Maturation of SARS-CoV-2 Spike-specific memory B cells drives resilience to viral escape
暂无分享,去创建一个
A. Telenti | A. Walls | D. Veesler | I. Bartha | F. Sallusto | A. Lanzavecchia | John E. Bowen | M. A. Tortorici | H. Virgin | E. Cameroni | M. McCallum | D. Corti | A. Riva | N. Czudnochowski | M. Tarkowski | L. Piccoli | O. Giannini | C. Fregni | C. Havenar-Daughton | K. Culap | P. Ferrari | A. Ceschi | M. Biggiogero | R. Marzi | C. Garzoni | J. Dillen | J. Bassi | A. Arvin | E. Dellota | Nicole Sprugasci | A. F. Pellanda | Valentino Lepori | F. Muoio | T. Terrot | J. Low | Christiane E. Saliba | Gloria Lombardo | A. Cassotta | Laura Pertusini
[1] A. Sette,et al. SARS-CoV-2 spike conformation determines plasma neutralizing activity elicited by a wide panel of human vaccines , 2022, Science immunology.
[2] P. Maes,et al. Imprinted antibody responses against SARS-CoV-2 Omicron sublineages , 2022, Science.
[3] A. Sette,et al. Omicron spike function and neutralizing activity elicited by a comprehensive panel of vaccines , 2022, Science.
[4] Qian Wang,et al. Antibody evasion by SARS-CoV-2 Omicron subvariants BA.2.12.1, BA.4 and BA.5 , 2022, Nature.
[5] O. Pybus,et al. Emergence of SARS-CoV-2 Omicron lineages BA.4 and BA.5 in South Africa , 2022, Nature Medicine.
[6] P. Maes,et al. Imprinted antibody responses against SARS-CoV-2 Omicron sublineages , 2022, bioRxiv.
[7] Yuxin Chen,et al. The Third dose of CoronVac vaccination induces broad and potent adaptive immune responses that recognize SARS-CoV-2 Delta and Omicron variants , 2022, Emerging microbes & infections.
[8] L. Walker,et al. Recall of preexisting cross-reactive B cell memory after Omicron BA.1 breakthrough infection , 2022, Science Immunology.
[9] M. Nussenzweig,et al. Increased memory B cell potency and breadth after a SARS-CoV-2 mRNA boost , 2022, Nature.
[10] Justine C. Williams,et al. Efficient recall of Omicron-reactive B cell memory after a third dose of SARS-CoV-2 mRNA vaccine , 2022, bioRxiv.
[11] Frances E. Muldoon,et al. Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity , 2022, Nature.
[12] M. Gale,et al. Imprinted SARS-CoV-2-specific memory lymphocytes define hybrid immunity , 2022, Cell.
[13] A. Walls,et al. SARS-CoV-2 breakthrough infections elicit potent, broad, and durable neutralizing antibody responses , 2022, Cell.
[14] A. Walls,et al. Structural basis of SARS-CoV-2 Omicron immune evasion and receptor engagement , 2021, bioRxiv.
[15] M. Kraemer,et al. Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa , 2021, Nature.
[16] A. Telenti,et al. Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift , 2021, Nature.
[17] Aaron M. Rosenfeld,et al. mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern , 2021, Science.
[18] A. Meola,et al. mRNA vaccination of naive and COVID-19-recovered individuals elicits potent memory B cells that recognize SARS-CoV-2 variants , 2021, Immunity.
[19] A. Telenti,et al. Lectins enhance SARS-CoV-2 infection and influence neutralizing antibodies , 2021, Nature.
[20] M. Beltramello,et al. Broad betacoronavirus neutralization by a stem helix–specific human antibody , 2021, Science.
[21] M. Beltramello,et al. SARS-CoV-2 RBD antibodies that maximize breadth and resistance to escape , 2021, Nature.
[22] S. Crotty. Hybrid immunity , 2021, Science.
[23] C. Rice,et al. Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection , 2021, Nature.
