CD4＋FoxP3＋ regulatory T cells （Tregs） are immunosuppressive cells that are critical for immune tolerance. Several studies have demonstrated that one of the anti-inflammatory mechanisms of action of intravenous imm...CD4＋FoxP3＋ regulatory T cells （Tregs） are immunosuppressive cells that are critical for immune tolerance. Several studies have demonstrated that one of the anti-inflammatory mechanisms of action of intravenous immunoglobulin （Wig） involves the expansion of Tregs. Recently, we demonstrated that IVIgmediated Treg expansion involves the cyclooxygenase-2 （COX-2）-dependent induction of prostaglandin E2 （PGE2） in human dendritic cells （DCs）. However, the validity of these findings in autoimmune patients is lacking.展开更多
MicroRNAs （miRNAs） are evolu- tionarily conserved small non-coding RNA sequences, approximately 22 nucleotides in length, that act as negative regulators of target genes via binding to the 3＇-untranslated region of...MicroRNAs （miRNAs） are evolu- tionarily conserved small non-coding RNA sequences, approximately 22 nucleotides in length, that act as negative regulators of target genes via binding to the 3＇-untranslated region of mRNAs,展开更多
文摘CD4＋FoxP3＋ regulatory T cells （Tregs） are immunosuppressive cells that are critical for immune tolerance. Several studies have demonstrated that one of the anti-inflammatory mechanisms of action of intravenous immunoglobulin （Wig） involves the expansion of Tregs. Recently, we demonstrated that IVIgmediated Treg expansion involves the cyclooxygenase-2 （COX-2）-dependent induction of prostaglandin E2 （PGE2） in human dendritic cells （DCs）. However, the validity of these findings in autoimmune patients is lacking.
文摘MicroRNAs （miRNAs） are evolu- tionarily conserved small non-coding RNA sequences, approximately 22 nucleotides in length, that act as negative regulators of target genes via binding to the 3＇-untranslated region of mRNAs,
