Single-dose, virus-vectored vaccine protection against Yersinia pestis challenge: CD4+ cells are required at the time of challenge for optimal protection

被引:25
作者
Chattopadhyay, Anasuya [1 ]
Park, Steven [2 ]
Delmas, Guillaume [2 ]
Suresh, Rema [2 ]
Senina, Svetlana [2 ]
Perlin, David S. [2 ]
Rose, John K. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[2] Publ Hlth Res Inst, Newark, NJ 07103 USA
关键词
Yersinia pestis; Vesicular stomatitis virus; CD4(+) cells;
D O I
10.1016/j.vaccine.2008.09.031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
We have developed an experimental recombinant vesicular stomatitis virus (VSV) vectored plague vaccine expressing a secreted form of Yersinia pestis low calcium response protein V (LcrV) from the first position of the VSV genome. This vector, given intramuscularly in a single dose, induced high-level antibody titers to LcrV and gave 90-100% protection against pneumonic plague challenge in mice. This single-dose protection was significantly better than that generated by VSV expressing the non-secreted LcrV protein. Increased protection correlated with increased anti-LcrV antibody and a bias toward IgG2a and away from IgG1 isotypes. We also found that the depletion of CD4(+) cells, but not CD8(+) cells, at the time of challenge resulted in reduced vaccine protection, indicating a role for cellular immunity in protection. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6329 / 6337
页数:9
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