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[Regulatory T cells]. 调节性T细胞。
Q4 Medicine Pub Date : 2006-12-01 DOI: 10.1142/9789813231719_0008
I. Marinić, A. Gagro, S. Rabatić
Regulatory T-cells are a subset of T cells that have beene extensively studied in modern immunology. They are important for the maintenance of peripheral tolerance, and have an important role in various clinical conditions such as allergy, autoimmune disorders, tumors, infections, and in transplant medicine. Basically, this population has a suppressive effect on the neighboring immune cells, thus contributing to the local modulation and control of immune response. There are two main populations of regulatory T cells - natural regulatory T cells, which form a distinct cellular lineage, develop in thymus and perform their modulatory action through direct intercellular contact, along with the secreted cytokines; and inducible regulatory T cells, which develop in the periphery after contact with the antigen that is presented on the antigen presenting cell, and their primary mode of action is through the interleukin 10 (IL-10) and transforming growth factor beta (TGF-alpha) cytokines. Natural regulatory T cells are activated through T cell receptor after contact with specific antigen and inhibit proliferation of other T cells in an antigen independent manner. One of the major difficulties in the research of regulatory T cells is the lack of specific molecular markers that would identify these cells. Natural regulatory T cells constitutively express surface molecule CD25, but many other surface and intracellular molecules (HLA-DR, CD122, CD45RO, CD62, CTLA-4, GITR, PD-1, Notch, FOXP3, etc.) are being investigated for further phenotypic characterization of these cells. Because regulatory T cells have an important role in establishing peripheral tolerance, their importance is manifested in a number of clinical conditions. In the IPEX syndrome (immunodysregulation, polyendocrinopathy and enteropathy, X-linked), which is caused by mutation in Foxp3 gene that influences the development and function of regulatory T cells, patients develop severe autoimmune reactions that involve autoimmune endocrine disorders (type 1 diabetes, thyroiditis), respiratory and nutritive allergy, eczema and severe infections. In different types of allergy (pollen allergy, dust mite, nutritive allergens, contact hypersensitivity, etc.) and autoimmune diseases (such as rheumatoid arthritis, multiple sclerosis and type 1 diabetes) a lower number or decreased functional capability of regulatory T cells have been described. In inflammatory conditions and infections, this cell population has an important task in restricting immune response and protecting the host from excessive damage. This ability of regulatory T cells can be used by some pathogens (Epstein Barr virus, Mycobacterium tuberculosis, Leishmania major, etc.) and tumor cells to avoid host response and therefore contribute to the development of some pathological conditions. The knowledge gained on the phenotype and function of regulatory T cells could be useful in many medical conditions. In allergy, autoimmune diseases and
