<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang C</submitter><funding>Shanghai Pudong Scientific and Technological development Projects</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><pagination>275-286</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9816240</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(2)</volume><pubmed_abstract>Radionuclides theranostic are ideal "partners" for bispecific antibodies to explore the immune response of patients and synergistic treatment. A bispecific single-domain antibody-Fc fusion protein, KN046, exhibits a good treatment effect by binding to programmed cell death-ligand 1 (PD-L1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). An ionizing-radiation stimulus mediated by a low-dose of [&lt;sup>131&lt;/sup>I] may be used for immunopotentiation. In this study, we established [&lt;sup>131&lt;/sup>I]-labeled KN046 as a novel radioimmunotherapy agent to treat malignant melanoma and explored the mechanism.&lt;h4>Methods&lt;/h4>After intravenous injection of [&lt;sup>131&lt;/sup>I]-KN046, SPECT/CT imaging was applied to identify candidate targets for KN046 immunotherapy. [&lt;sup>18&lt;/sup>F]-FDG and [&lt;sup></pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>Enhanced antitumor immune responses via a new agent [&lt;sup>131&lt;/sup>I]-labeled dual-target immunosuppressant.</pubmed_title><pmcid>PMC9816240</pmcid><funding_grant_id>PKJ2020-Y55</funding_grant_id><funding_grant_id>81971648</funding_grant_id><funding_grant_id>2020YFA0909000</funding_grant_id><pubmed_authors>He S</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Jiang C</pubmed_authors><pubmed_authors>Yao B</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Tian Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced antitumor immune responses via a new agent [&lt;sup>131&lt;/sup>I]-labeled dual-target immunosuppressant.</name><description>Radionuclides theranostic are ideal "partners" for bispecific antibodies to explore the immune response of patients and synergistic treatment. A bispecific single-domain antibody-Fc fusion protein, KN046, exhibits a good treatment effect by binding to programmed cell death-ligand 1 (PD-L1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). An ionizing-radiation stimulus mediated by a low-dose of [&lt;sup>131&lt;/sup>I] may be used for immunopotentiation. In this study, we established [&lt;sup>131&lt;/sup>I]-labeled KN046 as a novel radioimmunotherapy agent to treat malignant melanoma and explored the mechanism.&lt;h4>Methods&lt;/h4>After intravenous injection of [&lt;sup>131&lt;/sup>I]-KN046, SPECT/CT imaging was applied to identify candidate targets for KN046 immunotherapy. [&lt;sup>18&lt;/sup>F]-FDG and [&lt;sup></description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-21T16:16:21.983Z</modification><creation>2025-02-19T03:30:52.642Z</creation></dates><accession>S-EPMC9816240</accession><cross_references><pubmed>36242616</pubmed><doi>10.1007/s00259-022-05986-4</doi></cross_references></HashMap>