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PMID: 4377001 Published · ppublish English Journal Article

Observations on the type of infection by Epstein-Barr virus in peripheral lymphoid cells of patients with infectious mononucleosis.

International journal of cancer ·Vol. 14 ·No. 6 ·1974-12-15 ·Pages 704-15

Rickinson AB, Jarvis JE, Crawford DH, Epstein MA

Abstract

Transformation to continuous cell lines has been studied in cultures of peripheral leuckocytes from infectious mononucleosis (IM) patients and in co-cultures of IM leukocytes and foetal cord blood leukocytes of opposite sex. The transformed cells in the co-cultures were of mixed origin with foetal cells usually predominating. Neutralizing antisera to EB virus markedly reduced or abolished the incidence of transformation in IM leukocyte cultures. This effect was not due to cytotoxicity and followed the pattern seen with cultures where transformation was known to depend on the inter-cellular transfer of infectious EB virus. The findings suggest that EB virus is harboured in peripheral lymphocytes of IM patients as a non-productive unexpressed infection which is activated to produce virus in vitro, the particles released then infecting neighbouring cells to give transformed lines. The differences between this mechanism and the one whereby lines arise in culture from malignant cells of Burkitt's lymphoma are considered, and their significance is discussed.

MeSH Terms
Blood Cell Line Cell Transformation, Neoplastic Cells, Cultured Culture Media Female Fetus Herpesvirus 4, Human Humans Immune Sera Infectious Mononucleosis/pathology Lymphocyte Activation Lymphocytes/radiation effects,ultrastructure Male Radiation Effects Sex Chromosomes Time Factors Umbilical Cord
Chemicals
Culture Media Immune Sera
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rickinson A B
Jarvis J E
Crawford D H
Epstein M A
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1974-12-15
Pages
704-15
Language
English
Region
United States
NLM ID
0042124
Subset
IM
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