Literature DB >> 17541621

Prolongation of corneal allograft survival by CTLA4-FasL in a murine model.

Weiyun Shi1, Min Chen, Lixin Xie.   

Abstract

BACKGROUND: To investigate the therapeutic effect of CTLA4-FasL-B7 costimulatory pathway blockage-on graft survival in a murine model of corneal transplantation.
METHODS: Orthotopic penetrating keratoplasty was performed on BALB/c mice. The mice were randomized into four groups: the isograft group, untreated allograft group, cyclosporine A drug delivery system (CsA DDS)-anterior chamber implanted group, and 10 microg/mL CTLA4-FasL-treated group. Allografts were from C57BL/6 mice. Survival time of corneal grafts was evaluated. Immunohistological method and TdT-mediated dUTP Nick End Labeling (TUNEL) were applied for the detection of CD4+ T cells and apoptotic cells in corneal transplants. To assess whether peripheral immune tolerance appeared after the treatment of CTLA4-FasL, CsA DDS-implanted- and CTLA4-FasL-treated BALB/c mice with clear grafts received skin allografts at 4 weeks after keratoplasty, and the status of corneal transplants were observed when skin grafts were rejected.
RESULTS: Allografts in the CTLA4-FasL group (median survival time [MST] = 106 days, p = 0.0042) and the CsA DDS group (MST = 60 days, p = 0.0037) revealed extending survival time, compared with that in the untreated allograft group (MST = 14 days). There were significantly fewer CD4-positive T cells in both the isograft group and the CsA DDS group. In the untreated allograft group, the number of CD4+ T cells gradually increased from day 1 until the final day of observation (day 21). By contrast, it reached a peak on day 7 and then absolutely reduced in the CTLA4-FasL group. Many apoptotic cells were detected on day 7 in the CTLA4-FasL group, but very few were seen in the other groups. Within 30 days of skin-graft rejection, previously healthy and long-standing corneal grafts became rejected in the CsA DDS group but remained clear in the CTLA4-FasL group.
CONCLUSIONS: CTLA4-FasL can prolong the survival time of corneal allografts in mice, exerting a negative regulation on T-cell activation simultaneously by blocking B7 costimulatory signals and inducing Fas-FasL apoptotic pathway. Due to the adjunctive role of FasL, it also appears to be a potential activity of tolerance induction through T-cell apoptotic pathways.

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Year:  2007        PMID: 17541621     DOI: 10.1007/s00417-007-0606-5

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  31 in total

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Journal:  Clin Exp Immunol       Date:  1997-02       Impact factor: 4.330

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Journal:  Transplantation       Date:  1997-10-27       Impact factor: 4.939

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Journal:  Invest Ophthalmol Vis Sci       Date:  1988-02       Impact factor: 4.799

9.  Simultaneous stimulation of Fas-mediated apoptosis and blockade of costimulation prevent autoimmune diabetes in mice induced by multiple low-dose streptozotocin.

Authors:  Y Jin; A Qu; G M Wang; J Hao; X Gao; S Xie
Journal:  Gene Ther       Date:  2004-06       Impact factor: 5.250

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Journal:  Nature       Date:  1995-09-28       Impact factor: 49.962

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  2 in total

1.  Alloreactive CD8 T cells rescued from apoptosis during co-stimulation blockade by Toll-like receptor stimulation remain susceptible to Fas-induced cell death.

Authors:  Bhavana Priyadharshini; Thomas B Thornley; Keith A Daniels; Amy Cuthbert; Raymond M Welsh; Dale L Greiner; Michael A Brehm
Journal:  Immunology       Date:  2013-04       Impact factor: 7.397

Review 2.  Immunomodulatory Strategies Targeting Dendritic Cells to Improve Corneal Graft Survival.

Authors:  Alfrun Schönberg; Matthias Hamdorf; Felix Bock
Journal:  J Clin Med       Date:  2020-04-28       Impact factor: 4.241

  2 in total

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