An overview of key steps in developing regulatory guidelines was listed in a position paper published in Xenotransplantation in 2000 and a summary of regulatory documents for Xenotransplantation was presented in Osaka in 2013.

Click the buttom below for relevant publications and key regulatory documents related to xenotransplantation.

IXA has worked closely with WHO and various national regulatory bodies to establish detailed recommendations regarding safe, scientifically and ethically reasonable conditions that should be met in order to undertake a corneal xenotransplantation clinical trial.

An initial consensus statement on conditions for undertaking clinical trials of corneal xenotransplantation was published in Xenotransplantation in 2014. It is expected that this initial consensus statement will be revised over time in response to scientific advances in the field, and changes in the regulatory framework based on accumulating clinical experience.

A Xenotransplantation Advisory Committee lead by the president of the International Society for Heart and Lung Transplantation (ISHLT), Robert Kormos, considered the status of xenotransplantation and its potential role in the future treatment of patients with end-stage cardiac and pulmonary diseases in a global context. In particular, members considered the need for a new source of thoracic organs for transplantation, the potential of xenotransplantation to fulfill this need in comparison with other therapeutic modalities, the immune barriers and potential complications of clinical xenotransplantation, and some ethical, regulatory, and financial aspects. A position paper Report of the Xenotransplantation Advisory Committee of the International Society for Heart and Lung Transplantation: The Present Status of Xenotransplantation and Its Potential Role in the Treatment of End-Stage Cardiac and Pulmonary Diseases was published in Xenotransplantation in 2000. The authors emphasized that the field of xenotransplantation research, particularly that involving thoracic-organ transplantation, should be reviewed at intervals and revisions made to their conclusions and recommendations.

IXA has worked closely with WHO and various national regulatory bodies to establish detailed recommendations regarding safe, scientifically and ethically reasonable conditions that should be met in order to undertake an islet xenotransplantation clinical trial.

The 2^nd International Conference on Clinical Islet Xenotransplantation (ICCIX) took place in San Francisco on August 1, 2014. The objective of the 2^nd ICCIX was to update the IXA Consensus Statement on Conditions for Undertaking Clinical Trials of Porcine Islet Products in Type 1 Diabetes, which was published in Xenotransplantation in 2009. Topics discussed included the regulatory framework, source pigs, pig islet cell products, preclinical efficacy and safety studies, recipient monitoring, patient selection, and ethical consideration. The updated IXA Consensus Statement will incorporate the current thinking of the participating opinion leaders active in the respective fields and will be published in a future issue of Xenotransplantation.

Acivities
New activity list to come!

Lectures/Seminars
Members of the committee plan to launch monthly lectures or webinars which will cover different xenotransplantation topics. These lectures are intended for new or junior members who wish to broaden their knowledge on the current research in xenotransplantation.

Experimental Protocols
This section will catalog different protocols utilized by scientists in the field, such as cell isolation, antibody binding and more. They should provide valuable tools for students or new members in the field of xenotransplantation.

Some information about reagents reactive with pig or primate species is available through the following links:

• NIH Nonhuman Primate Reagent Resource


• DGIL Porcine Translational Research Database


• Current Status of the Swine Leukocyte Antigen (SLA) System


• First International Workshop to Define Swine Leukocyte Cluster of Differentiation (CD) Antigens

• Non-gal antibody assay

• Detection of porcine endogenous retrovirus in xenotransplantation


• Quantitative analysis of porcine endogenous retroviruses in different organs of transgenic pigs generated for xenotransplantation


• Sensitive and specific immunological detection methods for porcine endogenous retroviruses applicable to experimental and clinical xenotransplantation

• Pig thrombomodulin binds human thrombin but is a poor cofactor for activation of human protein C and TAFI


• Platelet aggregation in humans and nonhuman primates: relevance to xenotransplantation

The National Swine Resource and Research Center (NSRRC) was established in 2003 to develop the infrastructure to ensure that biomedical investigators across a variety of disciplines have access to critically needed swine models of human health and disease. The NSRRC will also serve as a central resource for reagents, creation of new genetically modified swine, and information and training related to use of swine models in biomedical research.