Central European Journal of Immunology最新文献

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Immunotherapy of B cell lymphoma with CD22-redirected CAR NK-92 cells. cd22重定向CAR - NK-92细胞对B细胞淋巴瘤的免疫治疗
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.126672
Xiaopeng Tian, Ruixi Zhang, Huimin Qin, Xiangru Shi, Wenhui Qi, Dongpeng Jiang, Tingting Zhu, Aining Sun
{"title":"Immunotherapy of B cell lymphoma with CD22-redirected CAR NK-92 cells.","authors":"Xiaopeng Tian,&nbsp;Ruixi Zhang,&nbsp;Huimin Qin,&nbsp;Xiangru Shi,&nbsp;Wenhui Qi,&nbsp;Dongpeng Jiang,&nbsp;Tingting Zhu,&nbsp;Aining Sun","doi":"10.5114/ceji.2023.126672","DOIUrl":"https://doi.org/10.5114/ceji.2023.126672","url":null,"abstract":"<p><strong>Introduction: </strong>Chimeric antigen receptor (CAR)-NK cells are considered safer than CAR-T cells due to their short lifetime and production of lower toxicity cytokines. By virtue of unlimited proliferative ability in vitro, NK-92 cells could be utilized as the source for CAR-engineered NK cells. CD22 is highly expressed in B cell lymphoma. The goal of our study was to determine whether CD22 could become an alternative target for CAR-NK-92 therapy against B cell lymphoma.</p><p><strong>Material and methods: </strong>We first generated m971-BBZ NK-92 that expressed a CAR for binding CD22 in vitro. The expression of CAR was assessed by flow cytometric analysis as well as immunoblotting. The cytotoxicity of the m971-BBZ NK-92 cells towards target lymphoma cells was determined by the luciferase-based cytolysis assay. The production of cytokines in CAR NK-92 cells in response to target cells was evaluated by ELISA assay. Lastly, the cytolytic effect was evaluated by the cytolysis assay mentioned above following irradiation. The level of inhibitory receptor of CAR-expressing cells was assessed by flow cytometry.</p><p><strong>Results: </strong>CD22-specific CAR was expressed on m971-BBZ NK-92 cells successfully. m971-BBZ NK-92 cells efficiently lysed CD22-expressing lymphoma cells and produced large amounts of cytokines after coculture with target cells. Meanwhile, irradiation did not apparently influence the cytotoxicity of m971-BBZ NK-92 cells. Inhibitory receptor detection exhibited a lower level of PD-1 in m971-BBZ NK-92 cells than FMC-63 BBZ T cells after repeated antigen stimulation.</p><p><strong>Conclusions: </strong>Our data show that adoptive transfer of m971-BBZ NK-92 could serve as a promising strategy for immunotherapy of B cell lymphoma.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 1","pages":"1-13"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/17/d1/CEJI-48-50550.PMC10189576.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9930543","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
Trigeminal neuralgia occurring after the third dose of Pfizer BioNTech COVID-19 vaccine. Complication or coincidence? An illustrative case report and literature review. 三叉神经痛发生在第三剂辉瑞BioNTech COVID-19疫苗后。复杂还是巧合?一篇说明性病例报告及文献回顾。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.125309
Kacper Chrostowski, Michał Piasecki, Joanna Bielewicz
{"title":"Trigeminal neuralgia occurring after the third dose of Pfizer BioNTech COVID-19 vaccine. Complication or coincidence? An illustrative case report and literature review.","authors":"Kacper Chrostowski,&nbsp;Michał Piasecki,&nbsp;Joanna Bielewicz","doi":"10.5114/ceji.2023.125309","DOIUrl":"https://doi.org/10.5114/ceji.2023.125309","url":null,"abstract":"<p><p>The coronavirus disease 2019 pandemic is an ongoing concern for medical care worldwide. Since its emergence, multiple COVID-19 vaccines have been designed, allowing for more effective control of the pandemic. COVID-19 vaccines, like any other form of medical intervention, may cause adverse and unforeseen side effects, varying in frequency and severity. Determining a correlation between the occurring symptoms and the vaccination is often a challenging task, requiring multiple data sources and reported cases. So far, there have been multiple reports of trigeminal neuralgia developing after COVID-19 vaccination. A 36-year-old woman was admitted to the Emergency Ward due to chronic pain attacks in the left side of her face. The pain appeared two months ago, on the day following the vaccination using the third dose of the Pfizer BioNTech COVID-19 vaccine. At the Neurology Department she was diagnosed with trigeminal neuralgia. Based on the lack of any obvious causes, relation to the vaccination, and other similar reports, we assumed that the trigeminal neuralgia was a complication of the vaccination. Hospital treatment consisted of oxcarbazepine, dexamethasone and pregabalin. Treatment was successful, with transient episodes of exacerbation. Six months after the onset of the disorder the patient remains without pain. We believe that the presented case supports the possibility of trigeminal neuralgia occurring in relation to the Pfizer BioNTech COVID-19 vaccine administration. Additional reports may further contribute to establishing a certain link.