Osiecka-Iwan A, Hyc A, Moskalewski S
Department of Histology and Embryology, Medical University of Warsaw, Poland.
Cell Transplant. 1999 Nov-Dec;8(6):627-36. doi: 10.1177/096368979900800609.
Rat syngeneic and allogeneic chondrocytes were transplanted intramuscularly or into defects prepared in articular cartilage (intracartilaginous transplants). Recipients of allogeneic transplants received cyclosporin A (CsA), cladribine (2-chlorodeoxyadenosine, 2-CdA), or both drugs in combination. Transplants were taken for examination after 5 weeks. Cartilage formed intramuscularly by syngeneic chondrocytes was ossified. Allogeneic cartilage was resorbed by infiltrating cells. CsA or 2-CdA partially suppressed, and both these agents in combination strongly suppressed, formation of infiltrations. Both syngeneic and allogeneic chondrocytes formed cartilage in joint surface defects but only allogeneic cartilage was attacked by infiltrating cells. CsA + 2-CdA treatment slightly decreased intensity of infiltrations but did not prevent cartilage resorption. Antichondrocyte response was studied by evaluation of spleen mononuclear cells (SMC) stimulation in mixed splenocyte-chondrocyte cultures and by detection of antichondrocyte cytotoxic antibodies. SMC stimulation index (SI) was calculated separately for syngeneic and allogeneic chondrocytes. Comparison of SMC SI for syngeneic and allogeneic chondrocytes indicated lack of stimulation of SMC from control or syngeneic transplant recipients and significant stimulation of SMC from recipients of allogeneic transplants. SMC from animals treated with CsA + 2-CdA were not stimulated. Additional experiments aiming at an explanation of the lack of stimulation of SMC from intact animals by syngeneic chondrocytes reported in this work and contrary to other findings disclosed that it was caused by the use of collagenase solution containing N alpha-p-tosyl-l-lysine chloromethyl ketone for chondrocyte isolation. Spontaneous antichondrocyte cytotoxic antibody activity was found in intact rats raised only in sera from recipients of allogeneic intramuscular transplants without immunosuppression. Thus, strong immunosuppressive treatment of rats with allogeneic chondrocyte transplants was more effective in relation to the general immunological response than to the local reaction.
将大鼠同基因和异基因软骨细胞进行肌肉内移植或移植到关节软骨制备的缺损处(软骨内移植)。异基因移植的受体接受环孢素A(CsA)、克拉屈滨(2-氯脱氧腺苷,2-CdA)或两种药物联合使用。移植5周后取出进行检查。同基因软骨细胞在肌肉内形成的软骨发生了骨化。异基因软骨被浸润细胞吸收。CsA或2-CdA部分抑制了浸润的形成,而这两种药物联合使用则强烈抑制了浸润的形成。同基因和异基因软骨细胞在关节面缺损处均形成了软骨,但只有异基因软骨受到浸润细胞的攻击。CsA + 2-CdA治疗略微降低了浸润强度,但并未阻止软骨吸收。通过评估混合脾细胞-软骨细胞培养物中脾单核细胞(SMC)的刺激情况以及检测抗软骨细胞细胞毒性抗体来研究抗软骨细胞反应。分别计算同基因和异基因软骨细胞的SMC刺激指数(SI)。同基因和异基因软骨细胞的SMC SI比较表明,来自对照或同基因移植受体的SMC未受到刺激,而异基因移植受体的SMC受到显著刺激。用CsA + 2-CdA处理的动物的SMC未受到刺激。本研究旨在解释同基因软骨细胞未刺激完整动物的SMC这一现象,与其他研究结果相反,额外的实验表明这是由于使用含有Nα-对甲苯磺酰-L-赖氨酸氯甲基酮的胶原酶溶液分离软骨细胞所致。在仅由未进行免疫抑制的异基因肌肉内移植受体血清饲养的完整大鼠中发现了自发的抗软骨细胞细胞毒性抗体活性。因此,对大鼠进行异基因软骨细胞移植的强免疫抑制治疗对全身免疫反应的效果比对局部反应的效果更显著。