Objective. To examine the functional capacity of dendritic cells (DCs) from a panel of HLA-B27/human  2 -microglobulin (Hu 2 m)-transgenic rat lines and crosses with varying susceptibilities to spondylarthritis (SpA)-like disease.Methods. Mature splenic DCs were isolated from HLA-B27-transgenic, HLA-B7-transgenic, and/or Hu 2 m-transgenic rats and tested for support of allogeneic proliferation, compared with nontransgenic controls (all male rats on Lewis background). Graded numbers of DCs were cultured with allogeneic lymph node CD4؉ T cells (dark agouti background). Proliferation was assayed by incorporation of tritiated deoxythymidine after 2-4 days of culture.Results. Allogeneic proliferation stimulated by DCs from the healthy HLA-B27/Hu 2 m-transgenic line 21-3 and from the healthy Hu 2 m-transgenic line 283-2 was weakly decreased (21-3) or close to normal (283-2) as compared with that observed with control nontransgenic Lewis rat DCs. In contrast, the ability of DCs from (21-3 ؋ 283-2)F 1 rats, which develop a dramatic SpA phenotype, to stimulate allogeneic proliferation was markedly defective. When DC-induced allogeneic proliferation was compared among different transgenic lines and crosses with distinct levels of susceptibility to SpA-like disease, stimulatory capacity was inversely correlated with disease susceptibility.Conclusion. In HLA-B27/Hu 2 m-transgenic rats, a defective functional capacity of DCs correlates with susceptibility to SpA. Since it was previously demonstrated that defective DC function is not a consequence of disease, it could well be a principal factor in the spontaneous development of SpA in these lines.