Chang Aileen Yu-Hen, Hernández Alfonso Sucerquia, Mejía Jose Forero, Tritsch Sarah Renee, Mendoza-Torres Evelyn, Encinales Liliana, Bonfanti Andres Cadena, Proctor Abigale Marie, Simon Gary Leonard, Simmens Samuel Joseph, Firestein Gary Steven
Department of Medicine, George Washington University, Washington, DC, USA.
Department of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC, USA.
J Cell Immunol. 2024;6(2):64-75. doi: 10.33696/immunology.6.191.
Chikungunya virus (CHIKV) is an alphavirus spread by mosquitos that causes arthralgias and arthritis that may last for years. The objective of this study was to describe the arthritis progression and T cell immunology over a two-year period.
A cohort of 40 cases of serologically confirmed CHIKV from Magdalena and Atlántico, Colombia were followed in 2019 and again in 2021. Arthritis disease severity, disability, pain, stiffness, physical function, mobility, fatigue, anxiety, sleep disturbances and depression were assessed. Serum cytokines and T-cell subsets were measured and tested for change. Correlations within each of the 2 time periods for laboratory parameters were also examined.
Although, arthritis disease severity, as measured by the Disease Activity Score-28 (DAS-28) did not change significantly over a two-year period, a new metric- the Chikungunya Disease Activity Score (CHIK-DAS)- was more sensitive to detect changes in disease severity than the Disease Activity Score-28 (DAS-28) and showed some improvement in average disease severity from moderate to mild over two years. Cases were characterized by moderate disability, pain, and stiffness with mild alterations of physical function, mobility, fatigue, anxiety, sleep disturbances and depression that did not change significantly over time. Small joints including the fingers and wrists were most affected without significant change over time. The percentage of effector T cells (Teffs) and regulatory T cells (Tregs) of CD4 T cells both decreased over time. Teff percentages decreased more significantly resulting in a halving of the Teff/Treg ratio two years later. Furthermore, markers of Treg immunosuppressive function such as CTLA4, Helios, CD28, CD45RA and 41bb decreased over time. Cytokines did not change significantly over time.
The presented data suggest that arthritis persists almost seven years after chikungunya infection in some patients with waning Teff and Treg numbers and activation markers over time. Treg activation may be a promising therapeutic target for further investigation.
基孔肯雅病毒(CHIKV)是一种由蚊子传播的甲病毒,可引起关节痛和关节炎,症状可能持续数年。本研究的目的是描述两年内关节炎的进展情况和T细胞免疫学特征。
对2019年从哥伦比亚马格达莱纳和大西洋省血清学确诊的40例基孔肯雅病毒感染病例进行随访,并于2021年再次随访。评估关节炎疾病的严重程度、残疾情况、疼痛、僵硬程度、身体功能、活动能力、疲劳、焦虑、睡眠障碍和抑郁情况。检测血清细胞因子和T细胞亚群,并测试其变化情况。还检查了两个时间段内各实验室参数之间的相关性。
尽管通过疾病活动评分-28(DAS-28)衡量的关节炎疾病严重程度在两年内没有显著变化,但一种新的指标——基孔肯雅疾病活动评分(CHIK-DAS)——比疾病活动评分-28(DAS-28)更能敏感地检测疾病严重程度的变化,并且显示出在两年内平均疾病严重程度从中度到轻度有一定改善。病例的特征是中度残疾、疼痛和僵硬,身体功能、活动能力、疲劳、焦虑、睡眠障碍和抑郁有轻度改变,且随时间没有显著变化。包括手指和手腕在内的小关节受影响最大,且随时间没有显著变化。CD4 T细胞的效应T细胞(Teffs)和调节性T细胞(Tregs)百分比均随时间下降。Teff百分比下降更显著,导致两年后Teff/Treg比值减半。此外,Treg免疫抑制功能标志物如CTLA4、Helios、CD28、CD45RA和41bb随时间下降。细胞因子随时间没有显著变化。
所呈现的数据表明,在一些患者中,基孔肯雅病毒感染后关节炎持续近七年,同时Teff和Treg数量以及激活标志物随时间逐渐减少。Treg激活可能是一个有前景的治疗靶点,值得进一步研究。