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HOME > ÇÐȸ°£Ç๰ >
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BCG Immunotherapy Trial in Lepromatous Leprosy |
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ÀúÀÚ |
Do Il Kim(±èµµÀÏ) |
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Korean Leprosy Institute |
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1979 |
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12 |
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1 |
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43 |
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50 |
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The most commonly used chemotherapeutic agent in leprosy is DDS. However, as could be expected with monotherapy, a considerable proportion of lepromatous cases will relapse with drug resistant strain of M. leprae. Other drugs, such as clofazimine and rifampicin, are so expensive that they have only a very limited use at present. Moreover, all chemotherapeutic agents, although they may be efficient in killing M. leprae, apparently do not alter the body's capacity to eliminate the dead bacilli, which may continue to release antigen for prolonged periods of time and thereby give rise to erythema nodosum leprosum. Finally, since the anergic state in lepromatous patients appears to be lifelong, such patients will have to remain permanently on anti-leprosy chemotherapy, unless cell-mediated immunity to M. leprae can be induced. For this reasons, there is a need for additional treatment methods such as immunotherapy. The aims of immunotherapy may to increase digestion of M. leprae and thereby reduce ENL reaction and the induce impunity in treated lepromatous patients, and thereby reduce the risk of development of DDS-resistant cases and make termination of anti-leprosy chemotherapy possible. On our histopathological study of lepromatous nodule eight weeks after BGG local injection into the leproma, it was observed that M. leprae was lysed rapidly and bacterial index became nearly negative and histological findings showed borderline leprosy. This results suggest that one might expect eventual systemic manifestations of cellular immunity to M. leprae by BCG immunotherapy in lepromatous leprosy. Therefore, the immunotherapy trial with BCG repeated injection to lepromatous patients being admitted in Korean Leprosy Institute has been carried out for more than fifteen months and the following results were obtained. |
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