调节性T细胞是T细胞的一个子集,在现代免疫学中得到了广泛的研究。它们对于外周耐受性的维持很重要,并且在各种临床疾病如过敏、自身免疫性疾病、肿瘤、感染和移植医学中发挥重要作用。基本上,这个群体对邻近的免疫细胞有抑制作用,从而有助于局部调节和控制免疫反应。调节性T细胞主要有两种:自然调节性T细胞,它们形成独特的细胞谱系,在胸腺中发育,并通过直接的细胞间接触以及分泌的细胞因子来发挥调节作用;和诱导调节性T细胞,它们与抗原呈递细胞上的抗原接触后在外周发育,它们的主要作用方式是通过白细胞介素10 (IL-10)和转化生长因子β (tgf - α)细胞因子。自然调节性T细胞与特异性抗原接触后,通过T细胞受体被激活,并以不依赖抗原的方式抑制其他T细胞的增殖。调节性T细胞研究的主要困难之一是缺乏特异性分子标记来识别这些细胞。自然调节性T细胞组成性地表达表面分子CD25,但许多其他表面和细胞内分子(HLA-DR、CD122、CD45RO、CD62、CTLA-4、GITR、PD-1、Notch、FOXP3等)正在被研究以进一步表征这些细胞的表型。由于调节性T细胞在建立外周耐受性方面起着重要作用,它们的重要性在许多临床条件中得到体现。IPEX综合征(免疫失调、多内分泌病和肠病,x连锁)是由Foxp3基因突变影响调节性T细胞的发育和功能引起的,患者会出现严重的自身免疫反应,包括自身免疫性内分泌紊乱(1型糖尿病、甲状腺炎)、呼吸和营养过敏、湿疹和严重感染。在不同类型的过敏(花粉过敏、尘螨、营养性过敏原、接触性超敏反应等)和自身免疫性疾病(如类风湿关节炎、多发性硬化症和1型糖尿病)中,调节性T细胞数量较少或功能能力下降已被描述。在炎症条件和感染中,这些细胞群在限制免疫反应和保护宿主免受过度损伤方面具有重要作用。调节性T细胞的这种能力可以被一些病原体(爱泼斯坦巴尔病毒、结核分枝杆菌、利什曼原虫等)和肿瘤细胞利用,以避免宿主反应,从而促进一些病理状况的发展。关于调节性T细胞的表型和功能的知识在许多医疗条件下可能是有用的。在过敏、自身免疫性疾病和医学上的移植手术中,希望增加它们的功能,从而部分抑制免疫系统的活性。另一方面,在某些感染和肿瘤中,最好是降低调节性T细胞的活性,增强效应T细胞的功能。调节性T细胞是一个非常活跃的免疫学领域,因此监测和调节其活性在广泛的临床条件下具有重要的潜在意义。通过开发和标准化监测方法,可以跟踪某些临床条件的附加参数,并可能将其用于治疗。
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引用次数: 1
[Word recognition test after general anesthesia: the influence of previous anesthesia]. 全麻后单词识别测试:既往麻醉的影响。
Q4 Medicine Pub Date : 2006-06-01 DOI: 10.1097/00003643-200606001-00346
I. Skok, A. Sekulić, S. Mikulandra
Among other higher brain functions such as consciousness and learning, general anesthesia also affects memory. A number of information retrieval tests are performed to determine the effects of drugs on explicit memory. In this study, we investigated the recognition of words before and after general anesthesia in subjects having and not having received anesthesia on one or more occasions before the present one. The study included 51 patients, ASA physical status I or II, median age 50, at least high-school graduates, without head trauma, known psychiatric or memory disorder, and taking no psychoactive medication. A standardized anesthesia technique, a single surgical procedure and a defined study-test interval were used. We designed our own test as a combination of story recall test and brief word learning test, both widely used in psychological and psychiatric examination. There was no significant difference in word recognition before and after general anesthesia in either patient group. Many studies indicate that anesthesia and surgery are associated with cognitive impairment lasting for 33 months in 10%-14% of elderly patients. We hypothesized that general anesthetics can cause prolonged cognitive alterations. Study results showed that previous anesthesia in addition to the current one had no significant influence on the word recognition test.
在意识和学习等其他高级大脑功能中,全身麻醉也会影响记忆。为了确定药物对外显记忆的影响,进行了一些信息检索测试。在本研究中,我们调查了在全麻之前接受过和未接受过一次或多次麻醉的受试者在全麻前后对单词的识别。该研究包括51名患者,ASA身体状态为I或II,中位年龄为50岁,至少高中毕业,无头部创伤,已知的精神或记忆障碍,未服用精神药物。采用标准化麻醉技术、单一手术程序和确定的研究试验间隔。我们设计了自己的测试,作为故事回忆测试和简短单词学习测试的结合,这两种测试在心理和精神检查中都被广泛使用。两组患者在全麻前后的单词识别能力无显著差异。许多研究表明,在10%-14%的老年患者中,麻醉和手术与持续33个月的认知障碍有关。我们假设全身麻醉会导致长期的认知改变。研究结果表明,除当前麻醉外,之前的麻醉对单词识别测试没有显著影响。
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引用次数: 0
[Uremic polyneuropathy]. (尿毒症多神经病)。
Q4 Medicine Pub Date : 2004-01-01 DOI: 10.1001/jama.1963.03700160135048
Ismail el Aklouk, V. Bašić Kes, N. Bašić-Jukić, B. Brunetta, P. Kes
Uremic polyneuropathy is probably the most common complication of chronic renal failure. About 70 percent of dialysis patients regularly have uremic polyneuropathy, in 30 percent the neuropathy is moderate or severe. Coexistence of muscle weakness and atrophy, areflexia, sensory loss and graded distribution of neurologic deficit in a patient with renal disease suggests the presence of uremic polyneuropathy. During longterm hemodialysis, the symptoms of polyneuropathy stabilize, but they improve only in relatively few patients. Complete recovery, occurring over a period of 6 to 12 months, usually follows successful renal transplantation.
