglycemic) versus groups that were implanted with 750 IEQ (7% normoglycemic) and 1000 IEQ (30% normoglycemic). In this study, we observed that the purity of porcine islet preparations (Pe0.001), islet pellet size in porcine preparations (Pe 0.01), and mice recipient body weight for human islet preparations (P=0.013) were independently associated with successful transplant outcome. NHP islets of 1000 IEQ were sufficient to achieve normoglycemic condition (83%). An islet mass of 2000 IEQ, high islet purity, increased recipient body weight, and high islet pellet volume increased the likelihood of successful reversal of diabetes in transplanted mice. Also, higher insulin secretory status of islets at basal stimulus was associated with a reduced mouse cure rate. The cumulative incidence of graft failure was significantly greater in human islets (56.12%) compared with porcine islets (35.57%; Pe0.001). Conclusion. Factors affecting NM bioassay were identified (islet mass, islet purity, pellet size, in vitro insulin secretory capability, and mouse recipient body weight) and should be considered when evaluating islet function.
KW - Human islets
KW - Islet cell transplantation
KW - Nude mice bioassay
KW - Nude mice transplant
KW - Porcine islets and nonhuman primate islets
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U2 - 10.1097/TP.0b013e318293b7b8
DO - 10.1097/TP.0b013e318293b7b8
M3 - Article
C2 - 23677052
AN - SCOPUS:84880136008
SN - 0041-1337
VL - 95
SP - 1439
EP - 1447
JO - Transplantation
JF - Transplantation
IS - 12
ER -