Effect of cyclosporine A treatment in vitro on pancreatic islet allograft rejection

1997 ◽  
Vol 29 (5) ◽  
pp. 2494-2497
Author(s):  
J. Mendola ◽  
H. Corominola ◽  
E. Esmatjes ◽  
A. Saenz ◽  
L. Fernandez-Cruz ◽  
...  
1997 ◽  
Vol 6 (1) ◽  
pp. 39-45 ◽  
Author(s):  
Josá F. Mendola ◽  
Helena Corominola ◽  
Enric Esmatjes ◽  
Alex Saenz ◽  
Laureano Fernandez-Cruz ◽  
...  

We examined in fully mismatched rats, the survival of pancreatic islet allografts in recipients treated with either fusidic acid (FA), an antistaphyllococcal antibiotic that has been shown to possess an immunosuppressive effect in vitro and in vivo, or cyclosporin-A (CsA). Islets were isolated by collagenase digestion, separated from acinar tissue by handpicking under a dissecting microscope and transplanted into the liver by portal vein injection of streptozotocin(STZ)-induced diabetic rats. The results indicated that while a temporary immunosuppression with CsA achieved an indefinite islet allograft survival, FA administered to recipients daily was not able to prevent islet allograft rejection across a major histocompatibility barrier. We conclude that despite the fact that fusidic acid has been claimed to act as an immunosuppressant drug in vitro with effects similar to those of CsA, unlike CsA, FA given either orally or by s.c. injection was not effective to prolong islet allograft survival in vivo. Copyright © 1997 Elsevier Science Inc.


2008 ◽  
Vol 86 (Supplement) ◽  
pp. 507
Author(s):  
M Hu ◽  
W J. Hawthorne ◽  
J M. OʼHara ◽  
K Hucker ◽  
J Wu ◽  
...  

2018 ◽  
Vol 102 (9) ◽  
pp. 1496-1504 ◽  
Author(s):  
Alix Besançon ◽  
Zeynep Demir ◽  
Tania Goncalves ◽  
Fabrice Valette ◽  
Emilie Panafieu ◽  
...  

Diabetes ◽  
1992 ◽  
Vol 41 (6) ◽  
pp. 771-775 ◽  
Author(s):  
A. M. Posselt ◽  
J. S. Odorico ◽  
C. F. Barker ◽  
A. Naji

2005 ◽  
Vol 114 (4) ◽  
pp. 279-288 ◽  
Author(s):  
Satish Govindaraj ◽  
Elena Fedorova ◽  
Eric M. Genden ◽  
Houtan Chaboki ◽  
Jonathan S. Bromberg ◽  
...  

Prior work has demonstrated that immunosuppressed orthotopic tracheal allografts undergo progressive reepithelialization over a 48-day period with recipient-derived tracheal epithelium. We hypothesized that reepithelialization of tracheal allografts would prevent rejection after withdrawal of immunosuppression. BALB/c murine tracheal grafts were transplanted orthotopically into either syngeneic or allogeneic C57/BL6 recipients. The recipients were either not immunosuppressed, immunosuppressed with cyclosporine A (10 mg/kg per day) continuously, or immunosuppressed for 48 days and then withdrawn from immunosuppression. The grafts were assessed for acute and chronic rejection 10 days and 50 days after immunosuppression withdrawal. The immunosuppressed allograft recipients maintained a ciliated epithelium acutely and chronically after immunosuppression withdrawal. Ten days after immunosuppression withdrawal, there was a mild cellular infiltrate, which resolved 50 days after withdrawal. Electron microscopy, lymphocyte subpopulation assays, and lamina propria analysis demonstrated that immunosuppression withdrawal did not result in tracheal allograft rejection. In vitro and in vivo assessments did not demonstrate evidence of systemic or local immune tolerance. We conclude that reepithelialization of orthotopic tracheal allografts with recipient-derived mucosa prevents rejection of allograft segments. Tracheal transplantation may require only transient immunosuppression, which can be withdrawn after tracheal reepithelialization.


1987 ◽  
Vol 6 (5) ◽  
pp. 649-658 ◽  
Author(s):  
Subrata Chakrabarti ◽  
Anders A.F. Sima ◽  
W. Jun Tze ◽  
Joseph Tai

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