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Mixture of Alum - Naloxone and Alum - Naltrexone as a novel adjuvant elicits immune responses for Toxoplasma gondii lysate antigen in BALB/c mice

机译:明矾-纳洛酮和明矾-纳曲酮的混合物作为新型佐剂引起BALB / c小鼠弓形虫溶菌抗原的免疫反应。

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Toxoplasma gondii (T gondii) is an obligate intracellular parasite. Treatment of the infection induced by this parasite is not straightforward due to the toxic side effects of the available drugs. Vaccine development could be a solution to this problem. In the present study, T.gondii Lysate Antigen (TLA), as a model vaccine, in combination with the Alum-NLT (Aluminum phosphate-Naltrexone) and Alum-NLX (Aluminum phosphate-Naloxone) were evaluated for immunization BALB/c. 147female BALB/c mice which were divided into seven groups of 21, were allocated to immunization experiments. The first group was selected as the negative control group, followed by the second, third, fourth, fifth, sixth and seventh groups which were immunized with Vac, Vac-Alum, Vac-NLX, Vac-NLT, Vac-Alum-NLX, Vac-Alum-NLT, respectively. Ten days after the final immunization, mice in all groups were divided into three groups for evaluating cellular immune responses, measuring the delayed-type hypersensitivity responses (DTHs) and evaluating survival. The DTH and cellular immune responses showed that in mice immunized with the TLA vaccine combined with the Alum-NLT mixture, the efficacy improved by increasing the production of Interleukin-5(IL-5) and Interferon gamma. This consequently shifted the immune responses toward a Th1 profile by increasing the IFN-gamma/IL-5 ratios. In challenge experiments, immunized mice with the Alum-NLT-Vac mixture survived for a longer period of time which indicated an improvement in protective immunity against T gondii. Administration of the Alum-NLT mixture adjuvant in combination with TLA vaccine enhanced the cellular immunity by shifting the immune response to a Th1 pattern. This shift to the Th1 pattern plays an important role in the induction of cellular. (C) 2016 Elsevier Inc. All rights reserved.
机译:弓形虫(T弓形虫)是专性的细胞内寄生虫。由于可用药物的毒副作用,这种寄生虫引起的感染的治疗并不简单。疫苗开发可以解决这个问题。在本研究中,评估了作为模型疫苗的冈氏锥虫溶血原抗原(TLA)与Alum-NLT(磷酸铝-纳曲酮)和Alum-NLX(磷酸铝-纳洛酮)的结合免疫BALB / c的能力。将147只雌性BALB / c小鼠分为7组,每组21只,进行免疫实验。选择第一组作为阴性对照组,然后第二,第三,第四,第五,第六和第七组分别用Vac,Vac-Alum,Vac-NLX,Vac-NLT,Vac-Alum-NLX免疫, Vac-Alum-NLT。最终免疫后十天,将所有组的小鼠分为三组,以评估细胞免疫反应,测量迟发型超敏反应(DTH)和评估存活率。 DTH和细胞免疫反应表明,在用TLA疫苗与明矾-NLT混合物联合免疫的小鼠中,通过增加白介素5(IL-5)和干扰素γ的产生来提高功效。因此,这会通过增加IFN-γ/ IL-5比值将免疫反应移向Th1谱。在激发实验中,用明矾-NLT-Vac混合物免疫的小鼠存活了更长的时间,这表明针对弓形虫的保护性免疫有所改善。通过将免疫应答转变为Th1型,将明矾-NLT混合物佐剂与TLA疫苗联合给药可增强细胞免疫力。这种向Th1模式的转变在细胞诱导中起重要作用。 (C)2016 Elsevier Inc.保留所有权利。

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