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HUGO-Mab™ Fully Human Monoclonal Antibody Mouse
Built on Cyagen’s proprietary TurboKnockout™ ES cell targeting technology, HUGO-Mab™ is engineered through full-length, in situ replacement of the heavy-chain, κ light-chain, and λ light-chain variable-region loci with human immunoglobulin sequences. This design supports uncompromised antibody diversity, robust antigen-driven immune responses, and efficient discovery of fully human monoclonal antibody candidates.
Overcoming Key Challenges in Fully Human Antibody Discovery

Antibody therapeutics remain central to modern biomedicine, with major applications across oncology, autoimmune diseases, metabolic diseases, infectious diseases, and chronic inflammatory disorders. Successful therapeutic antibody development requires more than antigen binding alone: discovery teams need diverse antibody repertoires, robust immune responses, functional screening, cross-species assessment, developability analysis, and translational validation.

Cyagen’s HUGO-Mab™ platform is designed to support this workflow from the earliest stage of antigen design and immunization through antibody sequence acquisition, recombinant expression, binding and blocking validation, affinity measurement, epitope analysis, and in vitro or in vivo pharmacology studies. The platform can be integrated with hybridoma screening, droplet microfluidics-based single B-cell screening, Beacon® single-cell optofluidic screening, AbSeek™ computational analysis, and Cyagen’s broader model and CRO validation capabilities.

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HUGO-Mab™: Engineered for Monoclonal Antibody Discovery

HUGO-Mab™ mice are designed to generate human variable-region monoclonal antibody candidates directly through in vivo immunization. By replacing mouse immunoglobulin variable-region loci with human sequences, the platform enables discovery of antibodies with human VH/Vκ/Vλ repertoires while preserving the biological context of antigen-driven B-cell activation and maturation.

Strain Name: Fully Human Monoclonal Antibody Mouse
Strain Abbreviation: HUGO-Mab™
Genetic Background: C57BL/6NCya, BALB/cAnCya, SJL
Coat Color: Black, White
Application: Fully human monoclonal antibody development
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HUGO-Ab™ Humanization Strategy

The schematic below illustrates the chain-specific humanization design of HUGO-Ab™ mouse models, showing how human immunoglobulin variable regions are incorporated across heavy-chain, κ light-chain, and λ light-chain loci to support fully human antibody generation in vivo.

Figure 1. HUGO-Ab™ Mouse Model: Scheme of Humanization Strategy of Heavy Chain and Light Chain.
Immunization Recommendations
Suggested Immunization Age: 6-8 weeks
Health Status: Specific Pathogen Free (SPF)
Key Features
Fully Humanized Antibody Variable Regions
Intact Immune Competence
Normal B-Cell Function
Preserved Native Antibody Function
Product Advantages
  • Developed using Cyagen's proprietary TurboKnockout gene editing technology for precise genomic replacement
  • Complete substitution of mouse heavy and light chain variable genes with human sequences,ensuring fully human antibodies
  • Retention of natural antibody effector functions (e.g., ADCC and CDC), facilitating biologically active antibody production
  • Robust immunogenicity, delivering high-affinity antibody molecules and streamlining therapeutic antibody development
HUGO-Mab™ mice show preserved B-cell development, serum IgG subclass profiles comparable to wild-type controls, and human-like heavy-chain V(D)J and κ/λ light-chain VJ rearrangement patterns.
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HUGO-Mab™ can be integrated with multiple discovery workflows, including hybridoma screening, microfluidic single-B-cell screening, and Beacon® single-cell optofluidic screening, followed by binding, blocking, affinity, functional, and in vivo validation.
Anti-H Antibody Discovery Using HUGO-Mab™ and Beacon® Single-Cell Optofluidics
To evaluate the antibody discovery potential of HUGO-Mab™ fully human monoclonal antibody mice, a comparative immunization study was performed using full-length Protein H and Target H peptide. Following immunization, antibody titers, Beacon® single-cell screening output, and antibody sequence diversity were assessed to compare the candidate discovery potential of different antigen formats.
(1) Full-Length Protein H Immunization
1,772 positive plasma cells | High HC/Kappa
(2) Target H Peptide Immunization
778 positive plasma cells | Restricted sequence diversity
Anti-PD-L1 Antibody Discovery via Microfluidic Single B Cell Platform utilizing HUGO-Mab™
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High-Homology Target: HUGO-Mab-eKO™ Accelerates ACVR2A Antibody Development
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Our Advantage
Comprehensive Human Antibody Diversity
Full-length, in situ replacement of human heavy-chain, κ light-chain, and λ light-chain variable-region loci enables broad human antibody repertoire coverage for diverse target discovery.
Accelerated Therapeutic Antibody Discovery
HUGO-Mab™ streamlines the generation, screening, and development of fully human antibody candidates, providing a reliable platform for early-stage therapeutic antibody discovery.
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Global Antibody Drug Industry Development BlueBook (Frost & Sullivan)
Key Insights
The industry is undergoing a rapid transformation driven by next-generation modalities, globalized markets, and upstream technological innovations.
  • Market Structural Shift: Monoclonal antibodies drive steady growth, but ADCs and bispecifics are rapidly accelerating, reshaping the market with higher-value innovations.
  • Chinese Market Globalization: China is actively expanding globally, evidenced by a surge in high-value cross-border license-out deals.
  • Technology-Driven Efficiency: Advanced discovery engines—exemplified by Cyagen's HUGO-Ab platform and AI algorithms—are streamlining candidate screening, optimizing molecular design, and localizing the upstream supply chain.
  • Oncology-Focused Innovation: R&D pipelines remain heavily concentrated on high-incidence malignancies like non-small cell lung cancer, utilizing complex modalities to combat clinical resistance.
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