Wittig B, Schwärzler C, Föhr N, Günthert U, Zöller M
Department of Tumor Progression and Immune Defense, German Cancer Research Center, Heidelberg.
J Immunol. 1998 Aug 1;161(3):1069-73.
Inflammatory bowel disease is a quite severe chronic inflammation, treated mainly by immunosuppression, which often has serious side effects. As CD44 is important in lymphocyte activation and migration, we asked whether Abs against CD44 isoforms influence trinitrobenzenesulfonic acid (TNBS)-induced colitis in mice. A lethal colitis (73/111 mice) could be prevented in 69 of 97 mice by anti-CD44v7 (CD44 variant isoform v7), whereas anti-CD44s (CD44 standard isoform) and anti-CD44v6 had no effect. Upon receiving anti-CD44v7 after the disease had been fully exacerbated, >90% of the mice recovered. TNBS plus anti-CD44v7-treated mice developed early signs of inflammation, with infiltration of leukocytes in the lamina propria and increased IFN-gamma production. However, while control mice developed a severe pancolitis, the intestine fully regenerated in anti-CD44v7-treated mice. Locally and systemically, a strong increase in IL-10 production was noted. Thus, anti-CD44v7 can be regarded as a highly efficient and specific therapeutic reagent in chronic colitis, which probably functions by regulating an overshooting Th1 reaction.
炎症性肠病是一种相当严重的慢性炎症,主要通过免疫抑制进行治疗,而免疫抑制往往会产生严重的副作用。由于CD44在淋巴细胞激活和迁移中起重要作用,我们研究了针对CD44异构体的抗体是否会影响三硝基苯磺酸(TNBS)诱导的小鼠结肠炎。在97只小鼠中,69只通过抗CD44v7(CD44变异异构体v7)预防了致命性结肠炎(73/111只小鼠),而抗CD44s(CD44标准异构体)和抗CD44v6则没有效果。在疾病完全加重后给予抗CD44v7,超过90%的小鼠恢复。TNBS加抗CD44v7治疗的小鼠出现早期炎症迹象,固有层有白细胞浸润且IFN-γ产生增加。然而,虽然对照小鼠发展为严重的全结肠炎,但抗CD44v7治疗的小鼠肠道完全再生。在局部和全身,均观察到IL-10产生显著增加。因此,抗CD44v7可被视为慢性结肠炎中一种高效且特异的治疗试剂,其可能通过调节过度的Th1反应发挥作用。