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Abstract 5615: YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling
PD-1/PD-L1 inhibition immunotherapy is very popular in cancer treatment and has become one of the most pursued therapeutic strategies in the field. Combination treatment using anti-PD-1/PD-L1 agents with other immunomodulators brings additional benefits, such as preventing refractory effects towards...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2022-06, Vol.82 (12_Supplement), p.5615-5615 |
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container_title | Cancer research (Chicago, Ill.) |
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creator | Liu, Baihong Yang, Hao Hui, Li Yang, Benny |
description | PD-1/PD-L1 inhibition immunotherapy is very popular in cancer treatment and has become one of the most pursued therapeutic strategies in the field. Combination treatment using anti-PD-1/PD-L1 agents with other immunomodulators brings additional benefits, such as preventing refractory effects towards PD-1/PD-L1 antibodies, and better inhibitory effects on tumor growth. Biocytogen developed YH008, a tetravalent anti PD-1/CD40 Fc-silenced IgG1 bispecific antibody (BsAb) that agonizes CD40 in a PD-1-dependent manner. Previously, YH008 demonstrated dose-dependent inhibitory efficacy against B16F10 engrafted tumors in PD-1/CD40 double humanized mice (established by Biocytogen: B-hPD1/CD40). Interestingly, in humanized CD40 mice that do not express human PD-1 expression, YH008 did not show tumor inhibition activity against the MC38 engrafted tumor. This observation indicates that YH008 activates the CD40 pathway in a PD-1 dependent manner. When compared with an anti-PD-L1/CD40 BsAb, YH008 showed superior tumor growth inhibition (TGI) against MC38 engrafted tumors in a triple humanized PD-1/PD-L1/CD40 mouse model (B-hPD-1/hPD-L1/hCD40). YH008 was observed to promote the proliferation and activation of dendritic cells, as well as increase CD8+/Treg ratio in B16F10 tumor-infiltrating lymphocytes (TILs). Furthermore, YH008 showed a superior liver toxicity profile compared to a selicrelumab analog. At a high dose of 100mg/kg, YH008 did not elevate liver enzymes in the blood of B-hPD1/hCD40 mice. Similarly, no significant adverse events were observed in a cynomolgus dose-escalation study. YH008 is currently in pre-clinical development with anticipated IND application in 2022.
Citation Format: Baihong Liu, Hao Yang, Li Hui, Benny Yang. YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 5615. |
doi_str_mv | 10.1158/1538-7445.AM2022-5615 |
format | article |
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Citation Format: Baihong Liu, Hao Yang, Li Hui, Benny Yang. YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 5615.</description><identifier>ISSN: 1538-7445</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/1538-7445.AM2022-5615</identifier><language>eng</language><ispartof>Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.5615-5615</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Liu, Baihong</creatorcontrib><creatorcontrib>Yang, Hao</creatorcontrib><creatorcontrib>Hui, Li</creatorcontrib><creatorcontrib>Yang, Benny</creatorcontrib><title>Abstract 5615: YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling</title><title>Cancer research (Chicago, Ill.)</title><description>PD-1/PD-L1 inhibition immunotherapy is very popular in cancer treatment and has become one of the most pursued therapeutic strategies in the field. Combination treatment using anti-PD-1/PD-L1 agents with other immunomodulators brings additional benefits, such as preventing refractory effects towards PD-1/PD-L1 antibodies, and better inhibitory effects on tumor growth. Biocytogen developed YH008, a tetravalent anti PD-1/CD40 Fc-silenced IgG1 bispecific antibody (BsAb) that agonizes CD40 in a PD-1-dependent manner. Previously, YH008 demonstrated dose-dependent inhibitory efficacy against B16F10 engrafted tumors in PD-1/CD40 double humanized mice (established by Biocytogen: B-hPD1/CD40). Interestingly, in humanized CD40 mice that do not express human PD-1 expression, YH008 did not show tumor inhibition activity against the MC38 engrafted tumor. This observation indicates that YH008 activates the CD40 pathway in a PD-1 dependent manner. When compared with an anti-PD-L1/CD40 BsAb, YH008 showed superior tumor growth inhibition (TGI) against MC38 engrafted tumors in a triple humanized PD-1/PD-L1/CD40 mouse model (B-hPD-1/hPD-L1/hCD40). YH008 was observed to promote the proliferation and activation of dendritic cells, as well as increase CD8+/Treg ratio in B16F10 tumor-infiltrating lymphocytes (TILs). Furthermore, YH008 showed a superior liver toxicity profile compared to a selicrelumab analog. At a high dose of 100mg/kg, YH008 did not elevate liver enzymes in the blood of B-hPD1/hCD40 mice. Similarly, no significant adverse events were observed in a cynomolgus dose-escalation study. YH008 is currently in pre-clinical development with anticipated IND application in 2022.
