Mowat A M, Hutton A K, Garside P, Steel M
Department of Immunology, University of Glasgow, Western Infirmary, U.K.
Immunology. 1993 Sep;80(1):110-5.
Interleukin-1 (IL-1) is an important mediator of inflammation and has been implicated in several forms of immunopathology. Here we have investigated whether IL-1 plays a role in the enteropathy which occurs during a graft-versus-host reaction (GVHR) in mice. Non-irradiated (CBA x BALB/c) F1 mice with GVHR had increased production of IL-1 and treatment with rabbit anti-IL-1 alpha antibodies abolished the crypt hyperplasia and significantly reduced the parallel increase in crypt length which occurs in the jejunum. Antibody treatment had no effect on the accompanying increase in intraepithelial lymphocyte (IEL) counts or on the splenomegaly. Recombinant IL-1 itself produced villus atrophy, crypt hyperplasia and increased IEL counts in normal mice and stimulated the proliferation of an intestinal epithelial cell line in vitro. We propose that IL-1 plays an effector role in immunologically mediated enteropathy, either via direct effects on epithelial cells or secondary to an action on other, stromal cells in the mucosa.
白细胞介素-1(IL-1)是炎症的重要介质,与多种免疫病理学形式有关。在此,我们研究了IL-1在小鼠移植物抗宿主反应(GVHR)期间发生的肠病中是否起作用。患有GVHR的未受照射的(CBA×BALB/c)F1小鼠IL-1产生增加,用兔抗IL-1α抗体治疗可消除隐窝增生,并显著降低空肠中伴随的隐窝长度平行增加。抗体治疗对上皮内淋巴细胞(IEL)计数的伴随增加或脾肿大没有影响。重组IL-1本身在正常小鼠中导致绒毛萎缩、隐窝增生和IEL计数增加,并在体外刺激肠道上皮细胞系的增殖。我们提出,IL-1在免疫介导的肠病中起效应作用,要么通过对上皮细胞的直接作用,要么继发于对黏膜中其他基质细胞的作用。