Author: Sacchi, Maria C.; Tamiazzo, Stefania; Stobbione, Paolo; Agatea, Lisa; De Gaspari, Piera; Stecca, Anna; Lauritano, Ernesto C.; Roveta, Annalisa; Tozzoli, Renato; Guaschino, Roberto; Bonometti, Ramona
Title: SARSâ€CoVâ€2 infection as a trigger of autoimmune response Cord-id: 2bpafcfh Document date: 2021_1_21
ID: 2bpafcfh
Snippet: ABSTRACT: Currently, few evidences have shown the possible involvement of autoimmunity in patients affected by coronavirus disease 2019 (COVIDâ€19). In this study, we elucidate whether severe acute respiratory syndrome coronavirus disease 2 (SARSâ€CoVâ€2) stimulates autoantibody production and contributes to autoimmunity activation. We enrolled 40 adult patients (66.8 years mean age) admitted to Alessandria Hospital between March and April 2020. All the patients had a confirmed COVIDâ€19 dia
Document: ABSTRACT: Currently, few evidences have shown the possible involvement of autoimmunity in patients affected by coronavirus disease 2019 (COVIDâ€19). In this study, we elucidate whether severe acute respiratory syndrome coronavirus disease 2 (SARSâ€CoVâ€2) stimulates autoantibody production and contributes to autoimmunity activation. We enrolled 40 adult patients (66.8 years mean age) admitted to Alessandria Hospital between March and April 2020. All the patients had a confirmed COVIDâ€19 diagnosis and no previously clinical record of autoimmune disease. Forty blood donors were analyzed for the same markers and considered as healthy controls. Our patients had high levels of common inflammatory markers, such as C reactive protein, lactate dehydrogenase, ferritin, and creatinine. Interleukinâ€6 concentrations were also increased, supporting the major role of this interleukin during COVIDâ€19 infection. Lymphocyte numbers were generally lower compared with healthy individuals. All the patients were also screened for the most common autoantibodies. We found a significant prevalence of antinuclear antibodies, antineutrophil cytoplasmic antibodies, and ASCA immunoglobulin A antibodies. We observed that patients having a de novo autoimmune response had the worst acute viral disease prognosis and outcome. Our results sustain the hypothesis that COVIDâ€19 infection correlates with the autoimmunity markers. Our study might help clinicians to: (a) better understand the heterogeneity of this pathology and (b) correctly evaluate COVIDâ€19 clinical manifestations. Our data explained why drugs used to treat autoimmune diseases may also be useful for SARSâ€CoVâ€2 infection. In addition, we highly recommend checking patients with COVIDâ€19 for autoimmunity markers, mainly when deciding on whether to treat them with plasma transfer therapy. STUDY HIGHLIGHTS: WHAT IS THE CURRENT KNOWLEDGE ON THE TOPIC? WHAT QUESTION DID THIS STUDY ADDRESS? WHAT DOES THIS STUDY ADD TO OUR KNOWLEDGE? HOW MIGHT THIS CHANGE CLINICAL PHARMACOLOGY OR TRANSLATIONAL SCIENCE? ☑ These results suggest that the drugs normally used to treat autoimmune diseases should also be considered during SARSâ€CoVâ€2, improving public health. In addition, before starting a transfer plasma therapy, it is important to also evaluate the autoimmunity conditions of the patients with COVIDâ€19. Transferring antibodies or trying to neutralize them should be done with precaution. It is possible that the risk of developing or increasing the autoimmune response may enhance.
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