Improved human islet isolation outcome from marginal donors following addition of oxygenated perfluorocarbon to the cold-storage solution

被引:115
作者
Ricordi, C [1 ]
Fraker, C [1 ]
Szust, J [1 ]
Al-Abdullah, I [1 ]
Poggioli, R [1 ]
Kirlew, T [1 ]
Khan, A [1 ]
Alejandro, R [1 ]
机构
[1] Univ Miami, Sch Med, Diabet Res Inst, Div Cellular Transplantat, Miami, FL 33136 USA
关键词
D O I
10.1097/01.TP.0000058813.95063.7A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Last year, from the approximately 6,000 organ donors, only approximately 1,500 pancreata were used for clinical transplantation. Factors that contribute to this poor pancreas use include strict donor selection criteria and the requirement for short cold-ischemia time (CIT). Numerous pancreata have not been used because of long ischemia times postprocurement. Given the oxygen-rich environment of the islets in the native pancreas, it is conceivable that islets are highly susceptible to irreversible damage following prolonged ischemia. The use of continuously oxygenated perfluorohydrocarbons (PFCs), known for their high oxygen-solubility coefficients, in a two-layer culture with standard University of Wisconsin preservation media, has extended the acceptable range CIT, and, furthermore, there has been no evidence of adverse effects from PFCs on the outcome of transplanted cells, whereas they often enhance islet cell function. The purpose of this study was to use the two-layer culture method to improve donor-organ use from marginal donors. Fifteen organs were procured using the two-layer method, and 18 without using it, from donors greater than 50 years of age. Despite nonsignificant differences in age, weight of the donors, weight of the organ and CIT, the PFC group yielded an average of twofold more islet equivalents than those harvested from the control group. As a result, from the control group, only 2 of 18 organs were used for clinical islet transplantation, whereas 8 of 15 were used from the PFC group. To this end, the two-layer method may help clinicians overcome the problem of organ underuse.
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收藏
页码:1524 / 1527
页数:4
相关论文
共 25 条
[1]   Increased antioxidant capacity, suppression of free radical damage and erythrocyte aggrerability after combined application of alpha-tocopherol and FC-43 perfluorocarbon emulsion in early postburn period in rats [J].
Bekyarova, G ;
Yankova, T ;
Galunska, B .
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND IMMOBILIZATION BIOTECHNOLOGY, 1996, 24 (06) :629-641
[2]   EFFECT OF EXCHANGE-TRANSFUSION WITH A RED-BLOOD-CELL SUBSTITUTE ON NEONATAL HEMODYNAMICS AND ORGAN BLOOD FLOWS [J].
BREUNINGER, HG ;
RUBENSTEIN, SD ;
WOLFSON, MR ;
SHAFFER, TH .
JOURNAL OF PEDIATRIC SURGERY, 1993, 28 (02) :144-150
[3]   Transabdominal oxygenation using perfluorocarbons [J].
Chiba, T ;
Harrison, MR ;
Ohkubo, T ;
Rollins, MD ;
Talbanese, CT ;
Jennings, RW .
JOURNAL OF PEDIATRIC SURGERY, 1999, 34 (05) :895-900
[4]   Perfluorocarbons: Future clinical possibilities [J].
Clark, MC ;
Weiman, DS ;
Pate, JW ;
Gir, S .
JOURNAL OF INVESTIGATIVE SURGERY, 1997, 10 (06) :357-365
[5]   ROLE OF PERFLUOROCHEMICAL EMULSIONS IN THE TREATMENT OF MYOCARDIAL REPERFUSION INJURY [J].
FORMAN, MB ;
INGRAM, DA ;
MURRAY, JJ .
AMERICAN HEART JOURNAL, 1992, 124 (05) :1347-1357
[6]   Possible role of heat shock protein 60 in reducing ischemic-reperfusion injury in canine pancreas grafts after preservation by the two-layer method [J].
Fujino, Y ;
Suzuki, Y ;
Tsujimura, T ;
Takahashi, T ;
Tanioka, Y ;
Tominaga, M ;
Ku, Y ;
Kuroda, Y .
PANCREAS, 2001, 23 (04) :393-398
[7]   The anti-inflammatory effects of perfluorocarbons: Let's get physical [J].
Heard, SO ;
Puyana, JC .
CRITICAL CARE MEDICINE, 2000, 28 (04) :1241-1242
[8]  
HIRAOKA K, 1994, TRANSPLANT P, V26, P953
[9]   USE OF CURRENT GENERATION PERFLUOROCARBON EMULSIONS IN CARDIAC-SURGERY [J].
HOLMAN, WL ;
MCGIFFIN, DC ;
VICENTE, WVA ;
SPRUELL, RD ;
PACIFICO, AD .
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND BIOTECHNOLOGY, 1994, 22 (04) :979-990
[10]   Hemodynamic effects of partial liquid ventilation with perfluorocarbon in acute lung injury [J].
Houmes, RJM ;
Verbrugge, SJC ;
Hendrik, ER ;
Lachmann, B .
INTENSIVE CARE MEDICINE, 1995, 21 (12) :966-972