Immunogenicity of biopharmaceuticals in laboratory animals
- PMID: 11164995
- DOI: 10.1016/s0300-483x(00)00410-8
Immunogenicity of biopharmaceuticals in laboratory animals
Abstract
The potential immunogenicity of new protein therapeutics raises concerns about the possibility of inducing untoward immune reactions in humans. It is generally assumed that all animals will make antibody to human proteins and therefore, there is sentiment among some scientists that this makes the issue of immunogenicity as a safety concern irrelevant. However, recent clinical trials with some proteins have detected the presence of autoantibodies that have resulted in clinical sequelae. These reactions were also observed in preclinical animal studies. In fact, non-human primate and transgenic mouse models can be useful for predicting the relative immunogenicity of human proteins. In addition, the characterization of the immunogenicity of biotechnology molecules provides a practical basis for determining the significance of antibody formation in preclinical safety studies.
Similar articles
-
Immunogenicity of biologically-derived therapeutics: assessment and interpretation of nonclinical safety studies.Regul Toxicol Pharmacol. 2009 Jul;54(2):164-82. doi: 10.1016/j.yrtph.2009.03.012. Epub 2009 Apr 2. Regul Toxicol Pharmacol. 2009. PMID: 19345250
-
Safety immunopharmacology: evaluation of the adverse potential of pharmaceuticals on the immune system.J Pharmacol Toxicol Methods. 2012 Sep;66(2):79-83. doi: 10.1016/j.vascn.2012.05.001. Epub 2012 May 14. J Pharmacol Toxicol Methods. 2012. PMID: 22587937 Free PMC article.
-
Predictive power of preclinical studies in animals for the immunogenicity of recombinant therapeutic proteins in humans.Curr Opin Mol Ther. 2004 Feb;6(1):10-6. Curr Opin Mol Ther. 2004. PMID: 15011776
-
Immunogenicity of therapeutic proteins: clinical implications and future prospects.Clin Ther. 2002 Nov;24(11):1720-40; discussion 1719. doi: 10.1016/s0149-2918(02)80075-3. Clin Ther. 2002. PMID: 12501870 Review.
-
The challenges of immunogenicity in developing biosimilar products.IDrugs. 2009 Jul;12(7):440-4. IDrugs. 2009. PMID: 19579165 Review.
Cited by
-
In vivo properties of an anti-GnRH Spiegelmer: an example of an oligonucleotide-based therapeutic substance class.Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8898-902. doi: 10.1073/pnas.132067399. Epub 2002 Jun 17. Proc Natl Acad Sci U S A. 2002. PMID: 12070349 Free PMC article.
-
Non-human primates in the PKPD evaluation of biologics: Needs and options to reduce, refine, and replace. A BioSafe White Paper.MAbs. 2022 Jan-Dec;14(1):2145997. doi: 10.1080/19420862.2022.2145997. MAbs. 2022. PMID: 36418217 Free PMC article. Review.
-
Immunogenicity of mAbs in non-human primates during nonclinical safety assessment.MAbs. 2013 Sep-Oct;5(5):810-6. doi: 10.4161/mabs.25234. Epub 2013 Jun 6. MAbs. 2013. PMID: 23924803 Free PMC article.
-
Muscle wasting associated with pathologic change is a risk factor for the exacerbation of joint swelling in collagen-induced arthritis in cynomolgus monkeys.BMC Musculoskelet Disord. 2013 Jul 9;14:205. doi: 10.1186/1471-2474-14-205. BMC Musculoskelet Disord. 2013. PMID: 23834772 Free PMC article.
-
A triple-transgenic immunotolerant mouse model.J Pharm Sci. 2013 Mar;102(3):1116-24. doi: 10.1002/jps.23447. Epub 2013 Jan 11. J Pharm Sci. 2013. PMID: 23316010 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical