Mohapatra P C, Sarangi Anshuman, Sarangi Ashok Kumar, Dalai R K, Sahoo Debashis
S.C.B. Medical College, Cuttack, India.
Department of Biochemistry, S.C.B. Medical College, Cuttack, Odisha India.
Indian J Clin Biochem. 2014 Jul;29(3):321-6. doi: 10.1007/s12291-013-0359-3. Epub 2013 Jul 14.
We investigated the prognostic role of TNF-alpha, IL-4 and IL-12 in a clinically well defined group of Plasmodium falciparum infected patients (n = 32) sequentially from Day 0 to Day 10 with a 2 day interval along with a control group of 16 healthy volunteers of same range of age and sex. Infection with malaria is often fatal because mitochondria are unable to generate enough ATP to maintain normal cellular function. ATP deficiency arises in malaria due to an inability of mitochondria through the effects of inflammatory cytokines on their function, to utilize available oxygen. In our study TNF-alpha and IL-12 levels were significantly elevated but IL-4 level showed persistent decline in Day 0, but subsequent measurement in Day 2, 4, 6, 8 and 10 showed persistent decline in levels of TNF-alpha and IL-12, an elevation in IL-4 levels which were associated with disease prognosis of the infected patients. These results again provide evidence that cytokines are very much a dominant partner in malaria pathogenesis with a specific prognostic role.
我们对一组临床诊断明确的恶性疟原虫感染患者(n = 32)进行了研究,从第0天到第10天,每隔2天依次检测肿瘤坏死因子-α(TNF-α)、白细胞介素-4(IL-4)和白细胞介素-12(IL-12)的预后作用,并设置了一个由16名年龄和性别范围相同的健康志愿者组成的对照组。疟疾感染通常是致命的,因为线粒体无法产生足够的三磷酸腺苷(ATP)来维持正常的细胞功能。疟疾中出现ATP缺乏是由于炎症细胞因子对线粒体功能产生影响,使其无法利用可用的氧气。在我们的研究中,TNF-α和IL-12水平显著升高,但IL-4水平在第0天持续下降,不过随后在第2、4、6、8和10天的测量显示,TNF-α和IL-12水平持续下降,IL-4水平升高,这与感染患者的疾病预后相关。这些结果再次证明,细胞因子在疟疾发病机制中是非常重要的因素,具有特定的预后作用。