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Contribution of the Microenvironment to the Pathogenesis of EBV-Positive Hodgkin and Nasal NK/T-cell Lymphomas

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Innate and Adaptive Immunity in the Tumor Microenvironment

Part of the book series: The Tumor Microenvironment ((TTME,volume 1))

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Depending on the differentiation and maturation of the EBV- carrying cell the virally encoded proteins can be expressed in various assortments. The expression of these proteins determines the fate of the EBV-harboring cell. Expression of the six nuclear and three membrane-associated EBV-encoded proteins, designated Type III latency, induces cell proliferation. This occurs only in B lymphocytes. In spite of the transforming capacity of EBV, humans are virus carriers without the emergence of B-cell malignancy, because the immune system recognizes and eliminates the cells which express the growth-promoting proteins. However, immunosuppressed individuals have a high risk for EBV-induced B-cell malignancies.

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Klein, E., Takahara, M., Kis, L.L. (2008). Contribution of the Microenvironment to the Pathogenesis of EBV-Positive Hodgkin and Nasal NK/T-cell Lymphomas. In: Yefenof, E. (eds) Innate and Adaptive Immunity in the Tumor Microenvironment. The Tumor Microenvironment, vol 1. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6750-1_10

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