Mice carrying the full-length human immunoglobulin loci produce antigen-specific human antibodies with the lambda light chain

The development of antibody drugs through animal immunization typically requires the humanization of host antibodies to address concerns about immunogenicity in humans. However, employing an animal model capable of producing human antibodies presents the opportunity to develop antibody drugs without the need for humanization. Despite the ratio of human immunoglobulin (Ig) κ to Igλ usage being approximately 60%:40%, the majority of approved antibody therapeutics are kappa antibodies, and the development of lambda antibodies as therapeutic agents has lagged behind. Therefore, in this study, we developed mice carrying the <i>IGH</i> and <i>IGL</i> loci (IGHL), which can produce human lambda antibodies, using mouse artificial chromosome (MAC) vectors. We demonstrated that IGHL mice consistently retain the human lambda antibody locus integrated on the MAC across generations and can be induced to produce specific antibodies upon antigen stimulation. These findings provide a promising platform for advancing lambda antibody drugs, which have historically been neglected.

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Publication Details

Journal
iScience
Published
2024-10-28
DOI
https://doi.org/10.1016/j.isci.2024.111258
Citations
7
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
2.83

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article

Mice carrying the full-length human immunoglobulin loci produce antigen-specific human antibodies with the lambda light chain

Yasuhiro Kazuki, Kazuto Shimoya, Yu Masuda, Kanako Kazuki et al.
7 citations
iScience
Monoclonal and Polyclonal Antibodies Research
2.83
article

Mice carrying the full-length human immunoglobulin loci produce antigen-specific human antibodies with the lambda light chain

Yasuhiro Kazuki, Kazuto Shimoya, Yu Masuda, Kanako Kazuki, Satoshi Abe, Takashi Moriwaki, S.S. Baba, Akane Okada
article en
7 citations

Abstract

The development of antibody drugs through animal immunization typically requires the humanization of host antibodies to address concerns about immunogenicity in humans. However, employing an animal model capable of producing human antibodies presents the opportunity to develop antibody drugs without the need for humanization. Despite the ratio of human immunoglobulin (Ig) κ to Igλ usage being approximately 60%:40%, the majority of approved antibody therapeutics are kappa antibodies, and the development of lambda antibodies as therapeutic agents has lagged behind. Therefore, in this study, we developed mice carrying the <i>IGH</i> and <i>IGL</i> loci (IGHL), which can produce human lambda antibodies, using mouse artificial chromosome (MAC) vectors. We demonstrated that IGHL mice consistently retain the human lambda antibody locus integrated on the MAC across generations and can be induced to produce specific antibodies upon antigen stimulation. These findings provide a promising platform for advancing lambda antibody drugs, which have historically been neglected.

iScienceVol. 27(12)
National Institutes of Natural Sciences (JP), Tottori University (JP)
Japan Agency for Medical Research and Development, Japan Science and Technology Corporation, Core Research for Evolutional Science and Technology, Exploratory Research Center on Life and Living Systems, National Institutes of Natural Sciences
Openalex Percentile: Top 9%
Monoclonal and Polyclonal Antibodies Research
2.83
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