Activated monocytes and platelet-monocyte aggregates in patients with sickle cell disease.
Activated monocytes and platelet-monocyte aggregates in patients with sickle cell disease.
复制标题
镰状细胞病患者的活化单核细胞和血小板单核细胞聚集体。
DOI:
10.1046/j.1365-2257.2002.00433.x
复制
发表时间:
2002
期刊:
影响因子:
--
通讯作者:
Paglieroni,Teresa
中科院分区:
文献类型:
--
作者:
Wun,Ted;Cordoba,Miguel;Rangaswami,Arun;Cheung,AnthonyW;Paglieroni,Teresa
Tumour necrosis factor‐α (TNF‐α) and interleukin‐1β (IL‐1β) increase endothelial surface receptors that mediate the adherence of sickle erythrocytes to the endothelium. Increased circulating levels of these cytokines have been found in patients with sickle cell disease (SCD). Monocytes are a source of both of these inflammatory mediators; we therefore determined whether circulating monocytes were activated in SCD, as defined by intracellular expression of these cytokines. Blood was also assayed for the presence of platelet–monocyte aggregates (PMAs), as platelet adherence is one possible mechanism for monocyte activation. The median percentages of monocytes expressing intracellular TNF‐α and IL‐1β in SCD patients were 6.8 (2.8–17.3) [median (range)] and 14.1 (1.3–44.8), respectively. In African‐American controls the corresponding percentages were 0.3 (0.1–0.5) and 0.4 (0.1–3.0), and in Caucasians 0.2 (0.1–0.5) and 0.8 (0.8–1.9) (P< 0.001, Kruskal–Wallis). The mean percentage (± SD) of PMA was 14.0 ± 8.3 for Caucasian controls, 25.7 ± 7.3 for African‐American controls, and 45.7 ± 21.6 for patients with SCD (P< 0.001, RM ANOVA;P< 0.05, Newman–Keuls posthoc test). We conclude that there are increased circulating PMAs and monocyte activation in patients with SCD.