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Plasticity of T cell memory responses to viruses

期刊

IMMUNITY
卷 20, 期 1, 页码 5-16

出版社

CELL PRESS
DOI: 10.1016/S1074-7613(03)00356-X

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资金

  1. NIAID NIH HHS [AI49320, AI46629, R01 AI017672, AI17672, AI46578, P01 AI046629, R01 AI046578, P01 AI049320, R37 AI017672] Funding Source: Medline
  2. NIAMS NIH HHS [R01 AR035506, AR35506] Funding Source: Medline
  3. NIDDK NIH HHS [DK32520, P30 DK032520] Funding Source: Medline
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI017672, R01AI046578, R37AI017672, P01AI049320, P01AI046629] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR035506] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK032520] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Virus-specific memory T cell populations demonstrate plasticity in antigenic and functional phenotype, in recognition of antigen, and in their ability to accommodate new memory T cell populations. The adaptability of complex antigen-specific T cell repertoires allows the host to respond to a diverse array of pathogens and accommodate memory pools to many pathogens in a finite immune system. This is in part accounted for by crossreactive memory T cells, which can be employed in immune responses and mediate protective immunity or life-threatening immunopathology.

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