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兔角膜移植排斥反应的体内共聚焦显微镜分析

In vivo confocal microscopic analysis of corneal allograft rejection in rabbits.

作者信息

Cho B J, Gross S J, Pfister D R, Holland E J

机构信息

Department of Ophthalmology, University of Minnesota, Minneapolis, USA.

出版信息

Cornea. 1998 Jul;17(4):417-22. doi: 10.1097/00003226-199807000-00013.

Abstract

PURPOSE

To demonstrate in vivo confocal microscopic features of corneal allograft rejection that may be useful for differentiating graft rejection from other conditions.

METHODS

Corneal donor buttons from Dutch Belted (DB) pigmented rabbits were transplanted orthotopically into New Zealand White (NZW) recipient corneal beds. Slit-lamp and confocal microscopic examinations were performed every 3 days thereafter until the time of graft failure.

RESULTS

Allograft-rejection signs began to appear during the fourth postoperative week. In epithelial rejection, small inflammatory cells were visualized forming a linear rejection line mixed with larger damaged epithelial cells. Subepithelial infiltrates (SEIs) could be discerned as aggregates of small and highly refractile inflammatory cells within the extracellular matrix. An area of stromal rejection showed increased reflectivity of stromal edema with numerous small infiltrated inflammatory cells. Keratic precipitate (KP) was visualized to be protruding into the anterior chamber with surrounding normal polygonal endothelial cells at its base. Endothelial rejection lines were formed by cellular aggregates of small inflammatory cells and damaged larger endothelial cells with pyknotic highly reflective nuclei. With the progression of endothelial rejection, damaged endothelial cells decreased in number, increased in size, and extended pseudopod-like cytoplasmic structures.

CONCLUSION

In vivo confocal microscopy can provide us with detailed histopathology of corneal graft rejection, which might be useful for differentiating immune rejection from other graft conditions and may provide a technique for early diagnosis of rejection before slit-lamp findings.

摘要

目的

展示角膜移植排斥反应的体内共聚焦显微镜特征,这些特征可能有助于将移植排斥反应与其他情况区分开来。

方法

将来自荷兰带兔(DB)的角膜供体纽扣原位移植到新西兰白兔(NZW)的受体角膜床中。此后每3天进行裂隙灯和共聚焦显微镜检查,直至移植失败。

结果

同种异体移植排斥反应体征在术后第四周开始出现。在上皮排斥反应中,可见小的炎性细胞形成一条线性排斥线,与较大的受损上皮细胞混合。上皮下浸润(SEIs)可被识别为细胞外基质内小的、高折射性炎性细胞的聚集。基质排斥反应区域显示基质水肿的反射率增加,伴有大量小的浸润性炎性细胞。角膜后沉着物(KP)可见突出进入前房,其底部有周围正常的多边形内皮细胞。内皮排斥线由小炎性细胞的细胞聚集体和受损的较大内皮细胞形成,这些内皮细胞核固缩且具有高反射性。随着内皮排斥反应的进展,受损内皮细胞数量减少、大小增加,并伸出伪足样细胞质结构。

结论

体内共聚焦显微镜可以为我们提供角膜移植排斥反应的详细组织病理学信息,这可能有助于将免疫排斥反应与其他移植情况区分开来,并可能提供一种在裂隙灯检查结果出现之前早期诊断排斥反应的技术。

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