@article{22072, keywords = {Adult, Coinfection, Female, HIV Infections, HIV-1, Humans, leprosy, Lymphocyte Count, Male, Middle Aged, tratamento, Natural Killer T-Cells, Young Adult}, author = {Tomimori J and Xavier M and Maeda SM and Carvalho KI and Kallas EG and Bruno FR and Snyder-Cappione J and Haslett P and Nixon D}, title = {Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients.}, abstract = {
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.
}, year = {2012}, journal = {Immunology}, volume = {136}, pages = {96-102}, month = {2012 May}, publisher = {Blackwell Publishing Ltd}, address = {Oxford}, issn = {1365-2567}, doi = {10.1111/j.1365-2567.2012.03563.x}, language = {eng}, }