DNA vaccines encoding proteins from wild-type and attenuated canine distemper virus protect equally well against wild-type virus challenge

被引:12
作者
Nielsen, Line [1 ]
Jensen, Trine Hammer [1 ]
Kristensen, Birte [1 ]
Jensen, Tove Dannemann [1 ]
Karlskov-Mortensen, Peter [1 ]
Lund, Morten [1 ]
Aasted, Bent [1 ]
Blixenkrone-Moller, Merete [2 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Vet Dis Biol, DK-1870 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Int Hlth Immunol & Microbiol, DK-1870 Copenhagen, Denmark
关键词
MONOCLONAL-ANTIBODIES; MEASLES-VIRUS; GENETIC-CHARACTERIZATION; HEMAGGLUTININ GENE; ROBUST PROTECTION; FUSION PROTEIN; INFLUENZA-A; H PROTEIN; DOGS; VACCINATION;
D O I
10.1007/s00705-012-1375-y
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Immunity induced by DNA vaccines containing the hemagglutinin (H) and nucleoprotein (N) genes of wild-type and attenuated canine distemper virus (CDV) was investigated in mink (Mustela vison), a highly susceptible natural host of CDV. All DNA-immunized mink seroconverted, and significant levels of virus-neutralizing (VN) antibodies were present on the day of challenge with wild-type CDV. The DNA vaccines also primed the cell-mediated memory responses, as indicated by an early increase in the number of interferon-gamma (IFN-gamma)-producing lymphocytes after challenge. Importantly, the wild-type and attenuated CDV DNA vaccines had a long-term protective effect against wild-type CDV challenge. The vaccine-induced immunity induced by the H and N genes from wild-type CDV and those from attenuated CDV was comparable. Because these two DNA vaccines were shown to protect equally well against wild-type virus challenge, it is suggested that the genetic/antigenic heterogeneity between vaccine strains and contemporary wild-type strains are unlikely to cause vaccine failure.
引用
收藏
页码:1887 / 1896
页数:10
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