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青蒿琥酯-姜黄素联合疗法治疗伯氏疟原虫感染小鼠通过免疫调节预防复发。

Curcumin-arteether combination therapy of Plasmodium berghei-infected mice prevents recrudescence through immunomodulation.

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore, India.

出版信息

PLoS One. 2012;7(1):e29442. doi: 10.1371/journal.pone.0029442. Epub 2012 Jan 20.

Abstract

Earlier studies in this laboratory have shown the potential of artemisinin-curcumin combination therapy in experimental malaria. In a parasite recrudescence model in mice infected with Plasmodium berghei (ANKA), a single dose of alpha,beta-arteether (ART) with three oral doses of curcumin prevented recrudescence, providing almost 95% protection. The parasites were completely cleared in blood with ART-alone (AE) or ART+curcumin (AC) treatments in the short-term, although the clearance was faster in the latter case involving increased ROS generation. But, parasites in liver and spleen were not cleared in AE or AC treatments, perhaps, serving as a reservoir for recrudescence. Parasitemia in blood reached up to 60% in AE-treated mice during the recrudescence phase, leading to death of animals. A transient increase of up to 2-3% parasitemia was observed in AC-treatment, leading to protection and reversal of splenomegaly. A striking increase in spleen mRNA levels for TLR2, IL-10 and IgG-subclass antibodies but a decrease in those for INFγ and IL-12 was observed in AC-treatment. There was a striking increase in IL-10 and IgG subclass antibody levels but a decrease in INFγ levels in sera leading to protection against recrudescence. AC-treatment failed to protect against recrudescence in TLR2(-/-) and IL-10(-/-) animals. IL-10 injection to AE-treated wild type mice and AC-treated TLR2(-/-) mice was able to prolong survival. Blood from the recrudescence phase in AE-treatment, but not from AC-treatment, was able to reinfect and kill naïve animals. Sera from the recrudescence phase of AC-treated animals reacted with several parasite proteins compared to that from AE-treated animals. It is proposed that activation of TLR2-mediated innate immune response leading to enhanced IL-10 production and generation of anti-parasite antibodies contribute to protective immunity in AC-treated mice. These results indicate a potential for curcumin-based combination therapy to be tested for prevention of recrudescence in falciparum and relapse in vivax malaria.

摘要

早期本实验室的研究表明,青蒿素-姜黄素联合疗法在实验性疟疾中有应用潜力。在感染伯氏疟原虫(ANKA)的小鼠寄生虫复发模型中,单次给予α,β-蒿甲醚(ART),并用 3 次口服姜黄素治疗可预防复发,提供近 95%的保护率。ART 单药(AE)或 ART+姜黄素(AC)治疗可在短期内完全清除血液中的寄生虫,但后者因增加 ROS 生成而清除速度更快。然而,AE 或 AC 治疗未能清除肝和脾中的寄生虫,这可能是寄生虫复发的一个潜在来源。在复发期,AE 治疗组的小鼠血液寄生虫载量上升至 60%,导致动物死亡。在 AC 治疗中观察到寄生虫载量短暂增加至 2-3%,从而产生保护作用并逆转脾肿大。AC 治疗显著增加了 TLR2、IL-10 和 IgG 亚类抗体的脾脏 mRNA 水平,而降低了 IFNγ和 IL-12 的水平。AC 治疗可显著增加 IL-10 和 IgG 亚类抗体水平,降低 INFγ水平,从而预防寄生虫复发。AC 治疗不能预防 TLR2(-/-)和 IL-10(-/-)动物的寄生虫复发。IL-10 注射到 AE 治疗的野生型小鼠和 AC 治疗的 TLR2(-/-)小鼠中,可延长其存活时间。AE 治疗的复发期血液,但不是 AC 治疗的复发期血液,能够重新感染和杀死未感染的动物。与 AE 治疗的动物相比,来自 AC 治疗动物复发期的血清与几种寄生虫蛋白发生反应。据推测,TLR2 介导的固有免疫反应的激活导致 IL-10 产生增加和抗寄生虫抗体的产生,这有助于 AC 治疗小鼠的保护性免疫。这些结果表明,姜黄素为基础的联合疗法有可能在恶性疟和间日疟复发中进行寄生虫复发预防的测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4fa/3262785/d1b83ca96807/pone.0029442.g001.jpg

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