The Cross-Species Mycobacterial Growth Inhibition Assay (MGIA) Project, 2010–2014
Author(s) -
Michael J. Brennan,
Rachel Tanner,
Sheldon L. Morris,
Thomas J. Scriba,
Jacqueline M. Achkar,
Andrea Zelmer,
David A. Hokey,
Angelo Izzo,
Sally Sharpe,
Ann Williams,
Adam PennNicholson,
Mzwandile Erasmus,
Elena Stylianou,
Daniel F. Hoft,
Helen McShane,
Helen A. Fletcher
Publication year - 2017
Publication title -
clinical and vaccine immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.649
H-Index - 77
eISSN - 1556-6811
pISSN - 1556-679X
DOI - 10.1128/cvi.00142-17
Subject(s) - mycobacterium tuberculosis , tuberculosis vaccines , tuberculosis , mycobacterium bovis , immune system , computational biology , biology , in vivo , medicine , immunology , microbiology and biotechnology , pathology
The development of a functional biomarker assay in the tuberculosis (TB) field would be widely recognized as a major advance in efforts to develop and to test novel TB vaccine candidates efficiently. We present preliminary studies using mycobacterial growth inhibition assays (MGIAs) to detect Mycobacterium bovis BCG vaccine responses across species, and we extend this work to determine whether a standardized MGIA can be applied in characterizing new TB vaccines. The comparative MGIA studies reviewed here aimed to evaluate robustness, reproducibility, and ability to reflect in vivo responses. In doing so, they have laid the foundation for the development of a MGIA that can be standardized and potentially qualified. A major challenge ahead lies in better understanding the relationships between in vivo protection, in vitro growth inhibition, and the immune mechanisms involved. The final outcome would be a MGIA that could be used with confidence in TB vaccine trials. We summarize data arising from this project, present a strategy to meet the goals of developing a functional assay for TB vaccine testing, and describe some of the challenges encountered in performing and transferring such assays.
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