Vaccine-Induced Antibody Responses Prevent the Induction of Interferon Type I Responses Upon a Homotypic Live Virus Challenge

被引:3
作者
Chan, J. [1 ]
Babb, R. [1 ]
David, S. C. [1 ]
McColl, S. R. [1 ]
Alsharifi, M. [1 ]
机构
[1] Univ Adelaide, Sch Biol Sci, Vaccine Res Grp, Ctr Mol Pathol, Adelaide, SA 5005, Australia
关键词
INFLUENZA-A VIRUS; DENDRITIC CELLS; VIRAL-INFECTION; M2; PROTEIN; ADJUVANT; IFN; ACTIVATION; IMMUNITY; MICE; HEMAGGLUTININS;
D O I
10.1111/sji.12410
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During acute viral infections, innate immunity provides essential protective measures to minimize virus dissemination and regulate adaptive immunity. This helps to successfully eliminate the pathogen and establish long-term memory. Here, we investigated the effect of vaccine-induced antibody responses on the induction of IFN-I responses and the associated lymphocyte activation using influenza A virus vaccination and challenge models. Mice were vaccinated with gamma-irradiated influenza A virus (-FLU) and challenged three weeks later with live virus. Our data show a significant reduction in IFN-I responses and lymphocyte activation following a homotypic virus challenge. We confirmed the role of vaccine-induced antibody responses in the observed impairment of IFN-I and the associated lymphocyte activation using adoptive transfer of immune sera and the administration of sera-treated viruses prior to challenge. Overall, we addressed a fundamental concept in immunology and provided experimental data illustrating the inhibition of IFN-I responses in vaccinated animals upon a homotypic virus challenge.
引用
收藏
页码:165 / 173
页数:9
相关论文
共 34 条
[1]   Type I Interferons trigger systemic, partial lymphocyte activation in response to viral infection [J].
Alsharifi, M ;
Lobigs, M ;
Regner, M ;
Lee, E ;
Koskinen, A ;
Müllbacher, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (07) :4635-4640
[2]   Interferon type I responses in primary and secondary infections [J].
Alsharifi, Mohammed ;
Muellbacher, Arno ;
Regner, Matthias .
IMMUNOLOGY AND CELL BIOLOGY, 2008, 86 (03) :239-245
[3]   Exhaustion of type I interferon response following an acute viral infection [J].
Alsharifi, Mohammed ;
Regner, Matthias ;
Blanden, Robert ;
Lobigs, Mario ;
Lee, Eva ;
Koskinen, Aulikki ;
Mullbacher, Arno .
JOURNAL OF IMMUNOLOGY, 2006, 177 (05) :3235-3241
[4]   The γ-irradiated influenza vaccine and the prospect of producing safe vaccines in general [J].
Alsharifi, Mohammed ;
Muellbacher, Arno .
IMMUNOLOGY AND CELL BIOLOGY, 2010, 88 (02) :103-104
[5]   Intranasal Flu Vaccine Protective against Seasonal and H5N1 Avian Influenza Infections [J].
Alsharifi, Mohammed ;
Furuya, Yoichi ;
Bowden, Timothy R. ;
Lobigs, Mario ;
Koskinen, Aulikki ;
Regner, Matthias ;
Trinidad, Lee ;
Boyle, David B. ;
Muellbacher, Arno .
PLOS ONE, 2009, 4 (04)
[6]   Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology [J].
Asselin-Paturel, C ;
Boonstra, A ;
Dalod, M ;
Durand, I ;
Yessaad, N ;
Dezutter-Dambuyant, C ;
Vicari, A ;
O'Garra, A ;
Biron, C ;
Brière, F ;
Trinchieri, G .
NATURE IMMUNOLOGY, 2001, 2 (12) :1144-1150
[7]   Gamma-irradiated influenza A virus provides adjuvant activity to a co-administered poorly immunogenic SFV vaccine in mice [J].
Babb, Rachelle ;
Chan, Jennifer ;
Khairat, Jasmine E. ;
Furuya, Yoichi ;
Alsharifil, Mohammed .
FRONTIERS IN IMMUNOLOGY, 2014, 5 :1-1
[8]   Type I IFN is a powerful mucosal adjuvant for a selective intranasal vaccination against influenza virus in mice and affects antigen capture at mucosal level [J].
Bracci, L ;
Canini, I ;
Puzelli, S ;
Sestili, P ;
Venditti, M ;
Spada, M ;
Donatelli, I ;
Belardelli, F ;
Proietti, E .
VACCINE, 2005, 23 (23) :2994-3004
[9]   IFN-α/β enhances BCR-dependent B cell responses [J].
Braun, D ;
Caramalho, I ;
Demengeot, J .
INTERNATIONAL IMMUNOLOGY, 2002, 14 (04) :411-419
[10]   DEVELOPMENT OF SUBTYPE-SPECIFIC AND HETEROSUBTYPIC ANTIBODIES TO THE INFLUENZA-A VIRUS HEMAGGLUTININ AFTER PRIMARY INFECTION IN CHILDREN [J].
BURLINGTON, DB ;
WRIGHT, PF ;
VANWYKE, KL ;
PHELAN, MA ;
MAYNER, RE ;
MURPHY, BR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 21 (05) :847-849