[Immunotherapy in the treatment of chronic polypous rhinosinusitis with comorbid bronchial asthma].

Q3 Medicine
E V Bezrukova, S A Artyushkin, E A Varyushina, A S Simbirtsev
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引用次数: 0

Abstract

The leading factors in the pathogenesis of chronic polyposis rhinosinusitis (CRSwNP) are dysfunction of the epithelial barrier of the nasal and sinus mucosa and dysregulation of the immune system, both at the systemic and local levels. A Th2-mediated immune response plays a central role in the development of disease in patients with CRSwNP CRPS, and CRSwNP is often associated with bronchial asthma (BA). At the present time, for the conservative treatment of patients with CRSwNP+BA, preference is given to drug therapy aimed at the correction of mucosal immunity. The use of interferon α2β (IFN α2β) and the dipeptide γ-D-glutamyl-L-tryptophan may reduce the severity of the long-term local inflammatory process. However, the clinical efficacy of these drugs in the context of chronic polyposis has not been studied. The aim of this study was to compare the efficacy of topical application of recombinant IFN α2β, recombinant IFN α2β in combination with γ-D-glutamyl-L-tryptophan and IL-4Rα receptor inhibitor in the treatment of patients with CRSwNP+BA. The patients were divided into three groups. In the first group (31 people), 1 million units of interferon alpha2b were injected into the polyposis tissue for five days. In the second group (31 people), interferon alpha2b at a dose of 1 million units and gamma-D-glutamyl-L-tryptophan at a dose of 0.1 mg were injected into the polypous tissue for five days. To assess the dynamics of clinical symptoms in the reference group (31 people), a drug with a known mechanism of action and efficacy - a genetically engineered IL-4Rα receptor inhibitor - was used. This drug was used 300 mg once every 2 weeks subcutaneously for 1 year. The obtained results showed that recombinant IFN α2β in combination with γ-D-glutamyl-L-tryptophan are pathogenetically appropriate preparations for conservative treatment of patients with the following initial indicators: severity of the polyposis process - 2.2+0.2 points, swelling - 2.8+0.4 points, and amount of discharge - 2.9+0.3 points. A single 5-day course of the above-mentioned preparations had a positive therapeutic effect, which was accompanied by a pronounced reduction in the clinical symptoms of the disease: the volume of polyposis tissue, nasal breathing difficulties and swelling of the nasal mucosa after one month and was maintained for one year. At the same time, the results of our study indicate the necessity of a longer period of application of recombinant IFN α2β in combination with γ-D-glutamyl-L-tryptophan in patients with CRSwNP+BA. The data obtained were comparable to the corresponding indicators when using the IL-4Ra inhibitor. In our opinion, the mechanism of action of the preparations is associated with a decrease in the activity of inflammatory and proliferative processes in the nasal and sinus mucosa.

[免疫疗法治疗慢性多囊鼻鼻窦炎合并支气管哮喘]。
慢性息肉病性鼻窦炎(CRSwNP)发病的主要因素是鼻腔和鼻窦黏膜上皮屏障功能障碍以及全身和局部水平的免疫系统失调。th2介导的免疫反应在CRSwNP CRPS患者的疾病发展中起核心作用,CRSwNP通常与支气管哮喘(BA)相关。目前,对于CRSwNP+BA患者的保守治疗,倾向于以纠正黏膜免疫为目的的药物治疗。使用干扰素α2β (IFN α2β)和二肽γ- d -谷氨酰胺- l-色氨酸可以减轻长期局部炎症过程的严重程度。然而,这些药物在慢性息肉病的临床疗效尚未研究。本研究旨在比较重组IFN α2β外用、重组IFN α2β联合γ- d -谷氨酰胺- l-色氨酸和IL-4Rα受体抑制剂治疗CRSwNP+BA患者的疗效。患者被分为三组。在第一组(31人)中,向息肉组织注射100万单位的干扰素α 2b,持续5天。在第二组(31人)中,干扰素α 2b的剂量为100万单位,γ - d -谷氨酰胺- l-色氨酸的剂量为0.1毫克,注射到息肉组织中5天。为了评估参照组(31人)临床症状的动态,使用了一种已知作用机制和疗效的药物——一种基因工程IL-4Rα受体抑制剂。本品每2周皮下注射一次,每次300毫克,连续1年。结果显示,重组IFN α2β联合γ- d -谷氨酰基- l-色氨酸对于息肉病程严重程度- 2.2+0.2分、肿胀- 2.8+0.4分、排液量- 2.9+0.3分的患者保守治疗是病理适宜的。上述制剂单次5天疗程具有积极的治疗效果,并伴有疾病临床症状的显著减轻:息肉组织体积、鼻呼吸困难和鼻黏膜肿胀一个月后,并持续一年。同时,我们的研究结果表明重组IFN α2β联合γ- d -谷氨酰胺- l-色氨酸在CRSwNP+BA患者中应用的时间较长是必要的。所获得的数据与使用IL-4Ra抑制剂时的相应指标相当。在我们看来,这些制剂的作用机制与降低鼻腔和鼻窦粘膜的炎症和增殖过程的活性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vestnik otorinolaringologii
Vestnik otorinolaringologii Medicine-Otorhinolaryngology
CiteScore
0.80
自引率
0.00%
发文量
69
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