Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors
Natural killer (NK) cells, key antitumor effectors of the innate immune system, are endowed with the unique ability to spontaneously eliminate cells undergoing a neoplastic transformation. Given their broad reactivity against diverse types of cancer and close association with cancer prognosis, NK ce...
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Veröffentlicht in: | BMB reports 2021-01, Vol.54 (1), p.44-58 |
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description | Natural killer (NK) cells, key antitumor effectors of the innate immune system, are endowed with the unique ability to spontaneously eliminate cells undergoing a neoplastic transformation. Given their broad reactivity against diverse types of cancer and close association with cancer prognosis, NK cells have gained considerable attention as a promising therapeutic target for cancer immunotherapy. NK cell-based therapies have demonstrated favorable clinical efficacies in several hematological malignancies but limited success in solid tumors, thus highlighting the need to develop new therapeutic strategies to restore and optimize anti-tumor activity while preventing tumor immune escape. The current therapeutic modalities yielding encouraging results in clinical trials include the blockade of immune checkpoint receptors to overcome the immune-evasion mechanism used by tumors and the incorporation of tumor-directed chimeric antigen receptors to enhance NK cell anti-tumor specificity and activity. These observations, together with recent advances in the understanding of NK cell activation within the tumor microenvironment, will facilitate the optimal design of NK cell-based therapy against a broad range of cancers and, more desirably, refractory cancers. [BMB Reports 2021; 54(1): 44-58] |
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Given their broad reactivity against diverse types of cancer and close association with cancer prognosis, NK cells have gained considerable attention as a promising therapeutic target for cancer immunotherapy. NK cell-based therapies have demonstrated favorable clinical efficacies in several hematological malignancies but limited success in solid tumors, thus highlighting the need to develop new therapeutic strategies to restore and optimize anti-tumor activity while preventing tumor immune escape. The current therapeutic modalities yielding encouraging results in clinical trials include the blockade of immune checkpoint receptors to overcome the immune-evasion mechanism used by tumors and the incorporation of tumor-directed chimeric antigen receptors to enhance NK cell anti-tumor specificity and activity. These observations, together with recent advances in the understanding of NK cell activation within the tumor microenvironment, will facilitate the optimal design of NK cell-based therapy against a broad range of cancers and, more desirably, refractory cancers. [BMB Reports 2021; 54(1): 44-58]</description><identifier>ISSN: 1976-6696</identifier><identifier>EISSN: 1976-670X</identifier><language>kor</language><publisher>생화학분자생물학회</publisher><subject>Cancer immunotherapy ; Chimeric antigen receptors ; Immune checkpoint receptors ; Immune escape ; Natural killer cells</subject><ispartof>BMB reports, 2021-01, Vol.54 (1), p.44-58</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881</link.rule.ids></links><search><creatorcontrib>Kim, Nayoung</creatorcontrib><creatorcontrib>Lee, Dong-Hee</creatorcontrib><creatorcontrib>Choi, Woo Seon</creatorcontrib><creatorcontrib>Yi, Eunbi</creatorcontrib><creatorcontrib>Kim, HyoJeong</creatorcontrib><creatorcontrib>Kim, Jung Min</creatorcontrib><creatorcontrib>Jin, Hyung-Seung</creatorcontrib><creatorcontrib>Kim, Hun Sik</creatorcontrib><title>Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors</title><title>BMB reports</title><addtitle>BMB Reports</addtitle><description>Natural killer (NK) cells, key antitumor effectors of the innate immune system, are endowed with the unique ability to spontaneously eliminate cells undergoing a neoplastic transformation. Given their broad reactivity against diverse types of cancer and close association with cancer