Zucca E, Roggero E, Maggi-Solcà N, Conconi A, Bertoni F, Reilly I, Castelli D, Pedrinis E, Piffaretti J C, Cavalli F
Istituto Oncologico della Svizzera Italiana, Divisione di Oncologia Medica, Ospedale San Giovanni, 6500 Bellinzona, Switzerland.
Haematologica. 2000 Feb;85(2):147-53.
Several recent studies have reported a high rate of previous hepatitis C virus (HCV) infection in patients with non-Hodgkin's lymphoma (NHL). However, it appears that there are marked geographical differences in the prevalence of HCV among NHL patients. There is further controversy concerning a possible pathogenetic link between HCV and certain histologic lymphoma subtypes, in particular MALT lymphomas, and it has recently been speculated that HCV might be involved in the multistep process of gastric lymphoma genesis, in addition to the well established role of chronic Helicobacter pylori infection. The aim of this study was to investigate the prevalence of HCV and H. pylori infections in patients with B-cell NHL in Southern Switzerland.
One hundred and eighty newly diagnosed HIV-negative B-cell NHL patients, consecutively seen at a referral oncology center in Southern Switzerland between 1990 and 1995 were prospectively studied. A microparticle enzyme immunoassay was used to detect antibodies to HCV. Serologic determination of HCV genotype was done by the Murex method. The quantitative detection of IgG anti-H. pylori was performed by the Biorad GAP test.
Infection with HCV was detected in 17/180 patients (9.4%; 95% C.I., 6%-15%). This prevalence is significantly higher than that observed in a large survey of 5424 new blood donors from the same area tested in 1992-97 (0.9%; 95% C.I., 0.7-1.2). Neither histologic subtypes nor specific extranodal presentations of NHL were associated with a higher prevalence of HCV. HCV serotype 2 (corresponding to genotypes 2a-c) was the most common. HCV infection was significantly associated with a shorter progression-free survival at both univariate and multivariate analysis. Anti-Helicobacter antibodies were detected in 81/180 patients (45%; 95% C.I., 38%-53%) and H. pylori infection was significantly associated with the development of primary lymphomas of the stomach.
A high prevalence of HCV infection was detected in NHL lymphoma patients and was associated with a shorter time to lymphoma progression. HCV infection was not correlated with primary gastric presentation or with MALT-type histology. Our findings further support the key role of H.pylori infection in the pathogenesis of primary gastric lymphoma of MALT-type. The possible role of HCV in the pathogenesis of NHL should be further investigated.
最近的几项研究报告称,非霍奇金淋巴瘤(NHL)患者既往丙型肝炎病毒(HCV)感染率很高。然而,NHL患者中HCV的患病率似乎存在显著的地域差异。关于HCV与某些组织学淋巴瘤亚型,特别是黏膜相关淋巴组织(MALT)淋巴瘤之间可能的致病联系,存在进一步的争议。最近有人推测,除了已确定的慢性幽门螺杆菌感染的作用外,HCV可能参与胃淋巴瘤发生的多步骤过程。本研究的目的是调查瑞士南部B细胞NHL患者中HCV和幽门螺杆菌感染的患病率。
对1990年至1995年间在瑞士南部一家转诊肿瘤中心连续就诊的180例新诊断的HIV阴性B细胞NHL患者进行前瞻性研究。采用微粒酶免疫测定法检测抗HCV抗体。通过Murex方法进行HCV基因型的血清学测定。采用Biorad GAP试验进行抗幽门螺杆菌IgG的定量检测。
180例患者中有17例检测到HCV感染(9.4%;95%置信区间,6%-15%)。这一患病率显著高于1992 - 1997年对同一地区5424名新献血者进行的大规模调查中观察到的患病率(0.9%;95%置信区间,0.7 - 1.2)。NHL的组织学亚型或特定的结外表现均与HCV的较高患病率无关。HCV 2型(对应于2a - c基因型)最为常见。在单因素和多因素分析中,HCV感染均与无进展生存期较短显著相关。81/180例患者检测到抗幽门螺杆菌抗体(45%;95%置信区间,38% - 53%),幽门螺杆菌感染与原发性胃淋巴瘤的发生显著相关。
在NHL淋巴瘤患者中检测到较高的HCV感染率,且与淋巴瘤进展时间较短相关。HCV感染与原发性胃表现或MALT型组织学无关。我们的研究结果进一步支持幽门螺杆菌感染在MALT型原发性胃淋巴瘤发病机制中的关键作用。HCV在NHL发病机制中的可能作用应进一步研究。