Snuggs Joseph W, Senter Rebecca K, Whitt Joshua P, Jackson J Derek, Le Maitre Christine L
Division of Clinical Medicine, The University of Sheffield, Sheffield, UK.
Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.
Gene Ther. 2025 Mar;32(2):93-105. doi: 10.1038/s41434-024-00504-7. Epub 2024 Nov 21.
Low back pain is the leading cause of global disability with intervertebral disc (IVD) degeneration a major cause. However, no current treatments target the underlying pathophysiological causes. PCRX-201 presents a novel gene therapy approach that addresses this issue. PCRX-201 codes for interleukin-1 receptor antagonist, the signalling inhibitor of the pro-inflammatory cytokine interleukin-1, which orchestrates the catabolic degeneration of the IVD. Here, the ability of PCRX-201 to transduce human nucleus pulposus cells to increase IL-1Ra production was assessed together with effects on catabolic pathways. When transduced with PCRX-201, the production and release of IL-1Ra was increased in degenerate human nucleus pulposus cells and tissue. Whereas, the production of downstream proteins, including IL-1β, IL-6, MMP3, ADAMTS4 and VEGF were decreased in both cells and tissue, indicating a reduction in IL-1-induced catabolic signalling. Here, a novel gene therapy vector, PCRX-201, was shown to transduce degenerate NP cells and tissue, increasing the production of IL-1Ra. The increased IL-1Ra resulted in decreased production of catabolic cytokines, enzymes and angiogenic factors, whilst also increasing aggrecan expression. This demonstrates PCRX-201 enables the inhibition of IL-1-driven IVD degeneration. The ability of PCRX-201 to elicit anti-catabolic responses is promising and warrants further development to determine the efficacy of this exciting, novel gene therapy.
腰痛是全球致残的主要原因,椎间盘(IVD)退变是其主要病因。然而,目前尚无针对潜在病理生理原因的治疗方法。PCRX - 201提出了一种解决这一问题的新型基因治疗方法。PCRX - 201编码白细胞介素 - 1受体拮抗剂,这是促炎细胞因子白细胞介素 - 1的信号抑制剂,它协调IVD的分解代谢退变。在此,评估了PCRX - 201转导人髓核细胞以增加IL - 1Ra产生的能力以及对分解代谢途径的影响。用PCRX - 201转导时,退变的人髓核细胞和组织中IL - 1Ra的产生和释放增加。而在细胞和组织中,包括IL - 1β、IL - 6、MMP3、ADAMTS4和VEGF在内的下游蛋白的产生均减少,表明IL - 1诱导的分解代谢信号传导减少。在此,一种新型基因治疗载体PCRX - 201被证明可转导退变的NP细胞和组织,增加IL - 1Ra的产生。IL - 1Ra的增加导致分解代谢细胞因子、酶和血管生成因子的产生减少,同时也增加了聚集蛋白聚糖的表达。这表明PCRX - 201能够抑制IL - 1驱动的IVD退变。PCRX - 201引发抗分解代谢反应的能力很有前景,值得进一步开发以确定这种令人兴奋的新型基因治疗的疗效。