Peptide-specific recognition of human cytomegalovirus strains controls adaptive natural killer cells
- Creators
- Hammer, Quirin
- Rückert, Timo
- Borst, Eva Maria
- Dunst, Josefine
- Haubner, André
- Durek, Pawel
- Heinrich, Frederik
- Gasparoni, Gilles
- Babic, Marina
- Tomic, Adriana
- Pietra, Gabriella
- Nienen, Mikalai
- Blau, Igor Wolfgang
- Hofmann, Jörg
- Na, Il-Kang
- Prinz, Immo
- Koenecke, Christian
- Hemmati, Philipp
- Babel, Nina
- Arnold, Renate
- Walter, Jörn
- Thurley, Kevin
- Mashreghi, Mir-Farzin
- Messerle, Martin
- Romagnani, Chiara
- Others:
- Hammer, Quirin
- Rückert, Timo
- Borst, Eva Maria
- Dunst, Josefine
- Haubner, André
- Durek, Pawel
- Heinrich, Frederik
- Gasparoni, Gille
- Babic, Marina
- Tomic, Adriana
- Pietra, Gabriella
- Nienen, Mikalai
- Blau, Igor Wolfgang
- Hofmann, Jörg
- Na, Il-Kang
- Prinz, Immo
- Koenecke, Christian
- Hemmati, Philipp
- Babel, Nina
- Arnold, Renate
- Walter, Jörn
- Thurley, Kevin
- Mashreghi, Mir-Farzin
- Messerle, Martin
- Romagnani, Chiara
Description
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.
Additional details
- URL
- http://hdl.handle.net/11567/917443
- URN
- urn:oai:iris.unige.it:11567/917443
- Origin repository
- UNIGE