Cargando…

Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells

Natural killer (NK) cells belong to the innate immune system and protect against cancers and a variety of viruses including retroviruses by killing transformed or infected cells. They express activating and inhibitory receptors on their cell surface and often become activated after recognizing virus...

Descripción completa

Detalles Bibliográficos
Autores principales: Littwitz-Salomon, Elisabeth, Dittmer, Ulf, Sutter, Kathrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100108/
https://www.ncbi.nlm.nih.gov/pubmed/27821119
http://dx.doi.org/10.1186/s12977-016-0311-8
_version_ 1782466070877044736
author Littwitz-Salomon, Elisabeth
Dittmer, Ulf
Sutter, Kathrin
author_facet Littwitz-Salomon, Elisabeth
Dittmer, Ulf
Sutter, Kathrin
author_sort Littwitz-Salomon, Elisabeth
collection PubMed
description Natural killer (NK) cells belong to the innate immune system and protect against cancers and a variety of viruses including retroviruses by killing transformed or infected cells. They express activating and inhibitory receptors on their cell surface and often become activated after recognizing virus-infected cells. They have diverse antiviral effector functions like the release of cytotoxic granules, cytokine production and antibody dependent cellular cytotoxicity. The importance of NK cell activity in retroviral infections became evident due to the discovery of several viral strategies to escape recognition and elimination by NK cells. Mutational sequence polymorphisms as well as modulation of surface receptors and their ligands are mechanisms of the human immunodeficiency virus-1 to evade NK cell-mediated immune pressure. In Friend retrovirus infected mice the virus can manipulate molecular or cellular immune factors that in turn suppress the NK cell response. In this model NK cells lack cytokines for optimal activation and can be functionally suppressed by regulatory T cells. However, these inhibitory pathways can be overcome therapeutically to achieve full activation of NK cell responses and ultimately control dissemination of retroviral infection. One effective approach is to modulate the crosstalk between NK cells and dendritic cells, which produce NK cell-stimulating cytokines like type I interferons (IFN), IL-12, IL-15, and IL-18 upon retrovirus sensing or infection. Therapeutic administration of IFNα directly increases NK cell killing of retrovirus-infected cells. In addition, IL-2/anti-IL-2 complexes that direct IL-2 to NK cells have been shown to significantly improve control of retroviral infection by NK cells in vivo. In this review, we describe novel approaches to improve NK cell effector functions in retroviral infections. Immunotherapies that target NK cells of patients suffering from viral infections might be a promising treatment option for the future.
format Online
Article
Text
id pubmed-5100108
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-51001082016-11-08 Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells Littwitz-Salomon, Elisabeth Dittmer, Ulf Sutter, Kathrin Retrovirology Review Natural killer (NK) cells belong to the innate immune system and protect against cancers and a variety of viruses including retroviruses by killing transformed or infected cells. They express activating and inhibitory receptors on their cell surface and often become activated after recognizing virus-infected cells. They have diverse antiviral effector functions like the release of cytotoxic granules, cytokine production and antibody dependent cellular cytotoxicity. The importance of NK cell activity in retroviral infections became evident due to the discovery of several viral strategies to escape recognition and elimination by NK cells. Mutational sequence polymorphisms as well as modulation of surface receptors and their ligands are mechanisms of the human immunodeficiency virus-1 to evade NK cell-mediated immune pressure. In Friend retrovirus infected mice the virus can manipulate molecular or cellular immune factors that in turn suppress the NK cell response. In this model NK cells lack cytokines for optimal activation and can be functionally suppressed by regulatory T cells. However, these inhibitory pathways can be overcome therapeutically to achieve full activation of NK cell responses and ultimately control dissemination of retroviral infection. One effective approach is to modulate the crosstalk between NK cells and dendritic cells, which produce NK cell-stimulating cytokines like type I interferons (IFN), IL-12, IL-15, and IL-18 upon retrovirus sensing or infection. Therapeutic administration of IFNα directly increases NK cell killing of retrovirus-infected cells. In addition, IL-2/anti-IL-2 complexes that direct IL-2 to NK cells have been shown to significantly improve control of retroviral infection by NK cells in vivo. In this review, we describe novel approaches to improve NK cell effector functions in retroviral infections. Immunotherapies that target NK cells of patients suffering from viral infections might be a promising treatment option for the future. BioMed Central 2016-11-08 /pmc/articles/PMC5100108/ /pubmed/27821119 http://dx.doi.org/10.1186/s12977-016-0311-8 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Littwitz-Salomon, Elisabeth
Dittmer, Ulf
Sutter, Kathrin
Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title_full Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title_fullStr Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title_full_unstemmed Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title_short Insufficient natural killer cell responses against retroviruses: how to improve NK cell killing of retrovirus-infected cells
title_sort insufficient natural killer cell responses against retroviruses: how to improve nk cell killing of retrovirus-infected cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100108/
https://www.ncbi.nlm.nih.gov/pubmed/27821119
http://dx.doi.org/10.1186/s12977-016-0311-8
work_keys_str_mv AT littwitzsalomonelisabeth insufficientnaturalkillercellresponsesagainstretroviruseshowtoimprovenkcellkillingofretrovirusinfectedcells
AT dittmerulf insufficientnaturalkillercellresponsesagainstretroviruseshowtoimprovenkcellkillingofretrovirusinfectedcells
AT sutterkathrin insufficientnaturalkillercellresponsesagainstretroviruseshowtoimprovenkcellkillingofretrovirusinfectedcells