Insights into the roles of cathepsins in antigen processing and presentation revealed by specific inhibitors

被引:43
作者
Katunuma, N [1 ]
Matsunaga, Y
Himeno, K
Hayashi, Y
机构
[1] Tokushima Bunri Univ, Inst Hlth Sci, Tokushima 7708514, Japan
[2] Fukuoka Univ, Sch Med, Jonan Ku, Fukuoka 8140180, Japan
[3] Kyushu Univ, Dept Parasitol, Grad Sch Med Sci, Higashi Ku, Fukuoka 8128582, Japan
[4] Univ Tokushima, Sch Dent, Tokushima 7708503, Japan
关键词
antigen presentation; antigen processing; autoantigen; cathepsin; cathepsin inhibitor; T cell response;
D O I
10.1515/BC.2003.099
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eleven human cathepsins have been identified, however, the in vivo roles of individual cathepsins are still largely unknown. In this brief review we will summarize the functions of individual cathepsins in antigen processing and presentation, which are the initial steps of the immune response. Two general inhibitors of papainlike cysteine proteases, E-64 and pyridoxal phosphate, can completely suppress antigen presentation in vivo. To evaluate the contribution of individual cathepsins, specific inhibitors have been developed based on cathepsin tertiary structures: CA-074 for cathepsin B, CLIK-148 and -195 for cathepsin L, CLIK-60 for cathepsin S. Administration of CA-074, a cathepsin B inhibitor, suppresses the response to exogenous antigens, such as hepatitis B virus antigen, ovalbumin and Leishmania major antigen, and induces switching of the helper T cell responses from Th-2 to Th-1 of CD4+ T cells, thereby downregulating the production of IgE and IgG1. Administration of the cathepsin S inhibitor CLIK-60 impairs presentation of an autoantigen, [alpha]fodrin, in Sjogrens syndrome and suppresses the Th-1 response and autoantibody production.
引用
收藏
页码:883 / 890
页数:8
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