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Mechanisms for decreased function of B cells in aged mice and humans

Journal

JOURNAL OF IMMUNOLOGY
Volume 180, Issue 5, Pages 2741-2746

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.180.5.2741

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Funding

  1. NIAID NIH HHS [AI-064591, R01 AI064591] Funding Source: Medline
  2. NIA NIH HHS [R01 AG025256, AG-17618, AG-025256, R37 AG023717, AG-23717, AG-28586] Funding Source: Medline
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI064591] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE ON AGING [R01AG025256, R01AG023717, R01AG017618, R21AG028586, R37AG023717] Funding Source: NIH RePORTER

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The immune system has been known for some time to be compromised in aged individuals, e.g., both mice and humans, and in both humoral and cellular responses. Our studies have begun to elucidate intrinsic B lymphocyte defects in Ig class switch recombination, activation-induced cytidine deaminase, and E47 transcription factor expression. These defects occur in both mice and humans. Our studies have also shown that tristetraprolin is one of the key players in regulating the decreased E47 mRNA stability in aged B lymphocytes. These and current studies should lead to improvements in B lymphocyte function in aged populations.

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