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Identification and characterization of the constituent human serum antibodies elicited by vaccination
by
Lungu, Oana I.
, Boutz, Daniel R.
, Murrin, Ellen M.
, Georgiou, George
, Wine, Yariv
, Ippolito, Gregory C.
, Horton, Andrew P.
, DeKosky, Brandon J.
, Lavinder, Jason J.
, Dörner, Thomas
, Giesecke, Claudia
, Marcotte, Edward M.
, Hoi, Kam Hon
, Wirth, Megan M.
, Ellington, Andrew D.
in
Amino Acid Sequence
/ Antibodies
/ Antibodies, Bacterial - biosynthesis
/ Antibodies, Bacterial - chemistry
/ Antigens
/ B lymphocytes
/ B-Lymphocytes - immunology
/ Binding sites
/ Biological Sciences
/ Blood
/ blood serum
/ Bone marrow
/ Cells
/ Chromatography
/ Chromatography, Liquid
/ Epitopes
/ genes
/ high-throughput nucleotide sequencing
/ Humans
/ Immunization
/ immunoglobulin G
/ immunologic memory
/ Immunophenotyping
/ Liquid chromatography
/ Memory
/ Molecular Sequence Data
/ Plasma cells
/ Proteomics
/ secondary immunization
/ Sequencing
/ Tandem Mass Spectrometry
/ tetanus
/ Tetanus Toxoid - administration & dosage
/ Toxins
/ Vaccination
/ vaccine development
/ Vaccines
2014
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Identification and characterization of the constituent human serum antibodies elicited by vaccination
by
Lungu, Oana I.
, Boutz, Daniel R.
, Murrin, Ellen M.
, Georgiou, George
, Wine, Yariv
, Ippolito, Gregory C.
, Horton, Andrew P.
, DeKosky, Brandon J.
, Lavinder, Jason J.
, Dörner, Thomas
, Giesecke, Claudia
, Marcotte, Edward M.
, Hoi, Kam Hon
, Wirth, Megan M.
, Ellington, Andrew D.
in
Amino Acid Sequence
/ Antibodies
/ Antibodies, Bacterial - biosynthesis
/ Antibodies, Bacterial - chemistry
/ Antigens
/ B lymphocytes
/ B-Lymphocytes - immunology
/ Binding sites
/ Biological Sciences
/ Blood
/ blood serum
/ Bone marrow
/ Cells
/ Chromatography
/ Chromatography, Liquid
/ Epitopes
/ genes
/ high-throughput nucleotide sequencing
/ Humans
/ Immunization
/ immunoglobulin G
/ immunologic memory
/ Immunophenotyping
/ Liquid chromatography
/ Memory
/ Molecular Sequence Data
/ Plasma cells
/ Proteomics
/ secondary immunization
/ Sequencing
/ Tandem Mass Spectrometry
/ tetanus
/ Tetanus Toxoid - administration & dosage
/ Toxins
/ Vaccination
/ vaccine development
/ Vaccines
2014
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Identification and characterization of the constituent human serum antibodies elicited by vaccination
by
Lungu, Oana I.
, Boutz, Daniel R.
, Murrin, Ellen M.
, Georgiou, George
, Wine, Yariv
, Ippolito, Gregory C.
, Horton, Andrew P.
, DeKosky, Brandon J.
, Lavinder, Jason J.
, Dörner, Thomas
, Giesecke, Claudia
, Marcotte, Edward M.
, Hoi, Kam Hon
, Wirth, Megan M.
, Ellington, Andrew D.
in
Amino Acid Sequence
/ Antibodies
/ Antibodies, Bacterial - biosynthesis
/ Antibodies, Bacterial - chemistry
/ Antigens
/ B lymphocytes
/ B-Lymphocytes - immunology
/ Binding sites
/ Biological Sciences
/ Blood
/ blood serum
/ Bone marrow
/ Cells
/ Chromatography
/ Chromatography, Liquid
/ Epitopes
/ genes
/ high-throughput nucleotide sequencing
/ Humans
/ Immunization
/ immunoglobulin G
/ immunologic memory
/ Immunophenotyping
/ Liquid chromatography
/ Memory
/ Molecular Sequence Data
/ Plasma cells
/ Proteomics
/ secondary immunization
/ Sequencing
/ Tandem Mass Spectrometry
/ tetanus
/ Tetanus Toxoid - administration & dosage
/ Toxins
/ Vaccination
/ vaccine development
/ Vaccines
2014
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Identification and characterization of the constituent human serum antibodies elicited by vaccination
Journal Article
Identification and characterization of the constituent human serum antibodies elicited by vaccination
2014
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Overview
Most vaccines confer protection via the elicitation of serum antibodies, yet more than 100 y after the discovery of antibodies, the molecular composition of the human serum antibody repertoire to an antigen remains unknown. Using high-resolution liquid chromatography tandem MS proteomic analyses of serum antibodies coupled with next-generation sequencing of the V gene repertoire in peripheral B cells, we have delineated the human serum IgG and B-cell receptor repertoires following tetanus toxoid (TT) booster vaccination. We show that the TT ⁺ serum IgG repertoire comprises ∼100 antibody clonotypes, with three clonotypes accounting for >40% of the response. All 13 recombinant IgGs examined bound to vaccine antigen with K d ∼ 10 ⁻⁸–10 ⁻¹⁰ M. Five of 13 IgGs recognized the same linear epitope on TT, occluding the binding site used by the toxin for cell entry, suggesting a possible explanation for the mechanism of protection conferred by the vaccine. Importantly, only a small fraction (<5%) of peripheral blood plasmablast clonotypes (CD3 ⁻CD14 ⁻CD19 ⁺CD27 ⁺⁺CD38 ⁺⁺CD20 ⁻TT ⁺) at the peak of the response (day 7), and an even smaller fraction of memory B cells, were found to encode antibodies that could be detected in the serological memory response 9 mo postvaccination. This suggests that only a small fraction of responding peripheral B cells give rise to the bone marrow long-lived plasma cells responsible for the production of biologically relevant amounts of vaccine-specific antibodies (near or above the K d). Collectively, our results reveal the nature and dynamics of the serological response to vaccination with direct implications for vaccine design and evaluation.
Publisher
National Academy of Sciences,National Acad Sciences
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