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 1","pages":"75-80"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d1/14/CEJI-48-50183.PMC10189574.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9930538","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
The role of monocytes in malaria infection. 单核细胞在疟疾感染中的作用。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.126650
Keh Min Xuan, Nurhidanatasha Abu Bakar, Khairul Mohd Fadzli Mustaffa, Maryam Azlan
{"title":"The role of monocytes in malaria infection.","authors":"Keh Min Xuan,&nbsp;Nurhidanatasha Abu Bakar,&nbsp;Khairul Mohd Fadzli Mustaffa,&nbsp;Maryam Azlan","doi":"10.5114/ceji.2023.126650","DOIUrl":"https://doi.org/10.5114/ceji.2023.126650","url":null,"abstract":"<p><p>Malaria remains one of the most common human infections worldwide. In endemic areas, malaria is a leading cause of morbidity and mortality and it imposes significant socioeconomic burdens on the people affected. Monocytes are part of the immune system controlling parasite burden and protecting the host against malaria infection. Monocytes play their protective roles against malaria via phagocytosis, cytokine production and antigen presentation. Though monocytes are crucial for clearance of malaria infection, they have also been shown to cause adverse clinical outcomes. In this review, we discuss recent findings regarding the role of monocytes in malaria via mechanisms such as parasite detection and clearance, pro-inflammatory activities, and activation of other immune components. We also highlight the role of different monocyte subsets, and other myeloid cells that are involved in malaria infection. However, more investigations are required in order to explore the exact roles of these monocytes in malaria infection.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 1","pages":"54-62"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7b/fc/CEJI-48-50545.PMC10189572.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9930541","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
Molecular regulatory mechanism of LILRB4 in the immune response. LILRB4在免疫应答中的分子调控机制。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.125238
Haiyin Liu, Jun Yang, Jing Zhang, Peiyue Zhang, Mengting Zhang, Chaojun Yang, Li Liu, Cuiyuan Huang, Wei Wang, Yuhong Zhai, Jian Yang
{"title":"Molecular regulatory mechanism of LILRB4 in the immune response.","authors":"Haiyin Liu,&nbsp;Jun Yang,&nbsp;Jing Zhang,&nbsp;Peiyue Zhang,&nbsp;Mengting Zhang,&nbsp;Chaojun Yang,&nbsp;Li Liu,&nbsp;Cuiyuan Huang,&nbsp;Wei Wang,&nbsp;Yuhong Zhai,&nbsp;Jian Yang","doi":"10.5114/ceji.2023.125238","DOIUrl":"https://doi.org/10.5114/ceji.2023.125238","url":null,"abstract":"<p><p>Immune diseases are caused by the imbalance of immune regulation. This imbalance is regulated by many factors, both negative and positive. Leukocyte immunoglobulin-like receptor B4 (LILRB4) is a member of leukocyte immunoglobulin-like receptors (LILRs). LILRs are expressed constitutively on the surface of multiple immune cells which associate with membrane adaptors to signal through multi- ple cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs) or immunoreceptor tyro-sine-based activation motifs (ITAMs). Through ITIM, LILRB4 could recruit the src homology domain type-2-containing tyrosine phosphatase 1 or 2 (SHP-1 or SHP-2) into the cell membrane. In addition, many factors can induce the expression of LILRB4, such as vitamin D, interferon and so on. Studies have demonstrated that LILRB4 had a negative regulatory role in various of immune diseases. The present review intends to expound the structure and function of LILRB4, as well as its regulators and receptors in the immune cells, so as to provide a theoretical basis for immune disease therapy.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 1","pages":"43-47"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c9/5e/CEJI-48-50171.PMC10189573.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9933154","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
