Rentzos M, Nikolaou C, Andreadou E, Paraskevas G P, Rombos A, Zoga M, Tsoutsou A, Boufidou F, Kapaki E, Vassilopoulos D
Department of Neurology, School of Medicine, Athens National University, Athens, Greece.
Acta Neurol Scand. 2009 May;119(5):332-7. doi: 10.1111/j.1600-0404.2008.01103.x. Epub 2008 Oct 23.
Interleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL-10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL-10. There is little information about the involvement of IL-12 or IL-10 in the pathophysiology of Parkinson's disease (PD).
The objective of our study was to assess the role of IL-12 as a potential marker of immune reactions in patients with PD and to investigate whether IL-10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD.
We measured using immunoassay serum IL-12 and IL-10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL-12 and IL-10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score.
The PD group presented with significantly increased IL-10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL-10 and IL-12 levels was observed in patients with PD (R(S) = 0.7, P < 0.000001).
Our findings suggest that IL-10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL-10 and the significant correlation between IL-10 and IL-12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
白细胞介素(IL)-12是一种由活化的血液单核细胞、巨噬细胞和神经胶质细胞产生的异源二聚体细胞因子。它可增强T细胞的分化和增殖,并增加促炎细胞因子的产生。IL-10是一种由淋巴细胞和包括小胶质细胞在内的单核吞噬细胞产生的多效性细胞因子。最近的研究证实了IL-10的神经保护作用。关于IL-12或IL-10参与帕金森病(PD)病理生理学的信息很少。
我们研究的目的是评估IL-12作为PD患者免疫反应潜在标志物的作用,并研究免疫抑制细胞因子IL-10是否可能在PD发病机制中具有神经保护作用。
我们采用免疫测定法测量了41例PD患者的血清IL-12和IL-10水平,并与19名年龄和性别匹配的健康受试者(对照组)的血清水平进行比较。检测IL-12和IL-10水平与性别、年龄、病程、Hoehn和Yahr分期以及统一帕金森病评定量表(UPDRS)III评分的相关性。
与对照组相比,PD组的IL-10水平显著升高(P = 0.02)。观察到的升高不受治疗状态的影响。在PD患者中观察到IL-10和IL-12水平之间存在强且显著的相关性(R(S) = 0.7,P < 0.000001)。
我们的研究结果表明IL-10可能参与PD的发病机制。IL-10的升高以及IL-10与促炎细胞因子IL-12之间的显著相关性可能表明免疫紊乱和神经保护机制参与了PD患者。