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浆细胞在华氏巨球蛋白血症中的作用。

Role of plasma cells in Waldenström macroglobulinaemia.

作者信息

El-Ayoubi Ali, Wang James Q, Hein Nadine, Talaulikar Dipti

机构信息

Haematology Translational Research Unit, Department of Haematology, Canberra Hospital, Canberra, Australia; Australian National University Medical School, College of Medicine, Biology and Environment, Canberra, Australia.

ACRF Department of Cancer Biology and Therapeutics, John Curtin School of Medical Research, College of Medicine, Biology and Environment, Australian National University, Canberra, ACT, Australia.

出版信息

Pathology. 2017 Jun;49(4):337-345. doi: 10.1016/j.pathol.2017.02.004. Epub 2017 May 6.

Abstract

Waldenström macroglobulinaemia (WM) is an indolent mature B cell lymphoma characterised by an infiltrate of heterogeneous B cells and hypersecretion of IgM. There are two distinct cellular populations that can be distinguished on morphology and immunophenotyping within the bone marrow. The predominant lymphoplasmacytic compartment arises at an earlier stage in ontogeny, and is responsible for the cytopenias noted during the symptomatic phase of the disease. This population is ably targeted by B cell immunodepletion. The smaller plasma cell compartment has been shown to be monotypic and to carry the MYD88L265P mutation noted in >90% of WM. Further, pathogenic IgM levels tend to correlate better with plasma cell burden as compared to lymphoplasmacytic cell burden within the bone marrow. B cell immunodepletion does not eradicate the plasma cell compartment resulting in persistent IgM levels and poor complete remission rates. In this review we discuss the different cellular compartments in WM and highlight evidence regarding the significance and impending function of the plasma cell compartment in WM. We suggest detection of plasma cells be incorporated into routine diagnostic algorithms, and highlight the need to trial incorporation of plasma cell depleting therapy into treatment algorithms to deepen responses and improve clinical outcomes.

摘要

华氏巨球蛋白血症(WM)是一种惰性成熟B细胞淋巴瘤,其特征为异质性B细胞浸润和IgM分泌过多。在骨髓中,通过形态学和免疫表型分析可区分出两种不同的细胞群。占主导的淋巴浆细胞群在个体发育的早期阶段出现,是疾病症状期出现血细胞减少的原因。该细胞群可通过B细胞免疫清除有效靶向。较小的浆细胞群已被证明是单克隆性的,并携带在90%以上的WM中发现的MYD88L265P突变。此外,与骨髓中的淋巴浆细胞负荷相比,致病性IgM水平往往与浆细胞负荷的相关性更好。B细胞免疫清除不能根除浆细胞群,导致IgM水平持续存在且完全缓解率较低。在这篇综述中,我们讨论了WM中的不同细胞群,并强调了有关WM中浆细胞群的重要性和潜在功能的证据。我们建议将浆细胞检测纳入常规诊断算法,并强调需要尝试将浆细胞清除疗法纳入治疗算法,以加深反应并改善临床结果。

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