Castellani M L, Bhattacharya K, Tagen M, Kempuraj D, Perrella A, De Lutiis M, Boucher W, Conti P, Theoharides T C, Cerulli G, Salini V, Neri G
Department of Internal Medicine and Science of Ageing, University of Chieti, Italy.
Int J Immunopathol Pharmacol. 2007 Jul-Sep;20(3):447-53. doi: 10.1177/039463200702000303.
Chemokines are inflammatory proteins acting via G-protein coupled chemokine receptors that trigger different signaling pathways. Monocyte chemoattractant protein-1 (CCL2/MCP-1) and regulated on activation, normal T expressed and secreted (CCL5/RANTES) are the two major members of the CC chemokine beta subfamily. The roles of RANTES and MCP-1 are emerging in regulating the recruitment of inflammatory cells into tissue during inflammation. The inhibition of MCP-1 and RANTES with corresponding antibodies or other inhibitors may provide benefits in different clinical scenarios including cancer, inflammation, CNS disorders, parasitic disease, autoimmune and heart diseases. RANTES and MCP-1 may represent targets for diagnostic procedures and therapeutic intervention, and may be useful as a prognostic factor in the above diseases.
趋化因子是通过G蛋白偶联趋化因子受体发挥作用的炎症蛋白,可触发不同的信号通路。单核细胞趋化蛋白-1(CCL2/MCP-1)和活化正常T细胞表达和分泌调节因子(CCL5/RANTES)是CC趋化因子β亚家族的两个主要成员。RANTES和MCP-1在炎症过程中调节炎症细胞向组织内募集方面的作用正在显现。用相应抗体或其他抑制剂抑制MCP-1和RANTES可能在包括癌症、炎症、中枢神经系统疾病、寄生虫病、自身免疫性疾病和心脏病等不同临床情况下带来益处。RANTES和MCP-1可能代表诊断程序和治疗干预的靶点,并且可能作为上述疾病的预后因素。