Tosca A, Lehou J, Hatjivasiliou M, Varelzidis A, Stratigos J D
Department of Dermatology, Andreas Sygros Hospital, School of Medicine, National University of Athens, Greece.
Genitourin Med. 1988 Oct;64(5):289-93. doi: 10.1136/sti.64.5.289.
An immunohistological study of skin biopsy specimens from patients with early syphilis was undertaken before and after treatment (one day after intramuscular administration of 2.4 MIU benzathine penicillin and eight days later, after a total administration of 3.6 MIU. In chancres from seronegative patients treatment with 3.6 MIU usually resulted in fewer immunocompetent cells in the infiltrate. In lesions of secondary syphilis treatment with 2.4 MIU benzathine penicillin produced a significant decrease in immunocompetent cells. After treatment with 3.6 MIU there was no further decrease. It was worth noticing that even eight to nine days after the initial pretreatment biopsy, when 3.6 MIU had been administered, the overall lymphohistiocytic infiltrate was not substantially diminished. Significantly more suppressor (T8+) cells were found in lesions of primary syphilis than of secondary syphilis, and they showed remarkable exocytosis. Activated local T8+ cells may release immunosuppressive lymphokines.
对早期梅毒患者的皮肤活检标本在治疗前后进行了免疫组织学研究(在肌肉注射240万单位苄星青霉素一天后以及八天后,总共注射360万单位后)。在血清阴性患者的硬下疳中,使用360万单位治疗通常会使浸润中的免疫活性细胞减少。在二期梅毒病变中,使用240万单位苄星青霉素治疗会使免疫活性细胞显著减少。使用360万单位治疗后没有进一步减少。值得注意的是,即使在初次预处理活检后的八到九天,当已经注射了360万单位时,总体淋巴细胞组织细胞浸润并没有显著减少。在一期梅毒病变中发现的抑制性(T8 +)细胞明显多于二期梅毒,并且它们表现出明显的胞吐作用。活化的局部T8 +细胞可能释放免疫抑制性淋巴因子。