Peptide-specific recognition of human cytomegalovirus strains controls adaptive natural killer cells View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-05

AUTHORS

Quirin Hammer, Timo Rückert, Eva Maria Borst, Josefine Dunst, André Haubner, Pawel Durek, Frederik Heinrich, Gilles Gasparoni, Marina Babic, Adriana Tomic, Gabriella Pietra, Mikalai Nienen, Igor Wolfgang Blau, Jörg Hofmann, Il-Kang Na, Immo Prinz, Christian Koenecke, Philipp Hemmati, Nina Babel, Renate Arnold, Jörn Walter, Kevin Thurley, Mir-Farzin Mashreghi, Martin Messerle, Chiara Romagnani

ABSTRACT

Natural killer (NK) cells are innate lymphocytes that lack antigen-specific rearranged receptors, a hallmark of adaptive lymphocytes. In some people infected with human cytomegalovirus (HCMV), an NK cell subset expressing the activating receptor NKG2C undergoes clonal-like expansion that partially resembles anti-viral adaptive responses. However, the viral ligand that drives the activation and differentiation of adaptive NKG2C+ NK cells has remained unclear. Here we found that adaptive NKG2C+ NK cells differentially recognized distinct HCMV strains encoding variable UL40 peptides that, in combination with pro-inflammatory signals, controlled the population expansion and differentiation of adaptive NKG2C+ NK cells. Thus, we propose that polymorphic HCMV peptides contribute to shaping of the heterogeneity of adaptive NKG2C+ NK cell populations among HCMV-seropositive people. More... »

PAGES

453-463

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41590-018-0082-6

DOI

http://dx.doi.org/10.1038/s41590-018-0082-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1103191381

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29632329


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