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- W4321168233 abstract "The high mortality of coronavirus disease 2019 is related to poor antigen presentation and lymphopenia. Cytomegalovirus and the herpes family encode a series of major histocompatibility complex (MHC)-like molecules required for targeted immune responses to achieve immune escape. In this present study, domain search results showed that many proteins of the severe acute respiratory syndrome coronavirus 2 virus had MHC-like domains, which were similar to decoys for the human immune system. MHC-like structures could bind to MHC receptors of immune cells (such as CD4 + T-cell, CD8 + T-cell, and natural killer-cell), interfering with antigen presentation. Then the oxygen free radicals generated by E protein destroyed immune cells after MHC-like of S protein could bind to them. Mutations in the MHC-like region of the viral proteins such as S promoted weaker immune resistance and more robust transmission. S 127–194 were the primary reason for the robust transmission of delta variants. The S 144–162 regulated the formation of S trimer. The mutations of RdRP: G671S and N: D63G of delta variant caused high viral load. S 62–80 of alpha, beta, lambda variants were the important factor for fast-spreading. S 616–676 and 1014–1114 were causes of high mortality for gamma variants infections. These sites were in the MHC-like structure regions." @default.
- W4321168233 created "2023-02-18" @default.
- W4321168233 creator A5038452401 @default.
- W4321168233 creator A5041366828 @default.
- W4321168233 date "2023-02-20" @default.
- W4321168233 modified "2023-09-24" @default.
- W4321168233 title "COVID-19: Attacks Immune Cells and Interferences With Antigen Presentation Through MHC-Like Decoy System" @default.
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- W4321168233 doi "https://doi.org/10.1097/cji.0000000000000455" @default.
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