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Translational immunology: Applying fundamental discoveries to human health and autoimmune diseases.转化免疫学:将基础发现应用于人类健康和自身免疫性疾病。
Eur J Immunol. 2023 Dec;53(12):e2250197. doi: 10.1002/eji.202250197. Epub 2023 May 15.
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本文引用的文献

1
Regulation of Cytotoxic CD8+ T Cells by the Circadian Clock.生物钟对细胞毒性CD8 + T细胞的调节
J Immunol. 2023 Jan 1;210(1):12-18. doi: 10.4049/jimmunol.2200516.
2
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.多民族全基因组关联分析确定类风湿关节炎的新遗传机制。
Nat Genet. 2022 Nov;54(11):1640-1651. doi: 10.1038/s41588-022-01213-w. Epub 2022 Nov 4.
3
Clonal IgA and IgG autoantibodies from individuals at risk for rheumatoid arthritis identify an arthritogenic strain of .来自类风湿关节炎风险个体的克隆 IgA 和 IgG 自身抗体可识别出一种致关节炎的 菌株。
Sci Transl Med. 2022 Oct 26;14(668):eabn5166. doi: 10.1126/scitranslmed.abn5166.
4
IL-6-targeted therapies to block the cytokine or its receptor drive distinct alterations in T cell function.针对白细胞介素 6 (IL-6) 的靶向治疗通过阻断细胞因子或其受体,可导致 T 细胞功能的显著改变。
JCI Insight. 2022 Nov 22;7(22):e159436. doi: 10.1172/jci.insight.159436.
5
Host and bacterial factors linking periodontitis and rheumatoid arthritis.牙周炎和类风湿性关节炎相关的宿主和细菌因素。
Front Immunol. 2022 Aug 25;13:980805. doi: 10.3389/fimmu.2022.980805. eCollection 2022.
6
Global epidemiology of rheumatoid arthritis.类风湿关节炎的全球流行病学。
Nat Rev Rheumatol. 2022 Oct;18(10):591-602. doi: 10.1038/s41584-022-00827-y. Epub 2022 Sep 6.
7
A survey of genome-wide association studies, polygenic scores and UK Biobank highlights resources for autoimmune disease genetics.一项全基因组关联研究、多基因评分和英国生物库的调查突显了自身免疫性疾病遗传学资源。
Front Immunol. 2022 Aug 5;13:972107. doi: 10.3389/fimmu.2022.972107. eCollection 2022.
8
Predictors of remission in rheumatoid arthritis patients treated with biologics: a systematic review and meta-analysis.生物制剂治疗类风湿关节炎患者缓解的预测因素:系统评价和荟萃分析。
Clin Rheumatol. 2022 Dec;41(12):3615-3627. doi: 10.1007/s10067-022-06307-8. Epub 2022 Aug 16.
9
Integrated single cell and spatial transcriptomics reveal autoreactive differentiated B cells in joints of early rheumatoid arthritis.单细胞和空间转录组学整合分析揭示早期类风湿关节炎关节中的自身反应性分化 B 细胞。
Sci Rep. 2022 Jul 13;12(1):11876. doi: 10.1038/s41598-022-15293-5.
10
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component.跨自身免疫性疾病和过敏性疾病的多性状及跨人群全基因组关联研究确定了共同和独特的遗传成分。
Ann Rheum Dis. 2022 Aug 11;81(9):1301-1312. doi: 10.1136/annrheumdis-2022-222460.

转化免疫学:将基础发现应用于人类健康和自身免疫性疾病。

Translational immunology: Applying fundamental discoveries to human health and autoimmune diseases.

机构信息

Center for Translational Immunology, Benaroya Research Institute, Virginia Mason Hospital, Seattle, WA, USA.

出版信息

Eur J Immunol. 2023 Dec;53(12):e2250197. doi: 10.1002/eji.202250197. Epub 2023 May 15.

DOI:10.1002/eji.202250197
PMID:37101346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10600327/
Abstract

Studying the human immune system is challenging. These challenges stem from the complexity of the immune system itself, the heterogeneity of the immune system between individuals, and the many factors that lead to this heterogeneity including the influence of genetics, environment, and immune experience. Studies of the human immune system in the context of disease are increased in complexity as multiple combinations and variations in immune pathways can lead to a single disease. Thus, although individuals with a disease may share clinical features, the underlying disease mechanisms and resulting pathophysiology can be diverse among individuals with the same disease diagnosis. This has consequences for the treatment of diseases, as no single therapy will work for everyone, therapeutic efficacy varies among patients, and targeting a single immune pathway is rarely 100% effective. This review discusses how to address these challenges by identifying and managing the sources of variation, improving access to high-quality, well-curated biological samples by building cohorts, applying new technologies such as single-cell omics and imaging technologies to interrogate samples, and bringing to bear computational expertise in conjunction with immunologists and clinicians to interpret those results. The review has a focus on autoimmune diseases, including rheumatoid arthritis, MS, systemic lupus erythematosus, and type 1 diabetes, but its recommendations are also applicable to studies of other immune-mediated diseases.

摘要

研究人类免疫系统具有挑战性。这些挑战源于免疫系统本身的复杂性、个体间免疫系统的异质性,以及导致这种异质性的许多因素,包括遗传、环境和免疫经验的影响。在疾病背景下研究人类免疫系统的复杂性增加了,因为多种免疫途径的组合和变化可能导致单一疾病。因此,尽管患有某种疾病的个体可能具有相似的临床特征,但同一疾病诊断的个体之间潜在的疾病机制和导致的病理生理学可能存在差异。这对疾病的治疗产生了影响,因为没有一种单一的治疗方法适用于所有人,治疗效果在患者之间存在差异,而且针对单一免疫途径的治疗很少能达到 100%的效果。本文讨论了如何通过识别和管理变异源、通过建立队列来改善高质量、精心管理的生物样本的获取、应用单细胞组学和成像技术等新技术来检测样本以及结合计算专业知识与免疫学家和临床医生来解释这些结果来应对这些挑战。本文重点讨论了自身免疫性疾病,包括类风湿关节炎、多发性硬化症、系统性红斑狼疮和 1 型糖尿病,但它的建议也适用于其他免疫介导的疾病的研究。