Pitzke P, Bujia J, Wilmes E, Hammer C
Klinik und Poliklinik für Hals-, Nasen- und Ohrenkranke, Ludwig-Maximilians-Universität München.
Laryngorhinootologie. 1993 Mar;72(3):147-52. doi: 10.1055/s-2007-997874.
Autologous and homologous cartilage grafts are often used in reconstructive head and neck surgery. Unfortunately, sometimes the outcome of such operations is endangered by graft rejection or resorption. Among other reasons, immunological reactions with HLA class II antigen expression are thought to be involved at least in failures of vitally grafted cartilage. Up to now, only one case of class II antigen expression in a cartilage graft "in vivo" has been reported. Nevertheless, it has already been demonstrated that stimulated cartilage cells are able to express "in vitro" class II antigens if grown in monolayer cultures. However, it has also repeatedly been shown that chondrocytes reveal strong dedifferentiating features if cultured in monolayers. Therefore, it was the aim of this study to examine whether isolated and stimulated chondrocytes also express class II antigens if cultured under in vitro conditions closer to the relevant in vivo situation. Hence monolayer, suspension, agar, alginate and organ cultures were prepared simultaneously and kept for up to 60 days. Chondrocytes were stimulated by the addition of IFN-gamma and tested for class II antigens. For the detection of the antigens immunocyto- and immunohistochemical APAAP stainings as well as flow cytometric measurements were made. In all examined culture systems a class II antigen induction could be observed. Any significant differences between the various cultures as to the intensity of antigen expression could not be detected. Consequently, the expression of class II antigens on stimulated human chondrocytes seems not to be a specificity of monolayer cultures. Therefore, class II antigen induction may be considered to play a role in the rejection/resorption of vitally grafted cartilage in reconstructive surgery.
自体和同种异体软骨移植常用于头颈重建手术。不幸的是,有时此类手术的结果会因移植排斥或吸收而受到威胁。除其他原因外,人们认为至少在活体移植软骨失败中涉及与HLA II类抗原表达相关的免疫反应。到目前为止,仅报道过1例软骨移植“体内”II类抗原表达的病例。然而,已经证明,刺激后的软骨细胞如果在单层培养中生长,能够“体外”表达II类抗原。但是,也反复表明,如果在单层中培养,软骨细胞会呈现出强烈的去分化特征。因此,本研究的目的是检测在更接近相关体内情况的体外条件下培养时,分离并经刺激的软骨细胞是否也表达II类抗原。因此,同时制备了单层、悬浮、琼脂、藻酸盐和器官培养物,并保存长达60天。通过添加γ干扰素刺激软骨细胞,并检测II类抗原。采用免疫细胞化学和免疫组织化学APAAP染色以及流式细胞术测量来检测抗原。在所有检测的培养系统中均观察到II类抗原诱导。未检测到不同培养物之间在抗原表达强度方面有任何显著差异。因此,刺激后的人软骨细胞上II类抗原的表达似乎不是单层培养的特异性表现。因此,可以认为II类抗原诱导在重建手术中活体移植软骨的排斥/吸收中起作用。