Gluckman J C, Klatzmann D, Triebel F, Rottembourg J, Foucault C, Brisson E, Assogba U, Metivier F
Proc Eur Dial Transplant Assoc. 1983;20:349-55.
We have investigated whether suppression of the allogeneic response after blood transfusion (BT) could be due to inhibition of the production or activity of Interleukin-2 (IL-2), a soluble mediator involved in T lymphocyte proliferation. Reduction of IL-2 production after BT was less frequent than, but significantly associated with, non specific MLR suppression. However, MLR suppressor cells did not inhibit the release of IL-2 from autologous pre-BT lymphocytes. In addition, post-BT soluble suppressor factors of the MLR did not affect the ability of IL-2 to promote cell proliferation. Thus, although MLR suppression after BT is associated with reduced IL-2 production, this is not a major mechanism involved in this effect.
我们研究了输血(BT)后同种异体反应的抑制是否可能归因于白细胞介素-2(IL-2)的产生或活性受到抑制,IL-2是一种参与T淋巴细胞增殖的可溶性介质。输血后IL-2产生的减少比非特异性混合淋巴细胞反应(MLR)抑制的频率更低,但与之显著相关。然而,MLR抑制细胞并不抑制自体输血前淋巴细胞释放IL-2。此外,输血后MLR的可溶性抑制因子并不影响IL-2促进细胞增殖的能力。因此,尽管输血后MLR抑制与IL-2产生减少有关,但这并不是参与该效应的主要机制。