Antibody feedback regulates immune memory after SARS-CoV-2 mRNA vaccination

[1]  M. Nussenzweig,et al.  Memory B cell responses to Omicron subvariants after SARS-CoV-2 mRNA breakthrough infection in humans , 2022, bioRxiv.

[2]  D. Burton,et al.  Antibodies from primary humoral responses modulate the recruitment of naive B cells during secondary responses , 2022, Immunity.

[3]  M. Nussenzweig,et al.  Increased memory B cell potency and breadth after a SARS-CoV-2 mRNA boost , 2022, Nature.

[4]  M. Nussenzweig,et al.  Anti-SARS-CoV-2 receptor-binding domain antibody evolution after mRNA vaccination , 2021, Nature.

[5]  C. Rice,et al.  Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection , 2021, Nature.

[6]  L. Stamatatos,et al.  Germinal center–dependent and –independent memory B cells produced throughout the immune response , 2021, The Journal of experimental medicine.

[7]  M. Nussenzweig,et al.  Broad cross-reactivity across sarbecoviruses exhibited by a subset of COVID-19 donor-derived neutralizing antibodies , 2021, bioRxiv.

[8]  M. Nussenzweig,et al.  Sequencing, cloning, and antigen binding analysis of monoclonal antibodies isolated from single mouse B cells , 2021, STAR protocols.

[9]  D. Burton,et al.  Structural and functional ramifications of antigenic drift in recent SARS-CoV-2 variants , 2021, Science.

[10]  M. Nussenzweig,et al.  mRNA vaccine-elicited antibodies to SARS-CoV-2 and circulating variants , 2021, bioRxiv.

[11]  C. Rice,et al.  Enhanced SARS-CoV-2 neutralization by dimeric IgA , 2020, Science Translational Medicine.

[12]  J. Beeson,et al.  Epitope masking may limit antibody boosting to malaria vaccines , 2020, Immunology and cell biology.

[13]  M. Nussenzweig,et al.  Antibody Affinity Shapes the Choice between Memory and Germinal Center B Cell Fates , 2020, Cell.

[14]  M. Nussenzweig,et al.  SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies , 2020, Nature.

[15]  S. Hoffman,et al.  Antibody Feedback Limits the Expansion of B Cell Responses to Malaria Vaccination but Drives Diversification of the Humoral Response. , 2020, Cell host & microbe.

[16]  C. Rice,et al.  Convergent Antibody Responses to SARS-CoV-2 in Convalescent Individuals , 2020, Nature.

[17]  C. Rice,et al.  Measuring SARS-CoV-2 neutralizing antibody activity using pseudotyped and chimeric viruses , 2020, bioRxiv.

[18]  M. Nussenzweig,et al.  Structures of human antibodies bound to SARS-CoV-2 spike reveal common epitopes and recurrent features of antibodies , 2020, bioRxiv.

[19]  J. Greenbaum,et al.  Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals , 2020, Cell.

[20]  M. V. van Breemen,et al.  Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability , 2020, Science.

[21]  Philip L. Felgner,et al.  A serological assay to detect SARS-CoV-2 seroconversion in humans , 2020, medRxiv.

[22]  M. Meyer-Hermann.  Injection of Antibodies against Immunodominant Epitopes Tunes Germinal Centers to Generate Broadly Neutralizing Antibodies. , 2019, Cell reports.

[23]  D. Irvine,et al.  Immunization expands B cells specific to HIV-1 V3 glycan in mice and macaques , 2019, Nature.

[24]  James E. Crowe,et al.  High frequency of shared clonotypes in human B cell receptor repertoires , 2019, Nature.

[25]  A. Arrick,et al.  Institutional Animal Care and Use Committee (IACUC) , 2018 .

[26]  J. Ravetch,et al.  Fcγ Receptor Function and the Design of Vaccination Strategies. , 2017, Immunity.

[27]  M. Shlomchik,et al.  Memory B Cells of Mice and Humans. , 2017, Annual review of immunology.

[28]  Rustom Antia,et al.  Multi-epitope Models Explain How Pre-existing Antibodies Affect the Generation of Broadly Protective Responses to Influenza , 2016, PLoS pathogens.

[29]  M. Shlomchik,et al.  A Temporal Switch in the Germinal Center Determines Differential Output of Memory B and Plasma Cells. , 2014, Immunity.

[30]  Steven H. Kleinstein,et al.  Change-O: a toolkit for analyzing large-scale B cell immunoglobulin repertoire sequencing data , 2015, Bioinform..

[31]  T. Kurosaki,et al.  Memory B cells , 2015, Nature Reviews Immunology.

[32]  M. Jenkins,et al.  A germinal center–independent pathway generates unswitched memory B cells early in the primary response , 2012, The Journal of experimental medicine.

[33]  R. Maul,et al.  Different B Cell Populations Mediate Early and Late Memory During an Endogenous Immune Response , 2011, Science.

[34]  G. A. Lazar,et al.  Enhanced antibody half-life improves in vivo activity , 2010, Nature Biotechnology.

[35]  T. Phan,et al.  High affinity germinal center B cells are actively selected into the plasma cell compartment , 2006, The Journal of experimental medicine.

[36]  B. Heyman,et al.  Regulation of antibody responses via antibodies, complement, and Fc receptors. , 2000, Annual review of immunology.

[37]  K. Rajewsky,et al.  Evidence for a large compartment of IgM-expressing memory B cells in humans. , 1997, Blood.

[38]  Theobald. Smith.  ACTIVE IMMUNITY PRODUCED BY SO CALLED BALANCED OR NEUTRAL MIXTURES OF DIPHTHERIA TOXIN AND ANTITOXIN , 1909, The Journal of experimental medicine.