Antimicrobial defense mechanisms are enhanced by antigen-specific T cell differentiation followed by activation of mononuclear phagocytes (1, 2). 3" Interferon (IFN-3,) ~ is an important mediator of both antimicrobial activity and hydrogen peroxide secretion in mononuclear phagocytes (3). A number of observations suggest that an immunological defect exists in lepromatous leprosy w_hich-allows the extensive replication of M. leprae within dermal macrophages (4). The skin lesions are relatively deprived of helper T cells (OKT4), which are an important source of IFN-3" (5-7). The exposure of peripheral blood T cells to M. leprae fails to result in appreciable T cell proliferation and synthesis of lymphokine, including IFN-3" (8-10). In contrast, the lymphocytes of patients with lepromatous leprosy can respond to l~ctins and other antigens to which they are sensitized (4,(8)(9)(10)(11)(12)(13). This had lead to the concept of selective anergy in which, either due to the absence ofM. leprae-reactive T cells and/or the activity of suppressor cells or factors, macrophage activation does not occur and microbial dissemination ensues (1 1-23).In the course of studies on the reversal of T cell nonresponsiveness with purified IL-2 in lepromatous leprosy patients (8), we were struck by the heterogeneous response to this T cell growth factor. We have therefore reexamined the responsiveness of T cells to M. leprae and other antigens, and evaluated their stimulation by recombinant IL-2 and their possible inhibition by suppressor cell populations.
Materials and MethodsPatients. Patients (see Table I Abbreviations used in this paper: BCG, bacillus Calmette Guerin; C*, rabbit complement; Con A, concanavalin A; IFN-3,, immune (gamma) interferon; IL-2, interleukin 2; mAb, monoclonal antibodies.J. ExP. MED.