TY - JOUR
T1 - Accelerating research and development of new vaccines against tuberculosis
T2 - a global roadmap
AU - Cobelens, Frank
AU - Suri, Rajinder Kumar
AU - Helinski, Michelle
AU - Makanga, Michael
AU - Weinberg, Ana L. cia
AU - Schaffmeister, Britta
AU - Deege, Frank
AU - TB Vaccine Roadmap Stakeholder Group
AU - Hatherill, Mark
N1 - Funding Information: The EDCTP commissioned and financially supported the roadmap and was consulted and involved in each development step. EDCTP's scientific advisory board provided input on a draft version. The authors wish to acknowledge the valuable input received from Nebiat Gebreselassie and Matteo Zignol (Global Tuberculosis Programme, WHO, Switzerland), Denise Arakaki (National TB Programme, Brazil), Alex Bowles and Nine Steensma (Clinton Health Access Initiative, USA), Grania Brigden (The Union, France), Julio Croda (Oswaldo Cruz Foundation, Brazil), Katrin Eichelberg (Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, USA), Karen Elkins (Food and Drug Administration, USA), Mike Frick (Treatment Action Group, USA), Bernard Fritzell, Leander Grohde (Vakzine Projekt Management GmbH, Germany), Sri Hadinegoro (Technical Advisory Group on Immunization, Indonesia), Bethan Hughes (Wellcome Trust, UK), Ashish Kohli (European Federation of Pharmaceutical Industries and Associations, UK), Prasad Kulkami (Serum Institute of India, India), Hannu Laang (European Commission, Brussels), Adam MacNeil (Centers for Disease Control and Prevention, USA), Sophie Mathewson (Gavi, Switzerland), Videlis Nduba (Kenya Medical Research Institute, Kenya), Jan Poolman (Janssen Vaccines, Netherlands), Jelle Thole (TBVI, Netherlands) and Johan Vekemans (then Initiative for Vaccine Research, WHO, Switzerland). The findings and conclusions in this article are those of the authors and do not necessarily represent the views of the US Agency for International Development or the US Government. Funding Information: Tuberculosis Vaccine Roadmap Stakeholder Group: AMG reports travel support from the International AIDS Vaccine Initiative (IAVI). GBG is employed by Sanofi Pasteur and reports stocks or stock options in Sanofi Pasteur. SHEK is coinventor of the tuberculosis vaccine VPM1002, which is licensed to Vakzine Projekt Management, Hannover, Germany, and sublicensed to Serum Institute of India, Pune, India, and is co-holder of a patent licensed to Serum Institute of India. RVL received funding from EDCTP for the present work. DML received travel support from the Stop TB Partnership. CM holds clinical trial grants from EDCTP, received travel support from EDCTP, and is co-inventor on a patent on a tuberculosis vaccine held by the University of Zaragoza. RM received support for the present work from the Statens Serum Institut, holds research grants from the US National Institutes of Health (NIH) and the Independent Research Fund Denmark, and is co-inventor on a patent application on a new tuberculosis vaccine candidate. EN holds research grants from the NIH and the the Bill & Melinda Gates Foundation. THMO holds research grants from the NIH, the European Commission, and the Netherlands Organization for Research. TRS and AS are employed by the Gates Medical Research Institute. DRT is employed by IAVI. GV reports stocks or stock options in GSK. RW holds research grants from the the Bill & Melinda Gates Foundation, the Wellcome Trust, WHO, and UK Research and Innovation. The other authors declare no competing interests. The development of the Roadmap was financially supported by EDCTP. Funding Information: FC received funding from the European & Developing Countries Clinical Trials Partnership (EDCTP) for the present work, holds research grants from EDCTP and the Bill & Melinda Gates Foundation, reports travel support from the Tuberculosis Vaccine Initiative (TBVI) and the Coalition for TB Vaccine Discovery, and is an advisory board member of TBVI. MHe, MM, and ALW are employees of EDCTP. BS and FD received funding from EDCTP for the present work. MHa holds institutional clinical trial grants to University of Cape Town, Cape Town, South Africa, and is an advisory board member of TBVI. Publisher Copyright: © 2022 Elsevier Ltd
PY - 2022/4/1
Y1 - 2022/4/1
N2 - To eliminate tuberculosis globally, a new, effective, and affordable vaccine is urgently needed, particularly for use in adults and adolescents in low-income and middle-income countries. We have created a roadmap that lists the actions needed to accelerate tuberculosis vaccine research and development using a participatory process. The vaccine pipeline needs more diverse immunological approaches, antigens, and platforms. Clinical development can be accelerated by validated preclinical models, agreed laboratory correlates of protection, efficient trial designs, and validated endpoints. Determining the public health impact of new tuberculosis vaccines requires understanding of a country's demand for a new tuberculosis vaccine, how to integrate vaccine implementation with ongoing tuberculosis prevention efforts, cost, and national and global demand to stimulate vaccine production. Investments in tuberculosis vaccine research and development need to be increased, with more diversity of funding sources and coordination between these funders. Open science is important to enhance the efficiency of tuberculosis vaccine research and development including early and freely available publication of study findings and effective mechanisms for sharing datasets and specimens. There is a need for increased engagement of industry vaccine developers, for increased political commitment for new tuberculosis vaccines, and to address stigma and vaccine hesitancy. The unprecedented speed by which COVID-19 vaccines have been developed and introduced provides important insight for tuberculosis vaccine research and development.
AB - To eliminate tuberculosis globally, a new, effective, and affordable vaccine is urgently needed, particularly for use in adults and adolescents in low-income and middle-income countries. We have created a roadmap that lists the actions needed to accelerate tuberculosis vaccine research and development using a participatory process. The vaccine pipeline needs more diverse immunological approaches, antigens, and platforms. Clinical development can be accelerated by validated preclinical models, agreed laboratory correlates of protection, efficient trial designs, and validated endpoints. Determining the public health impact of new tuberculosis vaccines requires understanding of a country's demand for a new tuberculosis vaccine, how to integrate vaccine implementation with ongoing tuberculosis prevention efforts, cost, and national and global demand to stimulate vaccine production. Investments in tuberculosis vaccine research and development need to be increased, with more diversity of funding sources and coordination between these funders. Open science is important to enhance the efficiency of tuberculosis vaccine research and development including early and freely available publication of study findings and effective mechanisms for sharing datasets and specimens. There is a need for increased engagement of industry vaccine developers, for increased political commitment for new tuberculosis vaccines, and to address stigma and vaccine hesitancy. The unprecedented speed by which COVID-19 vaccines have been developed and introduced provides important insight for tuberculosis vaccine research and development.
UR - http://www.scopus.com/inward/record.url?scp=85126840680&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/S1473-3099(21)00810-0
DO - https://doi.org/10.1016/S1473-3099(21)00810-0
M3 - Review article
C2 - 35240041
SN - 1473-3099
VL - 22
SP - e108-e120
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 4
ER -