尿毒症多发性神经病可能是慢性肾功能衰竭最常见的并发症。约70%的透析患者有尿毒症多发性神经病变,30%的患者有中度或重度神经病变。肾脏疾病患者同时出现肌肉无力和萎缩、反射性松弛、感觉丧失和神经功能缺陷的分级分布提示尿毒症多发性神经病的存在。在长期血液透析过程中,多神经病变的症状趋于稳定,但只有少数患者症状得到改善。完全恢复,发生在6至12个月期间,通常在成功的肾移植之后。
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引用次数: 0
[Proceedings of the Acute Coronary Syndrome Symposium--Myocardial Infarct and Unstable Angina. 4 July 2003, Zagreb]. [急性冠脉综合征研讨会论文集——心肌梗死和不稳定型心绞痛。2003年7月4日,萨格勒布]。
Q4 Medicine Pub Date : 2004-01-01
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引用次数: 0
[Asthma in children]. [儿童哮喘]。
Q4 Medicine Pub Date : 1900-01-01 DOI: 10.1097/00000441-192704000-00038
A. Gagro
Asthma is the most common chronic disease in childhood characterized by chronic bronchial inflammation of variable intensity accompanied by spontaneous or drug reversible airflow obstruction. The onset of asthma, clinical presentation and response to therapy are influenced by numerous genetic and environmental factors. Asthma in childhood is characterized by its heterogeneity in terms of possible etiology, degree of inflammation and airway obstruction, lung function as well as the natural course of disease that may persist and continue to adulthood. Protective factors linked to early life experiences have also been delineated which may impact the development of asthma. Pathophysiological mechanisms of allergic reaction as an excessive inflammation driven by T-helper-2 (Th2) immunity, offer poor understanding of the heterogeneity of clinical disease. A recently introduced approach defines asthma as a syndrome that comprises of several subtypes or endotypes based on entirely novel pathways to disease. Timely diagnosis and adequate treatment are necessary to prevent irreversible airway remodeling and consequent decrease in pulmonary function.
哮喘是儿童时期最常见的慢性疾病,其特征是慢性支气管炎症伴自发性或药物可逆性气流阻塞。哮喘的发病、临床表现和对治疗的反应受到许多遗传和环境因素的影响。儿童哮喘的特点是在可能的病因、炎症和气道阻塞程度、肺功能以及可能持续并持续到成年的疾病的自然过程方面具有异质性。与早期生活经历有关的保护因素也被描述为可能影响哮喘发展的因素。过敏反应的病理生理机制是由t -辅助物-2 (Th2)免疫驱动的过度炎症,对临床疾病的异质性了解不足。最近引入的一种方法将哮喘定义为基于全新疾病途径的几种亚型或内型组成的综合征。及时的诊断和适当的治疗是必要的,以防止不可逆的气道重塑和随之而来的肺功能下降。
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引用次数: 0
[Cervicogenic headache]. [颈源性头痛]。
Q4 Medicine Pub Date : 1900-01-01 DOI: 10.1111/j.1526-4610.2005.05171_6.x
A. Marčić
The aim of this report is to give information on the definition, clinical characteristics and therapy of cervical headache with comprehensive guidelines for patients on daily living activities with cervical pain and headache. This information has been designed to help the patients understand of their disability and in learn how to protect themselves.
本报告的目的是提供信息的定义,临床特点和治疗的颈痛和头痛患者的日常生活活动的综合指南。这些信息旨在帮助患者了解自己的残疾,并学习如何保护自己。
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引用次数: 0
[Acute coronary syndrome]. [急性冠脉综合征]。
Q4 Medicine Pub Date : 1900-01-01 DOI: 10.1093/med/9780199557462.003.0031
M. Bergovec
s will be excluded as it is expected there will be sufficient full text published studies available. 11 . Context N/A 12 . Primary outcomes (critical outcomes) • All-cause mortality short term (≤30 days) • All-cause mortalityintermediate term (up to 1 year) • All-cause mortalitylong term (>1 year) • Myocardial re-infarction short term (≤30 days) • Myocardial re-infarction intermediate term (up to 1 year) • Myocardial re-infarction short term (≤30 days) • stroke short term (≤30 days) • stroke long term (>1 year) • stroke short term (≤30 days) • Complications related to bleeding short term (≤30 days), intermediate term (up to 1 year), and long term (>1 year) including haemorrhagic stroke –(access bleeding and non-access bleeding need to be differentiated)the following hierarchy of bleeding scales will be used: o BARC o Author’s definition o TIMI o GUSTO Where possible, bleeding outcomes will be categorised into: o Major bleeding (including BARC 3-5 and as reported by author) o Minor bleeding (including BARC 2, TIMI and as reported by author). – 1 year • Health-related quality of life including EQ5D and SF-36. 