A rare cause of steroid-resistant nephrotic syndrome - a case report. 类固醇抵抗性肾病综合征的罕见病因- 1例报告。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.127534
Paulina Kuran, Emilia Platos, Małgorzata Mizerska-Wasiak, Małgorzata Pańczyk-Tomaszewska
{"title":"A rare cause of steroid-resistant nephrotic syndrome - a case report.","authors":"Paulina Kuran,&nbsp;Emilia Platos,&nbsp;Małgorzata Mizerska-Wasiak,&nbsp;Małgorzata Pańczyk-Tomaszewska","doi":"10.5114/ceji.2023.127534","DOIUrl":"https://doi.org/10.5114/ceji.2023.127534","url":null,"abstract":"<p><p>Steroid resistance is a common condition occurring in children with nephrotic syndrome. Until now, over 50 genes involved in steroid-resistant nephrotic syndrome (SRNS) pathogenesis have been identified, among which the most prevalent are NPHS1, NPHS2, CD2AP, and PTPRO. The patterns of inheritance of SRNS are autosomal recessive, autosomal dominant, or mitochondrial, and tissues of those patients show focal segmental glomerulosclerosis (FSGS) signs in histopathological image analysis. We present a case of a 6-year-old girl who was admitted to the pediatric nephrology department due to nephrotic range proteinuria and edema of the lower leg. We started therapy with prednisone at a dose of 45 mg (60 mg/m<sup>2</sup>), enalapril as a nephroprotection, and antihistamines as an additional treatment. During in-patient treatment, we detected increased blood pressure. Due to persistent proteinuria in spite of 6-week treatment with steroids at the maximal dose, we confirmed disease resistance to steroids. Additionally, FSGS signs were confirmed in kidney biopsy samples. After genetic screening for SRNS and detection of the rare gene mutation NUP93 we reduced prednisone but maintained nephroprotective treatment and administered cyclosporin A. The girl remains currently under the care of nephrologists with normal arterial blood pressure, trace proteinuria in follow-up examination, and normal kidney function. NUP93 mutation is extremely rare; therefore few cases have been described to date. The onset of the symptoms in all pediatric patients appeared before the age of 8 and they developed end stage kidney disease (ESKD). They might manifest symptoms from the other systems.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 2","pages":"158-162"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/48/a2/CEJI-48-50695.PMC10485693.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10220431","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
Effects of theophylline combined with inhaled corticosteroids on patients with moderate and severe asthma and changes of T lymphocyte subsets in peripheral blood. 茶碱联合吸入皮质类固醇对中重度哮喘患者外周血T淋巴细胞亚群的影响。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.127843
Xiaozhen Cai, Rong Rong, Yidan Huang, Xiaowen Pu, Nanhai Ge
{"title":"Effects of theophylline combined with inhaled corticosteroids on patients with moderate and severe asthma and changes of T lymphocyte subsets in peripheral blood.","authors":"Xiaozhen Cai,&nbsp;Rong Rong,&nbsp;Yidan Huang,&nbsp;Xiaowen Pu,&nbsp;Nanhai Ge","doi":"10.5114/ceji.2023.127843","DOIUrl":"https://doi.org/10.5114/ceji.2023.127843","url":null,"abstract":"<p><strong>Introduction: </strong>Asthma is a common respiratory disease. Theophylline combined with inhaled corticosteroids (ICS) is a promising therapy for asthma. This study explored the therapeutic effects of ICS combined with theophylline on moderate and severe asthma patients and T lymphocyte subsets (CD3<sup>+</sup>CD8<sup>+</sup> T cells) in peripheral blood.</p><p><strong>Material and methods: </strong>A total of 202 moderate and severe asthma patients were selected, with 101 treated with theophylline combined with ICS and 101 treated with ICS alone as controls. Lung function [forced expiratory volume within 1 second (FEV1), forced vital capacity (FVC), and peak expiratory flow (PEF)] were tested using a spirometer. Asthma symptom control was evaluated by asthma control tests (ACT). The life quality was evaluated using the Asthma Quality of Life Questionnaire (AQLQ). The number and percentage of CD3<sup>+</sup> T, CD3<sup>+</sup>CD4<sup>+</sup> T and CD3<sup>+</sup>CD8<sup>+</sup> T cells in peripheral blood mononuclear cells were assessed by flow cytometry. The correlation between CD3<sup>+</sup>CD8<sup>+</sup> T cells and lung function and asthma control of patients after combination therapy was analyzed by Pearson correlation analysis.