T-Cell Responses to Immunodominant LACK Antigen Do Not Play a Critical Role in Determining Susceptibility of BALB/c Mice to Leishmania mexicana

Although BALB/c mice develop lesions when infected with Leishmania mexicana , the mechanisms which are responsible for susceptibility to this parasite have not been elucidated. In contrast, susceptibility of BALB/c mice to Leishmania major has been shown to depend on the early production of interleukin-4 (IL-4) by T cells which react to the parasitic LACK antigen. Here, we demonstrate that the lesions induced by L. mexicana are delayed compared to those induced by L. major but rapidly develop at later time points. Interestingly, while LACK-tolerant BALB/c-derived IE-LACK transgenic mice were resistant to L. major , they were susceptible to L. mexicana and developed lesions similar to those observed in wild-type BALB/c mice. The latter result was observed despite the fact that (i) LACK was expressed by L. mexicana , (ii) splenocytes from BALB/c mice were able to stimulate LACK-specific T-cell hybridoma cells when incubated with live L. mexicana promastigotes, and (iii) LACK-specific T cells contributed to IL-4 production in L. mexicana -infected BALB/c mice. Thus, in contrast to what was observed for L. major -infected mice, LACK-specific T cells do not play a critical role in determining susceptibility to L. mexicana . Although BALB/c mice are susceptible to both L. major and L. mex- icana , the mechanisms which are responsible for susceptibility to these parasites are likely to be different. LMR16.2, producing IL-2 upon recognition of the immunodominant L. major LACK epitope in an I-A d major histocompatibility complex class II-restricted fashion, was used as previously described (17). IL-2 and IL-4 levels were determined by enzyme-linked immunosorbent assays using commercially available kits (duoset from Genzyme Diagnostics, Cambridge, Mass.). The limit of detection was 5 pg/ml for both cytokines.