Literature DB >> 12556396

Survival in high-risk eyes of epithelium-deprived orthotopic corneal allografts reconstituted in vitro with syngeneic epithelium.

Junko Hori1, J Wayne Streilein.   

Abstract

PURPOSE: In low-risk eyes of mice, most of the composite corneal grafts composed of syngeneic epithelium layered on allogeneic stroma and endothelium are accepted indefinitely. The study was undertaken to determine the fate of similar composite corneal grafts placed in high-risk mouse eyes.
METHODS: Epithelium-deprived allogeneic corneas (C57BL/6) were reconstituted in vitro with BALB/c epithelium, and then transplanted orthotopically into high-risk eyes of BALB/c mice. Graft survival was assessed clinically and evaluated histologically. Acquisition of donor-specific delayed hypersensitivity (DH) was also assessed in recipient mice. Recipients bearing healthy composite grafts were immunized subcutaneously with injected C57BL/6 spleen cells at 2 or 8 weeks after grafting, after which the fate of the grafts was evaluated.
RESULTS: Virtually all epithelium-deprived corneal allografts reconstituted in vitro with normal BALB/c corneal epithelium survived indefinitely when placed in high-risk eyes of BALB/c mice. Recipients of these composite grafts failed to acquire donor-specific DH when tested at both 2 and 8 weeks after grafting. Moreover, these recipients did not acquire the capacity to actively suppress donor-specific DH. Within 1 to 3 weeks of sensitization of recipient mice with spleen cells of donor origin, healthy composite grafts in residence for 2 or 8 weeks were rejected.
CONCLUSIONS: Replacement of donor epithelium with syngeneic epithelium protects orthotopic allogeneic corneal grafts (stroma plus endothelium) placed in high-risk eyes from sensitizing their recipients and from immune-mediated rejection. Recipients of composite corneal grafts containing syngeneic epithelial layers act as though they are immunologically ignorant of the graft's presence.

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Year:  2003        PMID: 12556396     DOI: 10.1167/iovs.02-0399

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  4 in total

1.  Corneal stromal cells selectively inhibit production of anti-inflammatory cytokines by activated T cells.

Authors:  V Holán; A Vítová; J Pindjáková; M Krulová; A Zajícová; M Filipec
Journal:  Clin Exp Immunol       Date:  2004-05       Impact factor: 4.330

2.  Gene Therapy for Modulation of T-Cell-Mediated Immune Response Provoked by Corneal Transplantation.

Authors:  Marko Pastak; Veronika Kleff; Daniel R Saban; Marta Czugala; Klaus-Peter Steuhl; Süleyman Ergün; Bernhard B Singer; Thomas A Fuchsluger
Journal:  Hum Gene Ther       Date:  2017-10-06       Impact factor: 5.695

3.  NK cell depletion delays corneal allograft rejection in baby rats.

Authors:  Johannes Schwartzkopff; Simona L Schlereth; Moritz Berger; Laura Bredow; Florian Birnbaum; Daniel Böhringer; Thomas Reinhard
Journal:  Mol Vis       Date:  2010-10-02       Impact factor: 2.367

4.  Mechanisms of immune privilege in the anterior segment of the eye: what we learn from corneal transplantation.

Authors:  Junko Hori
Journal:  J Ocul Biol Dis Infor       Date:  2008-08-08
  4 in total

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