</p><p><strong>Results: </strong>Compared with moderate and severe patients treated with ICS alone, theophylline improved the efficacy of ICS. Theophylline combined with ICS decreased IL-4 and IL-6 levels, and CD3<sup>+</sup> T and CD3<sup>+</sup>CD8<sup>+</sup> T cell number and percentage. After combined treatment, CD3<sup>+</sup> CD8<sup>+</sup> T cells in peripheral blood of patients were positively correlated with lung function and negatively correlated with asthma control.</p><p><strong>Conclusions: </strong>The additional use of theophylline improved the efficacy of corticosteroids in asthma patient treatment and reduced inflammation level and CD3<sup>+</sup> T and CD3<sup>+</sup>CD8<sup>+</sup> T cell contents in peripheral blood.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 2","pages":"135-143"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/09/09/CEJI-48-50786.PMC10485692.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10220434","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
Abnormal expression of CXCL13, MIF and IL-35 in patients with primary Sjögren's syndrome and its relationship with disease severity. 原发性Sjögren综合征患者CXCL13、MIF和IL-35的异常表达及其与病情严重程度的关系
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 DOI: 10.5114/ceji.2023.127536
Ronghua Wang, Yushu Yang, Xuying Liu, Lingyan Lei, Xuan Qi
{"title":"Abnormal expression of CXCL13, MIF and IL-35 in patients with primary Sjögren's syndrome and its relationship with disease severity.","authors":"Ronghua Wang,&nbsp;Yushu Yang,&nbsp;Xuying Liu,&nbsp;Lingyan Lei,&nbsp;Xuan Qi","doi":"10.5114/ceji.2023.127536","DOIUrl":"https://doi.org/10.5114/ceji.2023.127536","url":null,"abstract":"<p><strong>Introduction: </strong>The aim of the study was to detect the saliva chemokine (C-X-C motif) ligand 13 (CXCL13), macrophage migration inhibitory factor (MIF), and interleukin 35 (IL-35) levels in patients with primary Sjögren's syndrome (pSS) and pSS-associated interstitial lung disease (pSS-ILD), and to explore the relationship between CXCL13, MIF, IL-35 levels, and disease severity.</p><p><strong>Material and methods: </strong>ESSDAI score was used to evaluate the disease activity of pSS patients, and the levels of CXCL13, MIF and IL-35 in saliva of subjects were detected and analyzed, and the relationship between CXCL13, MIF, IL-35 and the occurrence of pSS was evaluated. Pearson's correlation coefficient was used to analyze the correlation between CXCL13, MIF, IL-35 and ESSDAI score. ROC curve analysis was conducted to assess the diagnostic value of CXCL13, MIF, IL-35 and their combined application in pSS.</p><p><strong>Results: </strong>The levels of CXCL13, MIF, and IL-35 in saliva were positively correlated with ESSDAI score. Saliva CXCL13 and IL-35 are risk factors for the development of pSS into pSS-ILD. The ROC curve shows that the combination of saliva CXCL13, MIF and IL-35 has the highest diagnostic efficiency for pSS-ILD.</p><p><strong>Conclusions: </strong>CXCL13, MIF and IL-35 are related to the activity of pSS, and the combined diagnosis of these three indexes is expected to be an important method to predict the occurrence and development of pSS.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 2","pages":"144-149"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/41/06/CEJI-48-50697.PMC10485687.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10587668","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
A biomarker and molecular mechanism investigation for thyroid cancer. 甲状腺癌症的生物标志物和分子机制研究。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 Epub Date: 2023-09-29 DOI: 10.5114/ceji.2023.132163
Keju Xie
{"title":"A biomarker and molecular mechanism investigation for thyroid cancer.","authors":"Keju Xie","doi":"10.5114/ceji.2023.132163","DOIUrl":"https://doi.org/10.5114/ceji.2023.132163","url":null,"abstract":"<p><strong>Introduction: </strong>This study aimed to reveal the potential molecular mechanism associated with thyroid cancer (THCA) prognosis, and investigate promising biomarkers for THCA.</p><p><strong>Material and methods: </strong>Differentially expressed genes (DEGs) were compared between THCA samples (THCA group) and normal samples (N group). Then, enrichment analysis and protein-protein interaction (PPI) network analysis were performed, followed by prognostic hub gene exploration from the PPI network. Furthermore, the prognostic and mutation analysis was performed on these hub genes. Finally, the associations of the hub gene with immune cells were investigated.