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Protocol for the first clinical trial to investigate safety and efficacy of corneal xenotransplantation in patients with corneal opacity, corneal perforation, or impending corneal perforation

Cited 9 time in Web of Science Cited 12 time in Scopus
Authors

Choi, Hyuk Jin; Yoon, Chang Ho; Hyon, Joon Young; Lee, Hyung Keun; Song, Jong-Suk; Chung, Tae-Young; Mo, Hyojung; Kim, Jaeyoung; Kim, Jae-eun; Hahm, Bong-Jin; Yang, Jaeseok; Park, Wan Beom; Kim, Mee Kum

Issue Date
2019-01
Publisher
Blackwell Publishing Inc.
Citation
Xenotransplantation, Vol.26 No.1, p. e12446
Abstract
Background Xenotransplantation using fresh porcine corneas has been suggested as a feasible alternative to overcome the shortage of human donor corneas. Successful long-term survival of grafts without evidence of xenozoonosis in clinically applicable pig-to-non-human primate corneal transplantation model has brought researchers close to human clinical trials. Accordingly, we aimed to prepare a clinical trial protocol to conduct the first corneal xenotransplantation. Methods We developed the clinical trial protocol based on international consensus statement on conditions for undertaking clinical trials of corneal xenotransplantation developed by the International Xenotransplantation Society. Detailed contents of the protocol have been modified with reference to comments provided by ophthalmologists and multidisciplinary experts, including an infectionist, an organ transplantation specialist, a clinical pharmacologist, a neuropsychiatrist, a laboratory medicine doctor, and a microbiologist. Results Two patients with bilateral legal corneal blindness (best-corrected visual acuity <= 20/200 in the better eye and <= 20/1000 in the candidate eye) or with (impending) corneal perforation will be enrolled. During the screening period, participants and their family members will have two separate deep consideration periods before signing informed consent forms. Each patient will undergo corneal xenotransplantation using fresh corneas from Seoul National University miniature pigs. Commercially available immunosuppressants will be administered and systemic infection prophylaxis will be performed according to the program schedule. After transplantation, each patient will be monitored at a specialized clinic to investigate safety up to 2 years and efficacy up to 1 year. Conclusions A detailed clinical trial protocol for the first corneal xenotransplantation reflecting the global guidelines is provided.
ISSN
0908-665X
URI
https://hdl.handle.net/10371/199652
DOI
https://doi.org/10.1111/xen.12446
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  • College of Medicine
  • Department of Medicine
Research Area Immunology, Infectious Diseases, Vaccination, 감염병, 바이러스질환, 예방접종

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