NSAIDs Reduce Therapeutic Efficacy of Mesenchymal Stromal Cell Therapy in a Rodent Model of Posttraumatic Osteoarthritis

被引:7
|
作者
Sok, Daniel [1 ]
Raval, Sarvgna [1 ,2 ]
McKinney, Jay [1 ,3 ]
Drissi, Hicham [1 ,2 ]
Mason, Amadeus [1 ]
Mautner, Ken [1 ]
Kaiser, Jarred M. [1 ,2 ]
Willett, Nick J. [1 ,3 ,4 ]
机构
[1] Emory Univ, Sch Med, Atlanta, GA USA
[2] Atlanta Vet Affairs Hosp, 1175 Univ Dr NE, Atlanta, GA 30306 USA
[3] Georgia Inst Technol, Atlanta, GA 30332 USA
[4] Univ Oregon, Phil & Penny Knight Campus Accelerating Sci Impac, Eugene, OR 97403 USA
基金
美国国家卫生研究院;
关键词
osteoarthritis; stromal cells; stem cells; NSAID; pain management; knee; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; STEM-CELLS; BONE-MARROW; INTRAARTICULAR INJECTION; MENISCAL REGENERATION; KNEE OSTEOARTHRITIS; PROSTAGLANDIN E-2; GENE-EXPRESSION; JOINT; DIFFERENTIATION;
D O I
10.1177/03635465221083610
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Intra-articular injections of human mesenchymal stromal cells (hMSCs) have shown promise in slowing cartilage degradation in posttraumatic osteoarthritis (PTOA). Clinical use of cell therapies for osteoarthritis has accelerated in recent years without sufficient scientific evidence defining best-use practices. Common recommendations advise patients to avoid nonsteroidal anti-inflammatory drug (NSAID) use before and after cell injection over concerns that NSAIDs may affect therapeutic efficacy. Recommendations to restrict NSAID use are challenging for patients, and it is unclear if patients are compliant. Hypothesis: NSAIDs will reduce the efficacy of hMSC therapy in treating a preclinical model of PTOA. Study Design: Controlled laboratory study. Methods: Lewis rats underwent medial meniscal transection (MMT) surgery to induce PTOA or a sham (sham group) surgery that did not progress to PTOA. Rats received naproxen solution orally daily before (Pre-NSAID group) or after (Post-NSAID group) hMSC treatment, throughout the course of the experiment (Full-NSAID group), or received hMSCs without NSAIDs (No NSAID). Cartilage morphology and composition were quantified using contrast-enhanced micro-computed tomography and histology. Pain (secondary allodynia) was measured using a von Frey filament. Results: Injection of hMSCs attenuated cartilage degeneration associated with MMT. hMSCs prevented proteoglycan loss, maintained smooth cartilage surfaces, reduced cartilage lesions, reduced mineralized osteophyte formation, and reduced pain by week 7. The Pre-NSAID group had decreased proteoglycan levels compared with the hMSC group, although there were no other significant differences. Thus, pretreatment with NSAIDs had minimal effects on the therapeutic benefits of hMSC injections. The Post-NSAID and Full-NSAID groups, however, exhibited significantly worse osteoarthritis than the hMSC-only group, with greater proteoglycan loss, surface roughness, osteophyte volume, and pain. Conclusion: Use of NSAIDs before hMSC injection minimally reduced the therapeutic benefits for PTOA, which included preservation of cartilage surface integrity as well as a reduction in osteophytes. Use of NSAIDs after injections, however, substantially reduced the therapeutic efficacy of cellular treatment.
引用
收藏
页码:1389 / 1398
页数:10
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