tein and/or its receptor binding domain NP PPARγ medchemexpress protein N protein Viral receptor binding domain (RBD) Receptor binding domain SIRT2 Species Principle Investigators Davide C, Katja F, Martina B, et al. Li Z, Xingsu G, Binyang Z, et al. Yaoqing C, Bing H, Shuning L, et al. Lei C, Tengsen G, Min D, et al. Xilin W, Zhiwei W.CN 112661841 AEpitope S1-RBD and S1-NTDLei Y, Yingfen W, Wenjing G, et al.CN 112625136 A 20210409 CN 112574300 A 20210330 CN 112521496 A 20210319 CN 112409488 A 20210226 CN 112225806 A 20210115 CN 112210004 A 20210112 CN 112175073 A 20210105 CN 112175071 A 20210105 CN 112159469 ATwo epitopes of SARS-CoV-2 spike protein Spike protein Spike protein RBD domain Human ACE2 Spike RBD protein Spike protein Spike protein Spike protein Spike S1-RBDGuojun L, Chanjuan L, Junbin S, et al. Xiaochun W, and Junxin L. Ke D, Zhaowei G, Xi W, et al. Chunhe W, Yuning C, Yili C, et al. Yafeng L. Yang W, Xuefeng N, Chunlin W, et al. Jinghe H, Fan W, Mei L, et al. Jingui Y, Lei Z, Lianjun M, et al. Jinghe H, Fan W, Mei L, et al.Note: SARS CoV-2–severe acute respiratory syndrome coronavirus-2; RBD–Receptor binding domain; S, N, proteins–Spike, Nucleocapsid, proteins; ACE2–Angiotensin converting enzyme-2.Int. J. Mol. Sci. 2021, 22,ten of5. Discussion Antibodies are developed by the immune method in response to infection. Monoclonal antibodies are created inside the laboratory and are designed to mimic and boost the all-natural method of immunity. These agents are increasingly becoming tested and employed against cancer and different kinds of infection [10]. Monoclonal antibodies are intended to target a specific infection method, and this tends to make them distinct from other chemotherapy drugs. Monoclonal antibodies are manufactured by exposing a viral component to white blood cells and after that the isolated proteins are mass made by a cloning method within the laboratory [56]. Presently, two big categories of MAbs are becoming tested for COVID-19. The initial category especially target and neutralize the virus (casirivimab, imdevimab, bamlanivimab) as well as the second group of MAbs acts on the immunological program and decreases inflammatory circumstances following infection (tocilizumab, sarilumab and siltuximab) [13]. Patents and patenting methods for biotechnological merchandise for instance monoclonal antibodies are cumbersome. The majority of the time, these complex biological molecules require much more than one particular patent to cover each of the aspects with the innovation [57]. Furthermore, the novelty in biotechnology originates largely from a university/public supported/research institution. Patenting such technological advancements for commercial purposes or technology transfer needs numerous legal and procedural concerns [58]. The accessible information indicated that till lately three classes of MAbs have received emergency use authorization. They may be bamlanivimab, casirivimab-imdevimab mixture and bamlanivimab-etesevimab combination [13]. Patent evaluation suggested that MAbs tested for the therapy of COVID-19 are manufactured by recombinant DNA technologies. The complexity inside the manufacturing technique includes the production of crude protein by means of cell culture in a bioreactor, followed by a series of purification methods and finally the sterile filling procedures. The course of action starts from the immunization of laboratory animals like BALB/c [59]. This sensitizes the B lymphocytes against the antigen necessary for the production of MAbs. Distinct B cells are identified, fused and hybridized. Hybrid cells are clon