02638nas a2200337 4500000000100000008004100001260000900042653002400051653001300075653003200088653001100120653002400131653001200155653002500167653002500192653001600217653002800233653001400261653001500275653001700290653001200307100001300319700001500332700001600347700001200363245008700375300001100462490000700473520180600480022001402286 1990 d c199010aAmino Acid Sequence10aBacteria10aBlood Bactericidal Activity10aHumans10aIn Vitro Techniques10aleprosy10aLeprosy, lepromatous10aLeprosy, Tuberculoid10aMacrophages10aMolecular Sequence Data10aMonocytes10aPhagocytes10aPhagocytosis10aTuftsin1 aIyer R R1 aPrasad H K1 aBhutani L K1 aRao D N00aModulation of human lepromatous monocyte-macrophage functions in vitro by tuftsin. a847-580 v123 a

Human peripheral blood monocytes/macrophages derived from normal donors, patients of tuberculoid leprosy (BT/TT) and lepromatous leprosy (BL/LL) were assayed for stimulated phagocytic responses to the potent macrophage stimulator "Tuftsin" (NH2-Thr-Lys-Pro-Arg-OH) after varying periods (6 h to 14 days) of culture in vitro. The assays consisted of visual scoring of ingested Mycobacterium leprae and radiometric measurement of ingested 14C-acetate labelled Staphylococcus aureus and Mycobacterium tuberculosis (H37Ra). While normal and BT/TT macrophages showed a progressively increasing ability for tuftsin-stimulated phagocytosis with increasing age of culture in vitro, BL/LL macrophages showed the opposite response so that 14-day cultures were refractory to a stimulatory dose of up to 7.0 microM (10 to 20 times the optimal dose for normal and BT/TT macrophages). The 14-day BL/LL macrophage cultures were, however, responsive to 35 microM tuftsin (100 times the optimal dose for normal macrophages). Analysis of the dose-response curves also indicates that BT/TT cultures despite exhibiting an apparent similarity to normal macrophages demonstrate a rightward shift for a maximal stimulated phagocytosis. Finally SEM photo-micrographs of 14-day macrophage cultures of the three groups revealed that while normal and BT/TT cultures demonstrated an increase in membrane ruffling and filopodia on stimulation with 0.8 microM tuftsin, BL/LL cultures exhibited none of the features associated with stimulation. From the above findings, we conclude that lepromatous macrophages may display an aberrant differentiation profile leading to a terminal state of unresponsiveness and that the defect may possibly lie at the level of tuftsin receptor expression or transmembrane signal transduction.

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