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Published in: Pediatric Cardiology 3/2009

01-04-2009 | Original Article

Cardiovascular Complications Associated with Chronic Active Epstein–Barr Virus Infection

Authors: Jun Muneuchi, Shouichi Ohga, Masataka Ishimura, Kazuyuki Ikeda, Kenichiro Yamaguchi, Akihiko Nomura, Hidetoshi Takada, Yasunobu Abe, Toshiro Hara

Published in: Pediatric Cardiology | Issue 3/2009

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Abstract

This study aimed to assess the outcome of cardiovascular diseases for patients with chronic active Epstein–Barr virus infection (CAEBV). The study enrolled 15 patients (7 boys and 8 girls) who fulfilled the diagnostic criteria for CAEBV, including 10 patients with T-cell type and 3 patients with natural killer (NK)-cell type. The median age at the CAEBV onset was 6.3 years (range, 1.2–17.8 years). Regular cardiologic studies were performed during the median follow-up period of 8 years (range, 2–20 years). Nine patients (60%) had cardiac diseases including coronary artery lesion (CAL) (n = 4, 44%), decreased left ventricular ejection fraction and pericardial effusion in (n = 3, 33%), complete atrioventricular block (n = 1), and sudden arrest (n = 1). The frequency of fever (78%, p = 0.04) or cytopenias (100%, p = 0.01), as the major symptom among patients with cardiac complications, was higher than among those without complications. The median time from disease onset to detection of CAL was 3.4 years (range, 1.8–8.6 years). The mean z-score increased to 3.98. Seven patients (78%) with cardiac complications died of disease progression, hematopoietic stem cell transplantation–related events, or both. In two patients, CAL regressed after allogeneic cord blood transplantation. Among CAEBV patients, CAL was the most common cardiac complication and could not be controlled without the eradication of EBV-infected T- and NK-cells.
Literature
1.
go back to reference Brown TJ, Crawford SE, Cornwall ML, Garcia F, Shulman ST, Rowley AH (2001) CD8 T lymphocytes and macrophages infiltrate coronary artery aneurysms in acute Kawasaki disease. J Infect Dis 184:940–943PubMedCrossRef Brown TJ, Crawford SE, Cornwall ML, Garcia F, Shulman ST, Rowley AH (2001) CD8 T lymphocytes and macrophages infiltrate coronary artery aneurysms in acute Kawasaki disease. J Infect Dis 184:940–943PubMedCrossRef
3.
go back to reference Chuang HC, Lay JD, Chuang SE et al (2007) Epstein–Barr virus (EBV) latent membrane protein-1 downregulates tumor necrosis factor-alpha (TNF-alpha) receptor-1 and confers resistance to TNF-alpha-induced apoptosis in T-cells: implication for the progression to T-cell lymphoma in EBV-associated hemophagocytic syndrome. Am J Pathol 170:1607–1617PubMedCrossRef Chuang HC, Lay JD, Chuang SE et al (2007) Epstein–Barr virus (EBV) latent membrane protein-1 downregulates tumor necrosis factor-alpha (TNF-alpha) receptor-1 and confers resistance to TNF-alpha-induced apoptosis in T-cells: implication for the progression to T-cell lymphoma in EBV-associated hemophagocytic syndrome. Am J Pathol 170:1607–1617PubMedCrossRef
4.
go back to reference Culora GA, Moore IE (1997) Kawasaki disease, Epstein–Barr virus, and coronary artery aneurysms. J Clin Pathol 50:161–163PubMedCrossRef Culora GA, Moore IE (1997) Kawasaki disease, Epstein–Barr virus, and coronary artery aneurysms. J Clin Pathol 50:161–163PubMedCrossRef
5.
go back to reference De Zorzi A, Colan SD, Gauvreau K et al (1998) Coronary artery dimensions may be misclassified as normal in Kawasaki disease. J Pediatr 133:254–258PubMedCrossRef De Zorzi A, Colan SD, Gauvreau K et al (1998) Coronary artery dimensions may be misclassified as normal in Kawasaki disease. J Pediatr 133:254–258PubMedCrossRef
6.
