Central European Journal of Immunology最新文献

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Toll-like receptor (TLR2, TLR4) polymorphisms and their influence on the incidence of urinary tract infections in children with and without urinary tract malformation. toll样受体(TLR2、TLR4)多态性及其对有和无尿路畸形儿童尿路感染发生率的影响
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.119625
Anna Krakowska, Maciej Cedzyński, Agnieszka Wosiak, Rafal Swiechowski, Adrian Krygier, Marcin Tkaczyk, Krzysztof Zeman
{"title":"Toll-like receptor (TLR2, TLR4) polymorphisms and their influence on the incidence of urinary tract infections in children with and without urinary tract malformation.","authors":"Anna Krakowska,&nbsp;Maciej Cedzyński,&nbsp;Agnieszka Wosiak,&nbsp;Rafal Swiechowski,&nbsp;Adrian Krygier,&nbsp;Marcin Tkaczyk,&nbsp;Krzysztof Zeman","doi":"10.5114/ceji.2022.119625","DOIUrl":"https://doi.org/10.5114/ceji.2022.119625","url":null,"abstract":"<p><strong>Introduction: </strong>Toll-like receptors (TLRs) contribute to the innate immune system. They are an element of non-specific immunity, which enables organisms to react quickly to foreign antigens, without being previously exposed to them. TLRs are pattern recognition receptors. TLR gene polymorphisms are widely investigated in connection with various infections. The aims of the study were: to investigate the role of TLR2 and TLR4 polymorphisms in the course of urinary tract infections (UTIs); to test for differences in distribution of these polymorphisms between children with urinary tract malformations suffering from recurrent UTI (rUTI), children with malformations but without rUTI and healthy controls; to determine whether these polymorphisms predispose to rUTI; and to analyse how polymorphisms and urine neutrophil gelatinase-associated lipocalin (NGAL) and interleukin 8 (IL-8) concentrations affect one another.</p><p><strong>Material and methods: </strong>The group consisted of 133 children (1-18 years old), 68 female and 65 male. The group was divided into 4 subgroups: A (rUTI with urinary tract malformations), B (urinary tract malformations without rUTI), C (rUTI) and D (healthy controls). Polymorphisms were analysed using PCR-RFLP. IL-8 and NGAL urine concentrations were established using immunoenzymatic methods.</p><p><strong>Results: </strong>TLR2 Arg753Gln and TLR4 Arg299Gly appeared significantly more often among children with rUTI. No correlation between urine IL-8 and urine NGAL and polymorphisms was found. Urine NGAL concentration was significantly higher among children with urinary tract malformations.</p><p><strong>Conclusions: </strong>TLR2 Arg753Gln and TLR4 Asp299Gly may predispose to rUTI. Urine NGAL concentration suggests the presence of kidney tissue injury, of varying degrees, among children with urinary tract malformations.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 3","pages":"260-266"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c7/f4/CEJI-47-47813.PMC9896986.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9315410","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Interleukin 25 and its biological features and function in intestinal diseases. 白细胞介素 25 及其在肠道疾病中的生物学特征和功能。
IF 1.5 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 Epub Date: 2023-01-31 DOI: 10.5114/ceji.2022.124416
Wei Jiang, Zehui Wang, Jun Zhang, Minghui Li
{"title":"Interleukin 25 and its biological features and function in intestinal diseases.","authors":"Wei Jiang, Zehui Wang, Jun Zhang, Minghui Li","doi":"10.5114/ceji.2022.124416","DOIUrl":"10.5114/ceji.2022.124416","url":null,"abstract":"<p><p>Interleukin 25 (IL-25), also known as IL-17E, is a member of the IL-17 cytokine family and an important regulator of the type 2 immune response. Accumulating evidence suggests that IL-25 interacts with diverse immune as well as non-immune cells and plays a rather complicated role in different backgrounds of multiple organs. IL-25 has been studied in the physiology and pathology of the intestine to some extent. With epithelial cells being an important source in the intestine, IL-25 plays a key role in intestinal immune responses and is associated with inappropriate allergic reactions, autoimmune diseases, and cancer tumorigenesis. In this review, we discuss the emerging comprehension of the biology of IL-25, as well as its cellular sources, targets, and signaling transduction. In particular, we discuss how IL-25 participates in the development of intestinal diseases including helminth infection, inflammatory bowel diseases, food allergy and colorectal cancer, as well as its underlying role in future therapy.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 4","pages":"362-372"},"PeriodicalIF":1.5,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/74/c9/CEJI-47-49997.PMC9901255.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9329905","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Characterization of 5-inflammatory-gene signature to affect the immune status and predict prognosis in breast cancer. 5-炎症基因特征对乳腺癌免疫状态的影响及预后的预测
