scholarly journals Tracheal Transplantation

2019 ◽  
Author(s):  
Pierre Delaere
Author(s):  
Eric M. Genden ◽  
Brett A. Miles ◽  
Timothy Harkin ◽  
Samuel DeMaria ◽  
Andrew J. Kaufman ◽  
...  

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immunosuppressed with cyclosporine A (10 mg/kg per day) continuously, or immunosuppressed for 48 days and then withdrawn from immunosuppression.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 Tracheal transplantation may require only transient immunosuppression, which can be withdrawn after tracheal reepithelialization.


2001 ◽  
Vol 111 (4) ◽  
pp. 657-662 ◽  
Author(s):  
Carlos Zagalo ◽  
Nuno R. Grande ◽  
Jos?? Martins dos Santos ◽  
Emanuel Monteiro ◽  
Jos?? Brito ◽  
...  

1996 ◽  
Vol 3 (2) ◽  
pp. 154-158
Author(s):  
Robert Hermans ◽  
Pierre R. Delaere ◽  
Ziying Liu ◽  
Yicheng Ni ◽  
Hilde Bosmans ◽  
...  

1996 ◽  
Vol 37 (2) ◽  
pp. 118 ◽  
Author(s):  
Young Sik Park ◽  
Doo Yun Lee ◽  
Hyo Chae Paik ◽  
Ki Man Bae ◽  
Sang Ho Cho

2004 ◽  
Vol 165 (4) ◽  
pp. 1223-1232 ◽  
Author(s):  
Allan M. Ramirez ◽  
Shinsuke Takagawa ◽  
Marin Sekosan ◽  
H. Ari Jaffe ◽  
John Varga ◽  
...  

2016 ◽  
Vol 4 (4) ◽  
pp. e12690
Author(s):  
Simona Nemska ◽  
François Daubeuf ◽  
Nelly Frossard

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Laura Pandolfi ◽  
Roberta Fusco ◽  
Vanessa Frangipane ◽  
Ramona D’Amico ◽  
Marco Giustra ◽  
...  

AbstractBronchiolitis Obliterans Syndrome seriously reduces long-term survival of lung transplanted patients. Up to now there is no effective therapy once BOS is established. Nanomedicine introduces the possibility to administer drugs locally into lungs increasing drug accumulation in alveola reducing side effects. Imatinib was loaded in gold nanoparticles (GNP) functionalized with antibody against CD44 (GNP-HCIm). Lung fibroblasts (LFs) were derived from bronchoalveolar lavage of BOS patients. GNP-HCIm cytotoxicity was evaluated by MTT assay, apoptosis/necrosis and phosphorylated-cAbl (cAbl-p). Heterotopic tracheal transplantation (HTT) mouse model was used to evaluate the effect of local GNP-HCIm administration by Alzet pump. GNP-HCIm decreased LFs viability compared to Imatinib (44.4 ± 1.8% vs. 91.8 ± 3.2%, p < 0.001), inducing higher apoptosis (22.68 ± 4.3% vs. 6.43 ± 0.29; p < 0.001) and necrosis (18.65 ± 5.19%; p < 0.01). GNP-HCIm reduced cAbl-p (0.41 GNP-HCIm, 0.24 Imatinib vs. to control; p < 0.001). GNP-HCIm in HTT mouse model by Alzet pump significantly reduced tracheal lumen obliteration (p < 0.05), decreasing apoptosis (p < 0.05) and TGF-β-positive signal (p < 0.05) in surrounding tissue. GNP-HCIm treatment significantly reduced lymphocytic and neutrophil infiltration and mast cells degranulation (p < 0.05). Encapsulation of Imatinib into targeted nanoparticles could be considered a new option to inhibit the onset of allograft rejection acting on BOS specific features.


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