Interleukin-2 from Adaptive T Cells Enhances Natural Killer Cell Activity against Human Cytomegalovirus-Infected Macrophages
Control of human cytomegalovirus (HCMV) requires a continuous immune surveillance, thus HCMV is the most important viral pathogen in severely immunocompromised individuals. Both innate and adaptive immunity contribute to the control of HCMV. Here, we report that peripheral blood natural killer cells...
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Veröffentlicht in: | Journal of virology 2015-06, Vol.89 (12), p.6435-6441 |
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description | Control of human cytomegalovirus (HCMV) requires a continuous immune surveillance, thus HCMV is the most important viral pathogen in severely immunocompromised individuals. Both innate and adaptive immunity contribute to the control of HCMV. Here, we report that peripheral blood natural killer cells (PBNKs) from HCMV-seropositive donors showed an enhanced activity toward HCMV-infected autologous macrophages. However, this enhanced response was abolished when purified NK cells were applied as effectors. We demonstrate that this enhanced PBNK activity was dependent on the interleukin-2 (IL-2) secretion of CD4(+) T cells when reexposed to the virus. Purified T cells enhanced the activity of purified NK cells in response to HCMV-infected macrophages. This effect could be suppressed by IL-2 blocking. Our findings not only extend the knowledge on the immune surveillance in HCMV-namely, that NK cell-mediated innate immunity can be enhanced by a preexisting T cell antiviral immunity-but also indicate a potential clinical implication for patients at risk for severe HCMV manifestations due to immunosuppressive drugs, which mainly suppress IL-2 production and T cell responsiveness.
Human cytomegalovirus (HCMV) is never cleared by the host after primary infection but instead establishes a lifelong latent infection with possible reactivations when the host's immunity becomes suppressed. Both innate immunity and adaptive immunity are important for the control of viral infections. Natural killer (NK) cells are main innate effectors providing a rapid response to virus-infected cells. Virus-specific T cells are the main adaptive effectors that are critical for the control of the latent infection and limitation of reinfection. In this study, we found that IL-2 secreted by adaptive CD4(+) T cells after reexposure to HCMV enhances the activity of NK cells in response to HCMV-infected target cells. This is the first direct evidence that the adaptive T cells can help NK cells to act against HCMV infection. |
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Human cytomegalovirus (HCMV) is never cleared by the host after primary infection but instead establishes a lifelong latent infection with possible reactivations when the host's immunity becomes suppressed. Both innate immunity and adaptive immunity are important for the control of viral infections. Natural killer (NK) cells are main innate effectors providing a rapid response to virus-infected cells. Virus-specific T cells are the main adaptive effectors that are critical for the control of the latent infection and limitation of reinfection. In this study, we found that IL-2 secreted by adaptive CD4(+) T cells after reexposure to HCMV enhances the activity of NK cells in response to HCMV-infected target cells. This is the first direct evidence that the adaptive T cells can help NK cells to act against HCMV infection.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.00435-15</identifier><identifier>PMID: 25855747</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>CD4-Positive T-Lymphocytes - immunology ; Cells, Cultured ; Cytomegalovirus Infections - immunology ; Human cytomegalovirus ; Humans ; Interleukin-2 - secretion ; Killer Cells, Natural - immunology ; Macrophages - virology ; Virus-Cell Interactions</subject><ispartof>Journal of virology, 2015-06, Vol.89 (12), p.6435-6441</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-5fc55adc7b547ab971412605ccdd483da043a120066f2dbfab4f29ea69e809753</citedby><cites>FETCH-LOGICAL-c417t-5fc55adc7b547ab971412605ccdd483da043a120066f2dbfab4f29ea69e809753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474314/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474314/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25855747$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Zeguang</creatorcontrib><creatorcontrib>Frascaroli, Giada</creatorcontrib><creatorcontrib>Bayer, Carina</creatorcontrib><creatorcontrib>Schmal, Tatjana</creatorcontrib><creatorcontrib>Mertens, Thomas</creatorcontrib><title>Interleukin-2 from Adaptive T Cells Enhances Natural Killer Cell Activity against Human Cytomegalovirus-Infected Macrophages</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>Control of human cytomegalovirus (HCMV) requires a continuous immune surveillance, thus HCMV is the most important viral pathogen in severely immunocompromised individuals. Both innate and adaptive immunity contribute to the control of HCMV. Here, we report that peripheral blood natural killer cells (PBNKs) from HCMV-seropositive donors showed an enhanced activity toward HCMV-infected autologous macrophages. However, this enhanced response was abolished when purified NK cells were applied as effectors. We demonstrate that this enhanced PBNK activity was dependent on the interleukin-2 (IL-2) secretion of CD4(+) T cells when reexposed to the virus. Purified T cells enhanced the activity of purified NK cells in response to HCMV-infected macrophages. This effect could be suppressed by IL-2 blocking. Our findings not only extend the knowledge on the immune surveillance in HCMV-namely, that NK cell-mediated innate immunity can be enhanced by a preexisting T cell antiviral immunity-but also indicate a potential clinical implication for patients at risk for severe HCMV manifestations due to immunosuppressive drugs, which mainly suppress IL-2 production and T cell responsiveness.
