Abstract 1653: FcRn humanized rats for pharmacokinetics assessment of antibody drugs

Abstract Introduction: Biocytogen's B-hFcRn rat model serves as a practical tool for assessing the pharmacokinetics/pharmacokinetics and safety of human IgG therapeutics. The model capitalizes on the rat's larger size, which allows for serial blood sampling and thus more efficient and continuous data collection compared to mice, where animal welfare considerations necessitate staggered sampling across subgroups. This is combined with the presence of human FcRn, a pH-dependent receptor that binds and recycles IgG, protecting it from lysosomal degradation to extend its plasma half-life. Methods: l B-hFcRn rats were generated by inserting a chimeric cDNA encoding full-length human FCGRT, followed by its 3'UTR and stop codon right after the rat Fcgrt start codon, thereby replacing exons 2-4 and placing human FcRn expression under the control of the endogenous rat promoter while disrupting the native rat gene.l For protein expression analysis, liver, kidney, and spleen tissue lysates were collected from wild-type SD rats (+/+), homozygous B-hFcRn rats (H/H), and then analyzed by western blot with species-specific anti-FcRn antibody. l SD rats and B-hFcRn rats were intravenously injected with Bevacizumab (commercial), and serum was collected for pharmacokinetic (PK) analysis. Results: l Western blot analysis results indicated that Rat FcRn was only detectable in wild-type SD rats. Human FcRn was exclusively detectable in the liver, kidney, and spleen of homozygous B-hFcRn rats.l Linear pharmacokinetics were observed in B-hFcRn rats after a single intravenous bolus administration of the monoclonal antibody and serial blood collection. PK data suggest that the B-hFcRn rat model enables reliable prediction of the FcRn-mediated pharmacokinetics and efficacy of IgG antibodies in humans. Conclusions: The B-hFcRn rat model is used for pharmacokinetics, pharmacodynamics, and safety evaluation of human immunoglobulin G (IgG) and is based on the Fc domain therapeutics. Citation Format: Kelvin Yin, Suman Zhao, Zhi Zhang, Yanling Wang, . FcRn humanized rats for pharmacokinetics assessment of antibody drugs [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1653.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1653
Primary Topic
Monoclonal and Polyclonal Antibodies Research
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article
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article

Abstract 1653: FcRn humanized rats for pharmacokinetics assessment of antibody drugs

Suman Zhao, Yanling Wang, Kelvin Yin, Zhi Zhang
Cancer Research
Monoclonal and Polyclonal Antibodies Research
article

Abstract 1653: FcRn humanized rats for pharmacokinetics assessment of antibody drugs

Suman Zhao, Yanling Wang, Kelvin Yin, Zhi Zhang
article en

Abstract

Abstract Introduction: Biocytogen's B-hFcRn rat model serves as a practical tool for assessing the pharmacokinetics/pharmacokinetics and safety of human IgG therapeutics. The model capitalizes on the rat's larger size, which allows for serial blood sampling and thus more efficient and continuous data collection compared to mice, where animal welfare considerations necessitate staggered sampling across subgroups. This is combined with the presence of human FcRn, a pH-dependent receptor that binds and recycles IgG, protecting it from lysosomal degradation to extend its plasma half-life. Methods: l B-hFcRn rats were generated by inserting a chimeric cDNA encoding full-length human FCGRT, followed by its 3'UTR and stop codon right after the rat Fcgrt start codon, thereby replacing exons 2-4 and placing human FcRn expression under the control of the endogenous rat promoter while disrupting the native rat gene.l For protein expression analysis, liver, kidney, and spleen tissue lysates were collected from wild-type SD rats (+/+), homozygous B-hFcRn rats (H/H), and then analyzed by western blot with species-specific anti-FcRn antibody. l SD rats and B-hFcRn rats were intravenously injected with Bevacizumab (commercial), and serum was collected for pharmacokinetic (PK) analysis. Results: l Western blot analysis results indicated that Rat FcRn was only detectable in wild-type SD rats. Human FcRn was exclusively detectable in the liver, kidney, and spleen of homozygous B-hFcRn rats.l Linear pharmacokinetics were observed in B-hFcRn rats after a single intravenous bolus administration of the monoclonal antibody and serial blood collection. PK data suggest that the B-hFcRn rat model enables reliable prediction of the FcRn-mediated pharmacokinetics and efficacy of IgG antibodies in humans. Conclusions: The B-hFcRn rat model is used for pharmacokinetics, pharmacodynamics, and safety evaluation of human immunoglobulin G (IgG) and is based on the Fc domain therapeutics. Citation Format: Kelvin Yin, Suman Zhao, Zhi Zhang, Yanling Wang, . FcRn humanized rats for pharmacokinetics assessment of antibody drugs [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1653.

Cancer ResearchVol. 86(7_Supplement)
Beijing Biocytogen (China) (CN)
Openalex Percentile: Top 5%
Monoclonal and Polyclonal Antibodies Research
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