A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates

Abstract We present a non-human primate mycobacterial growth inhibition assay (MGIA) using in vitro blood or cell co-culture with the aim of refining and expediting early tuberculosis vaccine testing. We have taken steps to optimise the assay using cryopreserved peripheral blood mononuclear cells, t...

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Main Authors: Rachel Tanner, Andrew D. White, Charelle Boot, Claudia C. Sombroek, Matthew K. O’Shea, Daniel Wright, Emily Hoogkamer, Julia Bitencourt, Stephanie A. Harris, Charlotte Sarfas, Rachel Wittenberg, Iman Satti, Helen A. Fletcher, Frank A. W. Verreck, Sally A. Sharpe, Helen McShane
Format: Article
Language:English
Published: Nature Publishing Group 2021-01-01
Series:npj Vaccines
Online Access:https://doi.org/10.1038/s41541-020-00263-7
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spelling doaj-68af0e0e83b24984a10595f180e34dba2021-01-10T12:46:10ZengNature Publishing Groupnpj Vaccines2059-01052021-01-016111110.1038/s41541-020-00263-7A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidatesRachel Tanner0Andrew D. White1Charelle Boot2Claudia C. Sombroek3Matthew K. O’Shea4Daniel Wright5Emily Hoogkamer6Julia Bitencourt7Stephanie A. Harris8Charlotte Sarfas9Rachel Wittenberg10Iman Satti11Helen A. Fletcher12Frank A. W. Verreck13Sally A. Sharpe14Helen McShane15The Jenner Institute, University of OxfordPublic Health EnglandTB Research Group, Department of Parasitology, Biomedical Primate Research CentreTB Research Group, Department of Parasitology, Biomedical Primate Research CentreThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordPublic Health EnglandThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordThe Jenner Institute, University of OxfordTB Research Group, Department of Parasitology, Biomedical Primate Research CentrePublic Health EnglandThe Jenner Institute, University of OxfordAbstract We present a non-human primate mycobacterial growth inhibition assay (MGIA) using in vitro blood or cell co-culture with the aim of refining and expediting early tuberculosis vaccine testing. We have taken steps to optimise the assay using cryopreserved peripheral blood mononuclear cells, transfer it to end-user institutes, and assess technical and biological validity. Increasing cell concentration or mycobacterial input and co-culturing in static 48-well plates compared with rotating tubes improved intra-assay repeatability and sensitivity. Standardisation and harmonisation efforts resulted in high consistency agreements, with repeatability and intermediate precision <10% coefficient of variation (CV) and inter-site reproducibility <20% CV; although some systematic differences were observed. As proof-of-concept, we demonstrated ability to detect a BCG vaccine-induced improvement in growth inhibition in macaque samples, and a correlation between MGIA outcome and measures of protection from in vivo disease development following challenge with either intradermal BCG or aerosol/endobronchial Mycobacterium tuberculosis (M.tb) at a group and individual animal level.https://doi.org/10.1038/s41541-020-00263-7
collection DOAJ
language English
format Article
sources DOAJ
author Rachel Tanner
Andrew D. White
Charelle Boot
Claudia C. Sombroek
Matthew K. O’Shea
Daniel Wright
Emily Hoogkamer
Julia Bitencourt
Stephanie A. Harris
Charlotte Sarfas
Rachel Wittenberg
Iman Satti
Helen A. Fletcher
Frank A. W. Verreck
Sally A. Sharpe
Helen McShane
spellingShingle Rachel Tanner
Andrew D. White
Charelle Boot
Claudia C. Sombroek
Matthew K. O’Shea
Daniel Wright
Emily Hoogkamer
Julia Bitencourt
Stephanie A. Harris
Charlotte Sarfas
Rachel Wittenberg
Iman Satti
Helen A. Fletcher
Frank A. W. Verreck
Sally A. Sharpe
Helen McShane
A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
npj Vaccines
author_facet Rachel Tanner
Andrew D. White
Charelle Boot
Claudia C. Sombroek
Matthew K. O’Shea
Daniel Wright
Emily Hoogkamer
Julia Bitencourt
Stephanie A. Harris
Charlotte Sarfas
Rachel Wittenberg
Iman Satti
Helen A. Fletcher
Frank A. W. Verreck
Sally A. Sharpe
Helen McShane
author_sort Rachel Tanner
title A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
title_short A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
title_full A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
title_fullStr A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
title_full_unstemmed A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates
title_sort non-human primate in vitro functional assay for the early evaluation of tb vaccine candidates
publisher Nature Publishing Group
series npj Vaccines
issn 2059-0105
publishDate 2021-01-01
description Abstract We present a non-human primate mycobacterial growth inhibition assay (MGIA) using in vitro blood or cell co-culture with the aim of refining and expediting early tuberculosis vaccine testing. We have taken steps to optimise the assay using cryopreserved peripheral blood mononuclear cells, transfer it to end-user institutes, and assess technical and biological validity. Increasing cell concentration or mycobacterial input and co-culturing in static 48-well plates compared with rotating tubes improved intra-assay repeatability and sensitivity. Standardisation and harmonisation efforts resulted in high consistency agreements, with repeatability and intermediate precision <10% coefficient of variation (CV) and inter-site reproducibility <20% CV; although some systematic differences were observed. As proof-of-concept, we demonstrated ability to detect a BCG vaccine-induced improvement in growth inhibition in macaque samples, and a correlation between MGIA outcome and measures of protection from in vivo disease development following challenge with either intradermal BCG or aerosol/endobronchial Mycobacterium tuberculosis (M.tb) at a group and individual animal level.
url https://doi.org/10.1038/s41541-020-00263-7
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