Safety and Immunogenicity of the Candidate Tuberculosis Vaccine MVA85A in West Africa

被引:43
作者
Brookes, Roger H. [1 ]
Hill, Philip C. [1 ]
Owiafe, Patrick K. [1 ]
Ibanga, Hannah B. [1 ]
Jeffries, David J. [1 ]
Donkor, Simon A. [1 ]
Fletcher, Helen A. [2 ]
Hammond, Abdulrahman S. [1 ]
Lienhardt, Christian [3 ]
Adegbola, Richard A. [1 ]
McShane, Helen [2 ]
Hill, Adrian V. S. [2 ,4 ]
机构
[1] MRC Labs, TB Div, Bacterial Dis Programme, Banjul, Gambia
[2] Univ Oxford, Ctr Clin Vaccinol & Trop Med, Oxford, England
[3] Inst Rech Dev, Paris, France
[4] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
来源
PLOS ONE | 2008年 / 3卷 / 08期
基金
英国医学研究理事会;
关键词
D O I
10.1371/journal.pone.0002921
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Vaccination with a recombinant modified vaccinia Ankara expressing antigen 85A from Mycobacterium tuberculosis, MVA85A, induces high levels of cellular immune responses in UK volunteers. We assessed the safety and immunogenicity of this new vaccine in West African volunteers. Methods and Findings: We vaccinated 21 healthy adult male subjects (11 BCG scar negative and 10 BCG scar positive) with MVA85A after screening for evidence of prior exposure to mycobacteria. We monitored them over six months, observing for clinical, haematological and biochemical adverse events, together with assessment of the vaccine induced cellular immune response using ELISPOT and flow cytometry. MVA85A was well tolerated with no significant adverse events. Mild local and systemic adverse events were consistent with previous UK trials. Marked immunogenicity was found whether individuals had a previous BCG scar or not. There was not enhanced immunogenicity in those with a BCG scar, and induced T cell responses were better maintained in apparently BCG-naive Gambians than previously studied BCG-naive UK vaccinees. Although responses were predominantly attributable to CD4+ T cells, we also identified antigen specific CD8+ T cell responses, in subjects who were HLA B-35 and in whom enough blood was available for more detailed immunological analysis. Conclusions: These data on the safety and immunogenicity of MVA85A in West Africa support its accelerated development as a promising booster vaccine for tuberculosis.
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页数:8
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