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Tumor cells can utilize immune checkpoint receptors to evade recognition and elimination by the host immune system; consequently, blocking these receptors holds promise as a broadly effective strategy for tumor immunotherapy. Currently, while anti-PD-1/PD-L1 antibodies—much like anti-CTLA-4 antibodies—represent a relatively mature therapeutic modality, their overall efficacy in patients remains limited due to the prevalence of drug resistance. Therefore, the identification of novel targets for tumor immunotherapy has become a matter of urgent necessity.

Programmed Cell Death Protein 1 (PD-1) is a receptor expressed on activated T cells that binds to its ligands, PD-L1 and PD-L2, thereby negatively regulating immune responses. PD-1 ligands are present in the majority of cancers; the interaction between PD-1 and its ligands (PD-L1/2) suppresses T-cell activity and enables cancer cells to evade immune surveillance. The PD-1/PD-L1 signaling pathway constitutes a critical component of the tumor-induced immunosuppressive microenvironment, serving to dampen T-lymphocyte activation and enhance immune tolerance toward tumor cells, thereby facilitating tumor immune evasion. The binding of PD-1 to PD-L1 attenuates T-cell-mediated immune surveillance, resulting in an impaired immune response and, in some instances, inducing T-cell apoptosis. PD-1/PD-L1 inhibitors function by releasing anti-tumor T cells from this state of immunosuppression, thereby promoting T-cell proliferation, infiltration into the tumor microenvironment, and the subsequent induction of anti-tumor immune responses. Furthermore, the PD-1/PD-L1/2 pathway plays a role in regulating autoimmune responses, rendering these proteins promising therapeutic targets not only for various cancers but also for autoimmune disorders such as multiple sclerosis, arthritis, lupus, and Type 1 diabetes. Tyrosine phosphatase SHP2 serves as a pivotal regulator of T-cell function, mediating both the downstream activation signals initiated by the T-cell receptor (TCR) and the downstream inhibitory signals triggered by PD-1.

The Raji Human PDL1 Target Cell(Suspension) Model—effectively simulates the signal transduction process of PD1&SHP1/SHP2 *in vivo*. The underlying principle is illustrated in the figure below.

Figure 1. Schematic Diagram of the Raji Human PDL1 Target Cell(Suspension) Model

Raji cell line expressing full length human PDL1. Expression is confirmed by flow cytometry.

Figure 2. Recombinant PDL1 Target Cell (Suspension) stably expressing PDL1.

Figure 3. Blocking of PD1 induced PD1 SHP2 Reporter Cell (C1) Activity by PD1 Neutralizing Antibody with PDL1 Target Cell (Suspension)(C4). Blocking of PDL1 induced PD1 SHP2 Reporter Cell (C1) Activity by Atezolizumab with PDL1 Target Cell (Suspension)(C4).Blocking of PD1 induced PD1 SHP2 Reporter Cell (C17) Activity by PD1 Neutralizing Antibody with PDL1 Target Cell (Suspension)(C4). Blocking of PDL1 induced PD1 SHP2 Reporter Cell (C17) Activity by Atezolizumab with PDL1 Target Cell (Suspension)(C4).

Cell Passage Procedures

1.This cell line grows in suspension.
2.Upon receipt, cells should be thawed immediately or stored in liquid nitrogen until use.
3.Before thawing, pre-warm the water bath and culture medium to 37 °C, and prepare a small amount of dry ice.
4.Remove the cryovial from storage and transport it to the cell culture laboratory on dry ice.
5.Rapidly thaw the cells in a 37 °C water bath. Once the cells are completely thawed, spray the cryovial with 70% ethanol for disinfection and transfer it to a biosafety cabinet.
6.Add 10 mL of pre-warmed culture medium into a 15 mL centrifuge tube. Transfer the contents of the cryovial into the tube and centrifuge at 1000 rpm for 5 minutes.
7.Carefully discard the supernatant. Resuspend the cell pellet in 5 mL of pre-warmed culture medium by gentle pipetting. Immediately perform cell counting and adjust the cell density to 3–6 × 10⁵ cells/mL based on the counting results, then transfer the cells into a culture flask.
8.Count the cells every 1–2 days. When the cell density exceeds 1 × 10⁶ cells/mL, passage the cells promptly or add fresh culture medium. Maintain the cell density between 2 × 10⁵ and 1 × 10⁶ cells/mL.

Suspension Cell Cryopreservation Procedure:

1.Collect 8 × 10⁶ cells, centrifuge, and discard the supernatant.
2.Add 1 mL of cell freezing medium (90% FBS + 10% DMSO) and gently pipette to mix thoroughly. Transfer the suspension into a cryovial.
3.Immediately place the cryovial into a controlled-rate freezing container (Nalgene 5100-0001), fill with isopropanol up to the indicated level, and store at −80 °C.
4.After 24 hours, transfer the cryovial to liquid nitrogen for long-term storage.