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Sequential monitoring of serum IL-6, TNF-α, and IFN-γ levels in a CAEBV patient treated by plasma exchange and immunochemotherapy

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An Erratum to this article was published on 08 January 2013

Abstract

We report the case of a female patient with chronic active Epstein–Barr virus infection (CAEBV) accompanied by hemophagocytic syndrome (HPS). On admission, she presented with severe liver dysfunction and disseminated intravascular coagulation with elevation of serum IL-6, TNF-α, and IFN-γ levels. Plasma exchange (PE) followed by immunochemotherapy with prednisolone, cyclosporine A, and VP16 was performed. PE decreased serum cytokine levels dramatically and improved liver function. Following immunochemotherapy, CAEBV became inactive. Four months after discharge, however, CAEBV relapsed with HPS, and serum cytokine levels were extremely elevated again. There was no response to immunochemotherapy, and the patient died 1 day after admission. We examined the cytokines in five additional untreated-CAEBV patients and determined that they were elevated above the normal level in all patients. These results suggest that inflammatory cytokines may have roles in the development of CAEBV, and that their depletion can be an effective treatment for this disease.

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References

  1. Kawa K. Epstein–Barr virus-associated diseases in humans. Int J Hematol. 2000;71:108–17.

    PubMed  CAS  Google Scholar 

  2. Quintanilla-Martinez L, Kimura H, Jaffe ES. EBV-positive T-cell lymphoproliferative disorders of childhood. In: Jaffe E, Harris N, Stein H, Vardiman JW, editors. World Health Organization classification of tumors pathology and genetics of tumours of haematopoietic and lymphoid tissues. Lyon: IARC Press; 2008. p. 278–80.

  3. Kimura H. Pathogenesis of chronic active Epstein–Barr virus infection: is this an infectious disease, lymphoproliferative disorder, or immunodeficiency? Rev Med Virol. 2006;16:251–61.

    Article  PubMed  Google Scholar 

  4. Lay JD, Tsao CJ, Chen JY, et al. Upregulation of tumor necrosis factor-alpha gene by Epstein–Barr virus and activation of macrophages in Epstein–Barr virus-infected T cells in the pathogenesis of hemophagocytic syndrome. J Clin Invest. 1997;100:1969–79.

    Article  PubMed  CAS  Google Scholar 

  5. Sato S, Kawashima H, Oshiro H, et al. Virological and immunological characteristics of a 19-year-old Japanese female with fatal outcome with Epstein–Barr virus-associated hemophagocytic syndrome. J Clin Virol. 2004;31:235–8.

    Article  PubMed  Google Scholar 

  6. Cohen JI, Jaffe ES, Dale JK, et al. Characterization and treatment of chronic active Epstein–Barr virus disease: a 28-year experience in the United States. Blood. 2011;117:5835–49.

    Article  PubMed  CAS  Google Scholar 

  7. Imadome K, Shimizu N, Arai A, et al. Coexpression of CD40 and CD40 ligand in Epstein–Barr virus-infected T and NK cells and their role in cell survival. J Infect Dis. 2005;192:1340–8.

    Article  PubMed  CAS  Google Scholar 

  8. Okano M, Kawa K, Kimura H, et al. Proposed guidelines for diagnosing chronic active Epstein–Barr virus infection. Am J Hematol. 2005;80:64–9.

    Article  PubMed  Google Scholar 

  9. Henter JI, Horne A, Aricó M, et al. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer. 2007;48:124–31.

    Article  PubMed  Google Scholar 

  10. Koyama M, Takeshita Y, Sakata A, et al. Cytotoxic chemotherapy successfully induces durable complete remission in 2 patients with mosquito allergy resulting from Epstein–Barr virus-associated T-/natural killer cell lymphoproliferative disease. Int J Hematol. 2005;82:437–40.

    Article  PubMed  CAS  Google Scholar 

  11. Imadome K, Yajima M, Arai A, et al. Novel mouse xenograft models reveal a critical role of CD4 T cells in the proliferation of EBV-infected T and NK cells. PLoS Pathog. 2011;7:e1002326.

    Article  PubMed  CAS  Google Scholar 

  12. Ogawa J, Koike R, Sugihara T, et al. An autopsied case of chronic active Epstein–Barr virus infection complicated in systemic lupus erythematosus and antiphospholipid antibody syndrome. Nihon Rinsho Meneki Gakkai Kaishi. 2002;25:458–65.

    Article  PubMed  Google Scholar 

  13. Young KH, Zhang D, Malik JT, et al. Fulminant EBV-driven CD8 T-cell lymphoproliferative disorder following primary acute EBV infection: a unique spectrum of T-cell malignancy. Int J Clin Exp Pathol. 2008;1:185–97.

    PubMed  Google Scholar 

  14. Tokuhira M, Hanzawa K, Watanabe R, et al. Co-existence of acute myeloid leukemia with multilineage dysplasia and Epstein–Barr virus-associated T-cell lymphoproliferative disorder in a patient with rheumatoid arthritis: a case report. J Hematol Oncol. 2009;2:27.

    Article  PubMed  Google Scholar 

  15. Arai A, Imadome K, Watanabe Y, et al. Clinical features of adult-onset chronic active Epstein–Barr virus infection: a retrospective analysis. Int J Hematol. 2011;93:602–9.

    Article  PubMed  Google Scholar 

  16. Kimura H, Morita M, Yabuta Y, et al. Quantitative analysis of Epstein–Barr virus load by using a real-time PCR assay. J Clin Microbiol. 1999;37:132–6.

    PubMed  CAS  Google Scholar 

  17. Roncella S, Cutrona G, Truini M, et al. Late Epstein–Barr virus infection of a hepatosplenic gamma delta T-cell lymphoma arising in a kidney transplant recipient. Haematologica. 2000;85:256–62.

    PubMed  CAS  Google Scholar 

  18. Kanno H, Watabe D, Shimizu N, et al. Adhesion of Epstein–Barr virus-positive natural killer cell lines to cultured endothelial cells stimulated with inflammatory cytokines. Clin Exp Immunol. 2008;151:519–27.

    Article  PubMed  CAS  Google Scholar 

  19. Kawa K, Sawada A, Sato M, et al. Excellent outcome of allogeneic hematopoietic SCT with reduced-intensity conditioning for the treatment of chronic active EBV infection. Bone Marrow Transpl. 2011;46:77–83.

    Article  CAS  Google Scholar 

  20. Henzan T, Nagafuji K, Tsukamoto H, et al. Success with infliximab in treating refractory hemophagocytic lymphohistiocytosis. Am J Hematol. 2006;81:59–61.

    Article  PubMed  Google Scholar 

  21. Kikuchi H, Yamamoto T, Asako K, et al. Etanercept for the treatment of intractable hemophagocytic syndrome with systemic lupus erythematosus. Mod Rheumatol 2011;22:308–11.

    Google Scholar 

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Acknowledgments

This study was supported by a grant from Ministry of Health, Labor and Welfare of Japan (H24-Nanchi-046) and a grant from Ministry of Education, Culture, Sports, Science, and Technology of Japan (23591375). The ethics committee of Tokyo Medical and Dental University Hospital approved this study, and written informed consent was obtained from the patient.

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Correspondence to Ayako Arai.

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Arai, A., Nogami, A., Imadome, KI. et al. Sequential monitoring of serum IL-6, TNF-α, and IFN-γ levels in a CAEBV patient treated by plasma exchange and immunochemotherapy. Int J Hematol 96, 669–673 (2012). https://doi.org/10.1007/s12185-012-1170-2

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  • DOI: https://doi.org/10.1007/s12185-012-1170-2

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