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.121046
Hongyan Zang, Gaofeng Ni, Liguo Gong
{"title":"Characterization of 5-inflammatory-gene signature to affect the immune status and predict prognosis in breast cancer.","authors":"Hongyan Zang,&nbsp;Gaofeng Ni,&nbsp;Liguo Gong","doi":"10.5114/ceji.2022.121046","DOIUrl":"https://doi.org/10.5114/ceji.2022.121046","url":null,"abstract":"<p><strong>Introduction: </strong>Breast cancer (BC) is associated with an inflammatory microenvironment. In BC, epidemiological evidence suggests that inflammation is associated with a poor prognosis. However, approaches to determine the extent of inflammation in the tumor microenvironment remain unclear.</p><p><strong>Material and methods: </strong>We downloaded the expression profiles and corresponding clinicopathological information of 1050 BC tissues and 59 cases of normal breast tissue from The Cancer Genome Atlas (TCGA) dataset. Similarly, data of 1050 BC tissues were downloaded from Gene Expression Omnibus (GEO) and 200 inflammation-related genes were downloaded from the MSigDB database. We developed an inflammatory risk model to reflect the immune microenvironment in BC.</p><p><strong>Results: </strong>Multivariate Cox analysis showed that the risk score was an independent predictor of overall survival (OS). Inflammatory signature was significantly associated with clinical and molecular features and could serve as an independent prognostic factor for BC patients. Furthermore, most immune cells were significantly less infiltrated in the high-risk group than in the low-risk group. There was a significant difference in survival time between the group with a high and low tumor mutational burden (TMB) score, and the survival time of the patients with a low TMB was significantly higher than that of the high-risk group. The risk scores were significantly lower in patients who responded to immunotherapy (complete response/partial response - CR/PR) than in patients who did not respond to immunotherapy (stable disease/progressive disease - SD/PD).</p><p><strong>Conclusions: </strong>We developed and validated an inflammatory risk model, which served as an independent prognostic indicator and reflected immune response intensity in the BC microenvironment.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 3","pages":"218-233"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/6e/86/CEJI-47-48153.PMC9896988.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10825146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The correlation between infiltration of FoxP3+ Tregs, CD66b+ TANs and CD163+ TAMs in colorectal cancer. 结直肠癌中FoxP3+ Tregs、CD66b+ TANs和CD163+ TAMs浸润的相关性
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.114004
Yuehan Ren, Zhiyuan Chen, Jiancheng Sun, Yiqi Cai, Zhejing Chen, Xiaolei Chen, Wenyi Wu
{"title":"The correlation between infiltration of FoxP3<sup>+</sup> Tregs, CD66b<sup>+</sup> TANs and CD163<sup>+</sup> TAMs in colorectal cancer.","authors":"Yuehan Ren,&nbsp;Zhiyuan Chen,&nbsp;Jiancheng Sun,&nbsp;Yiqi Cai,&nbsp;Zhejing Chen,&nbsp;Xiaolei Chen,&nbsp;Wenyi Wu","doi":"10.5114/ceji.2022.114004","DOIUrl":"https://doi.org/10.5114/ceji.2022.114004","url":null,"abstract":"Introduction The infiltration of immune cells in tumor tissue is affected by the tumor microenvironment. However, the relationship between the infiltration of regulatory T cells (Tregs), tumor-associated neutrophils (TANs) and tumor-associated macrophages (TAMs) in colorectal cancer (CRC) remains unclear. Material and methods Tissue microarray and immunohistochemistry were used to detect the infiltration of FoxP3+ Tregs, CD66b+ TANs and CD163+ TAMs in 249 CRC samples (training cohort) and 243 CRC samples (validation cohort). The relationship between two cells was evaluated by Spearman’s rank correlation coefficient and comparison between two groups was analyzed by Mann-Whitney U test. Results The continuous variable positive cell numbers were non-normally distributed. Spearman correlation analysis showed that CD66b+ TAN level in cancer tissues was negatively related to FoxP3+ Treg level (correlation coefficient: –0.495, p < 0.05) and CD163+ TAM level (correlation coefficient: –0.266, p < 0.05), and FoxP3+ Treg level was positively related to CD163+ TAM level (correlation coefficient: 0.467, p < 0.05) in the training cohort. The numbers of FoxP3+ Tregs were significantly different between low and high CD66b+ TAN level groups (p < 0.001), as well as that of CD66b+ TANs in low and high CD163+ TAM level groups and CD163+ TAMs in different FoxP3+ Treg level groups. The results of the validation cohort were similar to those of the training cohort. Conclusions There is a negative correlation between infiltration of CD66b+ TANs and that of FoxP3+ Tregs or CD163+ TAMs, and a positive correlation between infiltration of FoxP3+ Tregs and CD163+ TAMs in CRC tissues.","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 1","pages":"1-7"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/42/6a/CEJI-47-46493.PMC9115591.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10252887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Use of the derived isohemagglutinin parameter to predict patients with COVID-19 in need of an intensive care unit. 使用衍生的等血凝素参数预测需要重症监护病房的COVID-19患者
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.115091
Bülent Barış Güven, Fatih Özçelik, Alpaslan Tanoglu
{"title":"Use of the derived isohemagglutinin parameter to predict patients with COVID-19 in need of an intensive care unit.","authors":"Bülent Barış Güven,&nbsp;Fatih Özçelik,&nbsp;Alpaslan Tanoglu","doi":"10.5114/ceji.2022.115091","DOIUrl":"https://doi.org/10.5114/ceji.2022.115091","url":null,"abstract":"<p><p>Predicting which patients will need the intensive care unit (ICU) due to severe COVID-19 is critical in terms of disease treatment. In this study, the use of the derived isohemagglutinin (dIH) parameter calculated from isohemagglutinin (IH) values and neutrophil to lymphocyte ratios for prediction of clinical care (CLC), ICU admission and mortality status was investigated for the morbidity and mortality of COVID-19. The data of approximately 21,500 patients admitted to the hospital with the suspicion of COVID-19 were scanned retrospectively. A total of 352 patients with IH results were divided into three groups according to CLC, ICU admission and mortality. Isohemagglutinin, hemogram and biochemistry test results, demographic characteristics, chronic diseases, length of stay, treatments, ICU admission and mortality records were reviewed for all patients. The relationship between test results, demographic characteristics, clinical status and mortality was investigated using statistical methods. The dIH values of patients with ICU admission and mortality were much lower than those of CLC patients [median (min-max): 3.34 (0.14-95.8) and 0.82 (0.05-42.3) vs. 0.18 (0.01-20.6) titers, p < 0.01, respectively]. In the ROC analysis for the power of dIH to discriminate ICU admission, the cutoff was ≤ 0.68 with sensitivity 88.9%, and specificity 79.6%. It was determined that a 1-unit increase in dIH values decreased the need for ICU by 2.09 times and the mortality of those receiving ICU treatment by 2.02 times. dIH values calculated in the early stages of the disease in patients with COVID-19 can be used to estimate the clinical progression associated with ICU admission and mortality.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 1","pages":"73-83"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/62/64/CEJI-47-46768.PMC9115598.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10252888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
24-hour central blood pressure and immune system activation in adolescents with primary hypertension - a preliminary study. 原发性高血压青少年24小时中心血压与免疫系统激活的初步研究
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.117929
Piotr Skrzypczyk, Adam Bujanowicz, Anna Ofiara, Michał Szyszka, Małgorzata Pańczyk-Tomaszewska
{"title":"24-hour central blood pressure and immune system activation in adolescents with primary hypertension - a preliminary study.","authors":"Piotr Skrzypczyk,&nbsp;Adam Bujanowicz,&nbsp;Anna Ofiara,&nbsp;Michał Szyszka,&nbsp;Małgorzata Pańczyk-Tomaszewska","doi":"10.5114/ceji.2022.117929","DOIUrl":"https://doi.org/10.5114/ceji.2022.117929","url":null,"abstract":"<p><strong>Introduction: </strong>Adult and pediatric data suggest a positive relationship between the extent of subclinical inflammation, blood pressure, and hypertension-mediated organ damage (HMOD) in primary hypertension (PH). 24-hour (24-h) ambulatory blood pressure (ABPM) and central blood pressure (CBP) are strong predictors of HMOD. Our study aimed to analyze the relationship between 24-h central ABPM, subclinical inflammation, and clinical data in adolescents with PH.