Stephan R N, Kisala J M, Dean R E, Geha A S, Chaudry I H
Department of Surgery, Michigan State University, East Lansing 48824-1315.
Arch Surg. 1988 Feb;123(2):235-40. doi: 10.1001/archsurg.1988.01400260123016.
To study the effect of blood transfusion (BT) on cell-mediated immunity, we examined the antigen presentation function of peritoneal macrophages and interleukin 2 (IL-2) generation by splenocytes. C3H/HEJ mice were transfused with 0.2 mL of fresh allogeneic blood obtained from C57BL/6 mice; they were killed on days 1, 3, and 7 after BT. A second group of C3H/HEJ mice was transfused with 0.2 mL/d of the same allogeneic blood on three successive days; they were killed on day 7 following the last BT. The antigen presentation function of peritoneal macrophages was measured by utilizing a D10.G4.1 T-helper cell clone; IL-2 activity in supernatants of concanavalin A-stimulated splenocytes was tested by utilizing an IL-2-dependent HT-2 cell line. The results indicate that although antigen presentation function remains unaffected after single and multiple BTs, the ability of splenocytes to generate IL-2 decreases significantly even after a single BT. Thus, the increased susceptibility to infection and the additional immune perturbations in malignant neoplasms following BT may be due in part to decreased IL-2 generation.
为研究输血(BT)对细胞介导免疫的影响,我们检测了腹腔巨噬细胞的抗原呈递功能以及脾细胞产生白细胞介素2(IL-2)的情况。给C3H/HEJ小鼠输注0.2 mL从C57BL/6小鼠获取的新鲜同种异体血液;在输血后第1、3和7天处死小鼠。第二组C3H/HEJ小鼠连续三天每天输注0.2 mL相同的同种异体血液;在最后一次输血后第7天处死小鼠。利用D10.G4.1辅助性T细胞克隆检测腹腔巨噬细胞的抗原呈递功能;利用依赖IL-2的HT-2细胞系检测伴刀豆球蛋白A刺激的脾细胞上清液中的IL-2活性。结果表明,虽然单次和多次输血后抗原呈递功能未受影响,但即使单次输血后脾细胞产生IL-2的能力也显著下降。因此,输血后对感染易感性增加以及恶性肿瘤中额外的免疫紊乱可能部分归因于IL-2产生减少。