Human cytomegalovirus (HCMV) is never cleared by the host after primary infection but instead establishes a lifelong latent infection with possible reactivations when the host's immunity becomes suppressed. Both innate immunity and adaptive immunity are important for the control of viral infections. Natural killer (NK) cells are main innate effectors providing a rapid response to virus-infected cells. Virus-specific T cells are the main adaptive effectors that are critical for the control of the latent infection and limitation of reinfection. In this study, we found that IL-2 secreted by adaptive CD4(+) T cells after reexposure to HCMV enhances the activity of NK cells in response to HCMV-infected target cells. This is the first direct evidence that the adaptive T cells can help NK cells to act against HCMV infection.</description><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>Cells, Cultured</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Human cytomegalovirus</subject><subject>Humans</subject><subject>Interleukin-2 - secretion</subject><subject>Killer Cells, Natural - immunology</subject><subject>Macrophages - virology</subject><subject>Virus-Cell Interactions</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0Eokvhxhn5yIEU27Hj5IK0WhW6tMClIG7WxJnsGhJnsZ2VVuLH436qnHqawzx6Nc-8hLzm7IRzUb___GN9wpgsVcHVE7LgrKkLpbh8ShaMCVGosv55RF7E-IsxLmUln5MjoWqltNQL8nftE4YB59_OF4L2YRrpsoNdcnukl3SFwxDpqd-CtxjpV0hzgIGeu2HAcL2lS5tZlw4UNuB8TPRsHsHT1SFNI25gmPYuzLFY-x5two5-ARum3RY2GF-SZz0MEV_dzmPy_ePp5eqsuPj2ab1aXhRWcp0K1VuloLO6VVJD22guuaiYsrbrZF12kO2BC8aqqhdd20Mre9EgVA3WrNGqPCYfbnJ3cztiZ9GnbGF2wY0QDmYCZ_7feLc1m2lvpNSy5DIHvL0NCNOfGWMyo4s224PHaY6G6_xaXam6fBytat5wViqd0Xc3aH5IjAH7-4s4M1fdmtytue7W8CuLNw8t7uG7Mst_LVyhcA</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Wu, Zeguang</creator><creator>Frascaroli, Giada</creator><creator>Bayer, Carina</creator><creator>Schmal, Tatjana</creator><creator>Mertens, Thomas</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20150601</creationdate><title>Interleukin-2 from Adaptive T Cells Enhances Natural Killer Cell Activity against Human Cytomegalovirus-Infected Macrophages</title><author>Wu, Zeguang ; Frascaroli, Giada ; Bayer, Carina ; Schmal, Tatjana ; Mertens, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-5fc55adc7b547ab971412605ccdd483da043a120066f2dbfab4f29ea69e809753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>Cells, Cultured</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Human cytomegalovirus</topic><topic>Humans</topic><topic>Interleukin-2 - secretion</topic><topic>Killer Cells, Natural - immunology</topic><topic>Macrophages - virology</topic><topic>Virus-Cell Interactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Zeguang</creatorcontrib><creatorcontrib>Frascaroli, Giada</creatorcontrib><creatorcontrib>Bayer, Carina</creatorcontrib><creatorcontrib>Schmal, Tatjana</creatorcontrib><creatorcontrib>Mertens, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Zeguang</au><au>Frascaroli, Giada</au><au>Bayer, Carina</au><au>Schmal, Tatjana</au><au>Mertens, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-2 from Adaptive T Cells Enhances Natural Killer Cell Activity against Human Cytomegalovirus-Infected Macrophages</atitle><jtitle>Journal of virology</jtitle><addtitle>J Virol</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>89</volume><issue>12</issue><spage>6435</spage><epage>6441</epage><pages>6435-6441</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>Control of human cytomegalovirus (HCMV) requires a continuous immune surveillance, thus HCMV is the most important viral pathogen in severely immunocompromised individuals. Both innate and adaptive immunity contribute to the control of HCMV. Here, we report that peripheral blood natural killer cells (PBNKs) from HCMV-seropositive donors showed an enhanced activity toward HCMV-infected autologous macrophages. However, this enhanced response was abolished when purified NK cells were applied as effectors. We demonstrate that this enhanced PBNK activity was dependent on the interleukin-2 (IL-2) secretion of CD4(+) T cells when reexposed to the virus. Purified T cells enhanced the activity of purified NK cells in response to HCMV-infected macrophages. This effect could be suppressed by IL-2 blocking. Our findings not only extend the knowledge on the immune surveillance in HCMV-namely, that NK cell-mediated innate immunity can be enhanced by a preexisting T cell antiviral immunity-but also indicate a potential clinical implication for patients at risk for severe HCMV manifestations due to immunosuppressive drugs, which mainly suppress IL-2 production and T cell responsiveness.
Human cytomegalovirus (HCMV) is never cleared by the host after primary infection but instead establishes a lifelong latent infection with possible reactivations when the host's immunity becomes suppressed. Both innate immunity and adaptive immunity are important for the control of viral infections. Natural killer (NK) cells are main innate effectors providing a rapid response to virus-infected cells. Virus-specific T cells are the main adaptive effectors that are critical for the control of the latent infection and limitation of reinfection. In this study, we found that IL-2 secreted by adaptive CD4(+) T cells after reexposure to HCMV enhances the activity of NK cells in response to HCMV-infected target cells. This is the first direct evidence that the adaptive T cells can help NK cells to act against HCMV infection.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>25855747</pmid><doi>10.1128/JVI.00435-15</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | CD4-Positive T-Lymphocytes - immunology Cells, Cultured Cytomegalovirus Infections - immunology Human cytomegalovirus Humans Interleukin-2 - secretion Killer Cells, Natural - immunology Macrophages - virology Virus-Cell Interactions |
title | Interleukin-2 from Adaptive T Cells Enhances Natural Killer Cell Activity against Human Cytomegalovirus-Infected Macrophages |
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