Highlights of 2019 Protein Engineering Summit (PEGS) in Boston, USA: advancing antibody-based cancer therapies to the clinic
Abstract The 15th Annual Protein Engineering Summit (PEGS) organized by Cambridge Healthtech Institute was held in Boston, USA, from 8 to 12 April 2019. This report highlights the presentations in the Oncology Stream of this meeting with a focus on bispecific antibodies (BsAbs). A variety of BsAb fo...
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Veröffentlicht in: | Antibody therapeutics 2019-10, Vol.2 (4), p.79-87 |
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creator | Li, Hong Li, You Wang, Cheng Wang, Shouye Ho, Mitchell |
description | Abstract
The 15th Annual Protein Engineering Summit (PEGS) organized by Cambridge Healthtech Institute was held in Boston, USA, from 8 to 12 April 2019. This report highlights the presentations in the Oncology Stream of this meeting with a focus on bispecific antibodies (BsAbs). A variety of BsAb formats with different target antigens (CD3, CTLA4, PD-1, PD-L1, EGFR, HER2, BCMA, CD19, CD20, CD38, CD123, TGFβ, PSMA, etc.) have been discussed, in which the T-cell engaging (anti-CD3) BsAb is the most studied construct to exhibit promising immunotherapeutic activities. The BsAb formats include IgG-like structures or antibody fragments composed of antigen-binding sites only. Preclinical and clinical data from different BsAbs demonstrated the potential therapeutic applications in various solid tumors and hematological malignancies. The ongoing development of BsAb formats will help overcome current clinical issues, such as tumor selectivity and antigen coverage. This report also covers several presentations about emerging targets (e.g. mesothelin, CD47) and new technologies in the field of antibody engineering and therapeutics. |
doi_str_mv | 10.1093/abt/tbz010 |
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The 15th Annual Protein Engineering Summit (PEGS) organized by Cambridge Healthtech Institute was held in Boston, USA, from 8 to 12 April 2019. This report highlights the presentations in the Oncology Stream of this meeting with a focus on bispecific antibodies (BsAbs). A variety of BsAb formats with different target antigens (CD3, CTLA4, PD-1, PD-L1, EGFR, HER2, BCMA, CD19, CD20, CD38, CD123, TGFβ, PSMA, etc.) have been discussed, in which the T-cell engaging (anti-CD3) BsAb is the most studied construct to exhibit promising immunotherapeutic activities. The BsAb formats include IgG-like structures or antibody fragments composed of antigen-binding sites only. Preclinical and clinical data from different BsAbs demonstrated the potential therapeutic applications in various solid tumors and hematological malignancies. The ongoing development of BsAb formats will help overcome current clinical issues, such as tumor selectivity and antigen coverage. This report also covers several presentations about emerging targets (e.g. mesothelin, CD47) and new technologies in the field of antibody engineering and therapeutics.</description><identifier>ISSN: 2516-4236</identifier><identifier>EISSN: 2516-4236</identifier><identifier>DOI: 10.1093/abt/tbz010</identifier><identifier>PMID: 31844838</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Meeting Reports</subject><ispartof>Antibody therapeutics, 2019-10, Vol.2 (4), p.79-87</ispartof><rights>The Author(s) 2019. Published by Oxford University Press on behalf of Antibody Therapeutics. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3230-f617f5311fc4db78bae82d1428c067a9be4c43673c393858c18abd503cd5e4283</citedby><cites>FETCH-LOGICAL-c3230-f617f5311fc4db78bae82d1428c067a9be4c43673c393858c18abd503cd5e4283</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/PMC6913531/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913531/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,1605,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31844838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Hong</creatorcontrib><creatorcontrib>Li, You</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Wang, Shouye</creatorcontrib><creatorcontrib>Ho, Mitchell</creatorcontrib><title>Highlights of 2019 Protein Engineering Summit (PEGS) in Boston, USA: advancing antibody-based cancer therapies to the clinic</title><title>Antibody therapeutics</title><addtitle>Antib Ther</addtitle><description>Abstract
