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ABSTRACT: Background
Neonatal Natural Killer (NK) cells show functional impairment and expansion of a CD56 negative population of uncertain significance.Methods
NK cells were isolated from cord blood and from adult donors. NK subpopulations were identified as positive or negative for the expression of CD56 and characterized for expression of granzyme B and surface markers by multi-parameter flow cytometry. Cell function was assessed by viral suppression and cytokine production using autologous lymphocytes infected with HIV. Activating (NKp30, NKp46) and inhibitory (Siglec-7) markers in healthy infants and adults were compared with viremic HIV-infected adults.Results
Cord blood contained increased frequencies of CD56 negative (CD56neg) NK cells with reduced expression of granzyme B and reduced production of IFN? and the CC-class chemokines RANTES, MIP1? and MIP1? upon stimulation. Both CD56pos and CD56neg NK subpopulations showed impaired viral suppression in cord blood, with impairment most marked in the CD56neg subset. CD56neg NK cells from cord blood and HIV-infected adults shared decreased inhibitory and activating receptor expression when compared with CD56pos cells.Conclusions
CD56neg NK cells are increased in number in normal infants and these effectors show reduced anti-viral activity. Like the expanded CD56neg population described in HIV-infected adults, these NK cells demonstrate functional impairments which may reflect inadequate development or activation.
SUBMITTER: Jacobson A
PROVIDER: S-EPMC3689709 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
Jacobson Amanda A Bell Frank F Lejarcegui Nicholas N Mitchell Caroline C Frenkel Lisa L Horton Helen H
PloS one 20130621 6
<h4>Background</h4>Neonatal Natural Killer (NK) cells show functional impairment and expansion of a CD56 negative population of uncertain significance.<h4>Methods</h4>NK cells were isolated from cord blood and from adult donors. NK subpopulations were identified as positive or negative for the expression of CD56 and characterized for expression of granzyme B and surface markers by multi-parameter flow cytometry. Cell function was assessed by viral suppression and cytokine production using autolo ...[more]