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MHC expression in fragment and full-thickness allogeneic embryonic retinal transplants
Authors:F. Ghosh  Jörgen Larsson  Kennerth Wilke
Affiliation:(1) Department of Ophthalmology, Lund University Hospital, S-22185 Lund, Sweden e-mail: Fredrik.Ghosh@oft.lu.se Tel.: +46–46–172484 Fax: +46–46–172721, SE
Abstract:Background: The study was carried out to evaluate the expression of major histocompatibility complex (MHC) molecules in retinal transplants with different tissue integrity. Methods: Twelve adult rabbits received an allogeneic subretinal neuroretinal transplant, in the form of either fragmented embryonic cells or a complete full-thickness embryonic retina. A controlled transvitreal approach was used for both transplantation types. The grafts were examined histologically after 31 or 49 days with hematoxylin and eosin staining and immunohistochemical analysis of MHC class I and class II expression. Results: All five fragment transplants developed into rosettes. Two of them displayed MHC class I-labeled cells, and four MHC class II-labeled cells. The cells were concentrated on the scleral side of the graft, and there was also a marked increase of labeled cells in the choroid. MHC labeling was often associated with defects in the retinal pigment epithelium. Six of the seven full-thickness grafts displayed a laminated morphology with well-developed retinal layers. The seventh consisted of rosettes. None of these grafts displayed MHC class I- or class II-labeled cells. Conclusions: The findings suggest that host immune response against fragmented and intact neuroretinal grafts is different, indicating tissue integrity as one factor affecting graft-host immune interactions. The absence of immune response in full-thickness grafts is encouraging and important in the struggle to find therapies for retinal degenerative disease. Received: 17 November 1999 Revised: 6 January 2000 Accepted: 18 January 2000
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