02562nas a2200469 4500000000100000008004100001260001300042653001200055653002600067653002300093653002700116653000800143653001100151653002300162653001700185653002800202653002100230653001600251653000900267653002300276653002500299653001100324653001800335100001300353700001300366700001300379700001100392700001300403700001300416700001300429700001600442700001300458700001800471700001100489245012800500856007200628300001100700490000700711050001600718520134400734022001402078 2007 d c2007 Nov10aAnimals10aAntibodies, Bacterial10aAntibody Formation10aDisease Models, Animal10aEar10aFemale10aImmunity, Cellular10aInflammation10aInjections, Intradermal10aInterferon-gamma10aLymph Nodes10aMice10aMice, Inbred C57BL10aMycobacterium leprae10aSpleen10aT-Lymphocytes1 aDuthie M1 aReece ST1 aLahiri R1 aGoto W1 aRaman VS1 aKaplan J1 aIreton G1 aBertholet S1 aGillis T1 aKrahenbuhl JL1 aReed S00aAntigen-specific cellular and humoral responses are induced by intradermal Mycobacterium leprae infection of the mouse ear. uhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2168264/pdf/0564-07.pdf a5290-70 v75 aDUTHIE 20073 a

Leprosy is caused by infection with Mycobacterium leprae. The immune response of leprosy patients can be highly diverse, ranging from strong cellular responses accompanied by an apparent deficit of M. leprae-specific antibodies to strong humoral responses with a deficit of cell-mediated responses. Leprosy takes many years to manifest, and this has precluded analyses of disease and immune response development in infected humans. In an attempt to better define development of the immune response during leprosy we have developed an M. leprae ear infection model. Intradermal inoculation of M. leprae into the ear supported not only infection but also the development of a chronic inflammatory response. The inflammatory response was localized, comprising a T-cell infiltration into the ear and congestion of cells in the draining lymph nodes. The development of local chronic inflammation was prevented by rifampin treatment. Importantly, and in contrast to subcutaneous M. leprae footpad infection, systemic M. leprae-specific gamma interferon and antibody responses were detected following intradermal ear infection. These results indicate the utility of intradermal ear infection for both induction and understanding of the immune response during M. leprae infection and the identification or testing of new leprosy treatments.

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