Grassegger A, Rollinger-Holzinger I, Zelger B W, Heim K, Zwierzina H, Fritsch P O, Höpfl R M
Department of Dermatology and Venereology, University of Innsbruck, Austria.
Arch Dermatol Res. 1997 Apr;289(5):243-50. doi: 10.1007/s004030050187.
The purpose of the study was to investigate the cytokine gene expression patterns and immunohistochemical characteristics of genitoanal warts in order to obtain a clue as to the immunological mechanisms possibly relevant for wart regression or persistence. We analysed surgically removed warts from 11 patients, 2 of whom were immunosuppressed. Lesions of five of the nine otherwise healthy individuals were additionally treated with intralesional interferon-gamma (IFN gamma) prior to surgery. Invasion of CD4+ T cells into the papillomas and HLA-DR and ICAM-1 expression on keratinocytes were found in two otherwise healthy patients and were intensified by intralesional IFN gamma in four of five patients. The mRNA expression patterns in seven of eight non-recurrent warts were compatible with a predominant TH1 or mixed TH1/TH2 cytokine profile. In contrast, in recalcitrant warts of three patients (one healthy, two immunocompromised) histological signs of immunore-activity and TH1-like cytokine mRNA expression were not detected. In recurrent warts of a renal transplant patient, IL-4 and IL-5 mRNA expression was repeatedly found suggesting a predominant TH2 response. In conclusion, immunoreactivity to genitoanal warts such as T-cell infiltration, HLA-DR and ICAM-1 expression was associated with a predominant TH1 or mixed TH1/ TH2 cytokine mRNA expression profile.
本研究的目的是调查生殖器肛门疣的细胞因子基因表达模式和免疫组织化学特征,以便获得可能与疣体消退或持续存在相关的免疫机制线索。我们分析了11例患者手术切除的疣体,其中2例为免疫抑制患者。9例其他方面健康的个体中,有5例的病变在手术前还接受了病灶内注射γ干扰素(IFNγ)治疗。在2例其他方面健康的患者中发现CD4+T细胞侵入乳头瘤以及角质形成细胞上HLA-DR和ICAM-1表达,并且在5例患者中有4例通过病灶内注射IFNγ使其增强。8例非复发性疣体中有7例的mRNA表达模式与主要为TH1或混合性TH1/TH2细胞因子谱相符。相比之下,在3例患者(1例健康,2例免疫功能低下)的顽固性疣体中未检测到免疫反应的组织学迹象和TH1样细胞因子mRNA表达。在1例肾移植患者的复发性疣体中,反复发现IL-4和IL-5 mRNA表达,提示主要为TH2反应。总之,生殖器肛门疣的免疫反应,如T细胞浸润、HLA-DR和ICAM-1表达,与主要为TH1或混合性TH1/TH2细胞因子mRNA表达谱相关。