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HOME > ÇÐȸ°£Ç๰ >
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Antigenic Studies of Mycobacterium Leprae and Mycobacterium Lepraemurium by Immunodiffusion |
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Kim. J D., Lew, J. |
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Yonsei University College of Medicine, Seoul, Korea |
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1972 |
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Since G.A. Hansen discovered M. leprae as a causative organism of human lepresy, many inrestigtosrs have continued their effects to cultivate M. leprae in vivo. Although Shepard succeeded in multiplying it by animal inoculation in mouse foot pad, M. leprae still can not be cultured. An bartificial media. Therefore, immunologic studies of leprosy lag far behind these on other mycobaeterial infections, and the identification and establishment of relationships among various antigens associated with mycobacteria have been the subjects of numerous investigations. Recently the immunodiffusion methods Eave wren widely used for the antigenic analysis of mycobacteria. Since Parlett and Youmans applied the agar gel diffusion technique to identify the antigenic relationship between mycobacteria, many investigators have developed and applied the immunodiffusion methods to antigenic analysis of M. leprae and other mycobacteria. Burrell and Rheins studied antigenicity of lepremin and reported that the old tuberculin and Bepromin were shown to possess common as well as distinct antigens. Pepys et al. and Pepys observed that PPD preparation and lepromin had three common precipitating antigens. Sushida and Hirano, Navalkar et al., and Navalkar detected antibodies in the sera from leprosy patients against culture filtrates of various mycobacteria and lepromin. Tuma and Silva obtained positive Precipitating reaction between various mycobacterial antigens arid rabbit serum immunized with leprosy bacilli. However, only a few papers have been reported on the specific antigens of M. leprae because of difficulties in obtaining enough amount of purified leprosy bacilli. Some investigators suggested that leprosy nodule contained certain specific antigens by the studies of lepromin, unheated leprosy nodules and tissue culture filtrates of M. lepraemurium. Rees et al. reported that tissue culture filtrates of M. lepraemurium contained soluble antigens comparable to those in the culture filtrates of other cultivable mycobacteria, and they assumed that the intracellularly growing M. leprae and M. lepraemurium in vivo were equally able to produce soluble antigens which could be released into the surrounding tissue space or into the blood stream. Abe isolated a water soluble, heat labile, protein antigen from unheated leprosy nodules, which gave precipitation only with the rabbit anti-leprosy nodule-extract serum. Those studies suggested that leprosy module and murine leprosy infected tissues contained certain specific antigens. The present paper reports the antigenic analysis of unheated human leprosy nodule extract, purified leprosy bacilli, murine leprosy infected rat testicle extract and purified murine leprosy bacilli, and the detection of antibodies in the sera from leprosy patients against various mycobacterial antigens. |
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