prognosis, NK cells have gained considerable attention as a promising therapeutic target for cancer immunotherapy. NK cell-based therapies have demonstrated favorable clinical efficacies in several hematological malignancies but limited success in solid tumors, thus highlighting the need to develop new therapeutic strategies to restore and optimize anti-tumor activity while preventing tumor immune escape. The current therapeutic modalities yielding encouraging results in clinical trials include the blockade of immune checkpoint receptors to overcome the immune-evasion mechanism used by tumors and the incorporation of tumor-directed chimeric antigen receptors to enhance NK cell anti-tumor specificity and activity. These observations, together with recent advances in the understanding of NK cell activation within the tumor microenvironment, will facilitate the optimal design of NK cell-based therapy against a broad range of cancers and, more desirably, refractory cancers. [BMB Reports 2021; 54(1): 44-58]</description><subject>Cancer immunotherapy</subject><subject>Chimeric antigen receptors</subject><subject>Immune checkpoint receptors</subject><subject>Immune escape</subject><subject>Natural killer cells</subject><issn>1976-6696</issn><issn>1976-670X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNpFjLtOwzAYhSMEElXpE7B4YYzk-G62qgJKW9GlA1vkOL8bK4kT2WHo2xOpXKbznYvOTbYotBS5kPjz9peFFvfZKiVfYcYkLaTGi6zZmhhgDsMZfeyRha5LyA0RWRMsROT7_isMUwPRjJfnqwVkG7DtOPgwoQgWxmmICZlQz4XvIXo7m8mfIfzXD9mdM12C1Y8us9Pry2mzzQ_Ht_fN-pC3HJO8JhSoE9RoR2QlOHOgnNSiImomIAUoKjTDWGFcW1xrw6AqjDSWCUEEpcvs6Xrb-jT5MtSpK3fr_ZFgUmBZcC0lV4zMu8e_XSrH6HsTLyVVnHJN6Dd3yF4v</recordid><startdate>20210131</startdate><enddate>20210131</enddate><creator>Kim, Nayoung</creator><creator>Lee, Dong-Hee</creator><creator>Choi, Woo Seon</creator><creator>Yi, Eunbi</creator><creator>Kim, HyoJeong</creator><creator>Kim, Jung Min</creator><creator>Jin, Hyung-Seung</creator><creator>Kim, Hun Sik</creator><general>생화학분자생물학회</general><scope>HZB</scope><scope>Q5X</scope><scope>JDI</scope></search><sort><creationdate>20210131</creationdate><title>Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors</title><author>Kim, Nayoung ; Lee, Dong-Hee ; Choi, Woo Seon ; Yi, Eunbi ; Kim, HyoJeong ; Kim, Jung Min ; Jin, Hyung-Seung ; Kim, Hun Sik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-k502-d23e3f63a9f27b654fe8f796b28fe8e21e8369400800dc0d9a4eb1a7ac4662633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2021</creationdate><topic>Cancer immunotherapy</topic><topic>Chimeric antigen receptors</topic><topic>Immune checkpoint receptors</topic><topic>Immune escape</topic><topic>Natural killer cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Nayoung</creatorcontrib><creatorcontrib>Lee, Dong-Hee</creatorcontrib><creatorcontrib>Choi, Woo Seon</creatorcontrib><creatorcontrib>Yi, Eunbi</creatorcontrib><creatorcontrib>Kim, HyoJeong</creatorcontrib><creatorcontrib>Kim, Jung Min</creatorcontrib><creatorcontrib>Jin, Hyung-Seung</creatorcontrib><creatorcontrib>Kim, Hun Sik</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><collection>KoreaScience</collection><jtitle>BMB reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Nayoung</au><au>Lee, Dong-Hee</au><au>Choi, Woo Seon</au><au>Yi, Eunbi</au><au>Kim, HyoJeong</au><au>Kim, Jung Min</au><au>Jin, Hyung-Seung</au><au>Kim, Hun Sik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors</atitle><jtitle>BMB reports</jtitle><addtitle>BMB Reports</addtitle><date>2021-01-31</date><risdate>2021</risdate><volume>54</volume><issue>1</issue><spage>44</spage><epage>58</epage><pages>44-58</pages><issn>1976-6696</issn><eissn>1976-670X</eissn><abstract>Natural killer (NK) cells, key antitumor effectors of the innate immune system, are endowed with the unique ability to spontaneously eliminate cells undergoing a neoplastic transformation. 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source | PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Cancer immunotherapy Chimeric antigen receptors Immune checkpoint receptors Immune escape Natural killer cells |
title | Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors |
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