The non-classical HLA class I molecule HFE does not influence the NK-like activity contained in fresh human PBMCs and does not interact with NK cells

Steve Pascolo*, Florent Ginhoux, Nihay Laham, Steffen Walter, Oliver Schoor, Jochen Probst, Pierre Rohrlich, Florian Obermayr, Paul Fisch, Olivier Danos, Rachel Ehrlich, Francois A. Lemonnier, Hans Georg Rammensee

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

In humans, four β2-microglobulin-associated non-classical class I molecules are encoded in the MHC: HLA-E, -F, -G and -H. Three of them (HLA-E, -F and -G) were shown to inhibit NK activity. On the contrary, the fourth one, HLA-H, named HFE after it was found to be mutated in patients suffering from inherited hemochromatosis, has been shown to be involved only in the regulation of iron uptake. We tested the capacity of HFE to affect (enhance or reduce) specifically the NK activity contained in non-manipulated fresh human PBMCs. We showed that HFE expression by target cells does not affect their killing by the NK-like activity contained in PBMCs. Moreover, using fluorescent HFE tetramers, we could confirm that blood NK cells as well as blood γδ T cells do not bind HFE. Altogether, our data indicate that HFE does not affect the NK activity contained in the PBMCs.

Original languageEnglish
Pages (from-to)117-122
Number of pages6
JournalInternational Immunology
Volume17
Issue number2
DOIs
StatePublished - Feb 2005

Funding

FundersFunder number
HFE
European CommissionQLQ1-CT-1999-00665

    Keywords

    • HFE
    • Iron metabolism
    • NK cells
    • Non-classical MHC class I
    • Tetramer

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