Laboratório de Imunobiologia da Inflamação, Departamento de Ciências Biológicas, Instituto de Ciências Exatas e Biológicas (ICEB), Universidade Federal de Ouro Preto, Ouro Preto, Brazil.
Programa de Pós Graduação em Ecologia de Biomas Tropicais, Universidade Federal de Ouro Preto, Ouro Preto, Brazil.
Front Cell Infect Microbiol. 2021 Oct 13;11:673070. doi: 10.3389/fcimb.2021.673070. eCollection 2021.
The search for an effective etiologic treatment to eliminate , the causative agent of Chagas disease, has continued for decades and yielded controversial results. In the 1970s, nifurtimox and benznidazole were introduced for clinical assessment, but factors such as parasite resistance, high cellular toxicity, and efficacy in acute and chronic phases of the infection have been debated even today. This study proposes an innovative strategy to support the controlling of the using blue light phototherapy or blue light-emitting diode (LED) intervention. In assays, axenic cultures of Y and CL strains of were exposed to 460 nm and 40 µW/cm of blue light for 5 days (6 h/day), and parasite replication was evaluated daily. For experiments, C57BL6 mice were infected with the Y strain of and exposed to 460 nm and 7 µW/cm of blue light for 9 days (12 h/day). Parasite count in the blood and cardiac tissue was determined, and plasma interleukin (IL-6), tumoral necrosis factor (TNF), chemokine ligand 2 (CCL2), and IL-10 levels and the morphometry of the cardiac tissue were evaluated. Blue light induced a 50% reduction in (epimastigote forms) replication after 5 days of exposure. This blue light-mediated parasite control was also observed by the reduction in the blood (trypomastigote forms) and in the cardiac tissue (parasite DNA and amastigote nests) of infected mice. Phototherapy reduced plasma IL-6, TNF and IL-10, but not CCL2, levels in infected animals. This non-chemical therapy reduced the volume density of the heart stroma in the cardiac connective tissue but did not ameliorate the mouse myocarditis, maintaining a predominance of pericellular and perivascular mononuclear inflammatory infiltration with an increase in polymorphonuclear cells. Together, these data highlight, for the first time, the use of blue light therapy to control circulating and tissue forms of . Further investigation would demonstrate the application of this promising and potential complementary strategy for the treatment of Chagas disease.
寻找一种有效的病因治疗方法来消除克氏锥虫,这种寄生虫是恰加斯病的病原体,已经持续了几十年,但结果却存在争议。20 世纪 70 年代,硝呋莫司和苯并咪唑被引入临床评估,但寄生虫耐药性、高细胞毒性以及在感染的急性和慢性阶段的疗效等因素至今仍存在争议。本研究提出了一种创新策略,以支持使用蓝光光疗或蓝光发光二极管(LED)干预来控制克氏锥虫。在体外试验中,将 Y 和 CL 株的克氏锥虫的无共生培养物暴露于 460nm 和 40µW/cm 的蓝光下 5 天(每天 6 小时),并每天评估寄生虫复制情况。在体内实验中,C57BL6 小鼠感染 Y 株克氏锥虫,并暴露于 460nm 和 7µW/cm 的蓝光下 9 天(每天 12 小时)。测定血液和心脏组织中的寄生虫计数,并检测血浆白细胞介素(IL)-6、肿瘤坏死因子(TNF)、趋化因子配体 2(CCL2)和 IL-10 水平以及心脏组织的形态计量学。蓝光照射 5 天后,克氏锥虫(epimastigote 形式)的复制减少了 50%。这种蓝光介导的寄生虫控制也通过感染小鼠血液(锥虫形式)和心脏组织(寄生虫 DNA 和阿米巴样囊)中寄生虫数量的减少得到了观察。光疗降低了感染动物血浆中 IL-6、TNF 和 IL-10 的水平,但没有降低 CCL2 的水平。这种非化学疗法减少了心脏结缔组织中心脏间质的体积密度,但没有改善小鼠心肌炎,保持了细胞周和血管周围单核炎症浸润的优势,并且多形核细胞增多。综上所述,这些数据首次强调了蓝光疗法在控制循环和组织形式的克氏锥虫中的应用。进一步的研究将证明这种有前途和潜在互补的治疗恰加斯病的策略的应用。