Immunogenicity of engineered antibodies.
By W. Y. Hwang, J. Foote. Methods, 2005
612 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology, Radiology, Nuclear Medicine and Imaging
View Paper: https://www.semanticscholar.org/paper/54b6c5f26162643088767851e72fbac22573b381
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In Molecular Biology
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In Radiology, Nuclear Medicine and Imaging
Citations in the corpus
- Antibody Structure and Function: The Basis for Engineering Therapeutics (2019, background): “In many cases, chimeric antibodies demonstrated reduced immunogenicity but still elicited some human anti-therapeutic antibody response [93].”
- Potent antibody therapeutics by design (2006, background): “Immunogenicity data for chimeric humanized mouse antibodies strongly indicate that the replacement of mouse-antibody constant domains with human-antibody constant domains substantially reduces the immunogenicity of the antibody and that humanization might further reduce the immunogenicit”
- The immunogenicity of humanized and fully human antibodies (2010, background): “Whereas approximately 40% of chimeric antibodies containing human sequence-derived constant regions and murinesequence derived V regions induce marked anti-drug antibody responses in vivo, only 9% of humanized and antibodies containing human constant regions and human sequence derived VH and VL fram”
- Mining human antibody repertoires (2010, background): “Human and humanized mAbs have been found to be less immunogenic than nonhuman and chimeric mAbs, the latter of which trigger human anti-mouse antibody (HAMA), human anti-rat antibody (HARA) and human anti-chimeric antibody (HACA) responses.(1) It is expected, but remains to be substantiated, that hu”