Teixeira Antonio Lucio, Reis Helton Jose, Nicolato Rodrigo, Brito-Melo Gustavo, Correa Humberto, Teixeira Mauro Martins, Romano-Silva Marco Aurelio
Laboratory of Immunopharmacology, Department of Biochemistry and Immunology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Apr 1;32(3):710-4. doi: 10.1016/j.pnpbp.2007.11.019. Epub 2007 Nov 23.
Inflammatory and immune alterations occur and may be relevant in patients with schizophrenia. Chemokines are a subgroup of cytokines that play a major role in the recruitment of determined subsets of leukocytes into tissues. To date no study has evaluated whether levels of chemokines are altered in patients with schizophrenia.
To evaluate serum levels of CC and CXC chemokines of schizophrenic patients and age- and gender-matched controls.
Forty male institutionalized schizophrenic patients (mean+/-SD age, 52.3+/-9.9) and 20 asymptomatic matched controls were recruited for this study. Severity of symptoms was assessed using BPRS, PANSS and AIMS. All patients were under typical antipsychotic treatment. Serum concentrations of chemokines were measured by ELISA.
There was no statistical difference in serum levels of CCL2, CCL3, CCL24, CXCL9 and CXCL10 between controls and patients. Serum levels of CCL11 were increased in schizophrenic patients when compared to controls. Serum levels of chemokines were not correlated with the length of disease or hospitalization and the severity of involuntary movements, positive and/or negative symptoms.
CCL11 is a ligand for CCR3, a receptor expressed preferentially on Th2 lymphocytes, mast cells and eosinophils. Higher serum levels of CCL11 in schizophrenia reinforce the view that this disease may be associated with a Th1/Th2 imbalance with a shift toward a Th2 immune response.
炎症和免疫改变在精神分裂症患者中出现且可能具有相关性。趋化因子是细胞因子的一个亚群,在特定白细胞亚群募集到组织中起主要作用。迄今为止,尚无研究评估精神分裂症患者的趋化因子水平是否发生改变。
评估精神分裂症患者以及年龄和性别匹配的对照组的血清CC和CXC趋化因子水平。
本研究招募了40名住院男性精神分裂症患者(平均±标准差年龄,52.3±9.9岁)和20名无症状的匹配对照组。使用简明精神病评定量表(BPRS)、阳性和阴性症状量表(PANSS)及异常不自主运动量表(AIMS)评估症状严重程度。所有患者均接受典型抗精神病药物治疗。通过酶联免疫吸附测定法(ELISA)测量趋化因子的血清浓度。
对照组和患者之间CCL2、CCL3、CCL24、CXCL9和CXCL10的血清水平无统计学差异。与对照组相比,精神分裂症患者的CCL11血清水平升高。趋化因子的血清水平与病程、住院时间以及不自主运动、阳性和/或阴性症状的严重程度无关。
CCL11是CCR3的配体,CCR3是一种优先在Th2淋巴细胞、肥大细胞和嗜酸性粒细胞上表达的受体。精神分裂症患者中较高的CCL11血清水平强化了这种疾病可能与Th1/Th2失衡并向Th2免疫反应转变相关的观点。