Co-expressing GP5 and M proteins under different promoters in recombinant modified vaccinia virus ankara (rMVA)-based vaccine vector enhanced the humoral and cellular immune responses of porcine reproductive and respiratory syndrome virus (PRRSV).

Zheng, Qisheng

Co-expressing GP5 and M proteins under different promoters in recombinant modified vaccinia virus ankara (rMVA)-based vaccine vector enhanced the humoral and cellular immune responses of porcine reproductive and respiratory syndrome virus (PRRSV). [electronic resource] - Virus genes Dec 2007 - 585-95 p. digital

Publication Type: Journal Article

0920-8569

10.1007/s11262-007-0161-5 doi


Animals
Antibodies, Viral--blood
Genetic Vectors
Immunization, Secondary
Interferon-gamma--biosynthesis
Interleukin-2--biosynthesis
Interleukin-4--biosynthesis
Mice
Mice, Inbred BALB C
Neutralization Tests
Porcine Reproductive and Respiratory Syndrome--immunology
Porcine respiratory and reproductive syndrome virus--genetics
Promoter Regions, Genetic
Recombinant Fusion Proteins--biosynthesis
Recombinant Proteins--biosynthesis
Spleen--immunology
T-Lymphocytes--immunology
Vaccines, Synthetic--immunology
Vaccinia virus--genetics
Viral Envelope Proteins--genetics
Viral Matrix Proteins--genetics
Viral Vaccines--immunology