The 15th Annual Protein Engineering Summit (PEGS) organized by Cambridge Healthtech Institute was held in Boston, USA, from 8 to 12 April 2019. This report highlights the presentations in the Oncology Stream of this meeting with a focus on bispecific antibodies (BsAbs). A variety of BsAb formats with different target antigens (CD3, CTLA4, PD-1, PD-L1, EGFR, HER2, BCMA, CD19, CD20, CD38, CD123, TGFβ, PSMA, etc.) have been discussed, in which the T-cell engaging (anti-CD3) BsAb is the most studied construct to exhibit promising immunotherapeutic activities. The BsAb formats include IgG-like structures or antibody fragments composed of antigen-binding sites only. Preclinical and clinical data from different BsAbs demonstrated the potential therapeutic applications in various solid tumors and hematological malignancies. The ongoing development of BsAb formats will help overcome current clinical issues, such as tumor selectivity and antigen coverage. This report also covers several presentations about emerging targets (e.g. mesothelin, CD47) and new technologies in the field of antibody engineering and therapeutics.</description><subject>Meeting Reports</subject><issn>2516-4236</issn><issn>2516-4236</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kV1LHDEUhoNUVKw3_gDJjWBLp-ZjPjJeCFa2WhAUVq9DkjmzG5lJ1iQjWPrjm2Wt6E0vDufr4T0HXoQOKflOSctPlU6nSf8mlGyhPVbRuigZrz-9q3fRQYyPhBBGStHWYgftcirKUnCxh_5c28VyyJEi9j1mhLb4LvgE1uGZW1gHEKxb4Pk0jjbhk7vZ1fwLzssfPibvvuGH-cUZVt2zcmbNKZes9t1LoVWEDps8hoDTEoJaWYg4-XWDzWCdNZ_Rdq-GCAeveR89_JzdX14XN7dXvy4vbgrDGSdFX9OmrzilvSk73QitQLCOlkwYUjeq1VCaktcNN7zlohKGCqW7inDTVZApvo_ON7qrSY_QGXApqEGugh1VeJFeWflx4-xSLvyzrFvK8-EscPIqEPzTBDHJ0UYDw6Ac-ClKxlnT8oYTltGvG9QEH2OA_u0MJXLtmMyOyY1jGT56_9gb-s-fDBxvAD-t_if0FzbSnto</recordid><startdate>201910</startdate><enddate>201910</enddate><creator>Li, Hong</creator><creator>Li, You</creator><creator>Wang, Cheng</creator><creator>Wang, Shouye</creator><creator>Ho, Mitchell</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201910</creationdate><title>Highlights of 2019 Protein Engineering Summit (PEGS) in Boston, USA: advancing antibody-based cancer therapies to the clinic</title><author>Li, Hong ; Li, You ; Wang, Cheng ; Wang, Shouye ; Ho, Mitchell</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3230-f617f5311fc4db78bae82d1428c067a9be4c43673c393858c18abd503cd5e4283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Meeting Reports</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Hong</creatorcontrib><creatorcontrib>Li, You</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Wang, Shouye</creatorcontrib><creatorcontrib>Ho, Mitchell</creatorcontrib><collection>Access via Oxford University Press (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antibody therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Hong</au><au>Li, You</au><au>Wang, Cheng</au><au>Wang, Shouye</au><au>Ho, Mitchell</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highlights of 2019 Protein Engineering Summit (PEGS) in Boston, USA: advancing antibody-based cancer therapies to the clinic</atitle><jtitle>Antibody therapeutics</jtitle><addtitle>Antib Ther</addtitle><date>2019-10</date><risdate>2019</risdate><volume>2</volume><issue>4</issue><spage>79</spage><epage>87</epage><pages>79-87</pages><issn>2516-4236</issn><eissn>2516-4236</eissn><abstract>Abstract
The 15th Annual Protein Engineering Summit (PEGS) organized by Cambridge Healthtech Institute was held in Boston, USA, from 8 to 12 April 2019. This report highlights the presentations in the Oncology Stream of this meeting with a focus on bispecific antibodies (BsAbs). A variety of BsAb formats with different target antigens (CD3, CTLA4, PD-1, PD-L1, EGFR, HER2, BCMA, CD19, CD20, CD38, CD123, TGFβ, PSMA, etc.) have been discussed, in which the T-cell engaging (anti-CD3) BsAb is the most studied construct to exhibit promising immunotherapeutic activities. The BsAb formats include IgG-like structures or antibody fragments composed of antigen-binding sites only. Preclinical and clinical data from different BsAbs demonstrated the potential therapeutic applications in various solid tumors and hematological malignancies. The ongoing development of BsAb formats will help overcome current clinical issues, such as tumor selectivity and antigen coverage. This report also covers several presentations about emerging targets (e.g. mesothelin, CD47) and new technologies in the field of antibody engineering and therapeutics.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>31844838</pmid><doi>10.1093/abt/tbz010</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Meeting Reports |
title | Highlights of 2019 Protein Engineering Summit (PEGS) in Boston, USA: advancing antibody-based cancer therapies to the clinic |
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