AI Article Synopsis

  • - The study involved over 150 leprosy patients treated with a combination of multidrug therapy (MDT) and immunotherapy (IMT) using heat-killed Mycobacterium leprae and live BCG vaccines, assessing their immune responses over 5 to 10 years.
  • - Results indicated a significant reduction in antibody levels among multibacillary (MB) patients, along with a corresponding decrease in bacterial indexes (BIs), highlighting improved immune responses post-treatment.
  • - There was an increase in lymphoproliferative responses to M. leprae antigens and a remarkable rise in lepromin positivity from 5% to 75% among MB patients during the follow-up, showcasing effective long-term

Article Abstract

More than 150 leprosy patients treated with multidrug therapy (MDT) plus immunotherapy (IMT) with a mixture of heat-killed Mycobacterium leprae plus live BCG were studied in relation to humoral and cell-mediated immune responses. Many previously had received prolonged sulfone monotherapy. Patients received 2 to 10 doses of IMT in a period of 1 to 3 years, depending upon their clinical form of leprosy. The patients were followed up for 5 to 10 years with repeated determinations of antibody levels to phenolic glycolipid-I; lymphoproliferative (LTT) responses to soluble extract of M. leprae, to whole bacilli and to BCG, skin-test responses and bacterial indexes (BIs). After MDT plus IMT there was a statistically significant decrease of antibody levels in the multibacillary (MB) group. The BI decreased proportionally to the ELISA results. LTT increased to M. leprae antigens, especially to soluble extract, in a high percentage of these patients (34% of LL patients positive). Lepromin positivity in MB patients increased from 5% initially positive to 75% at the cut-off during this follow up. These results show substantial early and persistent cell-mediated reactivity to M. leprae in many MB patients treated with MDT-IMT, confirming and expanding previously published data.

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