Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Anti-self antibodies selected from a human IgD heavy chain repertoire: a novel approach to generate therapeutic human antibodies against tumor-associated differentiation antigens
by
Raum, Tobias
, Kufer, Peter
, Gruber, Rudi
, Riethmüller, Gert
in
Amino Acid Sequence
/ Animals
/ Antibodies
/ Antigen (tumor-associated)
/ Antigens, Neoplasm - immunology
/ Antineoplastic agents
/ Biological and medical sciences
/ Cancer Vaccines
/ Cell adhesion molecules
/ Cell Adhesion Molecules - immunology
/ CHO Cells
/ Clinical trials
/ Colorectal cancer
/ Colorectal Neoplasms - immunology
/ Colorectal Neoplasms - metabolism
/ Cricetinae
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Effector cells
/ Enzyme-Linked Immunosorbent Assay
/ Epithelial Cell Adhesion Molecule
/ Epithelial cells
/ Epitope Mapping
/ Evolutionary conservation
/ Flow Cytometry
/ Humans
/ Immunogenicity
/ Immunoglobulin D
/ Immunoglobulin D - immunology
/ Immunoglobulin G
/ Immunoglobulin G - immunology
/ Immunoglobulin G - metabolism
/ Immunotherapy
/ Kinetics
/ Lymphocytes
/ Medical sciences
/ Mice
/ Models, Genetic
/ Molecular Sequence Data
/ Neoplasms - immunology
/ Original
/ Peptide Library
/ Peptides - metabolism
/ Phage display
/ Pharmacology. Drug treatments
/ Protein Binding
/ Sequence Homology, Amino Acid
/ Surface Plasmon Resonance
/ Transfection
2001
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Anti-self antibodies selected from a human IgD heavy chain repertoire: a novel approach to generate therapeutic human antibodies against tumor-associated differentiation antigens
by
Raum, Tobias
, Kufer, Peter
, Gruber, Rudi
, Riethmüller, Gert
in
Amino Acid Sequence
/ Animals
/ Antibodies
/ Antigen (tumor-associated)
/ Antigens, Neoplasm - immunology
/ Antineoplastic agents
/ Biological and medical sciences
/ Cancer Vaccines
/ Cell adhesion molecules
/ Cell Adhesion Molecules - immunology
/ CHO Cells
/ Clinical trials
/ Colorectal cancer
/ Colorectal Neoplasms - immunology
/ Colorectal Neoplasms - metabolism
/ Cricetinae
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Effector cells
/ Enzyme-Linked Immunosorbent Assay
/ Epithelial Cell Adhesion Molecule
/ Epithelial cells
/ Epitope Mapping
/ Evolutionary conservation
/ Flow Cytometry
/ Humans
/ Immunogenicity
/ Immunoglobulin D
/ Immunoglobulin D - immunology
/ Immunoglobulin G
/ Immunoglobulin G - immunology
/ Immunoglobulin G - metabolism
/ Immunotherapy
/ Kinetics
/ Lymphocytes
/ Medical sciences
/ Mice
/ Models, Genetic
/ Molecular Sequence Data
/ Neoplasms - immunology
/ Original
/ Peptide Library
/ Peptides - metabolism
/ Phage display
/ Pharmacology. Drug treatments
/ Protein Binding
/ Sequence Homology, Amino Acid
/ Surface Plasmon Resonance
/ Transfection
2001
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Anti-self antibodies selected from a human IgD heavy chain repertoire: a novel approach to generate therapeutic human antibodies against tumor-associated differentiation antigens
by
Raum, Tobias
, Kufer, Peter
, Gruber, Rudi
, Riethmüller, Gert
in
Amino Acid Sequence
/ Animals
/ Antibodies
/ Antigen (tumor-associated)
/ Antigens, Neoplasm - immunology
/ Antineoplastic agents
/ Biological and medical sciences
/ Cancer Vaccines
/ Cell adhesion molecules
/ Cell Adhesion Molecules - immunology
/ CHO Cells
/ Clinical trials
/ Colorectal cancer
/ Colorectal Neoplasms - immunology
/ Colorectal Neoplasms - metabolism
/ Cricetinae
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Effector cells
/ Enzyme-Linked Immunosorbent Assay
/ Epithelial Cell Adhesion Molecule
/ Epithelial cells
/ Epitope Mapping
/ Evolutionary conservation
/ Flow Cytometry
/ Humans
/ Immunogenicity
/ Immunoglobulin D
/ Immunoglobulin D - immunology
/ Immunoglobulin G
/ Immunoglobulin G - immunology
/ Immunoglobulin G - metabolism
/ Immunotherapy
/ Kinetics
/ Lymphocytes
/ Medical sciences
/ Mice
/ Models, Genetic
/ Molecular Sequence Data
/ Neoplasms - immunology
/ Original
/ Peptide Library
/ Peptides - metabolism
/ Phage display
/ Pharmacology. Drug treatments
/ Protein Binding
/ Sequence Homology, Amino Acid
/ Surface Plasmon Resonance
/ Transfection
2001
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Anti-self antibodies selected from a human IgD heavy chain repertoire: a novel approach to generate therapeutic human antibodies against tumor-associated differentiation antigens
Journal Article
Anti-self antibodies selected from a human IgD heavy chain repertoire: a novel approach to generate therapeutic human antibodies against tumor-associated differentiation antigens
2001
Request Book From Autostore
and Choose the Collection Method
Overview
Human antibodies were isolated by phage display from a naturally expressed human antibody repertoire. Antibody selection was carried out against the epithelial cell adhesion molecule (EpCAM) or 17-1A antigen, that in a clinical trial had been successfully used as a target for antibody therapy of minimal residual colorectal cancer. VH chains were selected from the human IgD repertoire expressed on naive B2 and autoreactive B1 lymphocytes. By guiding the selection through a murine template antibody, two EpCAM-specific human antibodies, HD69 and HD70, were obtained that closely resembled the murine therapeutic 17-1A antibody in their binding properties when expressed as complete huIgG1 molecules in CHO cells. However, both human antibodies recruited human cytotoxic effector cells far more efficiently than the murine 17-1A antibody used for clinical trials. Therefore, and in view of the long in vivo half-life of human IgG1 antibodies, HD69 and HD70 are regarded as highly promising third generation versions of the murine therapeutic antibody. Because of their origin from an evolutionary conserved germline VH repertoire, they are expected to exhibit minimal immunogenicity in patients.
Publisher
Springer,Springer Nature B.V,Springer-Verlag
Subject
/ Animals
/ Antigens, Neoplasm - immunology
/ Biological and medical sciences
/ Cell Adhesion Molecules - immunology
/ Colorectal Neoplasms - immunology
/ Colorectal Neoplasms - metabolism
/ Dose-Response Relationship, Drug
/ Enzyme-Linked Immunosorbent Assay
/ Epithelial Cell Adhesion Molecule
/ Humans
/ Immunoglobulin D - immunology
/ Immunoglobulin G - immunology
/ Immunoglobulin G - metabolism
/ Kinetics
/ Mice
/ Original
/ Pharmacology. Drug treatments
MBRLCatalogueRelatedBooks
Related Items
Related Items
This website uses cookies to ensure you get the best experience on our website.