Skip to main content
Top
Published in: BMC Ophthalmology 1/2014

Open Access 01-12-2014 | Study protocol

Functional antigen matching in corneal transplantation: matching for the HLA-A, -B and -DRB1 antigens (FANCY) – study protocol

Authors: Daniel Böhringer, Gabriele Ihorst, Birgit Grotejohann, Julia Maurer, Eric Spierings, Thomas Reinhard

Published in: BMC Ophthalmology | Issue 1/2014

Login to get access

Abstract

Background

Penetrating keratoplasty can commonly restore vision in corneal blindness. However, immunological graft reactions may induce irreversible graft failure in a substantial percentage. Repeat keratoplasties in turn are associated with increased risk of graft failure and possibly irreversible blindness. Topical as well as systemic immunosuppressants are administered for prophylaxis. However, severe adverse effects limit long-term usage. By contrast, matching for transplantation antigens might be effective for a long time.

Methods

FANCY is a prospective, controlled, randomised, double-blind, multi-centre clinical trial with two parallel arms. The primary objective is to evaluate superiority of the proposed HLA matching strategy in comparison to random graft assignment with respect to the primary endpoint ‘time to first endothelial graft rejection’. Relevant inclusion criteria are age over 18 years and waiting for penetrating or endothelial lamellar keratoplasty. The most important exclusion criteria are abuse of medication and/or drugs and an anticipated waiting time for an HLA match longer than 6 months. After randomisation, patients either receive a HLA-matched graft (experimental intervention) or a random graft (control intervention). The calculated sample size is 620 patients. The trial started in 2009 with a recruitment period of 24 months. A total of 654 patients were included during this time.

Discussion

The primary goal of FANCY is to assess whether histocompatibility matching is feasible and effective in the broad clinical routine. However, during the course of the trial, the landscape of keratoplasty changed due to the rise of Descemet Membrane Endothelial Keratoplasty (DMEK). Nowadays, immune reactions are confined mostly to the ‘high-risk’ subgroups. If we would design FANCY in 2014, we would narrow down the inclusion criteria to include only the high risk patients and accept longer waiting times for a matching donor here.

Trial registration

The unique identifying number of the FANCY trial is NCT00810472.
Appendix
Available only for authorised users
Literature
1.
go back to reference Reis A, Birnbaum F, Reinhard T: Systemic immunosuppressives after penetrating keratoplasty. Ophthalmologe. 2007, 104: 373-380. 10.1007/s00347-007-1517-x.CrossRefPubMed Reis A, Birnbaum F, Reinhard T: Systemic immunosuppressives after penetrating keratoplasty. Ophthalmologe. 2007, 104: 373-380. 10.1007/s00347-007-1517-x.CrossRefPubMed
2.
go back to reference Boehringer D, Reinhard T, Godehardt E, Sundmacher R: Regression analysis of idiopathic endothelial cell loss after perforating normal risk keratoplasty: basic principles for long-term analysis of endothelial risk factors in a retrospective clinical study. Klin Monatsbl Augenheilkd. 2001, 218 (6): 412-417. 10.1055/s-2001-16254.CrossRef Boehringer D, Reinhard T, Godehardt E, Sundmacher R: Regression analysis of idiopathic endothelial cell loss after perforating normal risk keratoplasty: basic principles for long-term analysis of endothelial risk factors in a retrospective clinical study. Klin Monatsbl Augenheilkd. 2001, 218 (6): 412-417. 10.1055/s-2001-16254.CrossRef
3.
go back to reference Reinhard T, Boehringer D, Enczmann J, Koegler G, Wernet P, Boehringer S, Sundmacher R: HLA class I/II matching and chronic endothelial cell loss in penetrating normal risk keratoplasty. Acta Ophthalmol Scand. 2004, 82 (1): 13-18. 10.1046/j.1600-0420.2003.00188.x.CrossRefPubMed Reinhard T, Boehringer D, Enczmann J, Koegler G, Wernet P, Boehringer S, Sundmacher R: HLA class I/II matching and chronic endothelial cell loss in penetrating normal risk keratoplasty. Acta Ophthalmol Scand. 2004, 82 (1): 13-18. 10.1046/j.1600-0420.2003.00188.x.CrossRefPubMed
5.
go back to reference Hopkins KA, Maguire MG, Fink NE, Bias WB: Reproducibility of HLA-A, B, and DR typing using peripheral blood samples: results of retyping in the collaborative corneal transplantation studies. Collaborative Corneal Transplantation Studies Group (corrected). Hum Immunol. 1992, 33: 122-128. 10.1016/0198-8859(92)90062-R.CrossRefPubMed Hopkins KA, Maguire MG, Fink NE, Bias WB: Reproducibility of HLA-A, B, and DR typing using peripheral blood samples: results of retyping in the collaborative corneal transplantation studies. Collaborative Corneal Transplantation Studies Group (corrected). Hum Immunol. 1992, 33: 122-128. 10.1016/0198-8859(92)90062-R.CrossRefPubMed
6.
go back to reference Sano Y, Ksander BR, Streilein JW: Minor H, rather than MHC, alloantigens offer the greater barrier to successful orthotopic corneal transplantation in mice. Transpl Immunol. 1996, 4 (1): 53-56. 10.1016/S0966-3274(96)80035-9.CrossRefPubMed Sano Y, Ksander BR, Streilein JW: Minor H, rather than MHC, alloantigens offer the greater barrier to successful orthotopic corneal transplantation in mice. Transpl Immunol. 1996, 4 (1): 53-56. 10.1016/S0966-3274(96)80035-9.CrossRefPubMed
Metadata
Title
Functional antigen matching in corneal transplantation: matching for the HLA-A, -B and -DRB1 antigens (FANCY) – study protocol
Authors
Daniel Böhringer
Gabriele Ihorst
Birgit Grotejohann
Julia Maurer
Eric Spierings
Thomas Reinhard
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Ophthalmology / Issue 1/2014
Electronic ISSN: 1471-2415
DOI
https://doi.org/10.1186/1471-2415-14-156

Other articles of this Issue 1/2014

BMC Ophthalmology 1/2014 Go to the issue