Metcalfe R A, Tandon N, Tamatani T, Miyasaka M, Weetman A P
Department of Medicine, University of Sheffield, U.K.
Immunology. 1993 Nov;80(3):493-7.
To examine the role played by adhesion molecules in thyroid autoimmunity, we have assessed the effect of administering monoclonal antibodies (mAb) against intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1 (LFA-1) in experimental autoimmune thyroiditis, induced by immunizing rats with thyroglobulin in complete Freund's adjuvant. The antibody against LFA-1, but not against ICAM-1, reduced thyroglobulin antibody production (P < 0.01) and both antibodies caused a significant reduction (P < 0.002) in the severity of the thyroidal lymphocytic infiltration. In vitro, both mAb impaired the proliferative response of splenic and lymph node T cells to thyroglobulin, but only the antibody against LFA-1 reduced thyroid cell killing assessed using splenic lymphocytes as effectors. Monoclonal antibodies against both these adhesion molecules appear to inhibit cell-mediated autoimmunity in vivo, but only the LFA-1 mAb reduced the autoantibody response.
为研究黏附分子在甲状腺自身免疫中所起的作用,我们评估了给予抗细胞间黏附分子-1(ICAM-1)和淋巴细胞功能相关抗原-1(LFA-1)的单克隆抗体(mAb)对实验性自身免疫性甲状腺炎的影响,该甲状腺炎是通过用甲状腺球蛋白在完全弗氏佐剂中免疫大鼠诱导产生的。抗LFA-1的抗体而非抗ICAM-1的抗体可降低甲状腺球蛋白抗体的产生(P<0.01),并且两种抗体均使甲状腺淋巴细胞浸润的严重程度显著降低(P<0.002)。在体外,两种mAb均损害脾和淋巴结T细胞对甲状腺球蛋白的增殖反应,但只有抗LFA-1的抗体降低了以脾淋巴细胞作为效应细胞时对甲状腺细胞的杀伤作用。针对这两种黏附分子的单克隆抗体似乎在体内均抑制细胞介导的自身免疫,但只有抗LFA-1的mAb降低了自身抗体反应。