Citation Format: Baihong Liu, Hao Yang, Li Hui, Benny Yang. YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 5615.</description><issn>1538-7445</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqdj89KAzEYxINUsP55BOF7gKZ-2W7q4q20Si-CBy-eQnY3u_uVNlmSdKVv4GPbWBHPPc0wMDP8GLsXOBVCFg9Czgr-mOdyunjNMMu4nAt5wcZ_-eifv2LXIWwQUQqUY_a1KEP0uoqQSk_wsUYsJqDhbcUFX65yhJJCbypqqAJtI5WuPkyAbEclxQBxv3MeWu8-Y3dMYaDBQey827fdaaQ2vbG1sRGONzToSM6Ca-BnPFBr9ZZse8suG70N5u5Xb5h8eX5frnnlXQjeNKr3tNP-oASqhK0SkkpI6oStEsHs3N43UYdfYg</recordid><startdate>20220615</startdate><enddate>20220615</enddate><creator>Liu, Baihong</creator><creator>Yang, Hao</creator><creator>Hui, Li</creator><creator>Yang, Benny</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20220615</creationdate><title>Abstract 5615: YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling</title><author>Liu, Baihong ; Yang, Hao ; Hui, Li ; Yang, Benny</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-crossref_primary_10_1158_1538_7445_AM2022_56153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Baihong</creatorcontrib><creatorcontrib>Yang, Hao</creatorcontrib><creatorcontrib>Hui, Li</creatorcontrib><creatorcontrib>Yang, Benny</creatorcontrib><collection>CrossRef</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Baihong</au><au>Yang, Hao</au><au>Hui, Li</au><au>Yang, Benny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abstract 5615: YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><date>2022-06-15</date><risdate>2022</risdate><volume>82</volume><issue>12_Supplement</issue><spage>5615</spage><epage>5615</epage><pages>5615-5615</pages><issn>1538-7445</issn><eissn>1538-7445</eissn><abstract>PD-1/PD-L1 inhibition immunotherapy is very popular in cancer treatment and has become one of the most pursued therapeutic strategies in the field. Combination treatment using anti-PD-1/PD-L1 agents with other immunomodulators brings additional benefits, such as preventing refractory effects towards PD-1/PD-L1 antibodies, and better inhibitory effects on tumor growth. Biocytogen developed YH008, a tetravalent anti PD-1/CD40 Fc-silenced IgG1 bispecific antibody (BsAb) that agonizes CD40 in a PD-1-dependent manner. Previously, YH008 demonstrated dose-dependent inhibitory efficacy against B16F10 engrafted tumors in PD-1/CD40 double humanized mice (established by Biocytogen: B-hPD1/CD40). Interestingly, in humanized CD40 mice that do not express human PD-1 expression, YH008 did not show tumor inhibition activity against the MC38 engrafted tumor. This observation indicates that YH008 activates the CD40 pathway in a PD-1 dependent manner. When compared with an anti-PD-L1/CD40 BsAb, YH008 showed superior tumor growth inhibition (TGI) against MC38 engrafted tumors in a triple humanized PD-1/PD-L1/CD40 mouse model (B-hPD-1/hPD-L1/hCD40). YH008 was observed to promote the proliferation and activation of dendritic cells, as well as increase CD8+/Treg ratio in B16F10 tumor-infiltrating lymphocytes (TILs). Furthermore, YH008 showed a superior liver toxicity profile compared to a selicrelumab analog. At a high dose of 100mg/kg, YH008 did not elevate liver enzymes in the blood of B-hPD1/hCD40 mice. Similarly, no significant adverse events were observed in a cynomolgus dose-escalation study. YH008 is currently in pre-clinical development with anticipated IND application in 2022.
Citation Format: Baihong Liu, Hao Yang, Li Hui, Benny Yang. YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 5615.</abstract><doi>10.1158/1538-7445.AM2022-5615</doi></addata></record> |
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title | Abstract 5615: YH008, a PD-1-CD40 bispecific antibody, inhibits tumor growth in vivo through PD-1-dependent activation of CD40 signaling |
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