不同多组分疫苗方案对COVID-19患者IgA分泌的影响

M. P. Kostinov, N. D. Abramova, V. N. Osiptsov, V. R. Tatevosov, V. V. Gainitdinova, N. O. Kryukova, I. A. Baranova, E. A. Khromova, Elena S. Korovkina, A. G. Chuchalin, O. A. Svitich, K. V. Mashilov
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 The patients were divided into two groups: group 1 (n = 45), received basic therapy; group 2 (n = 33), in addition to basic therapy, received the bacterial vaccine Immunovac-VP-4 according to a combined scheme. The biomaterial sampling was carried out by scraping of epithelial cells from the nasal mucosa, pharyngeal scraping and salivary gland secretion on days 1, 14 and 30 of the study. sIgA levels in all biological fluids were studied using ELISA technique (JSC Vector-Best, Russia).
 14 days after the start of observation, the dynamics of sIgA levels in nasal scrapings in group 1showed a significant decrease relative to the baseline values (p = 0.02), whereas the level of sIgA remained unchanged during the specified period (p = 0.07) in the group of patients receiving, along with basic therapy, additional Immunovac-VP-4 treatment. The dynamics of sIgA level in pharyngeal scrapings in the group of patients receiving only basic therapy did not change throughout the study period. Menwhile, the group of patients receiving basic therapy supplemented with Immunovac-VP-4 showed a significant increase in sIgA levels by the 30th day of follow-up over the baseline values (p = 0.02). The level of sIgA in salivary gland secretions did not differ significantly between the study groups during the entire follow-up period.
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摘要

粘膜免疫在预防包括COVID-19在内的呼吸道感染中发挥着重要作用。寻找通过纠正新型冠状病毒感染患者呼吸道粘膜固有免疫和适应性免疫因素激活感染后抗体合成的方法,可能与COVID-19患者的治疗相关。本研究的目的是评估确诊为COVID-19冠状病毒感染的患者上呼吸道sIgA的浓度,并评估细菌源性免疫刺激药物对sIgA分泌的影响。 患者分为两组:1组(n = 45),接受基础治疗;2组(n = 33)在基础治疗的基础上,按联合方案接种细菌疫苗Immunovac-VP-4。在研究的第1、14和30天,通过刮取鼻黏膜上皮细胞、咽刮取和唾液腺分泌物进行生物材料取样。采用ELISA技术(俄罗斯JSC Vector-Best)研究所有生物体液中的sIgA水平。 观察开始后14天,第1组鼻刮屑中sIgA水平的动态变化相对于基线值有显著下降(p = 0.02),而在基础治疗的同时接受免疫novac- vp -4治疗的患者组在指定时间段内sIgA水平保持不变(p = 0.07)。在整个研究期间,仅接受基础治疗的患者组咽刮痕中sIgA水平的动态变化没有改变。同时,在基础治疗的基础上加用immunnovac - vp -4的患者在随访第30天sIgA水平较基线值显著升高(p = 0.02)。在整个随访期间,研究组之间唾液腺分泌物中sIgA的水平无显著差异。 我们的研究结果表明,为了评估COVID-19患者的粘膜免疫状态,可以建议检测鼻分泌物中的sIgA。在复杂的治疗中,immunnovac - vp -4的使用伴随着呼吸道粘膜表面sIgA水平的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Secretory IgA in patients with COVID-19 at different regimens of using multicomponent vaccine Immunovac-VP-4
The mucosal immunity performs an important function in prevention of respiratory infections including COVID-19. The search for approaches to activate the synthesis of post-infectious antibodies by correcting the factors of innate and adaptive immunity at mucous membranes of respiratory tract in patients with infection caused by the new coronavirus may be relevant for the treatment of patients with COVID-19. The aim of our study was to assess the concentrations of sIgA in the upper respiratory tract in patients with a confirmed diagnosis of Coronavirus infection caused by the COVID-19, and to evaluate the effect of an immunostimulating drug of bacterial origin upon the sIgA secretion. The patients were divided into two groups: group 1 (n = 45), received basic therapy; group 2 (n = 33), in addition to basic therapy, received the bacterial vaccine Immunovac-VP-4 according to a combined scheme. The biomaterial sampling was carried out by scraping of epithelial cells from the nasal mucosa, pharyngeal scraping and salivary gland secretion on days 1, 14 and 30 of the study. sIgA levels in all biological fluids were studied using ELISA technique (JSC Vector-Best, Russia). 14 days after the start of observation, the dynamics of sIgA levels in nasal scrapings in group 1showed a significant decrease relative to the baseline values (p = 0.02), whereas the level of sIgA remained unchanged during the specified period (p = 0.07) in the group of patients receiving, along with basic therapy, additional Immunovac-VP-4 treatment. The dynamics of sIgA level in pharyngeal scrapings in the group of patients receiving only basic therapy did not change throughout the study period. Menwhile, the group of patients receiving basic therapy supplemented with Immunovac-VP-4 showed a significant increase in sIgA levels by the 30th day of follow-up over the baseline values (p = 0.02). The level of sIgA in salivary gland secretions did not differ significantly between the study groups during the entire follow-up period. The results of our study showed that, in order to assess the state of mucosal immunity in patients with COVID-19, one may recommend determination of sIgA in nasal secretions. The Immunovac-VP-4 prescribed in complex therapy is accompanied by an increase in the sIgA levels at the mucous surfaces of the respiratory tract.
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