go back to reference Fujiwara M, Shimozono H, Ono H et al (2003) Polyclonal proliferation of lymphocytes containing the Epstein–Barr virus genome in a patient dying of myocarditis in chronic active Epstein–Barr virus infection. J Pediatr Hematol Oncol 25:85–88PubMedCrossRef Fujiwara M, Shimozono H, Ono H et al (2003) Polyclonal proliferation of lymphocytes containing the Epstein–Barr virus genome in a patient dying of myocarditis in chronic active Epstein–Barr virus infection. J Pediatr Hematol Oncol 25:85–88PubMedCrossRef
7.
go back to reference Gallot G, Hamidou MA, Clémenceau B et al (2006) T-cell repertoire and Epstein–Barr virus-specific T-cell response in chronic active Epstein–Barr virus infection: a case study. Clin Immunol 119:79–86PubMedCrossRef Gallot G, Hamidou MA, Clémenceau B et al (2006) T-cell repertoire and Epstein–Barr virus-specific T-cell response in chronic active Epstein–Barr virus infection: a case study. Clin Immunol 119:79–86PubMedCrossRef
8.
go back to reference Hauptmann S, Meru N, Schewe C et al (2001) Fatal atypical T-cell proliferation associated with Epstein–Barr virus infection. Br J Haematol 112:377–380PubMedCrossRef Hauptmann S, Meru N, Schewe C et al (2001) Fatal atypical T-cell proliferation associated with Epstein–Barr virus infection. Br J Haematol 112:377–380PubMedCrossRef
9.
go back to reference Ishimura M, Ohga S, Nomura A et al (2005) Successful umbilical cord blood transplantation for severe chronic Epstein–Barr virus infection after the double failure of hematopoietic stem cell transplantation. Am J Hemtol 80:207–212CrossRef Ishimura M, Ohga S, Nomura A et al (2005) Successful umbilical cord blood transplantation for severe chronic Epstein–Barr virus infection after the double failure of hematopoietic stem cell transplantation. Am J Hemtol 80:207–212CrossRef
10.
go back to reference Iwatsuki K, Satoh M, Yamamoto T et al (2006) Pathogenic link between hydroa vacciniforme and Epstein–Barr virus–associated hematologic disorders. Arch Dermatol 142:587–595PubMedCrossRef Iwatsuki K, Satoh M, Yamamoto T et al (2006) Pathogenic link between hydroa vacciniforme and Epstein–Barr virus–associated hematologic disorders. Arch Dermatol 142:587–595PubMedCrossRef
11.
go back to reference Jeanette JC (2006) Implication for pathogenesis of patterns of injury in small- and medium-sized vessel vasculitis. Cleveland Clin J Med 69:SII-33–SII-38 Jeanette JC (2006) Implication for pathogenesis of patterns of injury in small- and medium-sized vessel vasculitis. Cleveland Clin J Med 69:SII-33–SII-38
12.
go back to reference Kanamaru H, Sato Y, Takayama T et al (2005) Assessment of coronary artery abnormalities by multislice spiral computed tomography in adolescents and young adults with Kawasaki disease. Am J Cardiol 95:522–525PubMedCrossRef Kanamaru H, Sato Y, Takayama T et al (2005) Assessment of coronary artery abnormalities by multislice spiral computed tomography in adolescents and young adults with Kawasaki disease. Am J Cardiol 95:522–525PubMedCrossRef
13.