13 . Secondary outcomes (important outcomes) • Withdrawal of study drug due to any side effects • Probable and/or definite stent thrombosis at 1 year 14 . Data extraction (selection and coding) EndNote will be used for reference management, sifting, citations and bibliographies. Titles and/or abstracts of studies retrieved using the search strategy and those from additional sources will be screened for inclusion. The full text of potentially eligible studies will be retrieved and will be assessed for eligibility in line with the criteria outlined above. 10% of the abstracts will be reviewed by two reviewers, with any disagreements resolved by discussion or, if necessary, a third independent reviewer. Acute coronary syndromes: DRAFT FOR CONSULTATION Combination therapy © National Institute for Health and Care Excellence, 2020 45 An in-house developed database; EviBase, will be used for data extraction. A standardised form is followed to extract data from studies (see Developing NICE guidelines: the manual section 6.4) and for undertaking assessment of study quality. Summary evidence tables will be produced including information on: study setting; study population and participant demographics and baseline characteristics; details of the intervention and control interventions; study methodology’ recruitment and missing data rates; outcomes and times of measurement; critical appraisal ratings. A second reviewer will quality assure the extracted data. Discrepancies will be identified and resolved through discussion (with a third reviewer where necessary). 15 . Risk of bias (quality) assessment Risk of bias will be assessed using the appropriate checklist as described in Developing NICE guidelines: the manual. For Intervention reviews the following checklist will be used according to study design being assessed: • Systematic reviews: Risk of Bias in
S将被排除在外,因为预计将有足够的全文发表的研究。11 . 12 .单击“下一步”。主要结局(关键结局)•全因死亡率短期(≤30天)•全因死亡率中期(长达1年)•全因死亡率长期(>1年)•心肌再梗死短期(≤30天)•心肌再梗死中期(长达1年)•心肌再梗死短期(≤30天)•中风短期(≤30天)•中风长期(>1年)•中风短期(≤30天)•出血相关并发症短期(≤30天),包括出血性中风在内的中期(长达1年)和长期(bbb10 - 1年)-(需要区分可及性出血和非可及性出血)将使用以下出血量表等级:BARC至作者定义的TIMI至GUSTO在可能的情况下,出血结局将分为:o大出血(包括BARC 3-5并由作者报告)o小出血(包括BARC 2、TIMI并由作者报告)。•健康相关生活质量,包括EQ5D和SF-36。13。次要结局(重要结局)•由于任何副作用而退出研究药物•1年后可能和/或确定支架血栓形成。EndNote将用于参考文献管理、筛选、引用和参考书目。使用检索策略和其他来源检索的研究的标题和/或摘要将被筛选纳入。将检索可能符合条件的研究的全文,并根据上述标准对其资格进行评估。10%的摘要将由两名审稿人审稿,有任何分歧可以通过讨论解决,必要时可以由第三名独立审稿人审稿。急性冠脉综合征:会诊联合治疗草案©National Institute FOR Health and Care Excellence, 2020 45一个内部开发的数据库;EviBase,将用于数据提取。遵循标准化表格从研究中提取数据(见制定NICE指南:手册第6.4节)并进行研究质量评估。将编制简要证据表,包括以下信息:研究环境;研究人群和参与者人口统计和基线特征;干预和控制措施的细节;研究方法的招募和数据缺失率;结果和测量时间;关键的评估等级。第二审稿人将对提取的数据进行质量保证。差异将通过讨论确定并解决(必要时与第三方审稿人)。15。偏倚风险(质量)评估偏倚风险将使用《制定NICE指南:手册》中描述的适当检查表进行评估。对于干预评价,将根据所评估的研究设计使用以下清单:•系统评价:系统评价中的偏倚风险(ROBIS)•随机对照试验:Cochrane RoB(2.0)综述作者对特定研究偏倚风险的分歧将通过讨论解决,必要时第三方综述作者将参与其中。16 . 数据综合策略在可能的情况下,将对数据进行元分析。使用Cochrane Review Manager (RevMan5)进行两两荟萃分析,以结合上述每个结果的所有研究中给出的数据。将使用固定效应荟萃分析,对连续结果和二元结果的风险比采用加权平均差异,并为每个结果计算95%置信区间。将使用I2统计量和目视检验来评估效应测量中研究之间的异质性。我们将认为I2值大于50%表明存在实质性异质性。敏感性分析将基于预先指定的亚组,使用分层荟萃分析来探索效果估计的异质性。如果这不能解释异质性,结果将使用随机效应来呈现。GRADE pro将用于评估每个结果的质量,同时考虑到个体研究质量和荟萃分析结果。将对每个结果的4个主要质量要素(偏倚风险、间接性、不一致性和不精确性)进行评估。当一个结果有超过5项研究时,就会检验发表偏倚。急性冠状动脉综合征:会诊联合治疗草案©National Institute FOR Health and Care Excellence, 2020 46其他偏倚只有在明显的情况下才会在质量评估中考虑。在无法进行meta分析的情况下,将根据每个结果单独提供数据并评估其质量。如果有足够的数据来构建治疗网络,WinBUGS将用于网络元分析。17所示。 亚组分析•抗凝适应症(机械心脏值vs静脉血栓栓塞)•心肌梗死治疗类型(PCI或CABG或医学)•支架类型(裸金属支架vs药物洗脱支架)缺席缺席评估的类型和方法缺席缺席干预、诊断性、预后性、定性、流行病学、服务交付、其他(请指定)语言英语英格兰乡村预计或实际开始日期30/04/19 22。预计完工日期14/05/2023。本次提交时的审查阶段审查阶段开始完成初步搜索试验选择过程的试点对符合资格标准的搜索结果进行正式筛选急性冠状动脉综合征:会诊联合治疗草案©National Institute FOR Health and Care Excellence, 2020 47数据提取偏倚风险(质量)评估
