Second, as vitamin D is a known link between toll-like receptors (TLR) activation and innate immunity [26], and vitamin D receptors are expressed in T cells [27], activated B cells [28], and dendritic cells [29], vitamin D deficiency may increase the risk of inflammation and sepsis in the critically ill by the suppression of immune reactivity and stimulatory effects on innate immunity [30-32]. The gene discussed is VDR; the disease is Sepsis.