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10.4049/jimmunol.1203569

http://scihub22266oqcxt.onion/10.4049/jimmunol.1203569
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C3661195!3661195!23606541
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suck abstract from ncbi


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pmid23606541      J+Immunol 2013 ; 190 (11): 5454-8
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  • Antigen-stimulated CD4 T cell expansion can be limited by their grazing of peptide-MHC complexes1 #MMPMID23606541
  • De Boer RJ; Perelson AS
  • J Immunol 2013[Jun]; 190 (11): 5454-8 PMID23606541show ga
  • It was recently shown that the expansion of CD4+ T cells during a primary immune reaction to a peptide from cytochrome c decreases approximately 0.5 log for every log increase in the number of cognate precursor cells, and that this remains valid over more than four orders of magnitude [Quiel, et al., Antigen-stimulated CD4 T-cell expansion is inversely and log-linearly related to precursor number. PNAS, 2011, 108: 3312]. This observed ?power law? was explained by a mechanism where non-dividing mature T cells inhibit the proliferation of less-differentiated cells of the same specificity. Here we interpret the same data by a mechanism where CD4+ T cells acquire cognate peptide-MHC (pMHC) complexes from the surface of antigen presenting cells (APCs), thereby increasing the loss rate of pMHC. We show that a mathematical model implementing this ?T cell grazing" mechanism, and having a T cell proliferation rate that is determined by the concentration of pMHC, explains the data equally well. As a consequence, the data no longer unequivocally support the previous explanation, and the increased loss of pMHC complexes on APCs at high T cell densities is an equally valid interpretation of this striking data.
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