. These results confirm that NO plays a significant role as an effector molecule used by normal human AMs, but this capacity is suppressed in AMs from MS and CS because of a lack of intrinsic cytokine priming.Nitric oxide (NO) acts as an important effector molecule in activated rodent macrophages, and its inhibition reduces macrophage responses against fungi, bacteria, parasites, and tumor cells [1]. In addition to this role in innate immunity, NO functions as an important signaling and regulatory molecule in