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Immune remodeling: lessons from repertoire alterations during chronological aging and in immune-mediated disease

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TRENDS IN MOLECULAR MEDICINE
卷 13, 期 3, 页码 94-102

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ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2007.01.005

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资金

  1. NATIONAL CANCER INSTITUTE [P20CA103730] Funding Source: NIH RePORTER
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [C06RR014489] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE ON AGING [R01AG022379] Funding Source: NIH RePORTER
  4. NCI NIH HHS [P20 CA 103730] Funding Source: Medline
  5. NCRR NIH HHS [C06 RR 014489] Funding Source: Medline
  6. NIA NIH HHS [R01 AG 022379, R01 AG022379, R01 AG022379-06] Funding Source: Medline

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Immunological studies of aging and of patients with chronic immune-mediated diseases document overlap of immune phenotypes. Here, the term 'immune remodeling' refers to these phenotypes that are indicative of biological processes of deterioration and repair. This concept is explored through lessons from studies about the changes in the T-cell repertoire and the functional diversity of otherwise oligoclonal, senescent T cells. Immune remodeling suggests a gradual process that occurs throughout life. However, similar but more drastic remodeling occurs disproportionately among young patients with chronic disease. In this article, I propose that immune remodeling is a beneficial adaptation of aging to promote healthy survival beyond reproductive performance, but acute remodeling poses risk of premature exhaustion of the immune repertoire and, thus, is detrimental in young individuals.

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