{"title":"[Acute coronary syndrome].","authors":"M. Bergovec","doi":"10.1093/med/9780199557462.003.0031","DOIUrl":"https://doi.org/10.1093/med/9780199557462.003.0031","url":null,"abstract":"s will be excluded as it is expected there will be sufficient full text published studies available. 11 . Context N/A 12 . Primary outcomes (critical outcomes) • All-cause mortality short term (≤30 days) • All-cause mortalityintermediate term (up to 1 year) • All-cause mortalitylong term (>1 year) • Myocardial re-infarction short term (≤30 days) • Myocardial re-infarction intermediate term (up to 1 year) • Myocardial re-infarction short term (≤30 days) • stroke short term (≤30 days) • stroke long term (>1 year) • stroke short term (≤30 days) • Complications related to bleeding short term (≤30 days), intermediate term (up to 1 year), and long term (>1 year) including haemorrhagic stroke –(access bleeding and non-access bleeding need to be differentiated)the following hierarchy of bleeding scales will be used: o BARC o Author’s definition o TIMI o GUSTO Where possible, bleeding outcomes will be categorised into: o Major bleeding (including BARC 3-5 and as reported by author) o Minor bleeding (including BARC 2, TIMI and as reported by author). – 1 year • Health-related quality of life including EQ5D and SF-36. 13 . Secondary outcomes (important outcomes) • Withdrawal of study drug due to any side effects • Probable and/or definite stent thrombosis at 1 year 14 . Data extraction (selection and coding) EndNote will be used for reference management, sifting, citations and bibliographies. Titles and/or abstracts of studies retrieved using the search strategy and those from additional sources will be screened for inclusion. The full text of potentially eligible studies will be retrieved and will be assessed for eligibility in line with the criteria outlined above. 10% of the abstracts will be reviewed by two reviewers, with any disagreements resolved by discussion or, if necessary, a third independent reviewer. Acute coronary syndromes: DRAFT FOR CONSULTATION Combination therapy © National Institute for Health and Care Excellence, 2020 45 An in-house developed database; EviBase, will be used for data extraction. A standardised form is followed to extract data from studies (see Developing NICE guidelines: the manual section 6.4) and for undertaking assessment of study quality. Summary evidence tables will be produced including information on: study setting; study population and participant demographics and baseline characteristics; details of the intervention and control interventions; study methodology’ recruitment and missing data rates; outcomes and times of measurement; critical appraisal ratings. A second reviewer will quality assure the extracted data. Discrepancies will be identified and resolved through discussion (with a third reviewer where necessary). 15 . Risk of bias (quality) assessment Risk of bias will be assessed using the appropriate checklist as described in Developing NICE guidelines: the manual. For Intervention reviews the following checklist will be used according to study design being assessed: • Systematic reviews: Risk of Bias in","PeriodicalId":35756,"journal":{"name":"Acta Medica Croatica","volume":"58 2 1","pages":"87-90"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"61658695","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Primary biliary cirrhosis]. 原发性胆汁性肝硬化。
Q4 Medicine Pub Date : 1900-01-01 DOI: 10.1007/978-3-642-16483-5_4730
S. Cukovic-Cavka
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引用次数: 2
Pyoderma gangrenosum. 坏疽性脓皮病。
Q4 Medicine Pub Date : 1900-01-01 DOI: 10.1007/978-3-211-79280-3_952
T. Stipić, T. Gregurek-Novak, V. Cajkovac
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引用次数: 0
期刊
Acta Medica Croatica
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