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Oral Administration of Human Polyvalent IgG by Mouthwash as an Adjunctive Treatment of Chronic Oral Candidiasis

机译:漱口液口服人类多价IgG作为慢性口腔念珠菌病的辅助治疗

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摘要

Candida albicans is a commensal fungus that can cause disease ranging in severity from moderate to severe mucosal infections to more serious life-threating disseminated infections in severely immunocompromised hosts. Chronic mucocutaneous candidiasis (CMC) occurs in patients with mutations in genes affecting IL-17-mediated immunity, such as STAT3, AIRE, RORC, CARD9, IL12B, and IL12RB1, or gain of function (GOF) mutations in STAT1. New strategies for the treatment of candidiasis are needed because of the increased burden of infections and the emergence of drug-resistant strains. In this study, we investigated an aspect of the role of antibodies in the control of C. albicans infection. We tested in vitro the effects of C. albicans opsonization with commercial human polyvalent intravenous IgG (IV IgG) on NADPH oxidase activity and killing of the fungi by blood leukocytes from 11 healthy donors and found a significant enhancement in both phenomena that was improved by IV IgG opsonization. Then, we hypothesized that the opsonization of Candida in vivo could help its elimination by mucosal phagocytes in human patients with mucocutaneous candidiasis. We tested a novel adjunctive treatment for oral candidiasis in humans based on topical treatment with IV IgG. For this purpose, we choose two pediatric patients with well-characterized primary immunodeficiencies who are susceptible to CMC. Two 8-year-old female patients with an autosomal recessive mutation in the IL12RB1 gene (P1, with oral candidiasis) and a GOF mutation in STAT1 (P2, with severe CMC persistent since the age of 8 months and resistant to pharmacological treatments) were treated with IV IgG administered daily three times a day as a mouthwash over the course of 2 weeks. The treatment with the IV IgG mouthwash reduced C. albicans mouth infection by 98 and 70% in P1 and P2, respectively, after 13 days, and complete fungal clearance was observed after complementary nystatin and caspofungin treatments, respectively. Therefore, treatment of oral candidiasis with human polyvalent IgG administered as a mouthwash helps eliminate mucosal infection in humans, circumventing drug resistance, and opening its potential use in patients with primary or transient immunodeficiency.
机译:白色念珠菌是一种共生真菌,可在严重免疫功能低下的宿主中引起疾病​​,严重程度从中度到重度粘膜感染到更严重的威胁生命的弥漫性感染。慢性粘膜皮肤念珠菌病(CMC)发生在具有影响IL-17介导的免疫力的基因(例如STAT3,AIRE,RORC,CARD9,IL12B和IL12RB1)突变或STAT1功能获得性(GOF)突变的患者中。由于增加了感染负担和出现了耐药菌株,因此需要治疗念珠菌病的新策略。在这项研究中,我们调查了抗体在控制白色念珠菌感染中的作用。我们在体外测试了商用人多价静脉内IgG(IV IgG)对白色念珠菌调理作用对NADPH氧化酶活性和来自11位健康供体的白血球杀死真菌的影响,并发现两种现象均得到了显着增强,通过IV改善IgG调理作用。然后,我们假设在人皮肤粘膜念珠菌病患者中,念珠菌在体内的调理作用可以帮助其被粘膜吞噬细胞消除。我们基于静脉注射IgG的局部治疗,对人口腔念珠菌病的新型辅助治疗方法进行了测试。为此,我们选择了两名特征明确的原发性免疫缺陷病的小儿患者,他们易患CMC。两名8岁女性患者,其IL12RB1基因为常染色体隐性突变(P1,患有口腔念珠菌病),而STAT1则为GOF突变(P2,自8个月大时开始持续存在严重CMC,并且对药物治疗有抵抗力)在2周的过程中,每天用IV IgG口服3次,每次漱口。静脉注射IgG漱口水的处理在13天后分别在P1和P2中降低了白色念珠菌口腔感染的98%和70%,分别在补充制霉菌素和卡泊芬净治疗后观察到完全的真菌清除。因此,用人多价IgG漱口液治疗口腔念珠菌病有助于消除人的粘膜感染,避免耐药性,并开放其在原发性或短暂性免疫缺陷患者中的潜在用途。

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