@article{7547, keywords = {Animals, Immunotherapy, Infusions, Parenteral, Interleukin-1, Macrophage Activation, Mice, Mice, Inbred BALB C, Mycobacterium Infections, Mycobacterium lepraemurium}, author = {Denis M}, title = {Recombinant interleukin-1 infusion increases resistance of BALB/c mice to murine leprosy.}, abstract = {

BALB/c mice were infected by the subcutaneous route with 10(7) Mycobacterium lepraemurium (MLM), and the progression of the infection followed in mice injected i.p. with diluent or recombinant human recombinant interleukin-1 alpha (IL-1 alpha). It was observed that infusion of 1 microgram of IL-1 alpha per day led to a reduction of bacterial growth in the livers and popliteal lymph nodes of MLM injected mice (2-3-log reduction at 6 months, P less than 0.0001). There was no indication that IL-1 alpha infusion was acting by enhancing macrophage activation. Indeed, resident peritoneal macrophages from control infected mice were as competent as macrophages from infected mice treated with IL-1 alpha in generating superoxide anion (O2-) (approximately 400 nM O2-/h/mg at 2 months post-infection). Moreover, they were no more permissive than those of IL-1 alpha infused mice for MLM in vitro as both groups of cells allowed progressive MLM growth, i.e. a 20-fold enhancement of intramacrophage MLM growth. Infusion of IL-1 alpha during MLM infection was not associated with any abrogation of the suppression of the T-cell response to T-cell mitogens or specific stimulation with antigens which is complete at 1 month post-infection. It is concluded that IL-1 alpha has immunotherapeutic potential in leprosy with the mechanism(s) of action still unclear.

}, year = {1991}, journal = {International journal of immunopharmacology}, volume = {13}, pages = {897-902}, month = {1991}, issn = {0192-0561}, doi = {10.1016/0192-0561(91)90042-6}, language = {eng}, }