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Screening vaccine formulations for biological activity using fresh human whole blood

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 t...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896559/
https://www.ncbi.nlm.nih.gov/pubmed/24401565
http://dx.doi.org/10.4161/hv.27657
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author 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
author_facet 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
author_sort Brookes, Roger H
collection PubMed
description 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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spelling pubmed-48965592016-06-24 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 Hum Vaccin Immunother Commentary 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. Taylor & Francis 2014-01-08 /pmc/articles/PMC4896559/ /pubmed/24401565 http://dx.doi.org/10.4161/hv.27657 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
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
Screening vaccine formulations for biological activity using fresh human whole blood
title Screening vaccine formulations for biological activity using fresh human whole blood
title_full Screening vaccine formulations for biological activity using fresh human whole blood
title_fullStr Screening vaccine formulations for biological activity using fresh human whole blood
title_full_unstemmed Screening vaccine formulations for biological activity using fresh human whole blood
title_short Screening vaccine formulations for biological activity using fresh human whole blood
title_sort screening vaccine formulations for biological activity using fresh human whole blood
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896559/
https://www.ncbi.nlm.nih.gov/pubmed/24401565
http://dx.doi.org/10.4161/hv.27657
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