Taghinezhad-S Sedigheh, Mohseni Amir Hossein, Bermúdez-Humarán Luis G, Casolaro Vincenzo, Cortes-Perez Naima G, Keyvani Hossein, Simal-Gandara Jesus
Department of Microbiology, Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran 1477893855, Iran.
Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, 78350 Jouy-en-Josas, France.
Vaccines (Basel). 2021 May 6;9(5):466. doi: 10.3390/vaccines9050466.
Severe acute respiratory syndrome coronavirus 2 virus (SARS-CoV-2) infection, the causative agent of COVID-19, now represents the sixth Public Health Emergency of International Concern (PHEIC)-as declared by the World Health Organization (WHO) since 2009. Considering that SARS-CoV-2 is mainly transmitted via the mucosal route, a therapy administered by this same route may represent a desirable approach to fight SARS-CoV-2 infection. It is now widely accepted that genetically modified microorganisms, including probiotics, represent attractive vehicles for oral or nasal mucosal delivery of therapeutic molecules. Previous studies have shown that the mucosal administration of therapeutic molecules is able to induce an immune response mediated by specific serum IgG and mucosal IgA antibodies along with mucosal cell-mediated immune responses, which effectively concur to neutralize and eradicate infections. Therefore, advances in the modulation of mucosal immune responses, and in particular the use of probiotics as live delivery vectors, may encourage prospective studies to assess the effectiveness of genetically modified probiotics for SARS-CoV-2 infection. Emerging trends in the ever-progressing field of vaccine development re-emphasize the contribution of adjuvants, along with optimization of codon usage (when designing a synthetic gene), expression level, and inoculation dose to elicit specific and potent protective immune responses. In this review, we will highlight the existing pre-clinical and clinical information on the use of genetically modified microorganisms in control strategies against respiratory and non-respiratory viruses. In addition, we will discuss some controversial aspects of the use of genetically modified probiotics in modulating the cross-talk between mucosal delivery of therapeutics and immune system modulation.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染是新冠病毒病(COVID-19)的病原体,目前已成为世界卫生组织(WHO)自2009年以来宣布的第六次国际关注的突发公共卫生事件(PHEIC)。鉴于SARS-CoV-2主要通过黏膜途径传播,通过相同途径给药的疗法可能是对抗SARS-CoV-2感染的理想方法。现在人们普遍认为,包括益生菌在内的基因改造微生物是治疗分子口服或鼻黏膜递送的有吸引力的载体。先前的研究表明,治疗分子的黏膜给药能够诱导由特异性血清IgG和黏膜IgA抗体介导的免疫反应以及黏膜细胞介导的免疫反应,这些反应有效地协同中和并根除感染。因此,黏膜免疫反应调节方面的进展,特别是使用益生菌作为活递送载体,可能会促使前瞻性研究评估基因改造益生菌对SARS-CoV-2感染的有效性。疫苗开发这一不断发展的领域中的新趋势再次强调了佐剂的作用,以及密码子使用优化(在设计合成基因时)、表达水平和接种剂量对引发特异性和强效保护性免疫反应的作用。在这篇综述中,我们将重点介绍有关基因改造微生物在对抗呼吸道和非呼吸道病毒的控制策略中应用的现有临床前和临床信息。此外,我们还将讨论在调节治疗性黏膜递送与免疫系统调节之间的相互作用中使用基因改造益生菌的一些争议性方面。