Abstract
Adult mice resistant to infection with 10(6) plaque-forming units of a virulent strain of herpes simplex virus type 1 were treated with 89Sr to abrogate marrow-dependent cell functions. Treated mice were found to be much more susceptible to the herpes simplex virus type 1 infection than untreated mice. The virus persisted in the visceral tissues of 89Sr-treated mice for 3 or more days postinfection but not in those of untreated mice. The virus also spread to the spinal cords of treated but not untreated mice. A marrow-dependent cell appeared to mediate resistance to herpes simplex virus type 1 by controlling the infection early after inoculation and not allowing the infection spread to the central nervous system.
MeSH Terms
Animals
Antigens, Viral/isolation & purification
Bone Marrow/immunology,pathology
Fluorescent Antibody Technique
Herpes Simplex/genetics,immunology,pathology
Immunity, Innate
Mice
Simplexvirus/immunology,isolation & purification
Spinal Cord/immunology
Strontium Radioisotopes/administration & dosage
Chemicals
Antigens, Viral
Strontium Radioisotopes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lopez C
Ryshke R
Bennett M
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20 references, click to expand
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