Kasperkiewicz Michael, Bednarek Marta, Tukaj Stefan
Department of Dermatology, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Department of Molecular Biology, Faculty of Biology, University of Gdańsk, Gdańsk, Poland.
Front Med (Lausanne). 2021 Dec 20;8:807711. doi: 10.3389/fmed.2021.807711. eCollection 2021.
It is hypothesized that SARS-CoV-2 has the potential to elicit autoimmunity due to molecular mimicry between immunogenic proteins of the virus and human extracellular molecules. While and evaluation of such immune cross-reactivity of human antibodies to SARS-CoV-2 proteins with several different tissue antigens has been described, there is limited information specifically pertaining to the immunological effects of COVID-19 and vaccines against SARS-CoV-2 on the development of autoimmune bullous diseases (AIBDs). Twelve seropositive post-COVID-19 individuals and 12 seropositive healthy volunteers who received two doses of the mRNA COVID-19 vaccine from Pfizer-BioNTech have been included in this case series investigation. Serum samples of these blood donors were tested for autoantibodies to the main immunobullous autoantigens, i.e., desmoglein 1, desmoglein 3, envoplakin, BP180, BP230, and type VII collagen. Our study revealed that none of the 24 anti-SARS-CoV-2 IgG-positive subjects had concomitant antibody reactivity with any of the tested autoantigens. These results argue against a relationship between SARS-CoV-2 infection/vaccines and AIBDs with respect to disease-triggering antibody cross-reactivity.
据推测,由于新冠病毒的免疫原性蛋白与人类细胞外分子之间存在分子模拟,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)有可能引发自身免疫。虽然已有研究描述了人类抗体对SARS-CoV-2蛋白与几种不同组织抗原的这种免疫交叉反应性的 和 评估,但关于2019冠状病毒病(COVID-19)和抗SARS-CoV-2疫苗对自身免疫性大疱性疾病(AIBDs)发展的免疫影响的具体信息有限。本病例系列研究纳入了12名COVID-19康复后血清学阳性个体和12名接受了两剂辉瑞-生物科技公司mRNA COVID-19疫苗的血清学阳性健康志愿者。检测了这些献血者血清样本中针对主要免疫性大疱性自身抗原的自身抗体,即桥粒芯糖蛋白1、桥粒芯糖蛋白3、内披蛋白、BP180、BP230和VII型胶原蛋白。我们的研究表明,24名抗SARS-CoV-2 IgG阳性受试者中,没有一人对任何测试的自身抗原有伴随的抗体反应性。这些结果表明,就引发疾病的抗体交叉反应性而言,SARS-CoV-2感染/疫苗与AIBDs之间不存在关联。