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Screening vaccine formulations for biological activity using fresh human whole blood.
Brookes, Roger H; Hakimi, Jalil; Ha, Yukyung; Aboutorabian, Sepideh; Ausar, Salvador F; Hasija, Manvi; Smith, Steven G; Todryk, Stephen M; Dockrell, Hazel M; Rahman, Nausheen.
Afiliación
  • Brookes RH; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Hakimi J; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Ha Y; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Aboutorabian S; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Ausar SF; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Hasija M; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
  • Smith SG; Faculty of Infectious and Tropical Diseases; Department of Immunology and Infection; London School of Hygiene and Tropical Medicine; London, UK.
  • Todryk SM; Department of Applied Sciences; Faculty of Health & Life Sciences; Northumbria University; Newcastle upon Tyne, UK.
  • Dockrell HM; Faculty of Infectious and Tropical Diseases; Department of Immunology and Infection; London School of Hygiene and Tropical Medicine; London, UK.
  • Rahman N; Department of Bioprocess Research and Development; Formulation and Stability Platform; Sanofi Pasteur; Toronto, ON Canada.
Hum Vaccin Immunother ; 10(4): 1129-35, 2014.
Article en En | MEDLINE | ID: mdl-24401565
Understanding the relevant biological activity of any pharmaceutical formulation destined for human use is crucial. For vaccine-based formulations, activity must reflect the expected immune response, while for non-vaccine therapeutic agents, such as monoclonal antibodies, a lack of immune response to the formulation is desired. During early formulation development, various biochemical and biophysical characteristics can be monitored in a high-throughput screening (HTS) format. However, it remains impractical and arguably unethical to screen samples in this way for immunological functionality in animal models. Furthermore, data for immunological functionality lag formulation design by months, making it cumbersome to relate back to formulations in real-time. It is also likely that animal testing may not accurately reflect the response in humans. For a more effective formulation screen, a human whole blood (hWB) approach can be used to assess immunological functionality. The functional activity relates directly to the human immune response to a complete formulation (adjuvant/antigen) and includes adjuvant response, antigen response, adjuvant-modulated antigen response, stability, and potentially safety. The following commentary discusses the hWB approach as a valuable new tool to de-risk manufacture, formulation design, and clinical progression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sangre / Vacunas / Química Farmacéutica Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Hum Vaccin Immunother Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sangre / Vacunas / Química Farmacéutica Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Hum Vaccin Immunother Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos