Therapeutic outcomes, assessments, risk factors and mitigation efforts of immunogenicity of therapeutic protein products
•We review therapeutic protein immunogenicity and its impact on efficacy and safety.•Patient- and product-related risk factors for immunogenicity are discussed.•Immunogenicity measurement, prediction and mitigation are also reviewed.•Basic immunology can address key remaining questions on immunogeni...
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Veröffentlicht in: | Cellular immunology 2015-06, Vol.295 (2), p.118-126 |
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container_title | Cellular immunology |
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creator | Yin, Liusong Chen, Xiaoying Vicini, Paolo Rup, Bonita Hickling, Timothy P. |
description | •We review therapeutic protein immunogenicity and its impact on efficacy and safety.•Patient- and product-related risk factors for immunogenicity are discussed.•Immunogenicity measurement, prediction and mitigation are also reviewed.•Basic immunology can address key remaining questions on immunogenicity mechanisms.
Therapeutic protein products (TPPs) are of considerable value in the treatment of a variety of diseases, including cancer, hemophilia, and autoimmune diseases. The success of TPP mainly results from prolonged half-life, increased target specificity and decreased intrinsic toxicity compared with small molecule drugs. However, unwanted immune responses against TPP, such as generation of anti-drug antibody, can impact both drug efficacy and patient safety, which has led to requirements for increased monitoring in regulatory studies and clinical practice, termination of drug development, or even withdrawal of marketed products. We present an overview of current knowledge on immunogenicity of TPP and its impact on efficacy and safety. We also discuss methods for measurement and prediction of immunogenicity and review both product-related and patient-related risk factors that affect its development, and efforts that may be taken to mitigate it. Lastly, we discuss gaps in knowledge and technology and what is needed to fill these. |
doi_str_mv | 10.1016/j.cellimm.2015.03.002 |
format | Article |
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Therapeutic protein products (TPPs) are of considerable value in the treatment of a variety of diseases, including cancer, hemophilia, and autoimmune diseases. The success of TPP mainly results from prolonged half-life, increased target specificity and decreased intrinsic toxicity compared with small molecule drugs. However, unwanted immune responses against TPP, such as generation of anti-drug antibody, can impact both drug efficacy and patient safety, which has led to requirements for increased monitoring in regulatory studies and clinical practice, termination of drug development, or even withdrawal of marketed products. We present an overview of current knowledge on immunogenicity of TPP and its impact on efficacy and safety. We also discuss methods for measurement and prediction of immunogenicity and review both product-related and patient-related risk factors that affect its development, and efforts that may be taken to mitigate it. 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Therapeutic protein products (TPPs) are of considerable value in the treatment of a variety of diseases, including cancer, hemophilia, and autoimmune diseases. The success of TPP mainly results from prolonged half-life, increased target specificity and decreased intrinsic toxicity compared with small molecule drugs. However, unwanted immune responses against TPP, such as generation of anti-drug antibody, can impact both drug efficacy and patient safety, which has led to requirements for increased monitoring in regulatory studies and clinical practice, termination of drug development, or even withdrawal of marketed products. We present an overview of current knowledge on immunogenicity of TPP and its impact on efficacy and safety. We also discuss methods for measurement and prediction of immunogenicity and review both product-related and patient-related risk factors that affect its development, and efforts that may be taken to mitigate it. Lastly, we discuss gaps in knowledge and technology and what is needed to fill these.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>25880103</pmid><doi>10.1016/j.cellimm.2015.03.002</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4425-5502</orcidid></addata></record> |
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subjects | Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal - therapeutic use Antibody Formation - immunology Autoimmune Diseases - drug therapy Autoimmune Diseases - immunology Efficacy Humans Immunogenicity Prediction Risk assessment Risk Factors Safety Therapeutic protein Treatment Outcome |
title | Therapeutic outcomes, assessments, risk factors and mitigation efforts of immunogenicity of therapeutic protein products |
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