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Divergent immune responses and disease outcomes in piglets immunized with inactivated and attenuated H3N2 swine influenza vaccines in the presence of maternally-derived antibodies
- Source :
- Virology. :45-54
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- 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.
- Subjects :
- Male
Swine
Cross Protection
T-Lymphocytes
T cell
Whole inactivated virus
Heterologous
Influenza A
Antibodies, Viral
Virus
Heterologous immunity
Immune system
Orthomyxoviridae Infections
Immunity
Virology
medicine
Live attenuated influenza virus
Animals
Live attenuated influenza vaccine
Swine Diseases
Maternally derived antibodies
biology
Influenza A Virus, H3N2 Subtype
Vaccination
medicine.anatomical_structure
Influenza Vaccines
Immunology
biology.protein
Female
Immunization
Antibody
Immunity, Maternally-Acquired
Subjects
Details
- ISSN :
- 00426822
- Database :
- OpenAIRE
- Journal :
- Virology
- Accession number :
- edsair.doi.dedup.....28f81d4674c0a66f3bec7132749aa913