Adult and infant mesenteric lymph nodes contained comparable numbers of FoxP3 + cells, with a nonsignificant trend toward observation of more FoxP3 + cells in infant samples ( Fig. 4 B ).
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Suppression of SIV-specific CD4+ T cells by infant but not adult macaque regulatory T cells: implications for SIV disease progression.
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In fact, we observed a trend, which did not reach statistical significance, toward more frequent expression of Ki-67 by infant than adult CD4 + T cells.