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Transactions of the American Clinical and Climatological Association最新文献

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CONSTITUTION AND BY-LAWS: CONSTITUTION. 章程及细则:章程。
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引用次数: 0
EUGENE A. "PAT" HILDRETH: 1924 - 2018. 尤金。“pat”hildreth: 1924 - 2018。
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引用次数: 0
JEREMIAH METZGER LECTURES. Jeremiah metzger讲课。
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引用次数: 0
IMMUNOEDITING IN AUTOIMMUNE RHEUMATIC DISEASES. 自身免疫性风湿病的免疫编辑
Antony Rosen

The striking association of specific autoantibodies with distinct disease phenotypes and trajectories in human autoimmune rheumatic diseases provides a powerful opportunity to interrogate disease mechanism. In scleroderma, a subgroup of patients with autoantibodies to POLR3 have coincident onset of cancer and scleroderma. The majority of these patients have genetic changes (somatic mutations and loss of heterozygosity) in the POLR3A gene in their matched cancers, coupled with immune responses directed against the mutated and wild type autoantigen. In some individuals with scleroderma or dermatomyositis where specific immune responses mark a high risk of emergent cancer, cancer does not emerge. Such patients have a broader immune response that targets additional autoantigens, suggesting that the breadth and magnitude of the immune response regulates cancer, and that the rheumatic diseases provide a unique window into natural immunoediting of cancer in humans. This has implications for prediction and therapy in both autoimmunity and cancer.

在人类自身免疫性风湿性疾病中,特异性自身抗体与不同疾病表型和轨迹的显著关联为探究疾病机制提供了强有力的机会。在硬皮病中,具有POLR3自身抗体的患者亚组有癌症和硬皮病的同时发病。这些患者中的大多数在其匹配的癌症中具有POLR3A基因的遗传变化(体细胞突变和杂合性丧失),并且伴随着针对突变和野生型自身抗原的免疫反应。在一些患有硬皮病或皮肌炎的个体中,特定的免疫反应标志着出现癌症的高风险,癌症不会出现。这类患者具有针对其他自身抗原的更广泛的免疫反应,这表明免疫反应的广度和强度调节癌症,并且风湿性疾病为研究人类癌症的自然免疫编辑提供了一个独特的窗口。这对自身免疫和癌症的预测和治疗都有意义。
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引用次数: 0
ROBERT W. SCHRIER, MD: 1936 - 2021. 罗伯特w.施里尔,医学博士:1936 - 2021。
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引用次数: 0
INSIGHTS INTO THE REGULATION OF MAST CELL FUNCTION IN TYPE 2 INFLAMMATION. 深入了解 2 型炎症中肥大细胞功能的调控。
Joshua A Boyce

Type 2 inflammation (T2I) underlies the pathogenesis of asthma, chronic rhinosinusitis with nasal polyps, and eosinophilic esophagitis. Mast cells (MCs) are tissue resident hematopoietic effector cells thought to play major roles in T2I. Two subtypes of human MCs are recognized based on immunohistochemical differences. MCs expressing tryptase but not chymase (MCT) reside within mucosal epithelial surfaces, and MCs expressing tryptase, chymase, and cathepsin G (MCTC) reside in submucosal, perivascular and intraneural locations. During T2I, MCs (particularly MCT) increase markedly by unclear mechanisms. Single cell genomic studies reveal that traditional histochemical categorization vastly underestimates the extent of MC functional heterogeneity. MCT and MCTC likely reflect endpoints of a developmental continuum, emerging from a transitional stage of development in which MCs expand through in situ proliferation. This mechanism, likely driven by interleukin 4 and other cytokines, is unique among granulocytes and carries substantial implications for pathogenesis and therapy of T2I-associated diseases.

2型炎症(T2I)是哮喘、伴有鼻息肉的慢性鼻窦炎和嗜酸性粒细胞性食管炎的发病机理基础。肥大细胞(MCs)是组织常驻的造血效应细胞,被认为在 T2I 中发挥着重要作用。根据免疫组化的差异,人类肥大细胞有两种亚型。表达胰蛋白酶但不表达糜蛋白酶的 MCs(MCT)驻留在粘膜上皮表面,而表达胰蛋白酶、糜蛋白酶和酪蛋白酶 G 的 MCs(MCTC)驻留在粘膜下、血管周围和血管内。在 T2I 期间,MCs(尤其是 MCT)明显增加的机制尚不清楚。单细胞基因组研究显示,传统的组织化学分类方法大大低估了 MC 功能异质性的程度。MCT 和 MCTC 很可能反映了发育连续体的端点,它们出现于发育的过渡阶段,在这一阶段,MC 通过原位增殖而扩大。这种机制可能由白细胞介素 4 和其他细胞因子驱动,在粒细胞中是独一无二的,对 T2I 相关疾病的发病机制和治疗具有重大意义。
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引用次数: 0
RECORDER'S REPORT: The 133rd Meeting, The Charleston Place, Charleston, South Carolina, March 24th through March 27th, 2022. 记录员报告:第133次会议于2022年3月24日至3月27日在南卡罗来纳州查尔斯顿查尔斯顿广场举行。
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引用次数: 0
PRESENT MEMBERS. 目前的成员。
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引用次数: 0
THE GORDON WILSON LECTURES. 戈登·威尔逊的讲座。
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引用次数: 0
GERALD MEDOFF, MD: 1936 - 2019. 杰拉尔德·梅多夫,医学博士:1936 - 2019。
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引用次数: 0
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Transactions of the American Clinical and Climatological Association
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