Ramaprasad P, Cree I A, Oluwole M, Samson P D
Stanley Browne Laboratories, Richardson Leprosy Hospital, Leprosy Mission, Miraj, India.
J Immunol Methods. 1995 Dec 27;188(2):239-46. doi: 10.1016/0022-1759(95)00219-7.
There is little information about the mucosal immune response in leprosy. We have developed a nasal provocation test with leprosin A which will be used to investigate mucosal immunity to Mycobacterium leprae. Initial studies were performed with increasing doses of leprosin A (1.0 pg/ml-10 micrograms/ml) to determine the optimal safe dose of leprosin A. Anti-M. leprae IgA antibody and normal IgA concentrations were measured in the saliva of leprosy contacts and controls before and after instillation of leprosin A. Nasal leprosin A was well tolerated up to a concentration of 10 micrograms/ml without side effects. None of the six subjects who had not been exposed to leprosy had salivary IgA against whole M. leprae, whereas IgA was detected from 64 h to 140 h following instillation of leprosin A in all of the leprosy hospital workers and in 15 out of 18 healthy household contacts tested. There was no correlation between serum and salivary anti-M. leprae IgA levels before and after testing. Salivary IgA anti-lipoarabinomannan responses were seen in 12 out of 20 household contacts. Normal salivary IgA concentrations varied from 8 to 240 mg/l. The leprosin A nasal provocation test appears to be a safe method for the investigation of the role of mucosal immunity in the pathogenesis of leprosy.
关于麻风病黏膜免疫反应的信息很少。我们开发了一种用麻风菌素A进行的鼻腔激发试验,该试验将用于研究对麻风分枝杆菌的黏膜免疫。最初的研究使用递增剂量的麻风菌素A(1.0 pg/ml - 10微克/ml)来确定麻风菌素A的最佳安全剂量。在滴注麻风菌素A之前和之后,测量麻风病接触者和对照者唾液中的抗麻风分枝杆菌IgA抗体和正常IgA浓度。高达10微克/ml浓度的鼻腔麻风菌素A耐受性良好,无副作用。6名未接触过麻风病的受试者中,没有一人唾液中有针对完整麻风分枝杆菌的IgA,而在所有麻风病医院工作人员以及18名接受检测的健康家庭接触者中的15人中,在滴注麻风菌素A后64小时至140小时检测到了IgA。检测前后血清和唾液中抗麻风分枝杆菌IgA水平之间没有相关性。20名家庭接触者中有12人出现了唾液中抗脂阿拉伯甘露聚糖的反应。正常唾液IgA浓度在8至240 mg/l之间变化。麻风菌素A鼻腔激发试验似乎是一种安全的方法,可用于研究黏膜免疫在麻风病发病机制中的作用。