</p><p><strong>Results: </strong>A total of 802 DEGs were obtained between the THCA group and the N group. These DEGs were mainly enriched in pathways such as lysine degradation. From the PPI network, 20 hub genes, including CD44, CCND1, SNAI1, and KIT, were investigated. The survival analysis showed that the up-regulation of CD44 and down-regulation of SNAI1 contributed to the favorable and unfavorable outcomes of patients with THCA, respectively. Meanwhile, the diagnostic analysis showed that the AUC of KIT in THCA was larger than 0.9. Furthermore, the gene mutation analysis showed that the alternated CCND1 participated in the cell cycle pathway. Finally, the correlation analysis showed that prognostic genes such as CD44 were positively correlated with immune cells such as M1 macrophages.</p><p><strong>Conclusions: </strong>A total of 20 hub genes including CCND1, CD44, SNAI1, and KIT were revealed as potential biomarkers for the differential diagnosis, prognosis, and development of drug targets of THCA. The lysine degradation pathway and cell cycle pathway might take part in the progression of THCA.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 3","pages":"203-218"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604643/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71410893","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
Anticitrullinated antibodies recognize rheumatoid arthritis associated T-cell epitopes modified by bacterial L-asparaginase. 抗瓜氨酸抗体识别细菌L-天冬酰胺酶修饰的类风湿性关节炎相关T细胞表位。
IF 1.3 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 Epub Date: 2023-09-21 DOI: 10.5114/ceji.2023.131455
Tsvetelina Batsalova, Ivanka Teneva, Krum Bardarov, Dzhemal Moten, Balik Dzhambazov
{"title":"Anticitrullinated antibodies recognize rheumatoid arthritis associated T-cell epitopes modified by bacterial L-asparaginase.","authors":"Tsvetelina Batsalova,&nbsp;Ivanka Teneva,&nbsp;Krum Bardarov,&nbsp;Dzhemal Moten,&nbsp;Balik Dzhambazov","doi":"10.5114/ceji.2023.131455","DOIUrl":"https://doi.org/10.5114/ceji.2023.131455","url":null,"abstract":"<p><p>Citrullinated proteins and anti-citrullinated protein antibodies (ACPAs) play an important role in the pathogenesis of rheumatoid arthritis (RA). It has been suggested that during inflammation or dysbiosis, bacteria could initiate production of ACPAs. Most patients with RA are seropositive for ACPAs, but these antibodies have overlapping reactivity to different posttranslational modifications (PTMs). For initiation and development of RA, T lymphocytes and T cell epitopes are still required. In this study, we evaluated the ability of bacterial L-asparaginase to modify RA-related T cell epitopes within type II collagen (CII259-273 and CII311-325), as well as whether these modified epitopes are recognized by ACPAs from RA patients. We included 12 patients with early RA and 11 healthy subjects selected according to predefined specific criteria. LC-MS/MS analyses revealed that the bacterial L-asparaginase can modify investigated T cell epitopes. ELISA tests showed cross-reactivity of ACPA positive sera from early RA patients towards the enzymatically modified immunodominant T cell epitopes within type II collagen (CII), but not to the modified irrelevant peptides. These data suggest that the cross-reactive ACPAs recognize the \"carbonyl-Gly-Pro\" motif in CII. Moreover, the T cell recognition of the modified major immunodominant T cell epitope Gal264-CII259-273 was not affected. This epitope was still able to activate autoreactive T cells from early RA patients. It is likely that such modifications are the missing link between the T cell priming and the development of anti-modified protein antibodies (AMPAs). Our results provide additional information on the etiology and pathogenesis of RA.</p>","PeriodicalId":9694,"journal":{"name":"Central European Journal of Immunology","volume":"48 3","pages":"174-188"},"PeriodicalIF":1.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604640/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71410894","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
Novel inflammatory markers in patients with severe COVID-19 and a pulmonary thrombotic event. 严重新冠肺炎和肺血栓事件患者的新炎症标志物。
IF 1.5 4区 医学
Central European Journal of Immunology Pub Date : 2023-01-01 Epub Date: 2023-09-21 DOI: 10.5114/ceji.2023.131382
Jarosław Bakiera, Karolina Strzelec-Pawełczak, Katarzyna Czarnek, Ida Osuchowska-Grochowska, Jacek Bogucki, Agnieszka Markiewicz-Gospodarek, Aleksandra Górska, Zuzanna Chilimoniuk, Sebastian Radej, Mateusz Szymański, Piero Portincasa, Cezary Grochowski
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