Abstract
Viremia was produced by inoculating intravenously BALB/c mice with murine cytomegalovirus. Virus was detected in plasma and granulocytes only during the first 8 days after infection. Lymphocyte-associated viremia, detectable by cocultivation on syngeneic or allogeneic fibroblasts, persisted for at least 4 weeks. Eight to 10 days after infection, sonicated lymphocytes had no demonstrable free virus. When whole lymphocytes with no demonstrable free virus were enclosed in a Millipore chamber and placed on a fibroblastic feeder layer, T cells produced free virus but B cells did not. Compared to normal calf serum, specific hyperimmune serum reduced B cell-associated infectious centers by 74% and T cell-associated infectious centers by only 38%. Normal mouse sera reduced by 36% and 30% infectious center production by B cells and T cells, respectively. Lymphocytes enriched with Fc receptor-positive cells produced significantly more infectious centers than receptor-negative cells.
MeSH Terms
Animals
Antibodies, Viral/biosynthesis
B-Lymphocytes/microbiology
Cytomegalovirus/growth & development,immunology
Cytomegalovirus Infections/blood,immunology
Cytopathogenic Effect, Viral
Female
Immune Sera
Kinetics
Male
Mice
Mitogens/pharmacology
T-Lymphocytes/microbiology
Chemicals
Antibodies, Viral
Immune Sera
Mitogens
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wu B C
Ho M
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