A T Cell-Inducing Influenza Vaccine for the Elderly: Safety and Immunogenicity of MVA-NP+M1 in Adults Aged over 50 Years

被引:107
作者
Antrobus, Richard D. [1 ]
Lillie, Patrick J. [1 ]
Berthoud, Tamara K. [1 ]
Spencer, Alexandra J. [1 ]
McLaren, James E. [2 ]
Ladell, Kristin [2 ]
Lambe, Teresa [1 ]
Milicic, Anita [1 ]
Price, David A. [2 ]
Hill, Adrian V. S. [1 ]
Gilbert, Sarah C. [1 ]
机构
[1] Univ Oxford, Jenner Inst, Oxford, England
[2] Cardiff Univ, Sch Med, Inst Infect & Immun, Cardiff, S Glam, Wales
来源
PLOS ONE | 2012年 / 7卷 / 10期
关键词
IMMUNOSENESCENCE; PROTECTION; EFFICACY; INFECTION; FUTURE;
D O I
10.1371/journal.pone.0048322
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: Current influenza vaccines have reduced immunogenicity and are of uncertain efficacy in older adults. We assessed the safety and immunogenicity of MVA-NP+M1, a viral-vectored influenza vaccine designed to boost memory T cell responses, in a group of older adults. Methods: Thirty volunteers (aged 50-85) received a single intramuscular injection of MVA-NP+M1 at a dose of 1.5x10(8) plaque forming units (pfu). Safety and immunogenicity were assessed over a period of one year. The frequency of T cells specific for nucleoprotein (NP) and matrix protein 1 (M1) was determined by interferon-gamma (IFN-gamma) ELISpot, and their phenotypic and functional properties were characterized by polychromatic flow cytometry. In a subset of M1-specific CD8(+) T cells, T cell receptor (TCR) gene expression was evaluated using an unbiased molecular approach. Results: Vaccination with MVA-NP+M1 was well tolerated. ELISpot responses were boosted significantly above baseline following vaccination. Increases were detected in both CD4(+) and CD8(+) T cell subsets. Clonality studies indicated that MVA-NP+M1 expanded pre-existing memory CD8(+) T cells, which displayed a predominant CD27(+)CD45RO(+)CD57(-)CCR7(-) phenotype both before and after vaccination. Conclusions: MVA-NP+M1 is safe and immunogenic in older adults. Unlike seasonal influenza vaccination, the immune responses generated by MVA-NP+M1 are similar between younger and older individuals. A T cell-inducing vaccine such as MVA-NP+M1 may therefore provide a way to circumvent the immunosenescence that impairs routine influenza vaccination. Trial Registration: ClinicalTrials.gov NCT00942071
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页数:10
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