Anti-inflammatory actions of endogenous and exogenous interleukin-10 versus glucocorticoids on macrophage functions of the newly born.
Anti-inflammatory actions of endogenous and exogenous interleukin-10 versus glucocorticoids on macrophage functions of the newly born.
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DOI:
10.1038/jp.2014.16
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发表时间:
2014-05
影响因子:
2.9
通讯作者:
Davidson, D.
中科院分区:
文献类型:
--
作者:
Kasat, K.;Patel, H.;Predtechenska, O.;Vancurova, I.;Davidson, D.
To determine whether specific macrophage immune functions of the newly born are insensitive to the actions of therapeutic levels of dexamethasone (DEX), previously measured in infants with bronchopulmonary dysplasia (BPD), compared to betamethasone (BETA) and exogenous or endogenous interleukin-10 (IL-10). Macrophages were differentiated from cord blood monocytes (N=18). A serial dose response (around 10−8M), in vitro study was used to examine the effect of DEX, BETA and IL-10, on pro-inflammatory (PI) cytokine release, phagocytosis and respiratory burst. Exogenous IL-10 (10−8M) significantly (p<0.05) inhibited the endotoxin-stimulated release of IL-6, IL-8 and tumor necrosis factor by 63% to 82% with no significant effect by DEX and BETA. There was no inhibition by these 3 agents at 10−8M on phagocytosis and respiratory burst. Inhibition of endogenous IL-10 with a monoclonal antibody significantly raised endotoxin-stimulated cytokine release by at least 4 fold. Macrophages were relatively insensitive to therapeutic levels of DEX and BETA with regard to PI cytokine release. This study provides rationale for translational, preclinical research using airway instillation of IL-10 for the treatment of BPD.
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影响因子:
2.5
作者:
Chusid, Lina A.;Pereira-Argenziano, Lucy;Davidson, Dennis
通讯作者:
Davidson, Dennis
影响因子:
158.5
作者:
Clark, RH;Kueser, TJ;Kinsella, JP
通讯作者:
Kinsella, JP
DOI:
10.1016/0002-9378(88)90216-5
发表时间:
1988-05-01
影响因子:
9.8
作者:
ROMERO, R;ROSLANSKY, P;HOBBINS, JC
通讯作者:
HOBBINS, JC
DOI:
10.1152/ajplung.00251.2009
发表时间:
2010-01-01
影响因子:
4.9
作者:
Mokres, Lucia M.;Parai, Kakoli;Bland, Richard D.
通讯作者:
Bland, Richard D.
影响因子:
3.6
作者:
Jobe AH
通讯作者:
Jobe AH