Publications by authors named "Zhangyan Jing"

Immune-checkpoint blockade (ICB) reinvigorates T cells from exhaustion and potentiates T-cell responses to tumors. However, most patients do not respond to ICB therapy, and only a limited response can be achieved in a "cold" tumor with few infiltrated lymphocytes. Synthetic biology can be used to engineer bacteria as controllable bioreactors to synthesize biotherapeutics .

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Article Synopsis
  • Type 1 diabetes (T1D) development is linked to a lack of specific immune checkpoint ligands, PD-L1 and galectin-9, in β-cells, making it crucial to find ways to boost these proteins to protect the cells.
  • Researchers created artificial extracellular vesicles (aEVs) using genetically modified macrophages that overexpress PD-L1 and Gal-9 to inhibit harmful T lymphocytes and safeguard β-cells.
  • These PD-L1-Gal-9 aEVs showed promising results by reducing hyperglycemia and delaying T1D progression in mice, while also enhancing regulatory T cell formation and promoting the death of harmful effector T-cells.
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Immune intervention of B cell activation to blockade the production of autoantibodies provokes intense interest in the field of systemic lupus erythematosus (SLE) therapy development. Although the survival rate for SLE is improved, many patients die untimely. Engineered cell membrane vesicles manifest remarkable capacity of targeted drug delivery and immunomodulation of immune cells such as B cells.

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The pathogeny of type 1 diabetes (T1D) is mainly provoked by the β-cell loss due to the autoimmune attack. Critically, autoreactive T cells firsthand attack β-cell in islet, that results in the deficiency of insulin in bloodstream and ultimately leads to hyperglycemia. Hence, modulating immunity to conserve residual β-cell is a desirable way to treat new-onset T1D.

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