The OX22 monoclonal antibody recognizes the high molecular weight form
of the CD45 molecule on rat T cells encoded by the CD45RC exon of the
leukocyte common antigen gene. Its expression on CD4+ T cells is asso
ciated with virgin unprimed cells and primed cells which produce IL-2
and IFN-gamma on stimulation and participate in cell-mediated immune r
eactions. This suggested that CD45RC expression may be useful as a phe
notypic marker for cells expressing Th1 function. In view of our previ
ous data indicating heterogeneity of T-cell helper function in differe
nt lymphoid compartments in the gut, the helper activity of OX22-enric
hed or OX22-depleted cell populations prepared from Peyer's patches (P
P) of rats was compared. Following intestinal immunization with keyhol
e limpet haemocyanin, PP cells were isolated and separated by panning.
Recovery data indicated that the majority of T cells in rat PP expres
s the OX22+ phenotype and, after separation, the OX22-enriched populat
ion contained 4 times as many cells as the OX22-depleted population. F
unctional studies revealed that both subsets were capable of providing
cognate help for secondary IgM, IgG and IgA antibody responses indica
ting that on this basis the CD45RC marker does not correlate with Th1
function in rats.