Divergent immune responses and disease outcomes in piglets immunized with inactivated and attenuated H3N2 swine influenza vaccines in the presence of maternally-derived antibodies

被引:35
作者
Sandbulte, Matthew R. [1 ]
Platt, Ratree [1 ]
Roth, James A. [1 ]
Henningson, Jamie N. [2 ]
Gibson, Kathleen A. [3 ]
Rajao, Daniela S. [3 ]
Loving, Crystal L. [3 ]
Vincent, Amy L. [3 ]
机构
[1] Iowa State Univ, Dept Vet Microbiol & Prevent Med, Ames, IA USA
[2] Kansas State Univ, Dept Diagnost Med Pathobiol, Manhattan, KS 66506 USA
[3] USDA ARS, Virus & Prion Res Unit, Natl Anim Dis Ctr, Ames, IA 50010 USA
关键词
Influenza A; Maternally derived antibodies; Live attenuated influenza virus; Whole inactivated virus; Heterologous immunity; PORCINE T-LYMPHOCYTES; VIRUS VACCINE; PROTECTIVE IMMUNITY; A VIRUS; PIGS; LIVE; EFFICACY; CHALLENGE; INFECTION; CELLS;
D O I
10.1016/j.virol.2014.06.027
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Live-attenuated influenza virus (LAIV) prime-boost vaccination previously conferred protection against heterologous H3N2 swine influenza challenge, including in piglets with maternally derived antibodies (MDA). Conversely, a whole-inactivated virus (WIV) vaccine was associated with enhanced disease. This study was aimed at identifying immune correlates of cross-protection. Piglets with and without MDA received intramuscular adjuvanted WIV or intranasal LAIV, and were challenged with heterologous H3N2. WIV induced cross-reactive IgG, inhibited by MDA, and a moderate T cell response. LAIV elicited mucosal antibodies and T cells cross-reactive to the heterologous challenge strain. The presence of MDA at LAIV vaccination blocked lung and nasal antibody production, but did not interfere with T cell priming. Even without mucosal antibodies, MDA-positive LAIV vaccinates were protected, indicating a likely role for T cells. Based on the data, one LAIV dose can induce cell-mediated immunity against antigenically divergent H3N2 influenza virus despite passive antibody interference with humoral immune responses. Published by Elsevier Inc.
引用
收藏
页码:45 / 54
页数:10
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