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Published online 20 March 2006 doi:10.1084/jem.20051287
Rockefeller University Press, 0022-1007 $8.00
JEM, Volume 203, Number 4, 995-1006
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ARTICLE

Control of Epstein-Barr virus infection in vitro by T helper cells specific for virion glycoproteins

Dinesh Adhikary1,2, Uta Behrends1,2, Andreas Moosmann3,4, Klaus Witter5, Georg W. Bornkamm1, and Josef Mautner1,2

1 Clinical Cooperation Group, Institute for Clinical and Molecular Biology, GSF-National Research Center for Environment and Health and 2 Children's Hospital, Hematology-Oncology, Technical University Munich, 80804 Munich, Germany
3 Clinical Cooperation Group Molecular Oncology, Department of Gene Vectors, GSF-National Research Center for Environment and Health, 4 Department of Otorhinolaryngology, and 5 Laboratory of Immunogenetics, Ludwig Maximilians University, 81377 Munich, Germany

CORRESPONDENCE Josef Mautner: mautner{at}gsf.de

Epstein-Barr virus (EBV) establishes lifelong persistent infections in humans by latently infecting B cells, with occasional cycles of reactivation, virus production, and reinfection. Protective immunity against EBV is mediated by T cells, but the role of EBV-specific T helper (Th) cells is still poorly defined. Here, we study the Th response to the EBV lytic cycle proteins BLLF1 (gp350/220), BALF4 (gp110), and BZLF1 and show that glycoprotein-specific Th cells recognize EBV-positive cells directly; surprisingly, a much higher percentage of target cells than those expressing lytic cycle proteins were recognized. Antigen is efficiently transferred to bystander B cells by receptor-mediated uptake of released virions, resulting in recognition of target cells incubated with <1 virion/cell. T cell recognition does not require productive infection and occurs early after virus entry before latency is established. Glycoprotein-specific Th cells are cytolytic and inhibit proliferation of lymphoblastoid cell lines (LCL) and the outgrowth of LCL after infection of primary B cells with EBV. These results establish a novel role for glycoprotein-specific Th cells in the control of EBV infection and identify virion proteins as important immune targets. These findings have implications for the treatment of diseases associated with EBV and potentially other coated viruses infecting MHC class II–positive cells.


Abbreviations used: BL, Burkitt's lymphoma; EBV, Epstein-Barr virus; geq, genome equivalent; LCL, EBV-immortalized lymphoblastoid B cell lines; miniLCL, miniEBV LCL; PTLD, posttransplant lymphoproliferative disorder.


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