Emilie D, Crevon M C, Galanaud P
Clin Immunol Immunopathol. 1983 Dec;29(3):415-23. doi: 10.1016/0090-1229(83)90044-2.
The effect of exogeneous prostaglandin E2 (PGE2) on the specific plaque-forming cell (PFC) response in cultures of non-adherent human peripheral blood mononuclear cells (PBM) was tested. When added on Day 2 of the cultures PGE2 inhibits the induction of the PFC response, and the maximum inhibition (50%) is obtained with 300 nM PGE2. When PBM are cultured during the first 24 hr with the same concentration of PGE2 their PFC response is enhanced and the target of this enhancement is a T cell. When PGE2 is added on Day 0 it does not affect the response, probably because of a balance between these two opposing effects. However, in the latter conditions a prostaglandin-free monocyte supernatant can render PGE2 suppressive. The monocyte supernatant acts by inhibiting the stimulatory effect after the interaction between PGE2 and T cells. Thus the effect of PGE2 depends on its time of action and on the concomitant production of a nondialyzable factor by monocytes.
检测了外源性前列腺素E2(PGE2)对非贴壁人外周血单个核细胞(PBM)培养物中特异性空斑形成细胞(PFC)反应的影响。在培养第2天添加PGE2时,它会抑制PFC反应的诱导,300 nM PGE2可产生最大抑制作用(50%)。当PBM在最初24小时用相同浓度的PGE2培养时,其PFC反应增强,这种增强的靶点是T细胞。当在第0天添加PGE2时,它不会影响反应,这可能是由于这两种相反作用之间的平衡。然而,在后一种情况下,不含前列腺素的单核细胞上清液可使PGE2具有抑制作用。单核细胞上清液通过抑制PGE2与T细胞相互作用后的刺激作用发挥作用。因此,PGE2的作用取决于其作用时间以及单核细胞同时产生的一种不可透析因子。