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Critical role of CD4 T cells in PF4/heparin antibody production in mice.

Yongwei ZhengMei YuAnand PadmanabhanRichard H AsterLiudi YuanRenren WenDemin Wang
Published in: Blood (2015)
Antibodies specific for platelet factor 4 (PF4)/heparin complexes are central to the pathogenesis of heparin-induced thrombocytopenia. Marginal zone B cells appear to be the source of such antibodies, but whether T-cell help is required is unclear. Here, we showed that induction of PF4/heparin-specific antibodies by PF4/heparin complexes was markedly impaired in mice depleted of CD4 T cells by anti-CD4 antibodies. Furthermore, Rag1-deficient recipient mice produced PF4/heparin-specific antibodies upon PF4/heparin challenge when reconstituted with a mixture of wild-type splenic B cells and splenocytes from B-cell-deficient (μMT) mice but not splenocytes from T- and B-cell-deficient (Rag1 knockout) mice. Lastly, mice with B cells lacking CD40, a B-cell costimulatory molecule that helps T-cell-dependent B-cell responses, displayed a marked reduction of PF4/heparin-specific antibody production following PF4/heparin challenge. Together, these findings show that helper T cells play a critical role in production of PF4/heparin-specific antibodies.
Keyphrases
  • venous thromboembolism
  • wild type
  • growth factor
  • high fat diet induced
  • dendritic cells
  • immune response
  • high glucose
  • adipose tissue
  • drug induced
  • oxidative stress
  • stress induced
  • high density