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PMID: 2154620 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Epstein-Barr virus (EBV) antigens processed and presented by B cells, B blasts, and macrophages trigger T-cell-mediated inhibition of EBV-induced B-cell transformation.

Journal of virology ·Vol. 64 ·No. 3 ·1990-03-00 ·Pages 1398-401

Bejarano MT, Masucci MG, Morgan A, Morein B, Klein G, Klein E

Abstract

The ability of B cells, B blasts, and macrophages to present Epstein-Barr virion antigens to autologous T cells and trigger their capacity to inhibit Epstein-Barr virus-induced B-cell transformation was tested. Macrophages were as efficient as B cells and B blasts in presenting the virus to T lymphocytes. This function required antigen processing, because it was inhibited by chloroquine treatment and by fixation of the antigen-presenting cells immediately after viral exposure but not 18 h later. T cells exposed to the purified Epstein-Barr virus envelope antigen gp350 coupled to immunostimulating complexes also showed inhibitory function. These results suggest that recognition of processed virion antigens elicits the generation of T-cell-mediated inhibition of Epstein-Barr virus-induced B-cell transformation.

MeSH Terms
Antigens, Viral/immunology B-Lymphocytes/immunology Cells, Cultured Herpesvirus 4, Human/immunology Humans Lymphocyte Activation Macrophages/immunology T-Lymphocytes/immunology Virion/genetics
Chemicals
Antigens, Viral
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bejarano M T
Department of Tumor Biology, Karolinska Institutet, Stockholm, Sweden.
Masucci M G
Morgan A
Morein B
Klein G
Klein E
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1990-03-00
Pages
1398-401
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC249265
Subset
IM
Grants
NCI NIH HHS · 5ROI CA 30264 · United States
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