不同病因的生殖道慢性感染性和炎症性疾病免疫功能低下妇女CD11b+CD64-CD32+CD16+、CD11b+CD64+CD32+CD16+中性粒细胞亚群诊断意义的变化

S. Kovaleva, I. Nesterova, S. N. Pikturno, E. I. Dydyshko, N. S. Prosolypova, А. M. Chulkova
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引用次数: 0

摘要

慢性盆腔炎(PID)在妇女仍然是一个问题,由于医疗后果的重要性。研究中性粒细胞(NG)受体装置参与各种病因疾病的抗感染保护似乎是相关的。目的:阐明不同病因的慢性PID加重期免疫功能低下女性NG CD11b+CD64-CD32+CD16+、CD11b+CD64+CD32+CD16+亚群定量和表型变化的变异特征。我们对20-40岁的女性进行了测试:研究组1 (SG1, n = 20) -慢性PID加重期间伴有单一或混合潜伏/复发性各种病毒感染(慢性疱疹病毒感染,乳头瘤病毒感染,复发性ARVI);研究2组(SG2, n = 30):细菌性慢性PID;对照组(CG): 20名健康女性。测定CD11b+CD64-CD32+CD16+NG(主要)和CD11b+CD64+CD32+CD16+NG(次要)亚群数量、受体表达密度(MFI) (FC500, USA)。结果发现,在加重期的PID中,NG的亚群组成在诊断上存在显著差异。我们发现,与合并复发/持续性病毒感染SG1的慢性PID相比,患有细菌性慢性PID的SG2中CD11b+СD64-СD32+СD16+NG亚群减少,CD11b+CD64+CD32+CD16+NG亚群增加7.6倍。NG亚群的负转化与活化CD16表达水平的显著下降有关。结果显示,对感染和炎症过程缺乏足够的反应——在SG1的主要亚群中,以及在SG1和SG2组的次要亚群中,活化CD11b的表达没有增加。在NG的主要亚群中,SG2组活化标记CD11b的表达减少。在各种病毒感染和PID (SG1)中,在NG负改变的次要亚群中,CD16的表达减少,CD64和CD32的表达增加。CD11b+СD64-СD32+СD16+、CD11b+CD64+CD32+CD16+NG亚群及其表型的测定可作为病毒性和细菌性PID鉴别诊断的诊断标志物,并为开发靶向免疫调节治疗的新方法提供依据。
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Diagnostically significant changes in subsets CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+ neutrophilic granulocytes of immunocompromised women with chronic infectious and inflammatory diseases of the genital tract of various etiologies
Chronic pelvic inflammatory disease (PID) in women remains a problem due to the importance of medical consequences. The study of the receptor apparatus of neutrophilic granulocytes (NG) involved in anti-infective protection in diseases of various etiologies seems to be relevant. Aim: to clarify the features of variants of quantitative and phenotypic changes in subsets of NG CD11b+CD64-CD32+CD16+, CD11b+CD64+CD32+CD16+ of immunocompromised women during exacerbation of chronic PID of various etiologies. We were tested women 20-40 years: Study Group 1 (SG1, n = 20) – chronic PID during the exacerbation with mono- or mixed latent/recurrent various viral infections (chronic herpes-virus infections, papillomavirus infection, recurrent ARVI); Study Group 2 (SG2, n = 30) – chronic PID of bacterial etiologies; Comparison Group (CG)– 20 healthy women. The number of subsets CD11b+CD64-CD32+CD16+NG (major) and CD11b+CD64+CD32+CD16+NG (minor), receptor expression density (MFI) was determined (FC500, USA). It was found that in PID during the period of exacerbation, diagnostically significant differences in the subset composition of NG were revealed. We got a decrease in the CD11b+СD64-СD32+СD16+NG subset and in 7,6 times increase in the CD11b+CD64+CD32+CD16+NG subset in SG2 with chronic PID of bacterial etiology, in contrast to chronic PID occurring in combination with recurrent/persistent viral infection SG1. Negative transformation of NG subsets is associated with a predominant decrease in the level of expression of the activation CD16. The absence of an adequate response to the infectious and inflammatory process was revealed – the absence of an increase in the expression of the activation CD11b in the major subset in SG1, as well as in the minor subset in groups SG1 and SG2. In the major subset of NG in groups SG2 a decrease in the expression of the activation marker CD11b. In the various viral infections and PID (SG1), in the negatively altered minor subset of NG we got a decrease of expression of CD16, an increase of expression of CD64 and CD32. Determination of subsets of CD11b+СD64-СD32+СD16+, CD11b+CD64+CD32+CD16+NG and their phenotype can be used as diagnostic markers for the differential diagnosis of PID of viral and bacterial etiology, and for the development of new methods of targeted immunomodulatory therapy.
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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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