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A Human Erythrocyte-based Haemolysis Assay for the Evaluation of Human Complement Activity.
King, Ruby Anne N; Climacosa, Fresthel Monica M; Santos, Bobbie Marie M; Caoili, Salvador Eugenio C.
Afiliación
  • King RAN; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, 54733College of Medicine, University of the Philippines Manila, Philippines.
  • Climacosa FMM; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, 54733College of Medicine, University of the Philippines Manila, Philippines.
  • Santos BMM; Department of Medical Microbiology, College of Public Health, 54733University of the Philippines Manila, Philippines.
  • Caoili SEC; Biomedical Innovations Research for Translational Health Science (BIRTHS) Laboratory, Department of Biochemistry and Molecular Biology, 54733College of Medicine, University of the Philippines Manila, Philippines.
Altern Lab Anim ; 48(3): 127-135, 2020 May.
Article en En | MEDLINE | ID: mdl-33006498
The complement system consists of at least 50 proteins that serve as one of the first lines of defence against foreign, or damaged, cells and invading microorganisms. Its dysregulation underlies the pathophysiology of many different diseases, which makes functional assays of complement activity crucial; they are, however, underutilised. Standard haemolysis assays for the analysis of complement function employ sensitised non-human erythrocytes (e.g. from the sheep, guinea-pig or rabbit), the use of which raises animal welfare concerns. To provide an alternative to the use of such animal-derived products for complement function assays, we developed a method that employs modified human erythrocytes to evaluate the activity of complement pathways. Human erythrocytes were subjected to various chemical and/or proteolytic treatments involving 2,4,6-trinitrobenzene sulphonate (TNBS) and pancreatin. Haemolysis assays demonstrated that sequential treatment with TNBS and pancreatin resulted in significantly greater complement-mediated haemolysis, as compared to TNBS or pancreatin treatment alone. Evidence that lysis of the modified erythrocytes was complement-mediated was provided by the chelation and subsequent restoration of calcium in the plasma. Thus, such modified human erythrocytes could be used as an alternative to animal-derived erythrocytes in haemolysis assays, in order to evaluate complement activity in human plasma during, for example, the screening of patients for complement deficiencies and other abnormalities in a clinical setting.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Activación de Complemento / Hemólisis Límite: Animals / Humans Idioma: En Revista: Altern Lab Anim Año: 2020 Tipo del documento: Article País de afiliación: Filipinas Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Activación de Complemento / Hemólisis Límite: Animals / Humans Idioma: En Revista: Altern Lab Anim Año: 2020 Tipo del documento: Article País de afiliación: Filipinas Pais de publicación: Reino Unido