TY - JOUR KW - Immune Tolerance KW - Immunologic Deficiency Syndromes KW - Leprosy, lepromatous KW - Macrophages KW - Mycobacterium leprae KW - T-Lymphocytes AU - Bach M A AU - Launois P AB -

Patients suffering from lepromatous leprosy fail to develop an efficient cell-mediated immunity towards Mycobacterium leprae, the causative agent. The mechanism of such a specific T-cell tolerance to the bacillus remains a key question in the pathophysiology of leprosy. Macrophages do not show any intrinsic defect in phagocytizing and killing M. leprae or in presenting antigen to helper T-cells. On the other hand, M. leprae-reactive helper T-cells do persist in lepromatous patients, but their activation appears to prevented by active suppressor mechanisms, involving both suppressor T-cells and macrophages. The target of this specific suppression could be the interleukin 2-producing T-cell subset. A better molecular definition of M. leprae antigens, both by monoclonal antibodies and T-cell clones, should open new perspectives for further analysis of the regulation of immune responses to M. leprae.

BT - Biochimie C1 - http://www.ncbi.nlm.nih.gov/pubmed/3147697?dopt=Abstract CN - BACH1988 DA - 1988 Aug DO - 10.1016/0300-9084(88)90264-7 IS - 8 J2 - Biochimie LA - eng N2 -

Patients suffering from lepromatous leprosy fail to develop an efficient cell-mediated immunity towards Mycobacterium leprae, the causative agent. The mechanism of such a specific T-cell tolerance to the bacillus remains a key question in the pathophysiology of leprosy. Macrophages do not show any intrinsic defect in phagocytizing and killing M. leprae or in presenting antigen to helper T-cells. On the other hand, M. leprae-reactive helper T-cells do persist in lepromatous patients, but their activation appears to prevented by active suppressor mechanisms, involving both suppressor T-cells and macrophages. The target of this specific suppression could be the interleukin 2-producing T-cell subset. A better molecular definition of M. leprae antigens, both by monoclonal antibodies and T-cell clones, should open new perspectives for further analysis of the regulation of immune responses to M. leprae.

PY - 1988 SP - 1013 EP - 8 T2 - Biochimie TI - Mechanisms of Mycobacterium leprae-specific T-cell deficiency in lepromatous leprosy. VL - 70 SN - 0300-9084 ER -