Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola

The 2014-2016 Ebola outbreak in West Africa was the largest in history leading to 28,639 cases, of which 40% were fatal. Better treatments and effective vaccines against Ebola virus are needed to prevent future recurrence. Multiple, novel, treatment options were assessed during the outbreak, includi...

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Príomhchruthaitheoirí: Tan, T, Rijal, P, Townsend, A, Hyde, S, Gill, D
Formáid: Conference item
Foilsithe / Cruthaithe: Elsevier 2017
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author Tan, T
Rijal, P
Townsend, A
Hyde, S
Gill, D
author_facet Tan, T
Rijal, P
Townsend, A
Hyde, S
Gill, D
author_sort Tan, T
collection OXFORD
description The 2014-2016 Ebola outbreak in West Africa was the largest in history leading to 28,639 cases, of which 40% were fatal. Better treatments and effective vaccines against Ebola virus are needed to prevent future recurrence. Multiple, novel, treatment options were assessed during the outbreak, including ZMapp™ monoclonal antibody therapy, which showed promising results in some patients. However, widespread adoption of this approach is hindered by high costs of monoclonal antibody manufacturing and the relatively short half-life of antibody in the blood circulation. To circumvent such limitations, we propose to utilise recombinant adeno-associated virus (rAAV) delivered to the muscle to express the therapeutic monoclonal antibodies.
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spelling oxford-uuid:3dcbec8c-3e81-46c2-857b-90ecee9b574b2022-03-26T14:21:37ZDevelopment of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebolaConference itemhttp://purl.org/coar/resource_type/c_5794uuid:3dcbec8c-3e81-46c2-857b-90ecee9b574bSymplectic Elements at OxfordElsevier2017Tan, TRijal, PTownsend, AHyde, SGill, DThe 2014-2016 Ebola outbreak in West Africa was the largest in history leading to 28,639 cases, of which 40% were fatal. Better treatments and effective vaccines against Ebola virus are needed to prevent future recurrence. Multiple, novel, treatment options were assessed during the outbreak, including ZMapp™ monoclonal antibody therapy, which showed promising results in some patients. However, widespread adoption of this approach is hindered by high costs of monoclonal antibody manufacturing and the relatively short half-life of antibody in the blood circulation. To circumvent such limitations, we propose to utilise recombinant adeno-associated virus (rAAV) delivered to the muscle to express the therapeutic monoclonal antibodies.
spellingShingle Tan, T
Rijal, P
Townsend, A
Hyde, S
Gill, D
Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title_full Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title_fullStr Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title_full_unstemmed Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title_short Development of recombinant Adeno-Associated Viral vector (rAAV) for passive immunisation against ebola
title_sort development of recombinant adeno associated viral vector raav for passive immunisation against ebola
work_keys_str_mv AT tant developmentofrecombinantadenoassociatedviralvectorraavforpassiveimmunisationagainstebola
AT rijalp developmentofrecombinantadenoassociatedviralvectorraavforpassiveimmunisationagainstebola
AT townsenda developmentofrecombinantadenoassociatedviralvectorraavforpassiveimmunisationagainstebola
AT hydes developmentofrecombinantadenoassociatedviralvectorraavforpassiveimmunisationagainstebola
AT gilld developmentofrecombinantadenoassociatedviralvectorraavforpassiveimmunisationagainstebola