When looking at T-cell populations in PCa, studies have noted the presence of CD8+ CD25+ Treg cell clones that expressed FoxP3 and suppressed naive T-cell proliferation in prostate tumor-derived TILs, and there was a significant correlation between CD3+, CD8+, and FOXP3+ T-cell densities, but these were not associated with most clinical or pathologic variables. Here, CD8A is linked to prostate neoplasm.