<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fu Q</submitter><funding>Dengfeng project of Foshan First People’s Hospital</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>Dengfeng project of Foshan First People's Hospital</funding><pagination>973</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11514859</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Cancer immunotherapy, particularly immune checkpoint inhibitors (ICBs) such as anti-PD-1 antibodies, has revolutionised cancer treatment, although response rates vary among patients. Previous studies have demonstrated that caerin 1.1 and 1.9, host-defence peptides from the Australian tree frog, enhance the effectiveness of anti-PD-1 and therapeutic vaccines in a murine TC-1 model by activating tumour-associated macrophages intratumorally.&lt;h4>Methods&lt;/h4>We employed a murine B16 melanoma model to investigate the therapeutic potential of caerin 1.1 and 1.9 in combination with anti-CD47 and a therapeutic vaccine (triple therapy, TT). Tumour growth of caerin-injected primary tumours and distant metastatic tumours was assessed, and survival analysis conducted. Single-cell RNA</pubmed_abstract><journal>Journal of translational medicine</journal><pubmed_title>Caerin 1.1 and 1.9 peptides halt B16 melanoma metastatic tumours via expanding cDC1 and reprogramming tumour macrophages.</pubmed_title><pmcid>PMC11514859</pmcid><funding_grant_id>2020A1515010855</funding_grant_id><funding_grant_id>31971355</funding_grant_id><funding_grant_id>2019A008</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Fu Q</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Ni G</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Luo Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Caerin 1.1 and 1.9 peptides halt B16 melanoma metastatic tumours via expanding cDC1 and reprogramming tumour macrophages.</name><description>&lt;h4>Background&lt;/h4>Cancer immunotherapy, particularly immune checkpoint inhibitors (ICBs) such as anti-PD-1 antibodies, has revolutionised cancer treatment, although response rates vary among patients. Previous studies have demonstrated that caerin 1.1 and 1.9, host-defence peptides from the Australian tree frog, enhance the effectiveness of anti-PD-1 and therapeutic vaccines in a murine TC-1 model by activating tumour-associated macrophages intratumorally.&lt;h4>Methods&lt;/h4>We employed a murine B16 melanoma model to investigate the therapeutic potential of caerin 1.1 and 1.9 in combination with anti-CD47 and a therapeutic vaccine (triple therapy, TT). Tumour growth of caerin-injected primary tumours and distant metastatic tumours was assessed, and survival analysis conducted. Single-cell RNA</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-06T03:11:21.982Z</modification><creation>2026-07-06T03:08:44.41Z</creation></dates><accession>S-EPMC11514859</accession><cross_references><pubmed>39468595</pubmed><doi>10.1186/s12967-024-05763-x</doi></cross_references></HashMap>