<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE311nnn/GSE311159/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE311159</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Enhanced immune response of human iPSC-macrophages via animal-free manufacturing processes</name><description>Studying human macrophages in vitro is crucial for understanding their immune functions. Recent interest in macrophages derived from induced pluripotent stem cells (iPSC-Mac) has led to various differentiation protocols, often using undefined animal serum like fetal bovine serum (FBS). This study compared FBS-based media to the defined medium X-VIVO™ 15 containing human serum albumin (hSA). Both produced functional macrophages, but those in hSA displayed a neutral activation state, enhanced cholesterol metabolism, and more significant changes in surface phenotype after stimulation. They also had a stronger response to co-stimulatory signals, making them better for testing immunomodulatory drugs. In contrast, FBS-grown macrophages were more adherent and pre-activated, showing reduced sensitivity upon stimulation, which may pose challenges for drug screening and immunomodulatory evaluations.</description><dates><publication>2026/04/22</publication></dates><accession>GSE311159</accession><cross_references><GSM>GSM9320333</GSM><GSM>GSM9320334</GSM><GSM>GSM9320332</GSM><GSM>GSM9320337</GSM><GSM>GSM9320335</GSM><GSM>GSM9320336</GSM><GPL>34284</GPL><GSE>311159</GSE><taxon>Homo sapiens</taxon><PMID>[41964059]</PMID></cross_references></HashMap>