CONTRIBUTION OF ACTIVATED MACROPHAGES TO THE PROCESS OF DELAYED XENOGRAFT REJECTION

Background When hyperacute rejection, involving natural xenoreactive a ntibodies (XAb) and/or complement (C), can be prevented, xenografts (X gs) undergo delayed xenograft rejection associated with a progressive mononuclear cell infiltration, We have previously shown that XAb forma tion can be totally suppressed in leflunomide (LF)-treated, T-deficien t nude rats receiving hamster hearts. Hence, this model was well-suite d to study a role played by other factors, e,g,, natural killer (NK) c ells and macrophages (M phi). The relative contribution of M phi to de layed xenograft rejection was investigated, Methods. In addition to LF (20 mg/kg/24 hr p,o,), anti-asialoGM-1 serum (1 mg/48 hr i,v,) and N omega-nitro-L-arginine methyl ester (L-NAME; 100 mg/kg/24 hr i,v,) wer e given. Craft-infiltrating cells, deposition of cytokines (interferon -gamma [IFN-gamma] and tumor necrosis factor-alpha [TNF-alpha]), IgM a nd C, and expression of endothelial cell (EC) P- and E-selectins were investigated by immunohistochemistry. In some cases, rat rTNF-alpha or anti-TNF-alpha antibodies were injected intravenously. Results. Xgs r ejected after 3 days by LF-treated rats showed an absence of IgM, C, a nd T cells, but the infiltration of NK cells and M phi, together with the presence of IFN-gamma and TNF-alpha. Addition of NM cell depletion resulted in a significantly prolonged survival of Xgs (6 days; P<0.00 1) in which NK cells and IFN-gamma had disappeared, but M phi were sti ll prominent, Additional blockade of M phi nitric oxide (NO) with L-NA ME further prolonged Xg survival (11 days; P<0.001), In these rejected Xgs, M phi, TNF-alpha, and EC expression of P- and E-selectins was st ill found, together with platelet thrombi, neutrophil-EC adhesion, and vessel intima lesions, The role of TNF-alpha in initiating this Xg re jection was further demonstrated by the acceleration of Xg rejection a fter injection of rTNF-alpha and by a synergism between L-NAME and ant i-TNF-alpha antibodies in hampering the acceleration of Xg rejection s een after transfer of sensitized M phi. Conclusion. In the absence of XAb, T cells, and NM cells, M phi can still reject Xgs, Both NO-depend ent and NO-independent mechanisms are involved, In the latter case, M phi-derived, TNF-alpha-associated EC activation may play a role.