[24] M. Davenport,et al. Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection , 2021, Nature Medicine.
[25] Aaron M. Rosenfeld,et al. Distinct antibody and memory B cell responses in SARS-CoV-2 naïve and recovered individuals following mRNA vaccination , 2021, Science Immunology.
[26] T. Ndung’u,et al. Escape of SARS-CoV-2 501Y.V2 from neutralization by convalescent plasma , 2021, Nature.
[27] L. Stamatatos,et al. mRNA vaccination boosts cross-variant neutralizing antibodies elicited by SARS-CoV-2 infection , 2021, Science.
[28] A. Iafrate,et al. Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity , 2021, Cell.
[29] William T. Harvey,et al. Author Correction: Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies , 2021, Nature.
[30] Ravindra K. Gupta,et al. The effect of spike mutations on SARS-CoV-2 neutralization , 2021, Cell Reports.
[31] D. Fremont,et al. Resistance of SARS-CoV-2 variants to neutralization by monoclonal and serum-derived polyclonal antibodies , 2021, Nature Medicine.
[32] D. Stuart,et al. Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera , 2021, Cell.
[33] D. Stuart,et al. Reduced neutralization of SARS-CoV-2 B.1.1.7 variant by convalescent and vaccine sera , 2021, Cell.
[34] M. Boothby. Faculty Opinions recommendation of Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection. , 2021, Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature.
[35] A. Achiron,et al. SARS-CoV-2 antibody dynamics and B-cell memory response over time in COVID-19 convalescent subjects , 2021, Clinical Microbiology and Infection.
[36] B. Haynes,et al. SARS-CoV-2 variant B.1.1.7 is susceptible to neutralizing antibodies elicited by ancestral Spike vaccines , 2021, bioRxiv.
[37] D. Ho,et al. Antibody Resistance of SARS-CoV-2 Variants B.1.351 and B.1.1.7 , 2021, bioRxiv.
[38] M. Beltramello,et al. N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2 , 2021, bioRxiv.
[39] Bjoern Peters,et al. Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection , 2021, Science.
[40] A. Meola,et al. Maturation and persistence of the anti-SARS-CoV-2 memory B cell response , 2020, Cell.
[41] R. Tibshirani,et al. Defining the features and duration of antibody responses to SARS-CoV-2 infection associated with disease severity and outcome , 2020, Science Immunology.
[42] M. Nussenzweig,et al. Evolution of Antibody Immunity to SARS-CoV-2 , 2020, bioRxiv.
[43] M. Beltramello,et al. Mapping Neutralizing and Immunodominant Sites on the SARS-CoV-2 Spike Receptor-Binding Domain by Structure-Guided High-Resolution Serology , 2020, Cell.
[44] L. Carter,et al. Functional SARS-CoV-2-specific immune memory persists after mild COVID-19 , 2020, medRxiv.
[45] Colin Renfrew,et al. Phylogenetic network analysis of SARS-CoV-2 genomes , 2020, Proceedings of the National Academy of Sciences.
[46] A. Walls,et al. Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein , 2020, Cell.
[47] G. Herrler,et al. SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor , 2020, Cell.
[48] B. Graham,et al. Cryo-EM Structure of the 2019-nCoV Spike in the Prefusion Conformation , 2020, bioRxiv.
[49] A. Walls,et al. Unexpected Receptor Functional Mimicry Elucidates Activation of Coronavirus Fusion , 2019, Cell.
[50] Barney S. Graham,et al. Immunogenicity and structures of a rationally designed prefusion MERS-CoV spike antigen , 2017, Proceedings of the National Academy of Sciences.
[51] D. Jarrossay,et al. Clonal dissection of the human memory B‐cell repertoire following infection and vaccination , 2009, European journal of immunology.
[52] Martin Odersky,et al. An Overview of the Scala Programming Language , 2004 .
[53] Dr Ferdiye Taner,et al. The enzyme-linked immunosorbent assay (ELISA). , 1976, Bulletin of the World Health Organization.