Abstract
Mice carrying the gene Mx were resistant to the lethal action of a hepatotropic line of avian influenza A virus. In resistant animals, foci of liver necrosis were self-limiting, and maximal virus titers reached were much below those in susceptible animals. Resistance could not be abrogated by immunosuppressive treatment with cyclophosphamide, methotrexate, or procarbazine, although such treatment prevented cellular infiltration at sites of virus replication and appeared to delay virus clearance. Silica and thorium dioxide, thought to inhibit macrophage function, likewise failed to abolish resistance. Regenerating liver tissue did not support more extensive virus replication than did intact adult liver.
MeSH Terms
Animals
Antigens, Viral/analysis
Cyclophosphamide/pharmacology
Hepatectomy
Immunosuppression Therapy
Liver/microbiology,pathology
Liver Regeneration
Methotrexate/pharmacology
Mice
Mice, Inbred A
Mice, Inbred C57BL
Mice, Inbred ICR
Mononuclear Phagocyte System/microbiology
Orthomyxoviridae/growth & development,pathogenicity
Orthomyxoviridae Infections/genetics,prevention & control
Procarbazine/pharmacology
Silicon Dioxide/pharmacology
Thorium Dioxide/pharmacology
Chemicals
Antigens, Viral
Procarbazine
Silicon Dioxide
Cyclophosphamide
Thorium Dioxide
Methotrexate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Haller O
Arnheiter H
Lindenmann J
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