02633nas a2200385   4500000000100000008004100001260004700042653001000089653001600099653001100115653001900126653001000145653001100155653001200166653002100178653000900199653001600208653001500224653002700239653001600266100001500282700001300297700001300310700001600323700001400339700001300353700002200366700001400388700001200402245010000414300001100514490000800525520170000533022001402233       2012                            d  c2012 MaybBlackwell Publishing LtdaOxford10aAdult10aCoinfection10aFemale10aHIV Infections10aHIV-110aHumans10aleprosy10aLymphocyte Count10aMale10aMiddle Aged10atratamento10aNatural Killer T-Cells10aYoung Adult1 aTomimori J1 aXavier M1 aMaeda SM1 aCarvalho KI1 aKallas EG1 aBruno FR1 aSnyder-Cappione J1 aHaslett P1 aNixon D00aLower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients.  a96-1020 v1363 a<p>Natural killer T (NKT) cells are a heterogeneous population of lymphocytes that recognize antigens presented by CD1d and have attracted attention because of their potential role linking innate and adaptive immune responses. Peripheral NKT cells display a memory-activated phenotype and can rapidly secrete large amounts of pro-inflammatory cytokines upon antigenic activation. In this study, we evaluated NKT cells in the context of patients co-infected with HIV-1 and Mycobacterium leprae. The volunteers were enrolled into four groups: 22 healthy controls, 23 HIV-1-infected patients, 20 patients with leprosy and 17 patients with leprosy and HIV-1-infection. Flow cytometry and ELISPOT assays were performed on peripheral blood mononuclear cells. We demonstrated that patients co-infected with HIV-1 and M. leprae have significantly lower NKT cell frequencies [median 0.022%, interquartile range (IQR): 0.007-0.051] in the peripheral blood when compared with healthy subjects (median 0.077%, IQR: 0.032-0.405, P < 0.01) or HIV-1 mono-infected patients (median 0.072%, IQR: 0.030-0.160, P < 0.05). Also, more NKT cells from co-infected patients secreted interferon-γ after stimulation with DimerX, when compared with leprosy mono-infected patients (P = 0.05). These results suggest that NKT cells are decreased in frequency in HIV-1 and M. leprae co-infected patients compared with HIV-1 mono-infected patients alone, but are at a more activated state. Innate immunity in human subjects is strongly influenced by their spectrum of chronic infections, and in HIV-1-infected subjects, a concurrent mycobacterial infection probably hyper-activates and lowers circulating NKT cell numbers.</p>  a1365-2567