Sarangi Anshuman, Mohapatra P C, Dalai R K, Sarangi Ashok Kumar
Department of Biochemistry, S.C.B. Medical College, Cuttack, Odisha.
Department of Medicine, S.C.B. Medical College, Cuttack, Odisha.
J Parasit Dis. 2014 Jun;38(2):143-7. doi: 10.1007/s12639-013-0237-1. Epub 2013 Jan 9.
We investigated the role of IL-4, IL-12 and TNF-alpha in clinically well-defined groups of Plasmodium falciparum and vivax (Pf & Pv) infected patients belonging to Group I (++), Group II (+++) and Group III (++++). On the basis of hematological parameters, hyperparasitaemia, and evidence of neurological involvement, three different levels of severity were selected attributing a score from Group I (++) to Group III (++++). In each group 16 patients each of P. falciparum and P. vivax malaria were studied. As a control group for cytokine determination 30 healthy volunteers were included in the study. Serum samples were analyzed for IL-12, IL-4 and TNF-alpha using (ELISA) obtained commercially (Ray Biotech). Hb levels of Pf and Pv patients were 8 ± 1.94, 7.6 ± 1.64 g/dl and 3.6 ± 1.23 and 10.1 ± 1.21, 9.4 ± 1.43 and 7.1 ± 0.98 g/dl. Serum iron levels of Pf and Pv patients were 85.86 ± 0.86, 81.10 ± 0.70 and 70.1 ± 0.73 and 99.47 ± 0.85, 96.67 ± 1.13 and 91.7 ± 2.65 mg/dl. TNF-alpha levels of Pf and Pv patients were 155 ± 23.66, 307.5 ± 111.87 and 955 ± 261.32 and 72 ± 9.93, 140.88 ± 23.11 and 469.37 ± 416.99 pg/ml. IL-12 levels of Pf and Pv patients were 117.5 ± 8.16, 160.63 ± 20.81 and 293.13 ± 94.64 and 75.7 ± 9.25, 112.9 ± 12.05 and 200 ± 53.78 pg/ml. IL-4 levels of Pf and Pv patients were 3.7 ± 0.11, 3.2 ± 0.13 and 2.3 ± 0.63 and 5.33 ± 1.08, 4.8 ± 0.16 and 3.9 ± 0.48 pg/ml. In the control group the values of TNF-alpha, IL-12 and IL-4 were 42.9 ± 13.5, 49.8 ± 11.59 and 6.06 ± 1.32 pg/ml respectively. Cytokines and poor oxygen delivery should not be viewed as alternative theories of malarial disease pathophysiology instead poor oxygen delivery is one of the consequences of excessive release of inflammatory cytokines which is further augmented by the present work.
我们研究了白细胞介素-4(IL-4)、白细胞介素-12(IL-12)和肿瘤坏死因子-α(TNF-α)在临床明确划分的恶性疟原虫和间日疟原虫(Pf和Pv)感染患者组中的作用,这些患者分为第I组(++)、第II组(+++)和第III组(++++)。根据血液学参数、高疟原虫血症以及神经系统受累证据,选择了三种不同严重程度水平,从第I组(++)到第III组(++++)赋予相应分数。在每组中,分别对16例恶性疟和间日疟患者进行了研究。作为细胞因子测定的对照组,研究纳入了30名健康志愿者。使用市售(Ray Biotech)的酶联免疫吸附测定(ELISA)法分析血清样本中的IL-12、IL-4和TNF-α。Pf和Pv患者的血红蛋白水平分别为8 ± 1.94、7.6 ± 1.64 g/dl以及3.6 ± 1.23和10.1 ± 1.21、9.4 ± 1.43和7.1 ± 0.98 g/dl。Pf和Pv患者的血清铁水平分别为85.86 ± 0.86、81.10 ± 0.70和70.1 ± 0.73以及99.47 ± 0.85、96.67 ± 1.13和91.7 ± 2.65 mg/dl。Pf和Pv患者的TNF-α水平分别为155 ± 23.66、307.5 ± 111.87和955 ± 261.32以及72 ± 9.93、140.88 ± 23.11和469.37 ± 416.99 pg/ml。Pf和Pv患者的IL-12水平分别为117.5 ± 8.16、160.63 ± 20.81和293.13 ± 94.64以及75.7 ± 9.25、112.9 ± 12.05和200 ± 53.78 pg/ml。Pf和Pv患者的IL-4水平分别为3.7 ± 0.11、3.2 ± 0.13和2.3 ± 0.63以及5.33 ± 1.08、4.8 ± 0.16和3.9 ± 0.48 pg/ml。在对照组中,TNF-α、IL-12和IL-4的值分别为42.9 ± 13.5、49.8 ± 11.59和6.06 ± 1.32 pg/ml。细胞因子和氧输送不足不应被视为疟疾疾病病理生理学的替代理论,相反,氧输送不足是炎症细胞因子过度释放的后果之一,而本研究进一步证实了这一点。