“…A human host’s natural and unique complement of miRNAs, sncRNAs, mRNAs, and other small RNA and/or DNA sequences appears to contribute to the observed natural quantity, complexity, and variability of nucleic acids located within host cells, and hence, their individual susceptibility to viral infection [ 11 , 12 , 13 , 14 , 32 ]. More specifically, the targeting and inactivation of SARS-CoV-2 by natural and/or pre-existing miRNAs or sncRNAs: (i) Would provide a natural protective mechanism or ssRNA-based innate-immune type of ‘ host immunity ’ against SARS-CoV-2 invasion, replication and COVID-19 [ 36 , 37 ]; (ii) would help explain individual variability of innate-immunity and resistance to SARS-CoV-2 infection of some persons who naturally express sncRNAs or miRNAs antisense to SARS-CoV-2, or other miRNAs or ssRNAs that target pathological ssRNA viruses [ 36 , 37 , 38 , 39 , 40 ]; (iii) suggests that very specific artificially synthesized and chemically stabilized sncRNA and/or miRNAs may be of therapeutic value in the accelerated destabilization, depolymerization, and destruction of the invading SARS-CoV-2 viral RNA sequence itself, resulting in SARS-CoV-2 degradation and the rapid cessation and termination of SARS-CoV-2 pathogenic activity; (iv) may also be useful in the targeting and inactivation of other contagious and invasive viruses, including neurotrophic viruses, that possess ssRNA genomes; and (v) would present a series of useful biomarkers to assess the absence or specific stage of SARS-CoV-2 infection and the efficacy of anti-SARS-CoV-2 pharmaceutical intervention and treatment strategies [ 31 , 39 ].…”