副蛋白血症:病理生理学。

D Samson
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引用次数: 0

摘要

副蛋白贫血可能与淋巴细胞或浆细胞的良性或恶性增殖有关,包括多发性骨髓瘤、未确定意义的单克隆伽玛病(MGUS)和Waldenström的巨球蛋白血症。原发性淀粉样变性可能与多发性骨髓瘤有关,很少与淋巴样恶性肿瘤有关,但大多数病例可被认为是一种特殊形式的单克隆γ病,其意义尚不确定,其中副蛋白由于其淀粉样变性特性而引起损伤。本文讨论了多发性骨髓瘤生物学的最新进展。目前已知多发性骨髓瘤起源于淋巴结的生发后中心B细胞,该细胞是骨髓的归宿。与骨髓基质细胞的相互作用促进骨髓瘤细胞的归巢和生长。基质细胞产生IL-6,这是骨髓瘤细胞重要的生长因子,而骨髓瘤细胞产生tnf - α、IL-1 β等激活破骨细胞的因子,导致骨髓瘤骨病。骨髓瘤细胞也产生血管内皮生长因子,导致骨髓微血管形成增加,促进肿瘤生长。随着多发性骨髓瘤骨髓中病毒基因序列的证实,人们对卡波西肉瘤相关疱疹病毒(HHV8)在多发性骨髓瘤中的可能作用产生了兴趣。然而,进一步的研究结果是相互矛盾的,目前没有明确的证据表明HHV8在多发性骨髓瘤中的病因作用。使用现代技术的细胞遗传学研究表明,几乎所有多发性骨髓瘤病例都存在细胞遗传学异常,主要异常是涉及染色体14q的各种易位和染色体13的缺失。14q易位在意义不明的单克隆伽玛病中同样常见,但13号染色体缺失似乎与多发性骨髓瘤的进展有关,并且对多发性骨髓瘤患者的生存也具有强大的预后意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paraproteinaemias: pathophysiology.

Paraproteinaemias may be associated with benign or malignant proliferations of lymphocytes or plasma cells, including multiple myeloma, monoclonal gammopathy of undetermined significance (MGUS) and Waldenström's macroglobulinaemia. Primary amyloidosis may be associated with multiple myeloma and rarely with lymphoid malignancies, but most cases can be considered as a particular form of monoclonal gammopathy of undetermined significance, where the paraprotein causes damage by virtue of its amyloidogenic properties. This article discusses recent advances in understanding of the biology of multiple myeloma. Multiple myeloma is now known to arise from a post-germinal centre B cell in the lymph node which homes to the bone marrow. Interactions with stromal cells in the marrow facilitate homing and growth of the myeloma cells. The stromal cells produce IL-6, which is an important growth factor for myeloma cells, while the myeloma cells produce factors such as TNF-alpha and IL-1 beta that activate osteoclasts, resulting in myeloma bone disease. Myeloma cells also produce vascular endothelial growth factor which results in increased microvessel formation in the marrow, promoting tumour growth. There has been interest in the possible role of the Kaposi's sarcoma associated herpes virus (HHV8) in multiple myeloma, following the demonstration of viral gene sequences in multiple myeloma marrow. However, results of further studies have been conflicting and at present there is no clear evidence for an aetiological role of HHV8 in multiple myeloma. Cytogenetic studies using modern techniques have demonstrated that almost all multiple myeloma cases are cytogenetically abnormal, the predominant abnormalities being various translocations involving chromosome 14q and deletions of chromosome 13. 14q translocations are equally common in monoclonal gammopathy of undetermined significance, but deletions of chromosome 13 seem to be associated with progression to multiple myeloma, and also have powerful prognostic significance for survival in multiple myeloma patients.

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