Mami Naira Ben, Mohty Mohamad, Aurran-Schleinitz Thérèse, Olive Daniel, Gaugler Béatrice
Laboratoire d'Immunologie des Tumeurs, Institut Paoli-Calmettes, Université de la Méditerranée, 232 Bd. Ste. Marguerite, 13273 Marseille, Cedex 09, France.
Immunobiology. 2008;213(6):493-8. doi: 10.1016/j.imbio.2007.11.009. Epub 2008 Jan 7.
Myeloid and plasmacytoid dendritic cells (MDC, PDC) play a key role in the initiation of immune responses. We found a reduction of both DC subsets in 42 patients with chronic lymphocytic leukaemia (CLL) at diagnosis (P<0.0001 and 0.0001 vs. controls, respectively), likely related to the high secretion of CCL22 and CXCL12 (P=0.04 and 0.008 vs. controls, respectively) by leukaemic cells. However, CD14+ monocytes from CLL patients could give rise to functional IL-12p70-secreting monocyte-derived DCs, capable of inducing a type 1 polarization immunostimulatory profile. These monocyte-derived DCs from CLL patients efficiently migrate in response to CCL19/MIP-3beta chemokine, suggesting that functional autologous DCs can be generated for immunotherapeutic purposes to circumvent DC defects in CLL.
髓样和浆细胞样树突状细胞(MDC、PDC)在免疫反应的启动中起关键作用。我们发现42例慢性淋巴细胞白血病(CLL)患者在诊断时这两种树突状细胞亚群均减少(分别与对照组相比,P<0.0001和0.0001),这可能与白血病细胞高分泌CCL22和CXCL12有关(分别与对照组相比,P=0.04和0.008)。然而,CLL患者的CD14+单核细胞可分化为分泌功能性IL-12p70的单核细胞衍生树突状细胞,能够诱导1型极化免疫刺激谱。这些来自CLL患者的单核细胞衍生树突状细胞能有效响应CCL19/MIP-3β趋化因子而迁移,表明可为免疫治疗目的生成功能性自体树突状细胞以规避CLL中的树突状细胞缺陷。