The ability of splenic antigen-presenting cells (APC) from nine indepe
ndent mouse major histocompatibility complex (MKC) haplotypes to prese
nt recombinant streptococcal exotoxin A (rSPEA) to heterogeneous T cel
ls and mouse T cell clones were compared using proliferation assays. W
e report that there is marked variation between MHC haplotypes, which
can be ranked as follows: H2(z) > H2(s) = H2(f) = H2(p) = H2(r) = H2(k
) > H2(d) > H2(b) = H2(q). In some haplotypes both A and E molecules b
ind rSPEA with low affinity. In addition, we show that presentation is
preferentially by E molecules in haplotypes where A and E are co-expr
essed, but that A alleles also bind and present rSPEA, based on inhibi
tion of responses by anti-E and anti-A mAbs. Furthermore, using strain
s of mice which fail to express E, we demonstrate that A(s) and A(f) p
resent rSPEA with high efficiency, whereas A(q) and A(b) are the least
efficient of all haplotypes. The results suggest that there is signif
icant variation in the ability of different alleles of both E and A mo
lecules to bind and present rSPEA.