Miner Jonathan J, Cook Lindsey E, Hong Jun P, Smith Amber M, Richner Justin M, Shimak Raeann M, Young Alissa R, Monte Kristen, Poddar Subhajit, Crowe James E, Lenschow Deborah J, Diamond Michael S
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sci Transl Med. 2017 Feb 1;9(375). doi: 10.1126/scitranslmed.aah3438.
In 2013, chikungunya virus (CHIKV) transmission was documented in the Western Hemisphere, and the virus has since spread throughout the Americas with more than 1.8 million people infected in more than 40 countries. CHIKV targets the joints, resulting in symmetric polyarthritis that clinically mimics rheumatoid arthritis and can endure for months to years. At present, no approved treatment is effective in preventing or controlling CHIKV infection or disease. We treated mice with eight different disease-modifying antirheumatic drugs and identified CLTA4-Ig (abatacept) and tofacitinib as candidate therapies based on their ability to decrease acute joint swelling. CTLA4-Ig reduced T cell accumulation in the joints of infected animals without affecting viral infection. Whereas monotherapy with CTLA4-Ig or a neutralizing anti-CHIKV human monoclonal antibody provided partial clinical improvement, therapy with both abolished swelling and markedly reduced levels of chemokines, proinflammatory cytokines, and infiltrating leukocytes. Thus, combination CTLA4-Ig and antiviral antibody therapy controls acute CHIKV infection and arthritis and may be a candidate for testing in humans.
2013年,西半球记录到基孔肯雅病毒(CHIKV)传播,此后该病毒已在美洲各地传播,40多个国家有超过180万人感染。CHIKV侵袭关节,导致对称性多关节炎,临床上类似于类风湿性关节炎,可持续数月至数年。目前,尚无经批准的治疗方法能有效预防或控制CHIKV感染或疾病。我们用八种不同的改善病情抗风湿药物治疗小鼠,并根据其减轻急性关节肿胀的能力,确定CTLA4-Ig(阿巴西普)和托法替布为候选疗法。CTLA4-Ig减少了感染动物关节中的T细胞积聚,而不影响病毒感染。虽然CTLA4-Ig单药治疗或中和性抗CHIKV人单克隆抗体治疗能提供部分临床改善,但两者联合治疗可消除肿胀,并显著降低趋化因子、促炎细胞因子和浸润白细胞的水平。因此,CTLA4-Ig与抗病毒抗体联合治疗可控制急性CHIKV感染和关节炎,可能是一种可供人体试验的候选疗法。