Hepatitis C virus - Associated marginal zone lymphoma

被引:10
|
作者
Armand, Marine [1 ,2 ]
Besson, Caroline [3 ,4 ]
Hermine, Olivier [5 ,6 ,7 ]
Davi, Frederic [1 ,2 ]
机构
[1] Hop La Pitie Salpetriere, AP HP, Dept Hematol, Paris, France
[2] UPMC Univ Paris 06, UMRS 1138, Paris, France
[3] Ctr Hosp Versailles, Hematooncol Unit, Le Chesnay, France
[4] Univ Paris Saclay, Univ Versailles St Quentin Yvelines, Paris, France
[5] Hop Necker Enfants Malad, AP HP, Dept Hematol, Paris, France
[6] Inst Imagine, CNRS ERL 8254, Inserm UMR1163, Paris, France
[7] Univ Sorbonne Paris Cite, Paris, France
关键词
Hepatitis C virus; Marginal zone lymphoma; Lymphomagenesis; Treatment; B-CELL LYMPHOMA; NON-HODGKIN LYMPHOMAS; MIXED CRYOGLOBULINEMIA; HCV INFECTION; CORE PROTEIN; LOW-GRADE; LYMPHOPROLIFERATIVE DISORDERS; SOMATIC HYPERMUTATION; II CRYOGLOBULINEMIA; VILLOUS LYMPHOCYTES;
D O I
10.1016/j.beha.2017.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The link between hepatitis C virus (HCV) infection and the development of B-cell non Hodgkin lymphoma is now well established and based on a number of epidemiological studies. It is further supported by the observation of lymphoma regression after HCV eradication by antiviral treatment. The far most frequent entities are marginal zone lymphoma (MZL) and diffuse large B-cell lymphoma (DLBCL).MZL usually emerge on a background of mixed cryoglobulinemia, a low-grade lymphoproliferation, and often transform into DLBCL, thereby following a multistep oncogenesis process. The role of HCV in lymphomagenesis is not yet fully understood but several mechanisms have been proposed including (i) chronic external stimulation through the B-cell receptor and other surface receptors, and (ii) direct transformation by intracellular viral proteins, the former being probably predominant in MZL. Regression of HCV-associated MZL can be achieved with antiviral therapy and the novel generation of direct-acting antiviral agents appears highly effective and safe for the treatment of these lymphoma. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:41 / 49
页数:9
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