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Immunocytokines and bispecific antibodies: two complementary strategies for the selective activation of immune cells at the tumor site
Summary The activation of the immune system for a selective removal of tumor cells represents an attractive strategy for the treatment of metastatic malignancies, which cannot be cured by existing methodologies. In this review, we examine the design and therapeutic potential of immunocytokines and b...
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Published in: | Immunological reviews 2016-03, Vol.270 (1), p.178-192 |
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The activation of the immune system for a selective removal of tumor cells represents an attractive strategy for the treatment of metastatic malignancies, which cannot be cured by existing methodologies. In this review, we examine the design and therapeutic potential of immunocytokines and bispecific antibodies, two classes of bifunctional products which can selectively activate the immune system at the tumor site. Certain protein engineering aspects, such as the choice of the antibody format, are common to both classes of therapeutic agents and can have a profound impact on tumor homing performance in vivo of individual products. However, immunocytokines and bispecific antibodies display different mechanisms of action. Future research activities will reveal whether an additive of even synergistic benefit can be obtained from the judicious combination of these two types of biopharmaceutical agents. |
doi_str_mv | 10.1111/imr.12391 |
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The activation of the immune system for a selective removal of tumor cells represents an attractive strategy for the treatment of metastatic malignancies, which cannot be cured by existing methodologies. In this review, we examine the design and therapeutic potential of immunocytokines and bispecific antibodies, two classes of bifunctional products which can selectively activate the immune system at the tumor site. Certain protein engineering aspects, such as the choice of the antibody format, are common to both classes of therapeutic agents and can have a profound impact on tumor homing performance in vivo of individual products. However, immunocytokines and bispecific antibodies display different mechanisms of action. Future research activities will reveal whether an additive of even synergistic benefit can be obtained from the judicious combination of these two types of biopharmaceutical agents.</description><identifier>ISSN: 0105-2896</identifier><identifier>EISSN: 1600-065X</identifier><identifier>DOI: 10.1111/imr.12391</identifier><identifier>PMID: 26864112</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; Antibodies, Bispecific - chemistry ; Antibodies, Bispecific - genetics ; Antibodies, Bispecific - immunology ; Antibodies, Bispecific - therapeutic use ; antibody engineering ; Antibody Specificity ; Antigens, Neoplasm - immunology ; armed antibodies ; bispecific antibodies ; Clinical Trials as Topic ; Cytokines - chemistry ; Cytokines - genetics ; Cytokines - therapeutic use ; Humans ; Immune System - cytology ; Immune System - immunology ; Immune System - metabolism ; immunocytokines ; immunotherapy of cancer ; Neoplasms - drug therapy ; Neoplasms - immunology ; Neoplasms - metabolism ; Protein Binding ; Protein Engineering</subject><ispartof>Immunological reviews, 2016-03, Vol.270 (1), p.178-192</ispartof><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5521-2116dfbdd485966a113831bf7d817a01313a5644e9fe1b4c33a9ed5f109c65183</citedby><cites>FETCH-LOGICAL-c5521-2116dfbdd485966a113831bf7d817a01313a5644e9fe1b4c33a9ed5f109c65183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26864112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kiefer, Jonathan D.</creatorcontrib><creatorcontrib>Neri, Dario</creatorcontrib><title>Immunocytokines and bispecific antibodies: two complementary strategies for the selective activation of immune cells at the tumor site</title><title>Immunological reviews</title><addtitle>Immunol Rev</addtitle><description>Summary
The activation of the immune system for a selective removal of tumor cells represents an attractive strategy for the treatment of metastatic malignancies, which cannot be cured by existing methodologies. In this review, we examine the design and therapeutic potential of immunocytokines and bispecific antibodies, two classes of bifunctional products which can selectively activate the immune system at the tumor site. Certain protein engineering aspects, such as the choice of the antibody format, are common to both classes of therapeutic agents and can have a profound impact on tumor homing performance in vivo of individual products. However, immunocytokines and bispecific antibodies display different mechanisms of action. Future research activities will reveal whether an additive of even synergistic benefit can be obtained from the judicious combination of these two types of biopharmaceutical agents.