Cargando…

Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques

Natural killer (NK) cells classically typify the nonspecific effector arm of the innate immune system, but have recently been shown to possess memory-like properties against multiple viral infections, most notably CMV. Expression of the activating receptor NKG2C is elevated on human NK cells in resp...

Descripción completa

Detalles Bibliográficos
Autores principales: Ram, Daniel R., Manickam, Cordelia, Hueber, Brady, Itell, Hannah L., Permar, Sallie R., Varner, Valerie, Reeves, R. Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997355/
https://www.ncbi.nlm.nih.gov/pubmed/29851983
http://dx.doi.org/10.1371/journal.ppat.1007104
_version_ 1783331027887849472
author Ram, Daniel R.
Manickam, Cordelia
Hueber, Brady
Itell, Hannah L.
Permar, Sallie R.
Varner, Valerie
Reeves, R. Keith
author_facet Ram, Daniel R.
Manickam, Cordelia
Hueber, Brady
Itell, Hannah L.
Permar, Sallie R.
Varner, Valerie
Reeves, R. Keith
author_sort Ram, Daniel R.
collection PubMed
description Natural killer (NK) cells classically typify the nonspecific effector arm of the innate immune system, but have recently been shown to possess memory-like properties against multiple viral infections, most notably CMV. Expression of the activating receptor NKG2C is elevated on human NK cells in response to infection with CMV as well as HIV, and may delineate cells with memory and memory-like functions. A better understanding of how NKG2C+ NK cells specifically respond to these pathogens could be significantly advanced using nonhuman primate (NHP) models but, to date, it has not been possible to distinguish NKG2C from its inhibitory counterpart, NKG2A, in NHP because of unfaithful antibody cross-reactivity. Using novel RNA-based flow cytometry, we identify for the first time true memory NKG2C+ NK cells in NHP by gene expression (KLRC2), and show that these cells have elevated frequencies and diversify their functional repertoire specifically in response to rhCMV and SIV infections.
format Online
Article
Text
id pubmed-5997355
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-59973552018-06-21 Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques Ram, Daniel R. Manickam, Cordelia Hueber, Brady Itell, Hannah L. Permar, Sallie R. Varner, Valerie Reeves, R. Keith PLoS Pathog Research Article Natural killer (NK) cells classically typify the nonspecific effector arm of the innate immune system, but have recently been shown to possess memory-like properties against multiple viral infections, most notably CMV. Expression of the activating receptor NKG2C is elevated on human NK cells in response to infection with CMV as well as HIV, and may delineate cells with memory and memory-like functions. A better understanding of how NKG2C+ NK cells specifically respond to these pathogens could be significantly advanced using nonhuman primate (NHP) models but, to date, it has not been possible to distinguish NKG2C from its inhibitory counterpart, NKG2A, in NHP because of unfaithful antibody cross-reactivity. Using novel RNA-based flow cytometry, we identify for the first time true memory NKG2C+ NK cells in NHP by gene expression (KLRC2), and show that these cells have elevated frequencies and diversify their functional repertoire specifically in response to rhCMV and SIV infections. Public Library of Science 2018-05-31 /pmc/articles/PMC5997355/ /pubmed/29851983 http://dx.doi.org/10.1371/journal.ppat.1007104 Text en © 2018 Ram et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ram, Daniel R.
Manickam, Cordelia
Hueber, Brady
Itell, Hannah L.
Permar, Sallie R.
Varner, Valerie
Reeves, R. Keith
Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title_full Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title_fullStr Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title_full_unstemmed Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title_short Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV+ and rhCMV+ rhesus macaques
title_sort tracking klrc2 (nkg2c)+ memory-like nk cells in siv+ and rhcmv+ rhesus macaques
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997355/
https://www.ncbi.nlm.nih.gov/pubmed/29851983
http://dx.doi.org/10.1371/journal.ppat.1007104
work_keys_str_mv AT ramdanielr trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT manickamcordelia trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT hueberbrady trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT itellhannahl trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT permarsallier trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT varnervalerie trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques
AT reevesrkeith trackingklrc2nkg2cmemorylikenkcellsinsivandrhcmvrhesusmacaques