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. 2014 Jan;36(1):43-52.
doi: 10.1111/pim.12077.

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

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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

A Guilmot et al. Parasite Immunol. 2014 Jan.

Abstract

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.

Keywords: Interferon-gamma; T cell; Trypanosoma cruzi; human neonate and adult; innate immunity; natural killer cell.

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Figures

Figure 1
Figure 1
Kinetics of IFN-γ mRNA accumulation and protein secretion in/by cord and adult cells. Kinetics of IFN-γ mRNA accumulation and protein secretion following stimulation of PBMC (a,c,e) or CBMC (b,d,f) with Trypanosoma cruzi trypomastigotes at a ratio of 1 parasite per cell (a,b), IL-15 (20 ng/mL) (c,d) or both (e,f). mRNA amounts were calculated by the method of 2ΔΔCT in relation to unstimulated cells cultured for the same time and GAPDH. Results are shown as median of 5–6 independent experiments. †P < 0·05 as compared with the effect of IL-15 alone (Wilcoxon paired test), $P < 0·05 as compared with cord blood cells (Mann–Whitney U-test). CBMC, cord blood mononuclear cells; PBMC, peripheral blood mononuclear cells.
Figure 2
Figure 2
Kinetics of intracellular IFN-γ production in different CD56+ adult cells. Kinetics of IFN-γ production by CD56+ cells following stimulation of PBMC with Trypanosoma cruzi trypomastigotes at a ratio of 1 parasite per cell (a–d), IL-15 (20 ng/mL) (e–h) or both (i–l). Results are shown as box-and-whisker plots of proportions of blood CD56bright (a, e, i), CD56dim CD16+ (b, f, j), CD56dim CD16 (c, g, k) natural killer (NK) cells and CD3+CD56+ (d, h, l) NK-like T cells (n = 5). *P < 0·05 as compared with unstimulated cells, †P < 0·05 as compared with the effect of IL-15 alone (Wilcoxon paired test), $P < 0·05 as compared with cord blood cells (Mann–Whitney U-test). PBMC, peripheral blood mononuclear cells.
Figure 3
Figure 3
Kinetics of intracellular IFN-γ production in different CD56+ cord cells. Kinetics of IFN-γ production by CD56+ cells following stimulation of CBMC with Trypanosoma cruzi trypomastigotes at a ratio of 1 parasite per cell (a–d), IL-15 (20 ng/mL) (e–h) or both (i–l). Results are shown as box-and-whisker plots of proportions of blood CD56bright (a, e, i), CD56dim CD16+ (b, f, j), CD56dim CD16 (c, g, k) natural killer (NK) cells and CD3+CD56+ (d, h, l) NK-like T cells (n = 6). *P < 0·05 as compared with unstimulated cells, †P < 0·05 as compared with the effect of IL-15 alone (Wilcoxon paired test). CBMC, cord blood mononuclear cells.
Figure 4
Figure 4
IL-15 dose-dependent IFN-γ response by different cord blood natural killer (NK) cell subsets. IFN-γ production by NK cells following 24 h stimulation of CBMC with different concentrations of rhIL-15 (0–20 ng/mL) in the presence or absence of Trypanosoma cruzi trypomastigotes at a ratio of 1 parasite per cell. Results are shown as box-and-whisker plots of proportions of IFN-γ positive cells amongst blood CD56bright (a), CD56dim CD16+ (b) and CD56dim CD16 (C) NK cells (n = 6). †P < 0·05 as compared with the condition without parasite at the same concentration of IL-15 (Wilcoxon paired test). CBMC, cord blood mononuclear cells.
Figure 5
Figure 5
Relative proportions of different natural killer (NK) subsets, NK-like T cells and ‘classical’ T cells in total or IFN-γ+ mononuclear cells in adult and cord cells. Relative proportions of NK and T populations in total (a,b) or IFN-γ+ (c,d) adult (a,c) or neonatal (b,d) CD56+ and/or CD3+ mononuclear cells after 24 h stimulation with IL-15 and Trypanosoma cruzi. We determined the proportion of ‘classical’ T cells (CD3+CD56), natural killer (NK)-like T cells (CD56+CD3+) and the three subpopulations of NK cells (CD56+CD3): CD56bright CD16−/low cells, CD56dim CD16+ cells and CD56dim CD16 cells. Data are shown as medians of six donors. $P < 0·05 to neonates (Mann–Whitney U-test).

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References

    1. Torrico F, Heremans H, Rivera MT, Van Marck E, Billiau A. Carlier Y. Endogenous IFN-gamma is required for resistance to acute Trypanosoma cruzi infection in mice. J Immunol. 1991;146:3626–3632. - PubMed
    1. Shtrichman R. Samuel CE. The role of gamma interferon in antimicrobial immunity. Curr Opin Microbiol. 2001;4:251–259. - PubMed
    1. Cooper MA, Fehniger TA. Caligiuri MA. The biology of human natural killer-cell subsets. Trends Immunol. 2001;22:633–640. - PubMed
    1. Vitale M, Caruso A, Licenziati S, et al. Differential production of IFN-gamma, analyzed at the single-cell level, by specific subsets of human NK and T cells from healthy and HIV(+) subjects. Cytometry. 2000;39:189–194. - PubMed
    1. Godfrey DI. Kronenberg M. Going both ways: immune regulation via CD1d-dependent NKT cells. J Clin Invest. 2004;114:1379–1388. - PMC - PubMed

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