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1. Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity

2. Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2

3. SARS-CoV-2 evolution during treatment of chronic infection

4. Longitudinal analysis reveals that delayed bystander CD8+ T cell activation and early immune pathology distinguish severe COVID-19 from mild disease

5. Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies

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