go back to reference Kanno H, Onodera H, Endo M et al (2005) Vascular lesion in a patient of chronic active Epstein–Barr virus infection with hypersensitivity to mosquito bites: vasculitis induced by mosquito bite with the infiltration of nonneoplastic Epstein–Barr virus-positive cells and subsequent development of natural killer/T-cell lymphoma with angiodestruction. Human Pathol 36:212–218CrossRef Kanno H, Onodera H, Endo M et al (2005) Vascular lesion in a patient of chronic active Epstein–Barr virus infection with hypersensitivity to mosquito bites: vasculitis induced by mosquito bite with the infiltration of nonneoplastic Epstein–Barr virus-positive cells and subsequent development of natural killer/T-cell lymphoma with angiodestruction. Human Pathol 36:212–218CrossRef
14.
go back to reference Kasahara Y, Yachie A, Takei K et al (2001) Differential cellular targets of Epstein–Barr virus (EBV) infection between acute EBV-associated hemophagocytic lymphohistiocytosis and chronic active EBV infection. Blood 98:1882–1888PubMedCrossRef Kasahara Y, Yachie A, Takei K et al (2001) Differential cellular targets of Epstein–Barr virus (EBV) infection between acute EBV-associated hemophagocytic lymphohistiocytosis and chronic active EBV infection. Blood 98:1882–1888PubMedCrossRef
15.
go back to reference Kikuta H, Taguchi Y, Tomizawa K et al (1988) Epstein–Barr virus genome-positive T lymphocytes in a boy with chronic active EBV infection associated with Kawasaki-like disease. Nature 333:455–457PubMedCrossRef Kikuta H, Taguchi Y, Tomizawa K et al (1988) Epstein–Barr virus genome-positive T lymphocytes in a boy with chronic active EBV infection associated with Kawasaki-like disease. Nature 333:455–457PubMedCrossRef
16.
go back to reference Kikuta H, Sakiyama Y, Matsumoto S et al (1993) Detection of Epstein–Barr virus DNA in cardiac and aortic tissue from chronic, active Epstein–Barr virus infection associated with Kawasaki-disease like coronary artery aneurysms. J Pediatr 123:90–92PubMedCrossRef Kikuta H, Sakiyama Y, Matsumoto S et al (1993) Detection of Epstein–Barr virus DNA in cardiac and aortic tissue from chronic, active Epstein–Barr virus infection associated with Kawasaki-disease like coronary artery aneurysms. J Pediatr 123:90–92PubMedCrossRef
17.
go back to reference Kimura H, Hoshino Y, Kanegane H et al (2001) Clinical and virologic characteristics of chronic active Epstein–Barr virus infection. Blood 98:280–286PubMedCrossRef Kimura H, Hoshino Y, Kanegane H et al (2001) Clinical and virologic characteristics of chronic active Epstein–Barr virus infection. Blood 98:280–286PubMedCrossRef
18.
go back to reference Kimura H, Morishima T, Kanegane H et al (2003) Prognostic factors for chronic active Epstein–Barr virus infection. J Infect Dis 187:527–533PubMedCrossRef Kimura H, Morishima T, Kanegane H et al (2003) Prognostic factors for chronic active Epstein–Barr virus infection. J Infect Dis 187:527–533PubMedCrossRef
19.
go back to reference Kurotobi S, Nagai T, Kawakami N, Sano T (2002) Coronary diameter in normal infants, children, and patients with Kawasaki disease. Pediatr Int 44:1–4PubMedCrossRef Kurotobi S, Nagai T, Kawakami N, Sano T (2002) Coronary diameter in normal infants, children, and patients with Kawasaki disease. Pediatr Int 44:1–4PubMedCrossRef
20.
go back to reference Lay JD, Chuang SE, Rowe M, Su IJ (2003) Epstein–Barr virus latent membrane protein-1 mediates upregulation of tumor necrosis factor-alpha in EBV-infected T-cells: implications for the pathogenesis of hemophagocytic syndrome. J Biomed Sci 10:146–155PubMed Lay JD, Chuang SE, Rowe M, Su IJ (2003) Epstein–Barr virus latent membrane protein-1 mediates upregulation of tumor necrosis factor-alpha in EBV-infected T-cells: implications for the pathogenesis of hemophagocytic syndrome. J Biomed Sci 10:146–155PubMed
21.
