No evidence of infection with porcine endogenous retrovirus in recipients of porcine islet-cell xenografts

被引:294
作者
Heneine, W
Tibell, A
Switzer, WM
Sandstrom, P
Rosales, GV
Mathews, A
Korsgren, O
Chapman, LE
Folks, TM
Groth, CG
机构
[1] Ctr Dis Control & Prevent, HIV & Retrovirol Branch, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
[2] Karolinska Inst, Huddinge Hosp, Dept Transplantat Surg, S-10401 Stockholm, Sweden
[3] Univ Uppsala, Acad Hosp, Dept Clin Immunol, S-75105 Uppsala, Sweden
关键词
D O I
10.1016/S0140-6736(98)07145-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The study of whether porcine xenografts can lead to porcine endogenous retrovirus (PERV) infection of recipients is critical for evaluating the safety of pig-to-man xenotransplantation. PERV is carried in the pig germline, and all recipients of porcine tissues or organs will be exposed to the virus. Methods We studied 10 diabetic patients who had received porcine fetal islets between 1990 and 1993, looking for evidence of PERV infection by using PCR serology, PCR, and reverse transcriptase assays. Prolonged xenograft survival (up to a year) was confirmed in five patients by porcine C-peptide excretion and detection of pig mitochondrial DNA (mtDNA) in serum. Findings Despite the evidence for extended exposure to pig cells and despite concomitant immunosuppressive therapy, we were unable to detect markers of PERV infection in any patient, Screening for two PERV sequences in peripheral blood lymphocytes collected 4-7 years after the xenotransplantation was negative. Markers of PERV expression, including viral RNA and reverse transcriptase, were undetectable in sera from both early (day 3 to day 180) and late (4-7 years) time points. Western blot analysis for antibodies was consistently negative, Interpretation These results suggested the absence of PERV infection in these patients. Also this study establishes a minimum standard for post-transplant surveillance of patients given porcine xenografts.
引用
收藏
页码:695 / 699
页数:5
相关论文
共 26 条
[1]   Identification of a full-length cDNA for an endogenous retrovirus of miniature swine [J].
Akiyoshi, DE ;
Denaro, M ;
Zhu, HH ;
Greenstein, JL ;
Banerjee, P ;
Fishman, JA .
JOURNAL OF VIROLOGY, 1998, 72 (05) :4503-4507
[2]  
Bjoersdorff A., 1995, Xenotransplantation, V2, P26, DOI 10.1111/j.1399-3089.1995.tb00062.x
[3]  
Busch Michael P., 1997, American Journal of Medicine, V102, P117, DOI 10.1016/S0002-9343(97)00077-6
[4]   XENOTRANSPLANTATION AND XENOGENEIC INFECTIONS [J].
CHAPMAN, LE ;
FOLKS, TM ;
SALOMON, DR ;
PATTERSON, AP ;
EGGERMAN, TE ;
NOGUCHI, PD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (22) :1498-1501
[5]   BRIEF REPORT - TREATMENT OF HEPATIC-FAILURE WITH EX-VIVO PIG-LIVER PERFUSION FOLLOWED BY LIVER-TRANSPLANTATION [J].
CHARI, RS ;
COLLINS, BH ;
MAGEE, JC ;
DIMAIO, JM ;
KIRK, AD ;
HARLAND, RC ;
MCCANN, RL ;
PLATT, JL ;
MEYERS, WC .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (04) :234-237
[6]  
COFFIN J M, 1990, P1437
[7]   Histological evidence of fetal pig neural cell survival after transplantation into a patient with Parkinson's disease [J].
Deacon, T ;
Schumacher, J ;
Dinsmore, J ;
Thomas, C ;
Palmer, P ;
Kott, S ;
Edge, A ;
Penney, D ;
Kassissieh, S ;
Dempsey, P ;
Isacson, O .
NATURE MEDICINE, 1997, 3 (03) :350-353
[8]  
DUNNING JJ, 1994, PATHOL BIOL, V42, P231
[9]   INCREASED ANTI-GAL ACTIVITY IN DIABETIC-PATIENTS TRANSPLANTED WITH FETAL PORCINE ISLET-CELL CLUSTERS [J].
GALILI, U ;
TIBELL, A ;
SAMUELSSON, B ;
RYDBERG, L ;
GROTH, CG .
TRANSPLANTATION, 1995, 59 (11) :1549-1556
[10]   TRANSPLANTATION OF PORCINE FETAL PANCREAS TO DIABETIC-PATIENTS [J].
GROTH, CG ;
KORSGREN, O ;
TIBELL, A ;
TOLLEMAR, J ;
MOLLER, E ;
BOLINDER, J ;
OSTMAN, J ;
REINHOLT, FP ;
HELLERSTROM, C ;
ANDERSSON, A .
LANCET, 1994, 344 (8934) :1402-1404