Grönneberg R
Allergy. 1984 Feb;39(2):115-8. doi: 10.1111/j.1398-9995.1984.tb01942.x.
Pharmacological modulation of the immediate and late phase reaction (LPR) to anti-human IgE was further investigated in a double-blind cross-over study. Tranexamic acid (AMCA) 1 g t.i.d. 24 h prior to and following intradermal injection of anti-IgE produced an approximate 40% inhibition of the LPR (P less than 0.01) without affecting the early response as compared with placebo in 10 volunteers. Antagonistic effect on activation of fibrinolysis and possibly the complement system is suggested as a possible mode of action.
在一项双盲交叉研究中,进一步研究了对抗人IgE的速发相和迟发相反应(LPR)的药理学调节作用。在10名志愿者中,与安慰剂相比,在皮内注射抗IgE之前和之后24小时,氨甲环酸(AMCA)每日3次、每次1 g,对LPR产生了约40%的抑制作用(P<0.01),且不影响早期反应。提示对纤维蛋白溶解激活以及可能对补体系统的拮抗作用是一种可能的作用方式。