{"title":"免疫学做得好吗?100种免疫介导的炎症性疾病 《华尔街日报》的年份。","authors":"D Sean Riminton","doi":"10.1111/imcb.12695","DOIUrl":null,"url":null,"abstract":"<p>It is now 60 years since Ian Mackay and Macfarlane Burnet published their seminal text “The Autoimmune Diseases” in which they examined the full scope of human inflammatory pathology as a manifestation of the underlying structure and function of the immune system. Here I revisit this approach to ask to what extent has the promise of Mackay and Burnet's work been exploited in clinical medicine as currently practiced. In other words, is immunology doing well? Despite spectacular headline contributions of immunology in clinical medicine, I present evidence suggesting a performance ceiling in our capacity to answer the relatively straightforward questions that patients frequently ask about their own diseases and find that this ceiling exists across almost all of the 100 immune-mediated inflammatory diseases examined. I propose that these questions are difficult, not so much because the immune system is overwhelmingly complex but rather that we have more to learn about the relatively simple agents and rules that may underpin self-organizing complex interacting systems as revealed in studies from other disciplines. The way that the immune system has evolved to exploit the ancient machinery determining three independent cell fate timers as described in this Journal would be a great place to start to decode the self-organizing principles that underpin the emergent pathology that we observe in the clinic.</p>","PeriodicalId":179,"journal":{"name":"Immunology & Cell Biology","volume":"101 10","pages":"896-901"},"PeriodicalIF":3.2000,"publicationDate":"2023-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Is immunology doing well? A look at 100 immune-mediated inflammatory diseases for 100 years of the Journal\",\"authors\":\"D Sean Riminton\",\"doi\":\"10.1111/imcb.12695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>It is now 60 years since Ian Mackay and Macfarlane Burnet published their seminal text “The Autoimmune Diseases” in which they examined the full scope of human inflammatory pathology as a manifestation of the underlying structure and function of the immune system. Here I revisit this approach to ask to what extent has the promise of Mackay and Burnet's work been exploited in clinical medicine as currently practiced. In other words, is immunology doing well? Despite spectacular headline contributions of immunology in clinical medicine, I present evidence suggesting a performance ceiling in our capacity to answer the relatively straightforward questions that patients frequently ask about their own diseases and find that this ceiling exists across almost all of the 100 immune-mediated inflammatory diseases examined. I propose that these questions are difficult, not so much because the immune system is overwhelmingly complex but rather that we have more to learn about the relatively simple agents and rules that may underpin self-organizing complex interacting systems as revealed in studies from other disciplines. The way that the immune system has evolved to exploit the ancient machinery determining three independent cell fate timers as described in this Journal would be a great place to start to decode the self-organizing principles that underpin the emergent pathology that we observe in the clinic.</p>\",\"PeriodicalId\":179,\"journal\":{\"name\":\"Immunology & Cell Biology\",\"volume\":\"101 10\",\"pages\":\"896-901\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2023-10-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Immunology & Cell Biology\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/imcb.12695\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunology & Cell Biology","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/imcb.12695","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 1
摘要
现在是60 Ian Mackay和Macfarlane Burnet发表了他们的开创性著作《自身免疫性疾病》,在该书中,他们研究了作为免疫系统潜在结构和功能表现的人类炎症病理学的全部范围。在这里,我重新审视这种方法,想问Mackay和Burnet的工作在临床医学中的前景在多大程度上得到了利用。换句话说,免疫学做得好吗?尽管免疫学在临床医学中做出了引人注目的重大贡献,但我提出的证据表明,我们在回答患者经常问到的关于自己疾病的相对简单的问题方面存在表现上限,并发现几乎所有检查的100种免疫介导的炎性疾病都存在这种上限。我认为这些问题很困难,与其说是因为免疫系统极其复杂,不如说是因为我们需要更多地了解相对简单的代理和规则,这些代理和规则可能是其他学科研究中揭示的自组织复杂交互系统的基础。正如本杂志所描述的,免疫系统进化到利用决定三个独立细胞命运定时器的古老机制的方式,将是一个很好的开始解码自组织原理的地方,这些自组织原理是我们在临床上观察到的新兴病理学的基础。
Is immunology doing well? A look at 100 immune-mediated inflammatory diseases for 100 years of the Journal
It is now 60 years since Ian Mackay and Macfarlane Burnet published their seminal text “The Autoimmune Diseases” in which they examined the full scope of human inflammatory pathology as a manifestation of the underlying structure and function of the immune system. Here I revisit this approach to ask to what extent has the promise of Mackay and Burnet's work been exploited in clinical medicine as currently practiced. In other words, is immunology doing well? Despite spectacular headline contributions of immunology in clinical medicine, I present evidence suggesting a performance ceiling in our capacity to answer the relatively straightforward questions that patients frequently ask about their own diseases and find that this ceiling exists across almost all of the 100 immune-mediated inflammatory diseases examined. I propose that these questions are difficult, not so much because the immune system is overwhelmingly complex but rather that we have more to learn about the relatively simple agents and rules that may underpin self-organizing complex interacting systems as revealed in studies from other disciplines. The way that the immune system has evolved to exploit the ancient machinery determining three independent cell fate timers as described in this Journal would be a great place to start to decode the self-organizing principles that underpin the emergent pathology that we observe in the clinic.
期刊介绍:
The Australasian Society for Immunology Incorporated (ASI) was created by the amalgamation in 1991 of the Australian Society for Immunology, formed in 1970, and the New Zealand Society for Immunology, formed in 1975. The aim of the Society is to encourage and support the discipline of immunology in the Australasian region. It is a broadly based Society, embracing clinical and experimental, cellular and molecular immunology in humans and animals. The Society provides a network for the exchange of information and for collaboration within Australia, New Zealand and overseas. ASI members have been prominent in advancing biological and medical research worldwide. We seek to encourage the study of immunology in Australia and New Zealand and are active in introducing young scientists to the discipline.