4.7 Article

Lessons learned from the study of human inborn errors of innate immunity

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 143, 期 2, 页码 507-527

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2018.07.013

关键词

Infection; inborn error of immunity; immunodeficiency; innate immunity; signaling pathway; Toll-like receptors; nuclear factor kappa light-chain enhancer of activated B cells; interferon; phagocytes

资金

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIAID NIH HHS [R01 AI127564, R37 AI095983, U19 AI111143, R01 AI088364, P01 AI061093] Funding Source: Medline
  3. NINDS NIH HHS [R01 NS072381] Funding Source: Medline

向作者/读者索取更多资源

Innate immunity contributes to host defense through all cell types and relies on their shared germline genetic background, whereas adaptive immunity operates through only 3 main cell types, alpha beta T cells, gamma delta T cells, and B cells, and relies on their somatic genetic diversification of antigen-specific responses. Human inborn errors of innate immunity often underlie infectious diseases. The range and nature of infections depend on the mutated gene, the deleteriousness of the mutation, and other ill-defined factors. Most known inborn errors of innate immunity to infection disrupt the development or function of leukocytes other than T and B cells, but a growing number of inborn errors affect cells other than circulating and tissue leukocytes. Here we review inborn errors of innate immunity that have been recently discovered or clarified. We highlight the immunologic implications of these errors.

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