Merrin C, Han T, Klein E, Wajsman Z, Murphy G P
Cancer Chemother Rep. 1975 Jan-Feb;59(1):157-63.
Seventeen patients with histologically proven adenocarcinoma of the prostate were selected for evaluation of their immunologic competence and therapy with bacillus Calmette-Guérin (BCG). All patients were in stage D. The immune response was explored in two main aspects: cell-mediated and humoral immunity. Delayed skin hypersensitivity reaction with purified protein derivative (PPD), streptokinase-streptodornase (varidase), Candida, mumps antigen, and Trichophyton were tested. Lymphocyte reactivity was measured by in vitro blastogenesis. Serum immunoglobulin levels and serum protein electrophoresis were also measured. The patients were then divided in two groups according to the skin test response to PPD. Group 1 (PPD-positive) consisted of seven patients. Group 2 (PPD-negative) consisted of ten patients. In group 1, two patients were treated with intraprostatic injection of BCG every week in the following doses: 1 cc the first week, 2 cc the second week, 4 cc the third week, and 6 cc the fourth week. The five remaining patients in this group received only 1 cc every week for 4 weeks. The group 2 patients (PPD-negative) were stimulated by oral intake of BCG in an attempt to convert their skin tests to positive. All patients revealed varying degrees of immunodepression. None of the patients in group 2 (stimulated by oral intake of BCG) converted to positive skin tests. Three patients in group 1 treated with BCG showed necrosis of the tumor. The different aspects of immunodepression in this disease are analyzed and correlated to the clinical staging, histologic grading, and response to therapy. The mechanism of BCG action in advanced prostatic carcinoma is discussed.
选取17例经组织学证实为前列腺腺癌的患者,以评估其免疫功能并采用卡介苗(BCG)进行治疗。所有患者均处于D期。从两个主要方面探讨免疫反应:细胞介导免疫和体液免疫。检测了用纯化蛋白衍生物(PPD)、链激酶-链道酶(溶链菌酶)、念珠菌、腮腺炎抗原和毛癣菌进行的迟发型皮肤超敏反应。通过体外淋巴细胞转化试验测定淋巴细胞反应性。还测定了血清免疫球蛋白水平和血清蛋白电泳。然后根据对PPD的皮肤试验反应将患者分为两组。第1组(PPD阳性)有7例患者。第2组(PPD阴性)有10例患者。在第1组中,2例患者每周接受前列腺内注射BCG,剂量如下:第1周1毫升,第2周2毫升,第3周4毫升,第4周6毫升。该组其余5例患者每周仅接受1毫升,共4周。第2组患者(PPD阴性)通过口服BCG进行刺激,试图使其皮肤试验转为阳性。所有患者均表现出不同程度的免疫抑制。第2组中(通过口服BCG刺激)没有患者的皮肤试验转为阳性。第1组中接受BCG治疗的3例患者出现肿瘤坏死。分析了该疾病免疫抑制的不同方面,并将其与临床分期、组织学分级及治疗反应相关联。讨论了BCG在晚期前列腺癌中的作用机制。