Differential IFN-γ production by adult and neonatal blood CD56+ natural killer (NK) and NK-like-T cells in response to Trypanosoma cruzi and IL-15
Autor: | Guilmot, A, Carlier, Y, Truyens, C |
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Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
Adult
Interleukin-15 human neonate and adult Trypanosoma cruzi Infant Newborn T cell chemical and pharmacologic phenomena Original Articles natural killer cell Fetal Blood Flow Cytometry CD56 Antigen Killer Cells Natural Interferon-gamma Kinetics T-Lymphocyte Subsets Humans Chagas Disease RNA Messenger innate immunity |
Zdroj: | Parasite Immunology |
ISSN: | 1365-3024 0141-9838 |
Popis: | Early interferon-gamma (IFN-γ) release by innate cells is critical to direct type 1 immune response able to control intracellular pathogens like Trypanosoma cruzi. Although CD56(bright) natural killer (NK) cells are reported to be potent early IFN-γ producers, other CD56(+) cells like CD56(dim) NK cells and NK-like T cells have recently been shown to also release IFN-γ. We have here studied the contribution of each CD56(+) lymphocyte populations in early IFN-γ production in both adults and neonates. On this purpose, we analysed the kinetics of IFN-γ production by RT-PCR, ELISA and flow cytometry from 2 h onwards after T. cruzi and IL-15 stimulation and sought for the responding CD56(+) cells. CD56(bright) and CD56(dim) CD16(-) NK cells were the more potent IFN-γ early producers in response to IL-15 and parasites in adults and neonates. In both age groups, the majority of IFN-γ producing cells were NK cells. However, on the contrary to neonates, CD3(+) CD56(+) NK-like T cells and CD3(+) CD56(-) 'classical' T cells also contributed to early IFN-γ production in adults. Altogether, our results support that whereas NK cells responded almost similarly in neonates and adults, cord blood innate CD56(+) and CD56(-) T cells displayed major quantitative and qualitative defects that could contribute to the well-known neonatal immune immaturity. |
Databáze: | OpenAIRE |
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