Velasco-de Andrés María, Català Cristina, Casadó-Llombart Sergi, Martínez-Florensa Mario, Simões Inês, García-Luna Joaquín, Mourglia-Ettlin Gustavo, Zaragoza Óscar, Carreras Esther, Lozano Francisco
Immunoreceptors of the Innate and Adaptive System, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.
Área Inmunología, Facultad de Química/Facultad de Ciencias, DEPBIO/IQB, Universidad de la República, Montevideo, Uruguay.
Antimicrob Agents Chemother. 2020 Dec 16;65(1). doi: 10.1128/AAC.01103-20.
Invasive fungal diseases represent an unmet clinical need that could benefit from novel immunotherapeutic approaches. Host pattern recognition receptors (e.g., Toll-like receptors, C-type lectins, or scavenger receptors) that sense conserved fungal cell wall constituents may provide suitable immunotherapeutic antifungal agents. Thus, we explored the therapeutic potential of the lymphocyte class I scavenger receptor CD5, a nonredundant component of the antifungal host immune response that binds to fungal β-glucans. Antifungal properties of the soluble ectodomain of human CD5 (shCD5) were assessed in experimental models of systemic fungal infection induced by pathogenic species ( and ). mechanistic studies were performed by means of fungus-spleen cell cocultures. shCD5-induced survival of lethally infected mice was dose and time dependent and concomitant with reduced fungal load and increased leukocyte infiltration in the primary target organ. Additive effects were observed after shCD5 was combined with suboptimal doses of fluconazole. addition of shCD5 to fungus-spleen cell cocultures increased the release of proinflammatory cytokines involved in antifungal defense (tumor necrosis factor alpha and gamma interferon) and reduced the number of viable organisms. The results prompt further exploration of the adjunctive therapeutic potential of shCD5 in severe invasive fungal diseases.
侵袭性真菌病是一种尚未满足的临床需求,可能会从新型免疫治疗方法中获益。能够感知保守真菌细胞壁成分的宿主模式识别受体(如Toll样受体、C型凝集素或清道夫受体)可能会提供合适的免疫治疗抗真菌药物。因此,我们探索了淋巴细胞I类清道夫受体CD5的治疗潜力,它是抗真菌宿主免疫反应的一个非冗余成分,可与真菌β-葡聚糖结合。在由致病物种引起的系统性真菌感染的实验模型中评估了人CD5可溶性胞外域(shCD5)的抗真菌特性。通过真菌-脾细胞共培养进行机制研究。shCD5诱导的致死性感染小鼠存活呈剂量和时间依赖性,同时主要靶器官中的真菌负荷降低,白细胞浸润增加。在shCD5与次优剂量氟康唑联合使用后观察到相加效应。向真菌-脾细胞共培养物中添加shCD5增加了参与抗真菌防御的促炎细胞因子(肿瘤坏死因子α和γ干扰素)的释放,并减少了活生物体的数量。这些结果促使人们进一步探索shCD5在严重侵袭性真菌病中的辅助治疗潜力。