Epstein-Barr virus (EBV) is associated with two human tumors, Burkitt's lymphoma and nasopharyngeal carcinoma. In addition, reactivation of EBV infection in immunodeficient patients leads to a fatal lymphoproliferative disease. In vitro infection of B lymphocytes with EBV leads to a T-cell independent polyclonal activation and transformation of a smaller fraction of the infected cells. Although the molecular events underlying the processes of infection, transformation, and polyclonal activation are still unknown, the first step involves the interaction of the virus with a specific receptor in the cell membrane. Our long-term goal is to understand the effects of viral binding on subsequent cellular events. In pursuit of this, we have been developing methods for the isolation of the EBV binding component (EBVR) found on Raji human lymphoblastoid cells. We have extracted and partially purified the EBVR from Raji cells and an antibody specific for the receptor. We have significantly improved the purity of EBV virion preparations and have characterized the virion-associated protein kinase. We are continuing our purification of the EBVR using its affinity for the EBV membrane antigen and are using available monoclonal antibodies to CR?2? to determine the relationship between the two receptors. We have initiated studies to identify viral promoters utilized during superinfection of Raji cells and to investigate the contol of viral gene transcriptin. The data obtained should help to elucidate the role of the EBVR in viral infection, transformation, and triggering cells to immunoglobulin production. (MI)
| Fowler, E; Raab-Traub, N; Hester, S (1985) Purification of biologically active Epstein-Barr virus by affinity chromatography and non-ionic density gradient centrifugation. J Virol Methods 11:59-74 |