</description><subject>Animals</subject><subject>Antibodies, Bispecific - chemistry</subject><subject>Antibodies, Bispecific - genetics</subject><subject>Antibodies, Bispecific - immunology</subject><subject>Antibodies, Bispecific - therapeutic use</subject><subject>antibody engineering</subject><subject>Antibody Specificity</subject><subject>Antigens, Neoplasm - immunology</subject><subject>armed antibodies</subject><subject>bispecific antibodies</subject><subject>Clinical Trials as Topic</subject><subject>Cytokines - chemistry</subject><subject>Cytokines - genetics</subject><subject>Cytokines - therapeutic use</subject><subject>Humans</subject><subject>Immune System - cytology</subject><subject>Immune System - immunology</subject><subject>Immune System - metabolism</subject><subject>immunocytokines</subject><subject>immunotherapy of cancer</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - metabolism</subject><subject>Protein Binding</subject><subject>Protein Engineering</subject><issn>0105-2896</issn><issn>1600-065X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkc9u1DAQxi0EokvhwAsgH-GQ1hP_ScIBCa1gWWkLEgKVm-U4k9Y0iRfb27IvwHPj7bYrOCB8saz5zTfz-SPkObATyOfUjeEESt7AAzIDxVjBlPz2kMwYMFmUdaOOyJMYvzMGFS_FY3JUqloJgHJGfi3HcTN5u03-yk0YqZk62rq4Rut6Z_MzudZ3DuNrmm48tX5cDzjilEzY0piCSXiRq7T3gaZLpBEHtMldIzW7yyTnJ-p76nZzkFochjwk3bJpM-au6BI-JY96M0R8dncfk6_v332ZfyhWnxbL-dtVYaUsoSgBVNe3XSdq2ShlAHjNoe2rrobKMODAjVRCYNMjtMJybhrsZA-ssUpCzY_Jm73uetOO2NnsI5hBr4Mbsx_tjdN_VyZ3qS_8tZYgBa-aLPDyTiD4HxuMSY8u7kyZCf0maqgqpYTi-af_j-aVoGZKZPTVHrXBxxiwP2wETO8i1jlifRtxZl_8aeFA3meagdM9cOMG3P5bSS_PPt9LFvsOFxP-PHSYcKVVxSupzz8uNK8XK3Gm5vqc_wa188LC</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Kiefer, Jonathan D.</creator><creator>Neri, Dario</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>H94</scope><scope>5PM</scope></search><sort><creationdate>201603</creationdate><title>Immunocytokines and bispecific antibodies: two complementary strategies for the selective activation of immune cells at the tumor site</title><author>Kiefer, Jonathan D. ; Neri, Dario</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5521-2116dfbdd485966a113831bf7d817a01313a5644e9fe1b4c33a9ed5f109c65183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antibodies, Bispecific - chemistry</topic><topic>Antibodies, Bispecific - genetics</topic><topic>Antibodies, Bispecific - immunology</topic><topic>Antibodies, Bispecific - therapeutic use</topic><topic>antibody engineering</topic><topic>Antibody Specificity</topic><topic>Antigens, Neoplasm - immunology</topic><topic>armed antibodies</topic><topic>bispecific antibodies</topic><topic>Clinical Trials as Topic</topic><topic>Cytokines - chemistry</topic><topic>Cytokines - genetics</topic><topic>Cytokines - therapeutic use</topic><topic>Humans</topic><topic>Immune System - cytology</topic><topic>Immune System - immunology</topic><topic>Immune System - metabolism</topic><topic>immunocytokines</topic><topic>immunotherapy of cancer</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - metabolism</topic><topic>Protein Binding</topic><topic>Protein Engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kiefer, Jonathan D.</creatorcontrib><creatorcontrib>Neri, Dario</creatorcontrib><collection>Istex</collection><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>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Immunological reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kiefer, Jonathan D.</au><au>Neri, Dario</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunocytokines and bispecific antibodies: two complementary strategies for the selective activation of immune cells at the tumor site</atitle><jtitle>Immunological reviews</jtitle><addtitle>Immunol Rev</addtitle><date>2016-03</date><risdate>2016</risdate><volume>270</volume><issue>1</issue><spage>178</spage><epage>192</epage><pages>178-192</pages><issn>0105-2896</issn><eissn>1600-065X</eissn><abstract>Summary
The activation of the immune system for a selective removal of tumor cells represents an attractive strategy for the treatment of metastatic malignancies, which cannot be cured by existing methodologies. In this review, we examine the design and therapeutic potential of immunocytokines and bispecific antibodies, two classes of bifunctional products which can selectively activate the immune system at the tumor site. Certain protein engineering aspects, such as the choice of the antibody format, are common to both classes of therapeutic agents and can have a profound impact on tumor homing performance in vivo of individual products. However, immunocytokines and bispecific antibodies display different mechanisms of action. Future research activities will reveal whether an additive of even synergistic benefit can be obtained from the judicious combination of these two types of biopharmaceutical agents.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26864112</pmid><doi>10.1111/imr.12391</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies, Bispecific - chemistry Antibodies, Bispecific - genetics Antibodies, Bispecific - immunology Antibodies, Bispecific - therapeutic use antibody engineering Antibody Specificity Antigens, Neoplasm - immunology armed antibodies bispecific antibodies Clinical Trials as Topic Cytokines - chemistry Cytokines - genetics Cytokines - therapeutic use Humans Immune System - cytology Immune System - immunology Immune System - metabolism immunocytokines immunotherapy of cancer Neoplasms - drug therapy Neoplasms - immunology Neoplasms - metabolism Protein Binding Protein Engineering |
title | Immunocytokines and bispecific antibodies: two complementary strategies for the selective activation of immune cells at the tumor site |
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