</p><p><strong>Material and methods: </strong>In 28 untreated adolescents with PH (14.50 ±2.27 years) and 25 healthy peers (14.76 ±2.83 years), we analyzed 24-h peripheral and central ABPM, markers of subclinical inflammation (neutrophil-to-lymphocyte ratio - NLR, platelet-to-lymphocyte ratio - PLR, mean platelet volume - MPV), and clinical and biochemical data.</p><p><strong>Results: </strong>Patients with PH had higher 24-h peripheral and central blood pressure than healthy peers. In all 53 patients, we found significant (p < 0.05) positive correlations between NLR, PLR and 24-h central systolic, diastolic, and mean blood pressure (24-h cSBP, 24-h cDBP, 24-h cMAP), between 24-h central augmentation index corrected for heart rate 75 (24-h cAIx75HR) and platelet count. In 28 patients with PH, 24-h cAIx75HR correlated with low-density lipoprotein (LDL) cholesterol (R = 0.442), and ambulatory arterial stiffness index with body mass index (BMI) (R = 0.487), uric acid (R = 0.430), and high-density lipoprotein (HDL) cholesterol (R = -0.428).</p><p><strong>Conclusions: </strong>Increased central 24-h blood pressure may be associated with immune system activation in adolescents with primary hypertension. In adolescents with primary hypertension, dyslipidemia and hyperuricemia are risk factors for increased arterial stiffness. Further studies on central and peripheral blood pressure in terms of their relationship with inflammation in these patients are needed.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 2","pages":"160-167"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2f/1a/CEJI-47-47428.PMC9894090.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10672217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cancer immunoediting hypothesis: history, clinical implications and controversies. 癌症免疫编辑假说:历史、临床意义和争议。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.117376
Witold Lasek
{"title":"Cancer immunoediting hypothesis: history, clinical implications and controversies.","authors":"Witold Lasek","doi":"10.5114/ceji.2022.117376","DOIUrl":"https://doi.org/10.5114/ceji.2022.117376","url":null,"abstract":"<p><p>The main function of the immune system is to protect against infectious pathogens and to ensure tissue homeostasis. The latter function includes preventing autoimmune reactions, tolerizing cells to nonpathogenic environmental microorganisms, and eliminating apoptotic/damaged, transformed, or neoplastic cells. The process of carcinogenesis and tumor development and the role of the immune system in inhibiting progression of cancer have been the subject of intense research since the end of the 20<sup>th</sup> century and resulted in formulation of the cancer immunoediting hypothesis. The hypothesis postulates three steps in oncogenesis: 1) elimination - corresponding to immunosurveillance, 2) equilibrium in which the growth of transformed or neoplastic cells is efficiently controlled by immune effector mechanisms, and 3) escape in which cancer progresses due to an ineffective antitumor response. In parallel, a new field of science - immune-oncology - has arisen. Attempts are also being made to quantify intra-tumoral and peritumoral T cell infiltrations and to define optimal immunological parameters for prognostic/predictive purposes in several types of cancer. The knowledge of relationships between the tumor and the immune system has been and is practically exploited therapeutically in the clinic to treat cancer. Immunotherapy is a standard or supplementary treatment in various types of cancer.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 2","pages":"168-174"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/17/fe/CEJI-47-47287.PMC9894085.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10672219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Oxidized low-density lipoprotein contributes to injury of endothelial cells via the circ_0090231/miR-9-5p/TXNIP axis. 氧化低密度脂蛋白通过circ_0090231/miR-9-5p/TXNIP轴参与内皮细胞损伤。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2021.112521
Xiubing Lei, Yang Yang
