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淋巴增生性疾病中的自身免疫与结外淋巴细胞浸润

Autoimmunity and extranodal lymphocytic infiltrates in lymphoproliferative disorders.

作者信息

Jønsson V, Wiik A, Hou-Jensen K, Christiansen M, Ryder L P, Madsen H O, Geisler C, Hansen M M, Thomsen K, Vorstrup S, Svejgaard A

机构信息

Department of Haematology, Rigshospital, Denmark.

出版信息

J Intern Med. 1999 Mar;245(3):277-86. doi: 10.1046/j.1365-2796.1999.0443f.x.

Abstract

OBJECTIVE

To examine the relationship between autoimmunity and extranodal lymphocytic infiltrates in different lymphoproliferative disorders with immunoglobulin alterations.

SUBJECTS AND DESIGN

A clinical review combined with a retrospective cohort study of 380 patients, 28 with monoclonal gammopathy of undetermined significance, three with common variable immunodeficiency, 147 with chronic lymphocytic leukaemia, 57 with Waldenström's macroglobulinaemia and 145 with non-Hodgkin's malignant lymphoma.

SETTING

A university hospital and The State Serum Institute in Copenhagen.

INTERVENTION

Clinical examination of each patient with special attention to chronic inflammatory and autoimmune manifestations. Biopsies were taken from non-infectious infiltrates, some of which were additionally tested with PCR analysis for gene rearrangements. Serological screening with a test battery for various autoantibodies was used in combination with techniques for the detection of M-components and monoclonal B-cell proliferation.

MAIN OUTCOME MEASURES

Clinical and/or serological autoimmune manifestations, M-component and other immunoglobulin alterations, and inflammatory tissue changes were studied in patients with chronic inflammatory, polyclonal or oligoclonal pseudolymphomas and in monoclonal, malignant extranodal lymphomas.

RESULTS

In 380 consecutive patients, 49 (12.9%) had extranodal manifestations, of whom 47 also had autoimmune manifestations. Nearly half of the 47 patients had more than one autoimmune manifestation. There was a strong correlation between clinical signs and corresponding autoantibodies such as anti-SSA and -SSB antibodies in Sjögren's syndrome (10 cases), antithyroid peroxidase antibodies in thyroiditis and Graves' disease (10 cases), and parietal cell antibodies in gastric ulcers with maltoma (12 cases). Clinical and serological signs of autoimmunity correlated strongly with female sex (34, 72% women; and 13, 28% men) and with immunoglobulin alterations.

CONCLUSIONS

To our knowledge this is the first systematic review of B-lymphoproliferative and autoimmune disorders indicating that pseudolymphoma and malignant lymphomas, including maltomas, may develop in the context of a permanent autoantigenic drive.

摘要

目的

探讨自身免疫与不同免疫球蛋白改变的淋巴增殖性疾病中结外淋巴细胞浸润之间的关系。

研究对象与设计

一项临床综述,并对380例患者进行回顾性队列研究,其中28例意义未明的单克隆丙种球蛋白病患者、3例常见可变免疫缺陷患者、147例慢性淋巴细胞白血病患者、57例华氏巨球蛋白血症患者和145例非霍奇金恶性淋巴瘤患者。

研究地点

哥本哈根的一家大学医院和国家血清研究所。

干预措施

对每位患者进行临床检查,特别关注慢性炎症和自身免疫表现。从非感染性浸润部位取活检组织,其中一些还进行了聚合酶链反应(PCR)分析以检测基因重排。使用针对各种自身抗体的检测组合进行血清学筛查,并结合检测M成分和单克隆B细胞增殖的技术。

主要观察指标

研究慢性炎症、多克隆或寡克隆假性淋巴瘤患者以及单克隆恶性结外淋巴瘤患者的临床和/或血清学自身免疫表现、M成分和其他免疫球蛋白改变以及炎症组织变化。

结果

在380例连续患者中,49例(12.9%)有结外表现,其中47例也有自身免疫表现。47例患者中近一半有不止一种自身免疫表现。临床体征与相应自身抗体之间存在强相关性,如干燥综合征(10例)中的抗SSA和抗SSB抗体、甲状腺炎和格雷夫斯病(10例)中的抗甲状腺过氧化物酶抗体以及伴有黏膜相关淋巴组织淋巴瘤的胃溃疡中的壁细胞抗体(12例)。自身免疫的临床和血清学体征与女性(34例,72%为女性;13例,28%为男性)以及免疫球蛋白改变密切相关。

结论

据我们所知,这是首次对B淋巴细胞增殖性疾病和自身免疫性疾病进行的系统综述,表明假性淋巴瘤和恶性淋巴瘤,包括黏膜相关淋巴组织淋巴瘤,可能在持续的自身抗原驱动背景下发生。

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