CAJ | 학술논문

目的：探讨朗格汉斯细胞（LC）和浆细胞样树突细胞（pDC）在尖锐湿疣（CA）感染发病机制中的可能作用。方法免疫组化 SP 法检测23例 CA 患者皮损中 CD1a+LC 和 CD2AP+pDC、CD123+pDC 的表达和分布情况，以其中13例 CA 组织的边缘正常皮肤为对照，比较 CA 皮损和边缘正常皮肤中 CD1a+LC、CD2AP+pDC、CD123+pDC 表达密度和阳性率的差异。结果 CD1a+LC 主要位于表皮基底层上棘层，少数在真皮乳头层。 CA皮损中 CD1a+LC 在表皮层和真皮层的密度及阳性率与边缘正常对照组比较，差异无统计学意义（P >0.05）。CD2AP+pDC、CD123+pDC 主要位于真皮乳头层，CA 患者皮损中 CD2AP+pDC、CD123+pDC 的密度和阳性率均比边缘正常对照组显著增高（P <0.05）。结论人乳头瘤病毒感染影响局部黏膜的 pDC 数量，LC 数量未见变化。
목적：탐토랑격한사세포（LC）화장세포양수돌세포（pDC）재첨예습우（CA）감염발병궤제중적가능작용。방법면역조화 SP 법검측23례 CA 환자피손중 CD1a+LC 화 CD2AP+pDC、CD123+pDC 적표체화분포정황，이기중13례 CA 조직적변연정상피부위대조，비교 CA 피손화변연정상피부중 CD1a+LC、CD2AP+pDC、CD123+pDC 표체밀도화양성솔적차이。결과 CD1a+LC 주요위우표피기저층상극층，소수재진피유두층。 CA피손중 CD1a+LC 재표피층화진피층적밀도급양성솔여변연정상대조조비교，차이무통계학의의（P >0.05）。CD2AP+pDC、CD123+pDC 주요위우진피유두층，CA 환자피손중 CD2AP+pDC、CD123+pDC 적밀도화양성솔균비변연정상대조조현저증고（P <0.05）。결론인유두류병독감염영향국부점막적 pDC 수량，LC 수량미견변화。
Objective To investigate the possible roles of Langerhans cells(LCs) and plasmacytoid dendritic cells(pDCs)in the pathogenesis of condyloma acuminatum(CA). Methods Tissue specimens were obtained from the lesions of 23 patients with CA and from perilesional normal skin of 13 of the 23 patients. The expressions and distribution of CD1a, CD2AP and CD123 were analyzed using the streptavidin-peroxidase (SP) immunohistochemical method. Statistical analysis was carried out to compare the density and percentage of CD1a + LCs, CD2AP + pDCs and CD123 +pDCs between lesional skin and perilesional normal skin. Results Most CD1a + LCs were observed in the prickle cell layer of the epidermis, and a few in the papillary layer of the dermis. There was no significant difference in the density or percentage of CD1a+ LCs in the epidermis or dermis between the lesional and perilesional skin specimens (all P > 0.05). CD2AP + pDCs and CD123 + pDCs were distributed mainly in the papillary layer of the dermis, and their density and percentage were significantly higher in the lesional than in the perilesional skin specimens (all P < 0.05). Conclusion Human papillomavirus infection may affect the quantity of pDCs but not LCs in local mucous membranes.