The world continues to be in the midst of a distressing pandemic of
coronavirus disease 2019 (COVID-19)
infection caused by
severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a novel virus with multiple antigenic systems. The virus enters via nasopharynx, oral and infects cells by the expression of the spike
protein, and enters the lungs using the
angiotensin-converting enzyme-2 receptor. The spectrum of specific immune responses to SARS-CoV-2 virus
infection is increasingly challenging as frequent mutations have been reported and their
antigen specificity varies accordingly. The development of
monoclonal antibodies (mAbs) will have a more significant advantage in suppressing SARS-CoV-2 virus infectivity. Recently, mAbs have been developed to target included specific
neutralizing antibodies against
SARS-CoV-2 infection. The use of the therapeutic index of mAbs that can elicit neutralization by binding to the viral spike
protein and suppress the
cytokine network is a classic therapeutic approach for a potential cure. The development of mAbs against B-cell function as well as inhibition of the
cytokine network has also been a focus in recent research. Recent studies have demonstrated the efficacy of mAbs as
antibody cocktail preparations against
SARS-CoV-2 infection. Target specific therapeutic accomplishment with mAbs, a milestone in the modern therapeutic age, can be used to achieve a specific therapeutic strategy to suppress SARS-CoV-2 virus
infection. This review focuses on the molecular aspects of the
cytokine network and antibody formation to better understand the development of mAbs against SARS- CoV-2
infection along with recent patents.