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Epstein-Barr Virus (EBV)-Induced B-Cell Proliferative Disorder after Chemotherapy in a Patient with Hemophagocytic Lymphohistiocytosis with Associated EBV-Induced T-cell Proliferation

We report a case of Epstein-Barr virus (EBV)-associated lymphoproliferative disorder (LPD) which developed after chemotherapy for hemophagocytic lymphohistiocytosis (HLH), who had no history of immunodeficiency or familial X-linked LPD. In HLH, the presence of EBV in T-cells was confirmed by a combi...

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Bibliographic Details
Published in:Leukemia & lymphoma 2000-05, Vol.37 (5-6), p.593-604
Main Authors: Suzumiya, Junji, Ohshima, Koichi, Kanda, Motonobu, Kumagawa, Midori, Nagano, Mitsuyuki, Hirata, Masayuki, Nawa, Yukifumi, Tamura, Kazuo, Kikuchi, Masahiro
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Language:English
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Summary:We report a case of Epstein-Barr virus (EBV)-associated lymphoproliferative disorder (LPD) which developed after chemotherapy for hemophagocytic lymphohistiocytosis (HLH), who had no history of immunodeficiency or familial X-linked LPD. In HLH, the presence of EBV in T-cells was confirmed by a combination of in situ hybridization (ISH) and immunostaining. Southern blot analysis using EBV-TR and immunoglobulin JH probes revealed oligoclonal proliferation of B-cells in each organ involved by abnormal B-lymphoid cells at autopsy. Combined ISH and immunostaining disclosed the presence of EBV in proliferating B-cells. Cytokine analysis during the period of T-cell activation in HLH revealed marked elevation of interferon (IFN) m¨, interleukin (IL)-10 and soluble IL-2 receptor (sIL-2R) and mild to moderate increases of tumor necrosis factor (TNF)-α were observed, while IFNm , IL-10 and sIL-2R were elevated initially during the HLH phase, which then decreased as LPD developed and B-cell proliferation predominated. Immunosuppressive chemotherapy for HLH may then have allowed latent EBV in B lymphocytes to induce transformation and oligoclonal proliferation of B-cells, finally resulting in LPD. Mechanisms of EBV-induced cell proliferation remain unclear, but alteration of various cytokines may be responsible for it.
ISSN:1042-8194
1029-2403
DOI:10.3109/10428190009058512