{"title":"Oxidized low-density lipoprotein contributes to injury of endothelial cells via the circ_0090231/miR-9-5p/TXNIP axis.","authors":"Xiubing Lei,&nbsp;Yang Yang","doi":"10.5114/ceji.2021.112521","DOIUrl":"https://doi.org/10.5114/ceji.2021.112521","url":null,"abstract":"<p><p>Atherosclerosis (AS) has been reported to induce severe clinical complications. Circular RNA (circRNA) circ_0090231 was found to be aberrantly overexpressed in oxidized low-density lipoprotein (ox-LDL)-induced endothelial cells. This study was designed to explore the role and mechanism of circ_0090231 in ox-LDL-triggered endothelial cell injury in AS. Circ_0090231, microRNA-9-5p (miR-9-5p), and thioredoxin interacting protein (TXNIP) levels were detected by real-time quantitative polymerase chain reaction (RT-qPCR). Cell viability, angiogenesis, and apoptosis were detected by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT), tube formation, and flow cytometry assay. Bcl-2, Bax, and TXNIP protein levels were gauged by western blot assay. Malondialdehyde (MDA), lactate dehydrogenase (LDH), and superoxide dismutase (SOD) activity were determined by special kits. Tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), and interleukin 6 (IL-6) levels were analyzed using enzyme-linked immunosorbent assay (ELISA) kits. The binding relationship between miR-9-5p and circ_0090231 or TXNIP was predicted by starBase, and then verified by a dual-luciferase reporter and RNA immunoprecipitation (RIP) assays. Circ_0090231 and TXNIP were increased, and miR-9-5p was decreased in ox-LDL-treated HUVECs. Moreover, circ_0090231 knockdown mitigated ox-LDL-induced HUVEC injury by boosting angiogenesis, oxidative stress, and inflammation, and hindering apoptosis. The mechanical analysis revealed that circ_0090231 acted as a sponge of miR-9-5p to regulate TXNIP expression. Circ_0090231 could attenuate ox-LDL-mediated HUVEC damage by the miR-9-5p/TXNIP axis, providing a promising therapeutic strategy for AS treatment.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 1","pages":"41-57"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/77/f4/CEJI-47-46151.PMC9115597.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10306020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Serum and urine periostin and cytokeratin-18 in children with congenital obstructive nephropathy. 先天性阻塞性肾病患儿血清和尿骨膜蛋白和细胞角蛋白-18的研究。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.115687
Agnieszka Turczyn, Grażyna Krzemień, Elżbieta Górska, Urszula Demkow, Małgorzata Pańczyk-Tomaszewska
{"title":"Serum and urine periostin and cytokeratin-18 in children with congenital obstructive nephropathy.","authors":"Agnieszka Turczyn,&nbsp;Grażyna Krzemień,&nbsp;Elżbieta Górska,&nbsp;Urszula Demkow,&nbsp;Małgorzata Pańczyk-Tomaszewska","doi":"10.5114/ceji.2022.115687","DOIUrl":"https://doi.org/10.5114/ceji.2022.115687","url":null,"abstract":"<p><p>Congenital obstructive nephropathy (CON) is one of the most common causes of chronic kidney disease in children. The aim of the study was to investigate serum and urine periostin and cytokeratin-18 (CK-18) in children with CON in relation to CON etiology, treatment, and kidney injury. We evaluated 81 children with CON secondary to ureteropelvic junction obstruction (UPJO), ureterovesical junction obstruction (UVJO), posterior urethral valves (PUV) and 60 controls. Neither biomarker demonstrated any relation to CON etiology. However, all patients showed significantly higher urine periostin (uPeriostin) and uPeriostin/Cr levels than the controls. Also, UVJO patients showed higher sCK-18 and uCK-18/Cr levels, and PUV patients showed higher uCK-18/Cr levels than the controls. Neither biomarker was found to have any relation to CON treatment. However, conservatively treated children and those before and after surgery showed significantly higher uPeriostin and uPeriostin/Cr levels than the controls. uPeriostin strongly correlated with differential renal function (DRF) < 40%. The ROC analysis demonstrated the best area under the curve (AUC) for uPeriostin (0.831) and uPeriostin/Cr (0.768), and low for sPeriostin (0.656) and uCK-18 (0.615) for detecting renal injury. In conclusion, although serum and urine periostin and CK-18 did not display any relation to etiology or the type of CON treatment, uPeriostin seems to be a useful tool for detecting renal injury in children with CON, especially due to its strong negative correlation with DRF < 40%.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"47 1","pages":"63-72"},"PeriodicalIF":1.3,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/af/22/CEJI-47-46897.PMC9115600.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10306024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Pam2 lipopeptides enhance the immunosuppressive activity of monocytic myeloid-derived suppressor cells by STAT3 signal in chronic inflammation. Pam2脂肽通过STAT3信号增强单核髓源性抑制细胞在慢性炎症中的免疫抑制活性。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2022-01-01 DOI: 10.5114/ceji.2022.113086
Xiaoxia Zhan, Xiaobing Jiang, Qiuying He, Liangyin Zhong, Yichong Wang, Yulan Huang, Shitong He, Junli Sheng, Jianwei Liao, Zhijie Zeng, Shengfeng Hu
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