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The receptor binding domain of SARS-CoV-2 Omicron subvariants targets Siglec-9 to decrease its immunogenicity by preventing macrophage phagocytosis.

Xin HeXiantao ZhangBolin WuJieyi DengYongli ZhangAiru ZhuYaochang YuanYingtong LinAchun ChenJinzhu FengXiumei WangShijian WuYingying LiuJie LiuYalin WangRong LiChaofeng LiangQuyu YuanYu LiangQiannan FangZhihui XiWenjie LiLiting LiangZhenglai ZhangHui TangYi PengChangwen KeXiancai MaWei-Bin CaiTing PanBingfeng LiuKai DengJun ChenJin-Cun ZhaoXuepeng WeiRan ChenYiwen ZhangHui Zhang
Published in: Nature immunology (2024)
The development of a vaccine specific to severe acute respiratory syndrome coronavirus 2 Omicron has been hampered due to its low immunogenicity. Here, using reverse mutagenesis, we found that a phenylalanine-to-serine mutation at position 375 (F375S) in the spike protein of Omicron to revert it to the sequence found in Delta and other ancestral strains significantly enhanced the immunogenicity of Omicron vaccines. Sequence FAPFFAF at position 371-377 in Omicron spike had a potent inhibitory effect on macrophage uptake of receptor-binding domain (RBD) nanoparticles or spike-pseudovirus particles containing this sequence. Omicron RBD enhanced binding to Siglec-9 on macrophages to impair phagocytosis and antigen presentation and promote immune evasion, which could be abrogated by the F375S mutation. A bivalent F375S Omicron RBD and Delta-RBD nanoparticle vaccine elicited potent and broad nAbs in mice, rabbits and rhesus macaques. Our research suggested that manipulation of the Siglec-9 pathway could be a promising approach to enhance vaccine response.
Keyphrases
  • respiratory syndrome coronavirus
  • sars cov
  • binding protein
  • amino acid
  • adipose tissue
  • coronavirus disease
  • escherichia coli
  • crispr cas
  • dna binding
  • case report
  • insulin resistance
  • skeletal muscle
  • protein kinase