Abstract |
Protection against influenza A virus infection in mice immunized with recombinant nucleoprotein (rNP) was studied. Nucleoprotein-immune mice were protected against a lethal challenge with A/Puerto Rico/8/34 (A/PR8) virus but showed considerable morbidity before recovery. Local boosting of the immune system with rNP by intranasal immunization improved the protection in NP-immune mice, and the decrease in morbidity after infection was reflected in accelerated clearance of virus from lungs. However, immune, boosted mice also rapidly cleared an antigenically unrelated influenza B virus from their lungs. Mice immunized with rNP precipitated with alhydrogel, that subsequently developed significant resistance to virus infection, failed to generate detectable levels of class I major histocompatibility complex (MHC)-restricted killer cells. Furthermore, B10.A(5R) mice that are non-responders for NP-specific class I killer cells could also be protected by immunization with rNP. In contrast, rNP-immunized mice developed strong proliferative T-cell responses to rNP. These data argue for an important role for helper T cells rather than virus-specific class I cytotoxic T cells in protection against influenza virus infection induced by rNP.
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Authors | J P Tite, C Hughes-Jenkins, D O'Callaghan, G Dougan, S M Russell, X M Gao, F Y Liew |
Journal | Immunology
(Immunology)
Vol. 71
Issue 2
Pg. 202-7
(Oct 1990)
ISSN: 0019-2805 [Print] England |
PMID | 2172156
(Publication Type: Journal Article)
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Chemical References |
- Antigens, Viral
- Influenza Vaccines
- Nucleoproteins
- Recombinant Proteins
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Topics |
- Animals
- Antigens, Viral
(immunology)
- Influenza A virus
(immunology)
- Influenza Vaccines
(immunology)
- Mice
- Mice, Inbred BALB C
- Mice, Inbred Strains
- Nucleoproteins
(immunology)
- Orthomyxoviridae Infections
(immunology, prevention & control)
- Recombinant Proteins
(immunology)
- T-Lymphocytes, Cytotoxic
(immunology)
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