Fischer A, Durandy A, Griscelli C
J Immunol. 1981 Apr;126(4):1452-5.
Activated human monocytes and concanavalin A (Con A)-activated T lymphocytes are known to suppress T and B lymphocyte proliferation and B cell maturation into immunoglobulin-producing cells. We have now shown that monocyte suppressive activity is predominantly mediated through release of prostaglandin E2 (PGE2), which is active only in the presence of a "short-lived," radiosensitive T lymphocyte subset. PGE2, at high concentration, can activate T suppressor lymphocytes (TS), which display the same characteristics as Con A-activated TS lymphocytes. Moreover, Con A activation of TS lymphocytes was obtained only in the presence of PGE2, as specific anti-PGE2 antiserum or indomethacin prevented TS activation; this suggested a double signal as a prerequisite for activation of the nonspecific TS cell subset. We propose that TS lymphocytes modified by Con A become sensitive to small amounts of PGE2 produced by monocytes that must be present during the Con A-stimulated activation phase of suppressive cells.
已知活化的人单核细胞和伴刀豆球蛋白A(Con A)活化的T淋巴细胞可抑制T和B淋巴细胞增殖以及B细胞成熟为产生免疫球蛋白的细胞。我们现已表明,单核细胞的抑制活性主要通过前列腺素E2(PGE2)的释放介导,PGE2仅在存在“短命”的、对辐射敏感的T淋巴细胞亚群时才具有活性。高浓度的PGE2可激活T抑制淋巴细胞(TS),其表现出与Con A活化的TS淋巴细胞相同的特征。此外,仅在PGE2存在的情况下才能实现TS淋巴细胞的Con A活化,因为特异性抗PGE2抗血清或吲哚美辛可阻止TS活化;这表明双重信号是激活非特异性TS细胞亚群的先决条件。我们提出,被Con A修饰的TS淋巴细胞对单核细胞产生的少量PGE2变得敏感,而这些单核细胞必须在抑制性细胞的Con A刺激活化阶段存在。