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Modified vaccinia Ankara‐expressing Ag85A,a novel tuberculosis vaccine,is safe in adolescents and children,and induces polyfunctional CD4+ T cells
Authors:Thomas J Scriba  Michele Tameris  Nazma Mansoor  Erica Smit  Linda van der Merwe  Fatima Isaacs  Alana Keyser  Sizulu Moyo  Nathaniel Brittain  Alison Lawrie  Sebastian Gelderbloem  Ashley Veldsman  Mark Hatherill  Anthony Hawkridge  Adrian V S Hill  Gregory D Hussey  Hassan Mahomed  Willem A Hanekom
Institution:1. South African Tuberculosis Vaccine Initiative, Institute of Infectious Diseases and Molecular Medicine, and School of Child and Adolescent Health, University of Cape Town, Observatory, South Africa;2. Centre for Clinical Vaccinology and Tropical Medicine and The Jenner Institute Laboratories, Nuffield Department of Medicine, Oxford University, Oxford, UK;3. Aeras Global Tuberculosis Vaccine Foundation, Rondebosch, South Africa;4. South African Tuberculosis Vaccine Initiative, Institute of Infectious Diseases and Molecular Medicine, and School of Child and Adolescent Health, University of Cape Town, Observatory, South AfricaThese authors share senior authorship
Abstract:Modified vaccinia Ankara‐expressing Ag85A (MVA85A) is a new tuberculosis (TB) vaccine aimed at enhancing immunity induced by BCG. We investigated the safety and immunogenicity of MVA85A in healthy adolescents and children from a TB endemic region, who received BCG at birth. Twelve adolescents and 24 children were vaccinated and followed up for 12 or 6 months, respectively. Adverse events were documented and vaccine‐induced immune responses assessed by IFN‐γ ELISpot and intracellular cytokine staining. The vaccine was well tolerated and there were no vaccine‐related serious adverse events. MVA85A induced potent and durable T‐cell responses. Multiple CD4+ T‐cell subsets, based on expression of IFN‐γ, TNF‐α, IL‐2, IL‐17 and GM‐CSF, were induced. Polyfunctional CD4+ T cells co‐expressing IFN‐γ, TNF‐α and IL‐2 dominated the response in both age groups. A novel CD4+ cell subset co‐expressing these three Th1 cytokines and IL‐17 was induced in adolescents, while a novel CD4+ T‐cell subset co‐expressing Th1 cytokines and GM‐CSF was induced in children. Ag‐specific CD8+ T cells were not detected. We conclude that in adolescents and children MVA85A safely induces the type of immunity thought to be important in protection against TB. This includes induction of novel Th1‐cell populations that have not been previously described in humans.
Keywords:IL‐17  Modified vaccinia Ankara‐expressing Ag85A  Polyfunctional  Tuberculosis  Vaccine
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