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huCD86 Mouse
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huCD86 Mouse
Product Name
huCD86 Mouse
Product ID
C002003
Strain Name
C57BL/6NCya-Cd86tm1(hCD86)/Cya
Backgroud
C57BL/6NCya
Status
Live Mouse
When using this mouse strain in a publication, please cite “huCD86 Mouse (Catalog C002003) were purchased from Cyagen.”
HUGO-GT Humanized ModelsTumor Target Humanized Mouse ModelsImmune Target Humanized Mouse Models
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The standard delivery applies for a guaranteed minimum of three heterozygous carriers. Breeding services for homozygous carriers and/or specified sex are available.
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HUGO-GT Humanized ModelsTumor Target Humanized Mouse ModelsImmune Target Humanized Mouse Models
Basic Information
Related Resource
Basic Information
Gene Name
CD86
Gene Alias
B70, B7-2, B7.2, LAB72, CD28LG2
NCBI ID
942
Chromosome
Chr 3
MGI ID
MGI:101773
Datasheet
Click here to download >>
Strain Description
The CD86 gene (Cluster of Differentiation 86) encodes a critical type I transmembrane glycoprotein that serves as a potent costimulatory ligand in the adaptive immune response. Primarily expressed on the surface of antigen-presenting cells (APCs)—including activated B cells, macrophages, and dendritic cells—the CD86 protein (also known as B7-2) acts as a ligand for two distinct receptors on T cells: the stimulatory receptor CD28 and the inhibitory receptor CTLA-4 [1]. Its primary function is to provide the "second signal" necessary for T cell activation, proliferation, and cytokine production following the initial recognition of an antigen. Beyond lymphoid tissues, CD86 labeling is a hallmark of activated myeloid lineages and is often used to characterize M1-polarized macrophages [2]. Dysregulation of the CD86 pathway is significantly associated with various autoimmune diseases, such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), as well as the immune evasion mechanisms observed in several types of hematologic malignancies and solid tumors [3].
The huCD86 mouse model was generated by replacing the endogenous extracellular domain of mouse Cd86 with the extracellular domain of human CD86, while retaining the mouse signal peptide and aa.245~309. This model is suitable for the study of various autoimmune diseases—including systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA)—as well as multiple malignancies, and for the development of CD86-targeted therapeutics.
Reference
Barna G, Szalóki G, Márk Á, Hunyadi A, Kriston C. CD86, the double agent: Significance of CD86 expression in B-cell malignancies. Int J Cancer. 2025 Nov 1;157(9):1772-1780.
Smith TD, Tse MJ, Read EL, Liu WF. Regulation of macrophage polarization and plasticity by complex activation signals. Integr Biol (Camb). 2016 Sep 12;8(9):946-55.
Liu W, Yang Z, Chen Y, Yang H, Wan X, Zhou X, Liu R, Zhang Y. The Association Between CTLA-4, CD80/86, and CD28 Gene Polymorphisms and Rheumatoid Arthritis: An Original Study and Meta-Analysis. Front Med (Lausanne). 2021 Feb 2;8:598076.
Strain Strategy
The mouse Cd86 endogenous extracellular domain was replaced with the human CD86 extracellular domain. The murine signal peptide and aa.245~309 were preserved.
Figure 1. Gene editing strategy of huCD86 mice.
Figure 1. Gene editing strategy of huCD86 mice.
Application Area
Screening, development, and preclinical evaluation of CD86-targeted drugs;
Research on the various autoimmune diseases, such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA);
Research on the pathological mechanisms and treatment methods of malignant tumors.
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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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