Brief research report: OM-85 reduces SARS-COV-2 viral RNA expression in nasopharyngeal cells from COVID-19 patients

IF 2 Q4 VIROLOGY
Gisele Cassão, Krist Helen Antunes, João Ismael Budelon Gonçalvez, Leonardo Duarte Santos, Bruno Lopes Abbadi, Cristiano Valim Bizarro, Pablo Machado, Luiz Augusto Basso, Christian Pasquali, Renato T. Stein, Ana Paula Duarte de Souza
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Abstract

OM-85 is a bacterial lysate from common respiratory tract pathogens, with an excellent safety profile, widely used to prevent recurrent respiratory tract infections. Several studies have been reporting the immunomodulating properties and antiviral roles of OM-85. The COVID-19 pandemic, originating in 2019, has presented a significant global public health crisis. While effective vaccines have been developed, vaccination rates vary considerably, and numerous concerning viral variants continue to emerge. The challenge persists in creating early interventions to halt the progression of the disease to its severe stages. To examine the therapeutic effect of OM-85 after SARS-CoV-2 infection and compared to recombinant human (rhINF-β) we collected nasopharyngeal cells from COVID-19 patients. The cells were treated ex-vivo with OM-85 or hrINF-β and the response was analyzed after 24h for gene expression by real-time PCR. We found that OM-85 decreased the SARS-CoV-2 N1 gene expression and increased RIG-I (DDX58) in these cells. The expression of ACE2 was undetected in these samples. These data support the antiviral effect of OM-85 against SARS-CoV-2.
研究简述:OM-85可降低COVID-19患者鼻咽细胞中SARS-COV-2病毒RNA表达
OM-85是一种常见呼吸道病原体的细菌裂解物,具有良好的安全性,广泛用于预防复发性呼吸道感染。一些研究报道了OM-85的免疫调节特性和抗病毒作用。始于2019年的2019冠状病毒病大流行引发了一场重大的全球公共卫生危机。虽然已经研制出有效的疫苗,但疫苗接种率相差很大,而且许多有关的病毒变体继续出现。在制定早期干预措施以阻止疾病发展到严重阶段方面仍然存在挑战。为了检验OM-85在SARS-CoV-2感染后的治疗效果,并与重组人(rhINF-β)进行比较,我们收集了COVID-19患者的鼻咽细胞。体外分别用OM-85或hrINF-β处理细胞,24h后用real-time PCR检测基因表达情况。我们发现OM-85在这些细胞中降低了SARS-CoV-2 N1基因表达并增加了RIG-I (DDX58)。在这些样本中未检测到ACE2的表达。这些数据支持OM-85对SARS-CoV-2的抗病毒作用。
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