PB20* Target Overview

  • Regulatory T cells: Prevent autoimmune diseases by regulating the immune system and maintaining resistance to self-antigens

  • There are various ways to generate and expand antigen-specific Treg cells.



    Our pipeline :


    1. Endogenous antigen-specific Treg cells (stronger specificity than polyclonal Treg cells)


    2. CAR (Chimeric Antigen Receptor)-Treg (Applicable to various autoimmune disease treatments by introducing a synthetic receptor called CAR)

  • The global T cell-based therapy market size is expected to reach $6.4 billion this year in 2021, and the average annual growth rate of the therapy is very high at about 20%, so the sales forecast for 2028 is estimated at $20.3 billion, about three times the size.

Distinctive advantage of PB201

GMP-Grade Proliferation
Process of Tregs

High proliferation efficiency compared to other foreign institutions

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  • Registered a domestic patent related to Treg's GMP-Grade proliferation process
    (Self-proliferation efficiency: about 3,000 to 5,500 times in 14 days >> other organ proliferation efficiency: about 1000 times in 18 days)

  • Problems of Treg therapies to be overcome: difficulty in Treg proliferation process

  • Our solution: Solve the problem of autologous monocyte shortage by securing a patent for Treg's GMP-Grade proliferation process

  • Overseas patent application and improvement patent application related to the patent are scheduled

PB202, PB203

  • CAR (Chimeric antigen receptor): An artificial receptor containing the epitope (antigen binding site) of a monoclonal antibody (mAb), capable of recognizing all proteins expressed in target tissues without being restricted to antigens through engineering

  • CAR-Treg specifically binds to activated T cells to suppress their activation

  • Isolation of autologous-regulatory T cells from autoimmune patients and allogeneic-regulatory T cells from normal individuals → engineering and expansion of regulatory T cells for the treatment of target diseases → elimination of the root cause of disease through re-administration of regulatory T cells