Liang Fengting, Zou Yangyang, Huang Liangmei, Pang Dongxiao, Liang Xuelan
Bobai County People's Hospital, Yulin, China.
The Second Hospital of Shanxi Medical University, Taiyuan, China.
Int J Lab Hematol. 2025 Aug;47(4):698-706. doi: 10.1111/ijlh.14461. Epub 2025 Mar 16.
The main terms for typical BCR::ABL1-negative myeloproliferative neoplasms (MPNs) are essential thrombocythemia (ET), polycythemia vera (PV), and primary myelofibrosis (PMF). Monocytes in MPN patients are involved in their inflammation and form an important part of the pathophysiology of MPN patients.
We used flow cytometry to study the immunophenotype of bone marrow monocytes from MPN patients (N = 118) and to correlate it with clinical parameters (including genetics, pathology, blood counts, personal information).
The results showed that bone marrow monocyte cells from MPN patients expressed the inflammation-related marker CD16 at higher levels than healthy controls. Second, bone marrow monocytes from Overt-PMF patients expressed CD11b at higher levels than monocytes from ET patients. Finally, certain specific monocyte subpopulations in MPN patients correlated with their clinical parameters. For example, in patients with ET and PMF, CD64+ monocytes were positively correlated with WBC and LDH. In PMF patients, the proportion of bone marrow monocytes was positively correlated with the grade of myelofibrosis, and CD15+ monocytes positively correlated with WBC and IPSS scores.
Our results provide insights into the immune microenvironment of MPNs based on immunophenotypic features and provide potential immune markers for MPNs occurrence and development.
典型的BCR::ABL1阴性骨髓增殖性肿瘤(MPN)的主要类型为原发性血小板增多症(ET)、真性红细胞增多症(PV)和原发性骨髓纤维化(PMF)。MPN患者的单核细胞参与其炎症反应,是MPN患者病理生理学的重要组成部分。
我们使用流式细胞术研究MPN患者(N = 118)骨髓单核细胞的免疫表型,并将其与临床参数(包括遗传学、病理学、血细胞计数、个人信息)相关联。
结果显示,MPN患者的骨髓单核细胞表达炎症相关标志物CD16的水平高于健康对照。其次,显性PMF患者的骨髓单核细胞表达CD11b的水平高于ET患者的单核细胞。最后,MPN患者中某些特定的单核细胞亚群与其临床参数相关。例如,在ET和PMF患者中,CD64+单核细胞与白细胞(WBC)和乳酸脱氢酶(LDH)呈正相关。在PMF患者中,骨髓单核细胞的比例与骨髓纤维化程度呈正相关,CD15+单核细胞与WBC和国际预后评分系统(IPSS)评分呈正相关。
我们的结果基于免疫表型特征为MPN的免疫微环境提供了见解,并为MPN的发生和发展提供了潜在的免疫标志物。