Experience of using immunomodulatory therapy in the complex treatment of mild community-acquired pneumonia and its long-term results

Q4 Medicine
M. P. Kostinov, V. Gainitdinova, S. Kazharova, A. E. Vlasenko, V. B. Polishchuk, D. U. Allaberdina
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Abstract

A decrease of nonspecific body resistance, an imbalance of local and systemic immunity and a free-radical oxidation abnormality substantially contribute to the pathogenesis of community-acquired pneumonia (CAP).Purpose: To study the efficiency of including immunomodulators into the comprehensive treatment of nonsevere community-acquired pneumonia and assess the long-term effects of the treatment conducted.Patients (n = 55) with non-severe CAP (41 (31-48) years old, with CRB-65 score of 0.15 (0-1)) are included in the study. Group 1 (control) received only standard CAP therapy; the other two groups received immunomodulators concurrently with the standard therapy: bacterial lysate (BL) for group 2 and azoximer bromide (AzB) for group 3. TNFα and IL-6 concentration was determined on the day of visit, on day 13 and day 60 of follow-up. During 2 years, the incidence of low respiratory tract infections (LRTI) was studied in the same patients with CAP in past (n = 55). All patients (n = 55) had clinical signs of non-severe community-acquired pneumonia. The overall duration of all symptoms was lower in immunomodulators groups as compared to the control group: 12 (11-13) days in BL group (p < 0.001) and 12 (11-12) days in AzB group (p < 0.001) with no statistically significant difference between intervention groups (p = 0.36). During treatment, TNFα and IL-6 concentration decreased on day 13 and day 60 in all patients; in patients who received immunomodulators, TNFα and IL-6 were reliably lower as compared to the control. Changes of TNFα and IL-6 concentration in the groups on day 60 of the study as compared to the baseline showed a decrease in BL group by 85 (-89 – -82) % and 86 (-90 – -85) % (p < 0.001; p = 0.001 and control); in AzB group by 82 (-86 – -80) % and 86 (-88 – -84) % (p = 0.002; p = 0.007 and control). Intensity of IL-6 concentration decrease on day 60 in BL and AzB groups did not differ (p = 0.72). Gender- and age-adjusted odds ratio for the development of low respiratory tract diseases (during 2 years after CAP) in AzB group was 0.15 (0.02-0.93) (p = 0.04) suggesting its protective effect. Inclusion of immunomodulators in basic treatment of non-severe community-acquired pneumonia reduces duration of symptoms and is associated with improvement of the proinflammatory cytokine profile. In 2 years of follow-up, long-term effects of the immunomodulatory therapy showed statistically significant lower incidence of low respiratory tract infections in AzB group only.
使用免疫调节疗法综合治疗轻度社区获得性肺炎的经验及其长期效果
非特异性机体抵抗力下降、局部和全身免疫失衡以及自由基氧化异常是社区获得性肺炎(CAP)的主要发病机制。目的:研究将免疫调节剂纳入非重症社区获得性肺炎综合治疗的效率,并评估治疗的长期效果。第一组(对照组)只接受标准的 CAP 治疗;其他两组在接受标准治疗的同时接受免疫调节剂治疗:第二组接受细菌裂解液(BL)治疗,第三组接受溴化偶氮肟(AzB)治疗。在两年的时间里,还对过去的 CAP 患者(55 人)的低呼吸道感染(LRTI)发生率进行了研究。所有患者(55 人)均有非重症社区获得性肺炎的临床症状。与对照组相比,免疫调节剂组所有症状的总体持续时间较短:BL组为12(11-13)天(p < 0.001),AzB组为12(11-12)天(p < 0.001),干预组间差异无统计学意义(p = 0.36)。治疗期间,所有患者的 TNFα 和 IL-6 浓度在第 13 天和第 60 天均有所下降;与对照组相比,接受免疫调节剂治疗的患者 TNFα 和 IL-6 浓度明显降低。与基线相比,研究第 60 天各组的 TNFα 和 IL-6 浓度变化显示,BL 组分别下降了 85 (-89 -82) % 和 86 (-90 -85) %(p < 0.001;p = 0.001 和对照组);AzB 组分别下降了 82 (-86 -80) % 和 86 (-88 -84) %(p = 0.002;p = 0.007 和对照组)。BL组和AzB组在第60天IL-6浓度下降的强度没有差异(p = 0.72)。经性别和年龄调整后,AzB 组发生低呼吸道疾病(CAP 后 2 年内)的几率为 0.15 (0.02-0.93) (p = 0.04),这表明其具有保护作用。在非重症社区获得性肺炎的基础治疗中加入免疫调节剂可缩短症状持续时间,并改善促炎细胞因子谱。在 2 年的随访中,免疫调节疗法的长期效果显示,仅 AzB 组的低呼吸道感染发生率有显著统计学意义。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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