Vaccination Alters the Balance between Protective Immunity, Exhaustion, Escape, and Death in Chronic Infections

被引:26
作者
Johnson, Philip L. F. [1 ]
Kochin, Beth F. [1 ]
McAfee, Megan S. [2 ]
Stromnes, Ingunn M. [2 ]
Regoes, Roland R. [3 ]
Ahmed, Rafi [4 ]
Blattman, Joseph N. [2 ]
Antia, Rustom [1 ]
机构
[1] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] ETH, Inst Integrat Biol, Zurich, Switzerland
[4] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30322 USA
基金
瑞士国家科学基金会;
关键词
T-CELLS; VIRUS-INFECTION; VIRAL-INFECTION; DISEASE; MICE; DYNAMICS; TUBERCULOSIS; PATHOGENESIS; PERSISTENCE; BIOLOGY;
D O I
10.1128/JVI.00166-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
While T cell-based vaccines have the potential to provide protection against chronic virus infections, they also have the potential to generate immunopathology following subsequent virus infection. We develop a mathematical model to investigate the conditions under which T cells lead to protection versus adverse pathology. The model illustrates how the balance between virus clearance and immune exhaustion may be disrupted when vaccination generates intermediate numbers of specific CD8 T cells. Surprisingly, our model suggests that this adverse effect of vaccination is largely unaffected by the generation of mutant viruses that evade T cell recognition and cannot be avoided by simply increasing the quality (affinity) or diversity of the T cell response. These findings should be taken into account when developing vaccines against persistent infections.
引用
收藏
页码:5565 / 5570
页数:6
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