Matches in SemOpenAlex for { <https://semopenalex.org/work/W3135536140> ?p ?o ?g. }
- W3135536140 abstract "Abstract Genetic deficiency for acid sphingomyelinase or its pharmacological inhibition has been shown to increase Foxp3+ regulatory T-cell frequencies among CD4+ T cells in mice. We now investigated whether pharmacological targeting of the acid sphingomyelinase, which catalyzes the cleavage of sphingomyelin to ceramide and phosphorylcholine, also allows to manipulate relative CD4+ Foxp3+ regulatory T-cell frequencies in humans. Pharmacological acid sphingomyelinase inhibition with antidepressants like sertraline, but not those without an inhibitory effect on acid sphingomyelinase activity like citalopram, increased the frequency of Foxp3+ regulatory T cell among human CD4+ T cells in vitro. In an observational prospective clinical study with patients suffering from major depression, we observed that acid sphingomyelinase-inhibiting antidepressants induced a stronger relative increase in the frequency of CD4+ Foxp3+ regulatory T cells in peripheral blood than acid sphingomyelinase-non- or weakly inhibiting antidepressants. This was particularly true for CD45RA− CD25high effector CD4+ Foxp3+ regulatory T cells. Mechanistically, our data indicate that the positive effect of acid sphingomyelinase inhibition on CD4+ Foxp3+ regulatory T cells required CD28 co-stimulation, suggesting that enhanced CD28 co-stimulation was the driver of the observed increase in the frequency of Foxp3+ regulatory T cells among human CD4+ T cells. In summary, the widely induced pharmacological inhibition of acid sphingomyelinase activity in patients leads to an increase in Foxp3+ regulatory T-cell frequencies among CD4+ T cells in humans both in vivo and in vitro." @default.
- W3135536140 created "2021-03-15" @default.
- W3135536140 creator A5000655439 @default.
- W3135536140 creator A5006697799 @default.
- W3135536140 creator A5009640637 @default.
- W3135536140 creator A5013912756 @default.
- W3135536140 creator A5017698169 @default.
- W3135536140 creator A5020419000 @default.
- W3135536140 creator A5020748054 @default.
- W3135536140 creator A5021157620 @default.
- W3135536140 creator A5021323674 @default.
- W3135536140 creator A5021931614 @default.
- W3135536140 creator A5024992001 @default.
- W3135536140 creator A5036892744 @default.
- W3135536140 creator A5040262741 @default.
- W3135536140 creator A5047964995 @default.
- W3135536140 creator A5055060499 @default.
- W3135536140 creator A5057863942 @default.
- W3135536140 creator A5062019804 @default.
- W3135536140 creator A5080154745 @default.
- W3135536140 creator A5081551414 @default.
- W3135536140 date "2021-03-05" @default.
- W3135536140 modified "2023-10-15" @default.
- W3135536140 title "Inhibition of acid sphingomyelinase increases regulatory T cells in humans" @default.
- W3135536140 cites W1494329257 @default.
- W3135536140 cites W1564700799 @default.
- W3135536140 cites W1914215890 @default.
- W3135536140 cites W1944184780 @default.
- W3135536140 cites W1969889378 @default.
- W3135536140 cites W1978073168 @default.
- W3135536140 cites W2004684279 @default.
- W3135536140 cites W2007631222 @default.
- W3135536140 cites W2014060223 @default.
- W3135536140 cites W2021009347 @default.
- W3135536140 cites W2026694721 @default.
- W3135536140 cites W2027127436 @default.
- W3135536140 cites W2033805603 @default.
- W3135536140 cites W2038066039 @default.
- W3135536140 cites W2041257968 @default.
- W3135536140 cites W2045932062 @default.
- W3135536140 cites W2053858732 @default.
- W3135536140 cites W2061071534 @default.
- W3135536140 cites W2068639447 @default.
- W3135536140 cites W2087482409 @default.
- W3135536140 cites W2087998194 @default.
- W3135536140 cites W2091259554 @default.
- W3135536140 cites W2097533850 @default.
- W3135536140 cites W2108535958 @default.
- W3135536140 cites W2114613490 @default.
- W3135536140 cites W2118268169 @default.
- W3135536140 cites W2125872855 @default.
- W3135536140 cites W2126795224 @default.
- W3135536140 cites W2128011175 @default.
- W3135536140 cites W2130218253 @default.
- W3135536140 cites W2130473166 @default.
- W3135536140 cites W2136129817 @default.
- W3135536140 cites W2146659162 @default.
- W3135536140 cites W2150747144 @default.
- W3135536140 cites W2156150528 @default.
- W3135536140 cites W2156268588 @default.
- W3135536140 cites W2301336892 @default.
- W3135536140 cites W2327051359 @default.
- W3135536140 cites W2515145983 @default.
- W3135536140 cites W2525147287 @default.
- W3135536140 cites W2525291061 @default.
- W3135536140 cites W2620181344 @default.
- W3135536140 cites W2767335941 @default.
- W3135536140 cites W2768617092 @default.
- W3135536140 cites W2799339598 @default.
- W3135536140 cites W2800559178 @default.
- W3135536140 cites W2887690857 @default.
- W3135536140 cites W2979758888 @default.
- W3135536140 doi "https://doi.org/10.1093/braincomms/fcab020" @default.
- W3135536140 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8054263" @default.
- W3135536140 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33898989" @default.
- W3135536140 hasPublicationYear "2021" @default.
- W3135536140 type Work @default.
- W3135536140 sameAs 3135536140 @default.
- W3135536140 citedByCount "9" @default.
- W3135536140 countsByYear W31355361402021 @default.
- W3135536140 countsByYear W31355361402022 @default.
- W3135536140 countsByYear W31355361402023 @default.
- W3135536140 crossrefType "journal-article" @default.
- W3135536140 hasAuthorship W3135536140A5000655439 @default.
- W3135536140 hasAuthorship W3135536140A5006697799 @default.
- W3135536140 hasAuthorship W3135536140A5009640637 @default.
- W3135536140 hasAuthorship W3135536140A5013912756 @default.
- W3135536140 hasAuthorship W3135536140A5017698169 @default.
- W3135536140 hasAuthorship W3135536140A5020419000 @default.
- W3135536140 hasAuthorship W3135536140A5020748054 @default.
- W3135536140 hasAuthorship W3135536140A5021157620 @default.
- W3135536140 hasAuthorship W3135536140A5021323674 @default.
- W3135536140 hasAuthorship W3135536140A5021931614 @default.
- W3135536140 hasAuthorship W3135536140A5024992001 @default.
- W3135536140 hasAuthorship W3135536140A5036892744 @default.
- W3135536140 hasAuthorship W3135536140A5040262741 @default.
- W3135536140 hasAuthorship W3135536140A5047964995 @default.
- W3135536140 hasAuthorship W3135536140A5055060499 @default.
- W3135536140 hasAuthorship W3135536140A5057863942 @default.
- W3135536140 hasAuthorship W3135536140A5062019804 @default.