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Vox Sang ; 110(4): 329-35, 2016 May.
Article in English | MEDLINE | ID: mdl-26766162

ABSTRACT

BACKGROUND: Ebola virus disease is a public health emergency of international concern, and enormous efforts are being made in the development of vaccines and therapies. Ebola virus convalescent plasma is a promising anti-infective treatment of Ebola virus disease. Therefore, we developed and implemented a pathogen-reduced Ebola virus convalescent plasma concept in accordance with national, European and global regulatory framework. MATERIALS AND METHODS: Ebola virus convalescent plasma manufacture and distribution was managed by a collection centre, two medical centres and an expert group from the European Blood Alliance. Ebola virus convalescent plasma was collected twice with an interval of 61 days from a donor recovering from Ebola virus disease in Germany. After pathogen reduction, the plasma was analysed for Ebola virus-specific immunoglobulin G (IgG) antibodies and its Ebola virus neutralizing activity. RESULTS: Convalescent plasma could be collected without adverse events. Anti-Ebola virus IgG titres and Ebola-specific neutralizing antibodies in convalescent plasma were only slightly reduced after pathogen reduction treatment with S59 amotosalen/UVA. A patient in Italy with Ebola virus disease was treated with convalescent plasma without apparent adverse effects. DISCUSSION: As proof of principle, we describe a concept and practical implementation of pathogen-reduced Ebola virus convalescent plasma manufacture, quality control and its clinical application to an Ebola virus disease patient.


Subject(s)
Antibodies, Neutralizing/isolation & purification , Ebolavirus/immunology , Hemorrhagic Fever, Ebola/prevention & control , Immunoglobulin G/isolation & purification , Adult , Antibodies, Neutralizing/immunology , Antibodies, Neutralizing/therapeutic use , Blood Donors , Convalescence , Furocoumarins/pharmacology , Germany , Humans , Immunoglobulin G/immunology , Immunoglobulin G/therapeutic use , Male , Middle Aged , Photosensitizing Agents/pharmacology , Quality Control , Ultraviolet Rays , Virus Inactivation/drug effects , Virus Inactivation/radiation effects
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