The antigens of the Egypt virus have been detected by means of the fluorescent antibody technique in the neurons of the brain and spinal cord, in both sensory and motor areas, of infected mice. The antigens have also been observed in infected human epidermoid carcinoma cells in culture. In both cases the antigens occurred in the cytoplasm of the cells exclusively. In the early stages of infection the antigen was localized about the nucleus of the human cultured cells. In some cases the staining of the antigens produced a sponge-like effect, probably because of the numerous vacuoles of lipid material. The antigens were observed in the protoplasmic connections between cells and they probably served as a main route of spread of the agent in these human cell cultures. The number of cells initially infected and showing antigen was proportional to the amount of virus added, and titration with one substrain of cells proved much more sensitive than intracerebral titration in the mouse.
Skip Nav Destination
Article navigation
1 September 1955
Article|
September 01 1955
VISUALIZATION OF EGYPT 101 VIRUS IN THE MOUSE'S BRAIN AND IN CULTURED HUMAN CARCINOMA CELLS BY MEANS OF FLUORESCENT ANTIBODY
Wilbur Fiske Noyes
Wilbur Fiske Noyes
From the Virus Section, the Sloan-Kettering Institute for Cancer Research, New York
Search for other works by this author on:
Wilbur Fiske Noyes
From the Virus Section, the Sloan-Kettering Institute for Cancer Research, New York
Received:
March 14 1955
Online ISSN: 1540-9538
Print ISSN: 0022-1007
Copyright, 1955, by The Rockefeller Institute for Medical Research New York
1955
J Exp Med (1955) 102 (3): 243–248.
Article history
Received:
March 14 1955
Citation
Wilbur Fiske Noyes; VISUALIZATION OF EGYPT 101 VIRUS IN THE MOUSE'S BRAIN AND IN CULTURED HUMAN CARCINOMA CELLS BY MEANS OF FLUORESCENT ANTIBODY . J Exp Med 1 September 1955; 102 (3): 243–248. doi: https://doi.org/10.1084/jem.102.3.243
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement