Rodeo S A, Warren R F
Hospital for Special Surgery, Cornell University Medical College, New York, New York, USA.
Clin Sports Med. 1996 Jul;15(3):469-81.
Research during the past decade has elucidated the structure and function of the knee joint meniscus, and both clinical and experimental studies have demonstrated the importance of this structure. Recent advances, such as the use of an exogenous fibrin clot, have allowed preservation of an increasingly greater proportion of injured menisci. The success of these methods will be established only by long-term follow-up studies demonstrating a lower incidence of progression to degenerative joint disease. It is hoped that an increasing understanding meniscal fibrochondrocytes biology and response to injury will result in the development of novel therapeutic strategies for repair of the injured meniscus. Basic studies clearly have demonstrated that meniscal fibrochondrocytes possess intrinsic repair capability. Both in vitro cell culture studies and in vivo animal models have provided the basic scientific foundation for the use of fibrin clot in tears in the avascular portion of the meniscus. The use of fibrin clot has allowed further expansion of the proportion of meniscal tears that are potentially reparable. Tears in the central, avascular zone of the meniscus, formerly thought to be irreparable, now may undergo repair with an enhanced opportunity for healing. The factors associated with a good prognosis in the meniscal repair include acute tear; peripheral tear; a stable knee; and the presence of serum or factors derived from serum, such as the presence of a fibrin clot, or vascular access channel, or hemarthrosis. Cell culture and molecular biologic techniques currently are being used to improve our understanding of meniscal biology. Particular challenges for future research include determination of the source of the reparative cells in meniscal repair, exploration of the biomechanical properties of the reparative tissue, and demonstration of the potential use of growth factors in meniscal healing. A further potential use of fibrin clot in the future is as a carrier vehicle both for the delivery of growth factors to injured meniscal and for the transplantation of autogenous fibrochondrocytes in meniscal defects. Other avenues of investigation include the use of cytokines to enhance meniscal healing, studies of meniscal replacement with allografts and collagen-based prostheses for meniscal regeneration, and the potential to augment meniscal cell proliferation and matrix synthesis by gene therapy techniques.
过去十年的研究阐明了膝关节半月板的结构与功能,临床和实验研究均已证实该结构的重要性。近期的进展,如使用外源性纤维蛋白凝块,使得越来越多的损伤半月板得以保留。只有通过长期随访研究证明发展为退行性关节疾病的发生率更低,才能确定这些方法的成功与否。希望对半月板纤维软骨细胞生物学及损伤反应的深入了解将促成修复损伤半月板的新型治疗策略的开发。基础研究清楚地表明半月板纤维软骨细胞具有内在修复能力。体外细胞培养研究和体内动物模型都为在半月板无血管部分的撕裂处使用纤维蛋白凝块提供了基础科学依据。纤维蛋白凝块的使用使可潜在修复的半月板撕裂比例进一步扩大。半月板中央无血管区的撕裂,以前被认为无法修复,现在可能有更大的愈合机会进行修复。半月板修复预后良好相关的因素包括急性撕裂;周边撕裂;膝关节稳定;以及存在血清或血清衍生因子,如存在纤维蛋白凝块、血管通道或关节积血。细胞培养和分子生物学技术目前正用于增进我们对半月板生物学的理解。未来研究的特殊挑战包括确定半月板修复中修复细胞的来源、探索修复组织的生物力学特性以及证明生长因子在半月板愈合中的潜在用途。纤维蛋白凝块未来的另一个潜在用途是作为载体,用于将生长因子递送至损伤的半月板以及在半月板缺损处移植自体纤维软骨细胞。其他研究途径包括使用细胞因子促进半月板愈合、研究同种异体移植和基于胶原蛋白的假体进行半月板再生的半月板置换,以及通过基因治疗技术增强半月板细胞增殖和基质合成的潜力。