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Programmed Cell Death Ligand 1-Transfected Mouse Bone Marrow Mesenchymal Stem Cells as Targeted Therapy for
Qiong-Ying Hu1, Yun Yuan2, Yu-Chen Li2
1Department of Laboratory Medicine, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610072, China.
Biomed Research International
|September 9, 2021
Summary
Overexpressing Programmed cell death 1 ligand (PD-L1) in mesenchymal stem cells suppressed rheumatoid arthritis development in mice. This therapy reduced joint damage and modulated immune cell activity, offering a potential treatment strategy.
Area of Science:
- Immunology
- Regenerative Medicine
- Rheumatology
Background:
- Programmed cell death 1 ligand (PD-L1) and its receptor (PD-1) are critical for immune regulation and immunotherapy.
- PD-1/PD-L1 interactions modulate T and B cell immunity, showing therapeutic potential in autoimmune diseases like rheumatoid arthritis (RA).
Purpose of the Study:
- To investigate the therapeutic efficacy of overexpressing PD-L1 in mouse bone marrow mesenchymal stem cells (MBMMSCs) for treating collagen-induced arthritis (CIA).
Main Methods:
- Constructed a recombinant PD-L1-lentiviral vector to overexpress PD-L1.
- Transfected MBMMSCs with the PD-L1 vector (PD-L1-MBMMSCs).
- Administered PD-L1-MBMMSCs to DBA/1j mice with CIA and evaluated therapeutic effects.
Main Results:
- PD-L1-MBMMSCs significantly suppressed the development of CIA in mice.
- Treatment ameliorated joint damage, reduced pro-inflammatory cytokine levels, and inhibited T and B cell activation.
- PD-L1-MBMMSCs modulated immune cell populations in the joints, decreasing dendritic cells and increasing regulatory T and B cells.
Conclusions:
- Overexpression of PD-L1 in MBMMSCs presents a promising therapeutic strategy for rheumatoid arthritis.
- PD-L1-MBMMSC-targeted therapy effectively suppresses autoimmune arthritis by modulating immune responses and cell populations.

