TY - JOUR KW - Adolescent KW - Adult KW - Antigens, Bacterial KW - Enzyme-Linked Immunosorbent Assay KW - Female KW - Humans KW - Immunoglobulin A KW - Immunoglobulin A, Secretory KW - leprosy KW - Male KW - Middle Aged KW - Mycobacterium leprae KW - Nasal Mucosa KW - Nasal Provocation Tests KW - Saliva KW - Tuberculin AU - Ramaprasad P AU - Cree I A AU - Oluwole M AU - Samson P D AB -

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.

BT - Journal of immunological methods C1 - http://www.ncbi.nlm.nih.gov/pubmed/8551052?dopt=Abstract CN - RAMAPRASAD 1995 DA - 1995 Dec 27 DO - 10.1016/0022-1759(95)00219-7 IS - 2 J2 - J. Immunol. Methods LA - eng N2 -

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.

PY - 1995 SP - 239 EP - 46 T2 - Journal of immunological methods TI - Development of a mucosal challenge test for leprosy using leprosin A. VL - 188 SN - 0022-1759 ER -