go back to reference Murakami K, Ohsawa M, Hu SX et al (1998) Large-vessel arteritis associated with chronic active Epstein–Barr virus infection. Arthritis Rheum 41:369–373PubMedCrossRef Murakami K, Ohsawa M, Hu SX et al (1998) Large-vessel arteritis associated with chronic active Epstein–Barr virus infection. Arthritis Rheum 41:369–373PubMedCrossRef
22.
go back to reference Muso E, Fujiwara H, Yoshida H et al (1993) Epstein–Barr virus genome-positive tubulointerstitial nephritis associated with Kawasaki disease-like coronary aneurysms. Clin Nephrol 40:7–15PubMed Muso E, Fujiwara H, Yoshida H et al (1993) Epstein–Barr virus genome-positive tubulointerstitial nephritis associated with Kawasaki disease-like coronary aneurysms. Clin Nephrol 40:7–15PubMed
23.
go back to reference Nakagawa A, Ito M, Iwaki T et al (1996) Chronic active Epstein–Barr virus infection with giant coronary aneurysms. Am J Clin Pathol 105:733–736PubMed Nakagawa A, Ito M, Iwaki T et al (1996) Chronic active Epstein–Barr virus infection with giant coronary aneurysms. Am J Clin Pathol 105:733–736PubMed
24.
go back to reference Nakagawa A, Ito M, Saga S (2002) Fatal cytotoxic T-cell proliferation in chronic active Epstein–Barr virus infection in childhood. Am J Clin Pathol 117:283–290PubMedCrossRef Nakagawa A, Ito M, Saga S (2002) Fatal cytotoxic T-cell proliferation in chronic active Epstein–Barr virus infection in childhood. Am J Clin Pathol 117:283–290PubMedCrossRef
25.
go back to reference Newberger JW, Takahashi M, Gerber MA et al (2004) Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation 110:2747–2761CrossRef Newberger JW, Takahashi M, Gerber MA et al (2004) Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation 110:2747–2761CrossRef
26.
go back to reference Okano M, Kawa K, Kimura H et al (2005) Proposed guidelines for diagnosing chronic active Epstein–Barr virus infection. Am J Hematol 80:64–69PubMedCrossRef Okano M, Kawa K, Kimura H et al (2005) Proposed guidelines for diagnosing chronic active Epstein–Barr virus infection. Am J Hematol 80:64–69PubMedCrossRef
27.
go back to reference Ohga S, Nomura A, Takada H et al (2001) Epstein–Barr virus (EBV) load and cytokine gene expression in activated T-cells of chronic active EBV infection. J Infect Dis 183:1–7PubMedCrossRef Ohga S, Nomura A, Takada H et al (2001) Epstein–Barr virus (EBV) load and cytokine gene expression in activated T-cells of chronic active EBV infection. J Infect Dis 183:1–7PubMedCrossRef
28.
go back to reference Ohga S, Nomura A, Takada H et al (2004) Dominant expression of interleukin-10 and transforming growth factor-β genes in activated T-cells of chronic active Epstein–Barr virus infection. J Med Virol 74:449–458PubMedCrossRef Ohga S, Nomura A, Takada H et al (2004) Dominant expression of interleukin-10 and transforming growth factor-β genes in activated T-cells of chronic active Epstein–Barr virus infection. J Med Virol 74:449–458PubMedCrossRef
29.
go back to reference Ohshima K, Suzumiya J, Sugihara M et al (1998) Clinicopathological study of severe chronic active Epstein–Barr virus infection that developed in association with lymphoproliferative disorder and/or hemophagocytic syndrome. Pathol Int 48:934–943PubMedCrossRef Ohshima K, Suzumiya J, Sugihara M et al (1998) Clinicopathological study of severe chronic active Epstein–Barr virus infection that developed in association with lymphoproliferative disorder and/or hemophagocytic syndrome. Pathol Int 48:934–943PubMedCrossRef
30.
