4.8 Review

Antigen-specific therapeutic approaches for autoimmunity

期刊

NATURE BIOTECHNOLOGY
卷 37, 期 3, 页码 238-251

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41587-019-0015-4

关键词

-

资金

  1. Canadian Institutes of Health Research (CIHR)
  2. Diabetes Canada
  3. Crohn's and Colitis Foundation of Canada
  4. Multiple Sclerosis Society of Canada (MSSC)
  5. ISCIII
  6. FEDER [PIE14/00027, PI15/0797]
  7. NEURON-ERANET (European Research Projects on Neuroinflammation) [NEURON7-FP-715-018]
  8. Ministerio de Economia y Competitividad of Spain (MINECO)
  9. Generalitat de Catalunya (SGR Programme)
  10. Generalitat de Catalunya (CERCA Programme)
  11. JDRF Career Development Award
  12. Diabetes Association (Foothills)

向作者/读者索取更多资源

The main function of the immune system in health is to protect the host from infection by microbes and parasites. Because immune responses to nonself bear the risk of unleashing accidental immunity against self, evolution has endowed the immune system with central and peripheral mechanisms of tolerance, including regulatory T and B cells. Although the past two decades have witnessed the successful clinical translation of a whole host of novel therapies for the treatment of chronic inflammation, the development of antigen-based approaches capable of selectively blunting autoimmune inflammation without impairing normal immunity has remained elusive. Earlier autoantigen-specific approaches employing peptides or whole antigens have evolved into strategies that seek to preferentially deliver these molecules to autoreactive T cells either indirectly, via antigen-presenting cells, or directly, via major histocompatibility complex molecules, in ways intended to promote clonal deletion and/or immunoregulation. The disease specificity, mechanistic underpinnings, developability and translational potential of many of these strategies remain unclear.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据