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LAG3/CD223

Alpha Lifetech can provide LAG3/CD223 corresponding products, help each customer's research and development.

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Introduction To LAG3/CD223

Drug targets a biomolecule that can directly bind to drugs and then react. Generally, the target refers to a protein related to the cause of disease. The focus of the target began with focusing on tumors and then began to spread to various fields. Introduction to LAG3/CD223 protein is a common target in medicine.
LAG-3 (lymphocyte-activated gene-3, also known as CD223) is an inhibitory immune checkpoint molecule highly expressed on activated T cells, and it is a transmembrane protein. The LAG-3 protein consists of four extracellular immunoglobulin-like domains (D1-D4) with high homology with CD4. The LAG-3 protein consists of four extracellular domains, D1 – D4, similar to Ig, where, both D1 and D2 are involved in the FGL 1 – LAG-3 interaction.

Function of Target LAG3/CD223

On activated T cells, LAG-3 expression can be upregulated by interleukin (IL) -2 and IL-12, which acts primarily as a receptor to transmit inhibitory signals. LAG-3 negatively regulates the proliferation, activation, effector function, and homeostasis of CD8 + and CD4 + T cells. In chronic viral infection or cancer, LAG-3 similar to PD-1 may mark the exhaustion of CD8 + T cells upon repetitive antigen stimulation. Moreover, LAG-3 is also constitutively expressed in regulatory T cell subsets and is involved in its inhibitory function. LAG-3 also inhibits CD8 + T cells and natural killer (NK) cells function.FGL1 is upregulated in tumor tissues and associated with low responsiveness to PD-1 / PD-L1 antibody treatment, and combined blockade of PD-L1 and LAG-3 was also found to have good synergistic antitumor effects in clinical studies. Therefore, inhibitor screening targeting the LAG-3 / FGL 1 pathway is of great research value.

Gene Pathway of Target LAG3/CD223

LAG-3 intracellular directly suppresses downstream signaling of TCR-CD3 complex by its unique "KIEELE" sequence, repetitive glutamate-proline (EP) repeats and serine phosphorylation sites, exerting a non-redundant immunosuppressive function FGL 1 interacts with LAG-3 in an MHC-II-independent manner, involving the FGL 1 fibrinogen-like domain and the LAG-3 D1 D2 domain. The cytoplasmic tail of LAG-3 mediates the negative signaling in the cell. When LAG-3 binds to its ligand, it transmits inhibitory signals through its cytoplasmic domain, inhibiting the initial steps of the T-cell receptor (TCR) pathway, preventing the activation of transcription factors ( NFAT), and leading to a decrease in cytokine production and T-cell proliferation.
LAG-3
Fig 1: LAG-3 Gene Pathway. (Reference source: Kreidieh FY, Tawbi HA. The introduction of LAG-3 checkpoint blockade in melanoma: immunotherapy landscape beyond PD-1 and CTLA-4 inhibition. Ther Adv Med Oncol. 2023 Jul 17;15:17588359231186027.)

Alpha Lifetech Can Provide

At present, various drugs targeting LAG3/CD223 are constantly under development, and taking drugs alone or together with other products to treat diseases has become a new method and remarkable achievements have been made. LAG3/CD223 protein has shown important research value and application prospects in tumor biology, and drug research and development. With further research and technological advances, LAG3/CD223 protein products are also essential. Alpha Lifetech can provide LAG3/CD223 corresponding products and help each customer's research and development. Alpha Lifetech focuses on high-precision detection development and validation services to support drug screening and biosimilar discovery. Our detection methods, including ELISA, cell-based functional testing, and flow cytometry, have undergone rigorous sensitivity, specificity, and reproducibility testing. In addition to testing and development, our team also provides data analysis, scheme optimization, and cross-species reactivity testing to ensure reliable results.

Reference 

[1] Chocarro L, Blanco E, Zuazo M, Arasanz H, Bocanegra A, Fernández-Rubio L, Morente P, Fernández-Hinojal G, Echaide M, Garnica M, Ramos P, Vera R, Kochan G, Escors D. Understanding LAG-3 Signaling. Int J Mol Sci. 2021 May 17;22(10):5282   
[2] Maruhashi T, Sugiura D, Okazaki IM, Okazaki T. LAG-3: from molecular functions to clinical applications. J Immunother Cancer. 2020 Sep;8(2):e001014.  
[3] Wang J, Sanmamed MF, Datar I, Su TT, Ji L, Sun J, Chen L, Chen Y, Zhu G, Yin W, Zheng L, Zhou T, Badri T, Yao S, Zhu S, Boto A, Sznol M, Melero I, Vignali DAA, Schalper K, Chen L. Fibrinogen-like Protein 1 Is a Major Immune Inhibitory Ligand of LAG-3. Cell. 2019 Jan 10;176(1-2):334-347.e12. 

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