go back to reference Ottaviani G, Matturri L, Rossi L, Jones D (2003) Sudden death due to lymphomatous infiltration of the cardiac conduction system. Cardiovasc Pathol 12:77–81PubMedCrossRef Ottaviani G, Matturri L, Rossi L, Jones D (2003) Sudden death due to lymphomatous infiltration of the cardiac conduction system. Cardiovasc Pathol 12:77–81PubMedCrossRef
31.
go back to reference Sato Y, Tsuboi T, Mikami T et al (2006) Chronic active Epstein–Barr virus infection with dilatation of the Valsalva sinus. Pediatr Int 48:643–645PubMedCrossRef Sato Y, Tsuboi T, Mikami T et al (2006) Chronic active Epstein–Barr virus infection with dilatation of the Valsalva sinus. Pediatr Int 48:643–645PubMedCrossRef
32.
go back to reference Satoh M, Oyama N, Akiba H et al (2002) Hypersensitivity to mosquito bites with natural-killer cell lymphocytosis: the possible implication of Epstein–Barr virus reactivation. Eur J Dermatol 12:381–384PubMed Satoh M, Oyama N, Akiba H et al (2002) Hypersensitivity to mosquito bites with natural-killer cell lymphocytosis: the possible implication of Epstein–Barr virus reactivation. Eur J Dermatol 12:381–384PubMed
33.
go back to reference Takano H, Nakagawa K, Ishio N et al (2008) Active myocarditis in a patient with chronic active Epstein–Barr virus infection. Int J Cardiol 130:e11–e13PubMedCrossRef Takano H, Nakagawa K, Ishio N et al (2008) Active myocarditis in a patient with chronic active Epstein–Barr virus infection. Int J Cardiol 130:e11–e13PubMedCrossRef
34.
go back to reference Teruya-Feldstein J, Jaffe ES, Burd JP et al (1997) The role of Mig, the monokine induced by interferon-γ, and IP-10, the interferon-γ-inducible protein-10, in tissue necrosis and vascular damage associated with Epstein–Barr virus-positive lymphoproliferative disease. Blood 90:4099–4105PubMed Teruya-Feldstein J, Jaffe ES, Burd JP et al (1997) The role of Mig, the monokine induced by interferon-γ, and IP-10, the interferon-γ-inducible protein-10, in tissue necrosis and vascular damage associated with Epstein–Barr virus-positive lymphoproliferative disease. Blood 90:4099–4105PubMed
35.
go back to reference Toubo T, Ohga S, Takada H et al (2006) Rheumatic fever–mimicking carditis as a first presentation of chronic active Epstein–Barr virus infection. Acta Pediatr 95:614–621CrossRef Toubo T, Ohga S, Takada H et al (2006) Rheumatic fever–mimicking carditis as a first presentation of chronic active Epstein–Barr virus infection. Acta Pediatr 95:614–621CrossRef
36.
go back to reference Tsuda E, Kamiya T, Kimura K et al (2002) Coronary artery dilatation exceeding 4.0 mm during acute Kawasaki disease predicts a high probability of subsequent late intima-medial thickening. Pediatr Cardiol 23:9–14PubMedCrossRef Tsuda E, Kamiya T, Kimura K et al (2002) Coronary artery dilatation exceeding 4.0 mm during acute Kawasaki disease predicts a high probability of subsequent late intima-medial thickening. Pediatr Cardiol 23:9–14PubMedCrossRef
Metadata
Title
Cardiovascular Complications Associated with Chronic Active Epstein–Barr Virus Infection
Authors
Jun Muneuchi
Shouichi Ohga
Masataka Ishimura
Kazuyuki Ikeda
Kenichiro Yamaguchi
Akihiko Nomura
Hidetoshi Takada
Yasunobu Abe
Toshiro Hara
Publication date
01-04-2009
Publisher
Springer-Verlag
Published in
Pediatric Cardiology / Issue 3/2009
Print ISSN: 0172-0643
Electronic ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-008-9343-8

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