|
|
 |
|
¡¡ |
|
¡¡ |
|
|
|
¡¡ |
HOME > ÇÐȸ°£Ç๰ >
¿ë¾î»çÀü |
|
Á¦¸ñ |
Studios on chemoprophylaxis of leprosy with DDS |
|
|
|
|
ÀúÀÚ |
Joon Lew, young Soo Kim |
¼Ò¼Ó |
Dept. of Microbiology Yonsei University College of Medicine and World Vision Special Skin Clinic |
|
|
³âµµ |
1975 |
±Ç |
9 |
|
|
È£ |
1 |
¹øÈ£ |
|
|
|
½ÃÀÛÆäÀÌÁö |
75 |
³¡ÆäÀÌÁö |
84 |
|
|
÷ºÎ |
|
|
|
¿ä¾à |
Since G.A. Hansen (1874) discovered M. leprae from leprosy tissue, it has been accepted that leprosy is a chronic contageous disease, and occurs chiefly among poorer people in poverty striven countries. In the treatment of leprosy, although chaulmoogra oil had been used from ancient times, it has now been abandoned. Faget et al. (1943) introduced promin, one of the derivatives of DDS, in the chemotherapy of leprosy and since then many investigators have been interested in chemotherapeutic agents for leprosy. Cochrane et al. (1949). Loweand Smith (1949), and Lowe (1950) reported that DDS is more potentially active against mycobacteria than promin, and it has been acceptcd that DDS is the drug of choice in the treatment of leprosy. However, DDS has still many limitations in the treatment of leprosy. Davey (1964) pointed out its rather strong toxicity, precipitation of hypersensitivity and prolonged period of medication. Therefore, many investigators haute attempted to find an ideal chemotherapeutic agent for leprosy (Buu-Hoi et al, 1955; Schneider et at, 1958; Davey & Hogerzeil, 1959; Lew et at, 1968). Many leprosy workers believe that leprosy control will be provided not only by effective treatment, but also by effective prophylactic measures. Fernandez (1939) suggested the possibility of leprosy prevention with BCG vaccination. Numerous clinical and field trials have been carried out in the attempt to prove the effectiyeness of BCG vaccination both as a stimulant for lepromin positive conversion, and as a prophylactic measure against leprosy (Azulay, 1949: Convict et at, 1952: Souza Campos, 1953: Brown et at, 1968; Bechelli et al, 1968). As chemoprophylactic agents, chloroquine has been used for malaria (Bolding, 1960), penicillin for syphilis (Andrew & Domonkos, 1963), and INH for tuberculosis (Payne, 1957; WHO, 1965). Leprosy is also a chronic disease and has a long incubation period. The idea is to eliminate the causative agent in the host tissue or to interfere with the host parasite relationship during its incubation period by the administration of DDS as a chemoprophylactic measure in leprosy contacts. The possibility of chemopjophylaxis of leprosy with DDS has been suggested and reported by some leprosy workers (Lee & Lew, 1960; Lew & Kim, 1966; Dharmendra et at, 1967). The purpose of this study is to prove the effective chemoprophylactic vague of DDS against leprosy contacts and to analyze she epidemiologic factors in leprosy families. |
|
|
³»¿ë |
|
 | |
¡¡ |
|
|
|
|
|
|
|
|