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干燥综合征中B细胞淋巴增殖性疾病淋巴瘤前期阶段的特征分析

Characterization of prelymphomatous stages of B cell lymphoproliferation in Sjögren's syndrome.

作者信息

De Vita S, Boiocchi M, Sorrentino D, Carbone A, Avellini C, Dolcetti R, Marzotto A, Gloghini A, Bartoli E, Beltrami C A, Ferraccioli G

机构信息

Centro di Riferimento Oncologico, Aviano, Italy.

出版信息

Arthritis Rheum. 1997 Feb;40(2):318-31. doi: 10.1002/art.1780400217.

Abstract

OBJECTIVE

To determine whether the prelymphomatous stages of B cell lymphoproliferation in Sjögren's syndrome (SS) may be better characterized by the integration of clinical, pathologic, and molecular data, the latter focusing on the expansion, persistence, and dissemination of clonal B cells in the course of the disease.

METHODS

Multiple tissue lesions (synchronous from different tissues and metachronous from the same tissue) were evaluated in biopsy specimens obtained from 6 consecutive patients with SS who had an associated lymphoproliferative disorder. Fully benign gastric lesions were evaluated in tissue from an additional 11 patients with SS who had no associated lymphoproliferative disorder. Multiple and complementary molecular analyses of B cell clonality were used: Southern blot, polymerase chain reaction, single-strand conformation polymorphism, DNA sequencing, and hybridization with clonospecific oligoprobes. All the patients were then strictly followed up for the appearance of lymphoma.

RESULTS

Different scenarios of SS-associated B cell lymphoproliferation were identified: 1) the ongoing expansion of the same dominant clone, localized or disseminated, in tissue from 2 patients, 1 of whom later developed an overt B cell lymphoma; 2) different dominant clones in different synchronous or metachronous tissues from the remaining 4 patients with an associated lymphoproliferative disorder; and 3) small oligoclonal expansions in 7 of the 11 benign gastric lymphoid infiltrates.

CONCLUSION

Prelymphomatous B cell lymphoproliferation in SS was better characterized following integration of the findings. The different types of B cell clonal expansion (oligoclonal or monoclonal, smaller or larger in size, fluctuating or established, localized or disseminated) may imply a different risk of lymphoma progression. An accurate clinical, histopathologic, and molecular characterization may therefore be crucial in future studies aimed at clarifying the pathobiology of SS-associated lymphoproliferation.

摘要

目的

通过整合临床、病理和分子数据来确定干燥综合征(SS)中B细胞淋巴增殖的淋巴瘤前期阶段是否能得到更好的特征描述,后者聚焦于疾病过程中克隆性B细胞的扩增、持续存在和播散。

方法

对6例患有相关淋巴增殖性疾病的连续性SS患者活检标本中的多个组织病变(来自不同组织的同步病变和来自同一组织的异时病变)进行评估。对另外11例无相关淋巴增殖性疾病的SS患者的组织中的完全良性胃病变进行评估。采用多种互补的B细胞克隆性分子分析方法:Southern印迹法、聚合酶链反应、单链构象多态性分析、DNA测序以及与克隆特异性寡核苷酸探针杂交。然后对所有患者进行严格随访以观察淋巴瘤的出现。

结果

确定了SS相关B细胞淋巴增殖的不同情况:1)2例患者组织中同一优势克隆的持续扩增,局限或播散,其中1例后来发展为明显的B细胞淋巴瘤;2)其余4例患有相关淋巴增殖性疾病的患者不同同步或异时组织中的不同优势克隆;3)11例良性胃淋巴浸润中的7例存在小的寡克隆扩增。

结论

整合研究结果后能更好地描述SS中淋巴瘤前期B细胞淋巴增殖的特征。不同类型的B细胞克隆性扩增(寡克隆或单克隆、大小较小或较大、波动或稳定、局限或播散)可能意味着淋巴瘤进展的不同风险。因此,准确的临床、组织病理学和分子特征描述对于未来旨在阐明SS相关淋巴增殖病理生物学的研究可能至关重要。

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