Medicine, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada
McCaig Institute for Bone and Joint Health, Calgary, Alberta, Canada.
Lupus Sci Med. 2022 Apr;9(1). doi: 10.1136/lupus-2022-000667.
Cytokine autoantibodies, particularly those directed to type I interferon (T1IFN), have been reported to portend an increased risk of severe COVID-19. Since SLE is one of the conditions historically associated with T1IFN autoantibodies, we sought to determine the prevalence of cytokine autoantibodies in our local cohort of 173 patients with SLE prepandemic and intrapandemic, of which nine had confirmed exposure to SARS-CoV-2. Autoantibodies to 16 different cytokines, including T1IFN, were measured by an addressable laser bead immunoassay. None of the 9 patients with confirmed exposure to SARS-CoV-2 had autoantibodies to T1IFN and none had severe COVID-19 symptoms, necessitating hospitalisation. Hence, we could not confirm that TIIFN autoantibodies increase the risk for severe COVID-19. In addition, the cytokine autoantibody pattern did not differ between those with and without evidence of SARS-CoV-2 exposure.
细胞因子自身抗体,特别是针对 I 型干扰素 (T1IFN) 的自身抗体,已被报道预示着 COVID-19 重症风险增加。由于 SLE 是历史上与 T1IFN 自身抗体相关的疾病之一,我们试图确定在我们的 173 例 SLE 患者队列中,包括 9 例已确诊接触 SARS-CoV-2 的患者,细胞因子自身抗体的流行率。通过可寻址激光珠免疫分析测定了针对 16 种不同细胞因子(包括 T1IFN)的自身抗体。在 9 例已确诊接触 SARS-CoV-2 的患者中,均未发现 T1IFN 自身抗体,且均未出现 COVID-19 重症症状,无需住院治疗。因此,我们无法确认 TIIFN 自身抗体是否会增加 COVID-19 重症风险。此外,在有或无 SARS-CoV-2 暴露证据的患者中,细胞因子自身抗体模式没有差异。