(Circulation. 1995;92:1919-1926.)
© 1995 American Heart Association, Inc.
Articles |
From the Division of Vascular Surgery of the General Surgical Services (G.M.L., F.A.), Department of Pathology (T.J.F.), Department of Dermatology (N.A.M., T.J.F.), and Wellman Laboratories of Photomedicine (G.M.L., F.A., N.A.M., T.J.F.), Massachusetts General Hospital and Harvard Medical School, Boston, and the Department of Surgery, University of Cologne (T.S.-R.), Germany.
Correspondence to Glenn M. LaMuraglia, MD, Division of Vascular Surgery, Massachusetts General Hospital, Boston, MA 02114.
Background Biological vascular allografts have proved unsatisfactory because of thrombosis, occlusion, and aneurysmal degeneration during chronic rejection. Photodynamic therapy (PDT), a technique that leads to the production of cytotoxic free radicals, was investigated as a novel method to prepare arterial allografts.
Methods and Results Shortly after impregnation with the photosensitizer drug chloroaluminum sulfonated phthalocyanine, infrarenal aortas of ACI rats were PDT-treated and orthotopically grafted in Lewis rats (PDT). The transplanted grafts were sequentially analyzed at 2, 4, and 8 weeks by morphometry, immunohistochemistry, and scanning electron microscopy. Of 25 untreated allografts, 4 (16%) developed aneurysms compared with 0 of 33 in PDT or untreated isografts (ISO, P<.001). PDT treatment of allografts significantly inhibited intimal hyperplasia (P<.001) and resulted in intimal areas comparable to those in ISO. However, medial thickness in both control allografts and PDT grafts was markedly decreased compared with ISO. External graft diameters of control allografts at 8 weeks were significantly enlarged (P<.02) compared with PDT or ISO. At all time points, T lymphocytes were found in a substantially larger number in untreated control grafts than in PDT or ISO. Scanning electron microscopy at 4 weeks confirmed complete repopulation with endothelial cells in PDT, which was not seen in the control allografts.
Conclusions Our findings suggest that local PDT treatment of arterial allografts inhibits inflammatory infiltration, aneurysmal dilatation, and development of intimal hyperplasia and may be used to develop vascular bioprostheses for use in humans.
Key Words: photodynamic therapy arteries free radicals allografts rejection
This article has been cited by other articles:
![]() |
D. J. Granville, B. A. Cassidy, D. O. Ruehlmann, J. C. Choy, C. Brenner, G. Kroemer, C. van Breemen, P. Margaron, D. W. Hunt, and B. M. McManus Mitochondrial Release of Apoptosis-Inducing Factor and Cytochrome c During Smooth Muscle Cell Apoptosis Am. J. Pathol., July 1, 2001; 159(1): 305 - 311. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Heckenkamp and G. M. Lamuraglia Intimal Hyperplasia, Arterial Remodeling, and Restenosis: An Overview Perspectives in Vascular Surgery and Endovascular Therapy, January 1, 1999; 11(2): 71 - 94. [Abstract] [PDF] |
||||
![]() |
T. Tojo, K. Niwaya, N. Sawabata, K. Kushibe, K. Nezu, S. Taniguchi, and S. Kitamura Tracheal replacement with cryopreserved tracheal allograft: experiment in dogs Ann. Thorac. Surg., July 1, 1998; 66(1): 209 - 213. [Abstract] [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |