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免疫抑制受体LILRB4在肿瘤和炎症性疾病中的研究进展

Advances in immunosuppressive receptor LILRB4 in tumors and inflammatory diseases
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摘要 白细胞免疫球蛋白样受体LILRB4(ILT3或CD85k)是免疫抑制受体家族成员,主要表达于髓系来源免疫细胞的细胞膜,在免疫调节中通过激活自身抑制基序(ITIM)或抑制Fc受体激活基序(ITAM)发挥免疫抑制作用。在肿瘤中,LILRB4受体被激活后产生免疫抑制性的肿瘤微环境协助肿瘤的侵袭和转移。在炎症疾病中,LILRB4在单核细胞、巨噬细胞、肥大细胞等多种细胞上表达并减轻炎症反应。目前LILRB4已成为肿瘤以及多种炎症性疾病的治疗靶点,针对急性髓细胞性白血病(AML)的抗LILRB4单克隆抗体已进入临床试验。本综述从LILRB4的结构分布、信号转导、治疗靶点、新药开发等几方面进行探讨。 The leukocyte immunoglobulin-like receptor LILRB4(ILT3 or CD85k),a member of the immunosuppressive receptor family,is expressed predominantly on the cell membranes of immune cells of myeloid origin,and exerts an immunosuppressive effect in immune regulation by activating either the autoinhibitory motif(ITIM)or by inhibiting Fc receptor activation motif(ITAM).In tumors,activation of LILRB4 receptor generates an immunosuppressive tumor microenvironment that assists in tumor invasion and metastasis,and in inflammatory diseases,LILRB4 is expressed on a variety of cells,such as monocytes,macrophages,mast cells,etc.,and attenuates inflammatory responses.Currently,LILRB4 has become a therapeutic target for tumors and various inflammatory diseases,and anti-LILRB4 monoclonal antibodies against acute myeloid leukemia(AML)have entered clinical trials.This review discusses LILRB4 in terms of its structural distribution,signaling,therapeutic targets,and new drug development.
作者 陈静怡 刘奕鎏 茹克亚·吐尔逊江 丁瑞 尹金平 梁作文 赵佳 李晶 CHEN Jingyi;LIU Yiliu;RUKEYA·Tu'erxunjiang;DING Rui;YIN Jinping;LIANG Zuowen;ZHAO Jia;LI Jing(China-Japan Union Hospitalof Jilin University,Changchun 130031,China;School of Public Health,Jilin University,Changchun 130012,China;School of Basic Medicine,Jilin University,Changchun 130012,China)
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2024年第7期1559-1564,共6页 Chinese Journal of Immunology
基金 大学生创新创业国家级项目(202310183314) 吉林省卫生健康科技提升项目(2023JC004) 吉林省教育厅科学技术研究项目(JJKH20241350KJ)。
关键词 白细胞免疫球蛋白样受体B4 免疫受体酪氨酸抑制基序 免疫抑制受体 肿瘤 炎症 Leukocyte immunoglobulin-like receptor B4 Immunoreceptor tyrosine inhibitory motif Immunosuppressive receptor Tumor Inflammation
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  • 1Daeron M,Latour S,Malbec O,Espinosa E,Pina P,Pasmans S,Fridman WH. The same tyrosine-based inhibition motif,in the intracytoplasmic domain of Fc gamma RⅡB,regulates negatively BCR-,TCR-,and FcR-dependent cell activation. Immunity,1995,3:635-646.
  • 2Takai T,Nakamura A,Endo S. Role of PIR-B in autoimmune glomerulonephritis. J Biomed Biotechnol,2011,2011:275302.
  • 3Daeron M,Jaeger S,Du Pasquier L,Vivier E. Immunoreceptor tyrosine-based inhibition motifs:a quest in the past and future. Immunol Rev,2008,224:11-43.
  • 4Katz HR. Inhibition of inflammatory responses by leukocyte Ig-like receptors. Adv Immunol,2006,91:251-272.
  • 5Bruhns P,Vely F,Malbec O,Fridman WH,Vivier E,Daeron M. Molecular basis of the recruitment of the SH2domain-containing inositol 5-phosphatases SHIP1and SHIP2by fcgamma RⅡB. J Biol Chem,2000,275:37357-37364.
  • 6Huang ZY,Hunter S,Kim MK,Indik ZK,Schreiber AD. The effect of phosphatases SHP-1and SHIP-1on signaling by the ITIM-and ITAM-containing Fcgamma receptors FcgammaRⅡB and FcgammaRⅡA. J Leukoc Biol,2003,73:823-829.
  • 7Binstadt BA,Brumbaugh KM,Dick CJ,Scharenberg AM,Williams BL,Colonna M,Lanier LL,Kinet JP,Abraham RT,Leibson PJ. Sequential involvement of Lck and SHP-1with MHC-recognizing receptors on NK cells inhibits FcR-initiated tyrosine kinase activation. Immunity,1996,5:629-638.
  • 8Daigle I,Yousefi S,Colonna M,Green DR,Simon HU. Death receptors bind SHP-1and block cytokine-induced anti-apoptotic signaling in neutrophils. Nat Med,2002,8:61-67.
  • 9Stebbins CC,Watzl C,Billadeau DD,Leibson PJ,Burshtyn DN,Long EO. Vav1dephosphorylation by the tyrosine phosphatase SHP-1as a mechanism for inhibition of cellular cytotoxicity. Mol Cell Biol,2003,23:6291-6299.
  • 10Staub E,Rosenthal A,Hinzmann B. Systematic identification of immunoreceptor tyrosine-based inhibitory motifs in the human proteome. Cell Signal,2004,16:435-456.

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