Tsubota K, Fujita H, Tsuzaka K, Takeuchi T
Department of Ophthalmology, Tokyo Dental College, Chiba, Japan.
Invest Ophthalmol Vis Sci. 2000 Jun;41(7):1666-73.
To characterize lacrimal gland function and lymphocyte infiltration in patients with Mikulicz's disease (MD) and Sjögren's syndrome (SS).
Four patients with MD and 5 with SS were recruited, on whom were performed Schirmer test I (Schirmer test without anesthesia), Schirmer test with nasal stimulation, and vital staining of the ocular surface. The lacrimal gland was then biopsied and the tissues stained with CD3, CD4, CD8, B220, APO2.7, Fas, and Fas ligand (Fas-L) antibodies.
Although regular Schirmer test results in the MD group were less than 10 mm, those with nasal stimulation, 38.1 +/- 3.4 mm, were significantly greater than the SS group. There were minimal ocular surface changes in MD. Morphologic staining with hematoxylin and eosin was identical in both groups, but the acinar cells were stained with APO2.7 only in the SS group. There was strong Fas and Fas-L staining in SS patients but not in those with MD.
Lacrimal gland acinar cells in those with MD maintained their function and were not programmed for cell death. The sicca syndrome was not observed in MD patients. Although the pathology is similar for MD and SS, the difference in acinar cell apoptosis and function can explain clinical differences.
对米库利奇病(MD)和干燥综合征(SS)患者的泪腺功能及淋巴细胞浸润情况进行特征描述。
招募了4例MD患者和5例SS患者,对其进行了I型泪液分泌试验(无麻醉的泪液分泌试验)、鼻刺激泪液分泌试验以及眼表活体染色。随后对泪腺进行活检,并用抗CD3、CD4、CD8、B220、APO2.7、Fas和Fas配体(Fas-L)抗体对组织进行染色。
尽管MD组常规泪液分泌试验结果小于10毫米,但鼻刺激后的结果为38.1±3.4毫米,显著高于SS组。MD患者眼表变化极小。两组苏木精和伊红形态学染色相同,但仅SS组腺泡细胞被APO2.7染色。SS患者Fas和Fas-L染色强,而MD患者则无。
MD患者的泪腺腺泡细胞保持其功能,未被编程发生细胞死亡。MD患者未观察到干燥综合征。尽管MD和SS的病理相似,但腺泡细胞凋亡和功能的差异可以解释临床差异。