MACS GMP Recombinant Human IL-12，170-076-175，美天旎

MACS GMP Recombinant Human Interleukin-12 (IL-12) is a recombinant protein optimized as an ancillary material for ex vivo cell processing. It is not intended for human in vivo applications.

Biological activity

IL-12 is a heterodimeric cytokine composed of two subunits (p35 and p40), which are encoded by two different genes, IL-12A (p35) and IL-12B (p40). The complete heterodimeric protein complex is termed IL-12p70. IL-12 is the most prominent member of the IL-12 cytokine family, which also contains other heterodimeric cytokines such as IL-23, IL-27 and IL-35⁶.

The p35 subunit of IL-12 contains 4 α-helix bundles, while the p40 subunit is structurally related to soluble IL-6 receptor alpha (sIL-6Rα). Hence, the structure of IL-12 is in essence that of a cytokine bound to a soluble receptor, and the ability to secrete the cytokine-like subunit (p35) depends upon association with the receptor-like subunit (p40)⁷.

IL-12 can affect many cell types, but its influence on T-cell-dependent responses has been most extensively studied: It is secreted by professional antigen presenting cells (mostly dendritic cells, but also macrophages and B cells) upon activation by microbial pathogens and binds to the IL-12 receptor complex (comprised IL-12Rβ1 and IL-12Rβ2) on T and NK cells. Receptor engagement induces the upregulation of transcription factor T-bet in CD4⁺ and CD8⁺ T cells and promotes their differentiation into Th1 cells or CTLs respectively. These activated T cells then secrete IFNγ and TNFα. IL-12 can also induce IFNγ production by NK cells⁷.

Naïve T cells express the IL-12 receptor subunit IL-12Rβ1, however expression of IL-12Rβ2 - and thereby responsiveness of naïve T cells to IL-12 - is dependent on TCR engagement, co-stimulation by CD28 and IL-2 signaling⁸. Signaling through the IL-12 receptor seems to be necessary for full-fledged T cell effector functions of the T cells and for IL-2 dependent proliferation².

MACS GMP Recombinant Human IL-12 can be used for a variety of applications, including:

Optimization of ex vivo expansion protocols for adoptive cell transfer. Studies have demonstrated that ex vivo activation of T cells in the presence of IL-12 can improve expansion and effector function and prevent in vivo T cell exhaustion in animal models.¹

Generation of cytokine-induced memory-like natural killer cells (CIML NK). Memory-like NK cells can be generated ex vivo by cultivating human NK cells with a combination of IL-12, IL-15 and IL-18. Such CIML NK cells demonstrated an increased longevity and enhanced anticancer functionality compared to normal effector NK cells.²

In vitro differentiation of naive CD4⁺ T cells towards Th1 cells. After activation, naïve CD4⁺ T cells can be differentiated into Th1 effector cells when cultured with a combination of IL-2, IL-12 and IFNγ.³

MACS GMP Products are manufactured and tested under a quality management system (ISO 13485) and are in compliance with relevant GMP guidelines. They are designed following the recommendations of USP <1043> on ancillary materials.

MACS GMP Products are for ex vivo cell processing only, and are not intended for human in vivo applications. For regulatory status in the USA, please contact your local representative.