Role of Steroids in Modulating Levels of Cytokines in Patients of Dengue Fever and Warning Signs

K. PannuA, A. Bhalla
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Abstract

Dengue fever (DF), also known as break-bone fever, is a tropical infectious disease caused by the dengue virus. Dengue virus is a member of Flaviviridae family in the genus Flavivirus [1,2]. The dengue virus complex comprises of four antigenic ally related viruses designated dengue virus serotypes 1 through 4. Although DF is a self-limited febrile illness, it can progress to dengue hemorrhagic fever (DHF) in a number of patients. DHF is characterized by thrombocytopenia and increased vascular permeability leading to prominent hemorrhagic manifestations and a increased mortality [3]. Analysis of serum from patients infected with dengue virus indicates that concentrations of IL10 [4], TNF-α [5], IL-8 [6], IL-12 [7], IFN-Υ [8], IFN-α [9]. And soluble TNF and IL-2 receptors are increased during DF and DHF. Cell cultures infected with the dengue virus release increased concentrations of inflammatory cytokines and other mediators. Prior studies have also correlated increased levels of several cytokines with disease severity and may have prognostic value [10-15]. In addition, these studies show that levels of cytokines adversely affecting the coagulation cascade tend to be higher in DHF versus DF [10, 16]. Given the critical role of cytokines in the inflammatory process and Coagulopathy, there have been numerous attempts to suppress their levels in an attempt to control various diseases [17-19]. Glucocorticoids have an inhibitory effect on a broad range of immune responses mediated by T cells and B cells, as well as potent suppressive effect on the effector functions of phagocytes. They inhibit the synthesis of almost all known cytokines (IL 1, 2, 3, 4, 5, 6, 8, 10, 13, GMCSF, TNF-α and IFN-Υ). Since inflammatory cytokines have been proposed to play an important role in pathogenesis of dengue fever and its various complications there has been considerable interest in studying the potential role of corticosteroids as a potential therapy for DF and DHF. We conducted a study to see the effect of corticosteroids on the levels of cytokines in dengue patients and hence provide an immuno pathological basis for the use of corticosteroids in DF, a highly debated practice with many studies giving conflicting results.
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类固醇对登革热患者细胞因子水平的调节作用及预警
登革热(DF),又称骨折热,是一种由登革热病毒引起的热带传染病。登革热病毒是黄病毒属黄病毒科的一个成员[1,2]。登革热病毒复合体包括四种抗原盟友相关病毒,命名为登革热病毒血清型1至4。尽管DF是一种自限性发热性疾病,但在许多患者中,它可以发展为登革热出血热(DHF)。DHF的特点是血小板减少和血管通透性增加,导致显著的出血表现和死亡率增加[3]。对登革热病毒感染患者血清的分析表明,IL10[4]、TNF-α[5]、IL-8[6]、IL-12[7]、IFN-γ[8]、IFNα[9]的浓度。可溶性TNF和IL-2受体在DF和DHF过程中增加。感染登革热病毒的细胞培养物释放出浓度增加的炎性细胞因子和其他介质。先前的研究也将几种细胞因子水平的升高与疾病严重程度相关,并可能具有预后价值[10-15]。此外,这些研究表明,与DF相比,DHF中对凝血级联产生不利影响的细胞因子水平往往更高[10,16]。鉴于细胞因子在炎症过程和凝血病中的关键作用,为了控制各种疾病,已经有许多尝试抑制其水平[17-19]。糖皮质激素对T细胞和B细胞介导的广泛免疫反应具有抑制作用,并对吞噬细胞的效应功能具有强大的抑制作用。它们抑制几乎所有已知细胞因子(IL 1、2、3、4、5、6、8、10、13、GMCSF、TNF-α和IFN-γ)的合成。由于炎性细胞因子已被认为在登革热及其各种并发症的发病机制中发挥重要作用,因此研究皮质类固醇作为DF和DHF潜在治疗方法的潜在作用引起了人们的极大兴趣。我们进行了一项研究,以观察皮质类固醇对登革热患者细胞因子水平的影响,从而为在DF中使用皮质类固醇提供免疫病理学基础,这是一种备受争议的做法,许多研究给出了相互矛盾的结果。
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