Corticosteroids Opportunist Higher Toxoplasma gondii Brain Cysts in Latent Infected Mice

Hasan A. El-Fadaly, M. A. Hassanain, R. Shaapan, N. Hassanain, A. M. Barakat
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引用次数: 11

Abstract

Toxoplasma gondii is an opportunistic zoonotic protozoan, distinguish superior brain parasite load in immune-suppressed patients. Corticosteroids are popular anti-inflammatory with immune-suppressive long course, it possible opportunist higher T. gondii brain parasite load and reverts encephalitis in latent infected personals. The present study concerns this concept and preferred for recognize different levels of T. gondii brain parasite load and immunoglobulin titers in both corticosteroids treated and untreated latent infected mice groups. A total number of 70 Swiss-Webster mice (12-18 g) were divided into four groups, the first and second ones are 30 each (infected-untreated and infected-treated group), the third and fourth 5 each (uninfected-untreated and uninfected-treated control). Administration of glucocorticoid (hydrocortisone sodium succinate) at a dose of 50 mg kgG1 (I.M) injection 3 times a week with oral administration of dexamethasone sodium phosphate in dose of 2.5 mg kgG1 dayG1 per mouse in drinking water for sequence 2 months. The 103 bradyzoites from mice brain of cystogenic ME-49 strain was used for inducing latent infected mice groups at 30 days before corticosteroids therapy. Serum and brain tissue samples were collected for serological assay and parasite load estimation from sacrificed mice. The results showed significance elevation of average percent of brain parasite load and IgM/IgG titers. All values exceeds higher and parallel to the progression of corticosteroids term in infected treated group than the infected-untreated one. In conclusion, long-term corticosteroids therapy possible opportunist higher T. gondii brain parasite load and induce encephalitis in latent infected murine model, imitate this serious condition in T. gondii infected patients who received corticosteroids therapy.
潜伏感染小鼠的机会性高级刚地弓形虫脑囊肿
刚地弓形虫是一种机会性人畜共患原虫,在免疫抑制患者中表现出较高的脑寄生负荷。皮质类固醇是常用的抗炎药,具有长期的免疫抑制作用,可能会增加弓形虫脑寄生虫载量,使潜伏感染者的脑炎恢复。本研究关注这一概念,并倾向于在皮质类固醇治疗和未治疗的潜伏感染小鼠组中识别不同水平的弓形虫脑寄生虫载量和免疫球蛋白滴度。将70只瑞士韦氏小鼠(12-18 g)分为四组,第一组和第二组各30只(感染未治疗组和感染治疗组),第三组和第四组各5只(未感染未治疗组和未感染治疗组)。给药糖皮质激素(氢化可的松磺酸钠)50 mg kgG1 (I.M)注射,每周3次,同时口服地塞米松磷酸钠2.5 mg kgG1天g1 /只,饮水,连续2个月。在糖皮质激素治疗前30天,用小鼠脑内生ME-49菌株103个缓殖子诱导潜伏感染小鼠组。采集小鼠血清和脑组织标本进行血清学检测和寄生虫负荷估算。结果显示,脑寄生虫平均负荷百分比和IgM/IgG滴度显著升高。治疗组的所有数值均高于未治疗组,且与皮质激素期进展平行。综上所述,长期糖皮质激素治疗可能会增加弓形虫脑内寄生虫载量并诱发潜伏感染小鼠模型脑炎,模拟接受糖皮质激素治疗的弓形虫感染患者出现这种严重情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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