{"id":5165,"date":"2026-05-13T15:07:21","date_gmt":"2026-05-13T19:07:21","guid":{"rendered":"https:\/\/oge.mit.edu\/msrp\/?post_type=profiles&#038;p=5165"},"modified":"2026-08-11T17:31:29","modified_gmt":"2026-08-11T21:31:29","slug":"adeline-schmidt","status":"publish","type":"profiles","link":"https:\/\/oge.mit.edu\/msrp\/profiles\/adeline-schmidt\/","title":{"rendered":"Adeline Schmidt"},"content":{"rendered":"<div class=\"wp-block-image\">\n<figure class=\"alignleft size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"599\" src=\"https:\/\/oge.mit.edu\/msrp\/wp-content\/uploads\/sites\/2\/2026\/05\/Schmidt-Adeline.jpg\" alt=\"by Corban Swain\" class=\"wp-image-5634\" style=\"aspect-ratio:1;object-fit:cover;width:200px;height:auto\" srcset=\"https:\/\/oge.mit.edu\/msrp\/wp-content\/uploads\/sites\/2\/2026\/05\/Schmidt-Adeline.jpg 400w, https:\/\/oge.mit.edu\/msrp\/wp-content\/uploads\/sites\/2\/2026\/05\/Schmidt-Adeline-200x300.jpg 200w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><\/figure>\n<\/div>\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<p class=\"wp-block-paragraph\"><strong>University of Florida<\/strong><br>Faculty Advisor: Prof. Jessica Stark<br>Research Supervisor: Tran Luu<br>Department: Biological Engineering<\/p>\n<\/div><\/div>\n\n\n\n<div style=\"height:0px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Biography<\/strong><\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">Adeline Schmidt is a rising junior at the University of Florida, majoring in Chemical<br>Engineering with a Biomolecular Engineering minor. Driven by a fascination with molecular<br>mechanisms, she conducts undergraduate research in the Denard Group, utilizing a yeast surface<br>display platform to identify inhibitors for SARS-CoV-2 variants. Previously, in the Rinaldi-<br>Ramos Lab, she focused on encapsulating superparamagnetic iron oxide nanoparticles in a PEG<br>polymer matrix. By minimizing Brownian relaxation to enable rapid magnetic responses for<br>higher-resolution imaging, this experience in microfluidics sparked her passion for programmable<br>polymers. Specifically, she is interested in cross-linking substrates into microgel matrices for<br>enzyme-triggered, site-specific drug delivery traceable via magnetic particle imaging.<\/p>\n\n\n\n<p class=\"has-text-align-center wp-block-paragraph\"><br><strong>Computational Validation of the CD44\/Siglec-9 Glyco-Immune Checkpoint in<br>Various Human Cancers<\/strong><br>Adeline O. Schmidt1, Tran Luu2,3, Jessica C. Stark2,3,4<br>1Department of Chemical Engineering, University of Florida<br>2Department of Biological Engineering, Massachusetts Institute of Technology<br>3Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology<br>4Department of Chemical Engineering, Massachusetts Institute of Technology<\/p>\n\n\n\n<p class=\"has-text-align-center wp-block-paragraph\"><br>Immune checkpoint blockades have advanced cancer treatment. However, many patients<br>remain unresponsive, motivating a need to identify other pathways that contribute to resistance.<br>Siglec-9, a glycan-binding immune receptor, has emerged as a glyco-immune checkpoint<br>that suppresses antitumor immunity in multiple cancers. The Stark lab recently discovered<br>CD44 as a high-affinity and cancer-associated ligand for Siglec-9 that dampens macrophage<br>phagocytosis, highlighting the CD44\/Siglec-9 axis as a promising myeloid checkpoint target.<br>Because direct studies of Siglec-9 interactions in humans are limited, further validation using<br>human datasets is needed. To address this, we analyzed published scRNA-seq and spatial<br>transcriptomic data of breast, renal, and colorectal cancers. We used ST3GAL4, a key enzyme<br>mediating Siglec-9 ligand synthesis, as a proxy for the Siglec-9-binding glycoform of CD44.<br>In three cancers, scRNA-seq shows CD44\/ST3GAL4 co-expression in epithelial and stromal<br>tumor cells, and SIGLEC9 concentrated in myeloid cells. In colorectal and breast cancers,<br>CD44\/ST3GAL4 co-expression is higher in tumor than matched normal epithelium, and<br>myeloid SIGLEC9 is increased in cancer. Interestingly, patients with higher myeloid SIGLEC9<br>also show higher epithelial CD44\/ST3GAL4 co-expression. Spatial transcriptomics confirmed<br>the tumor-enriched CD44 expression in colorectal cancer. Our analyses support CD44\/Siglec-9<br>as a cancer-associated glyco-immune axis across human cancers.<\/p>\n","protected":false},"featured_media":5423,"template":"","profile_category":[25],"class_list":["post-5165","profiles","type-profiles","status-publish","has-post-thumbnail","hentry","profile_category-2026-interns"],"acf":[],"_links":{"self":[{"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles\/5165","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles"}],"about":[{"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/types\/profiles"}],"version-history":[{"count":2,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles\/5165\/revisions"}],"predecessor-version":[{"id":5756,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles\/5165\/revisions\/5756"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/media\/5423"}],"wp:attachment":[{"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/media?parent=5165"}],"wp:term":[{"taxonomy":"profile_category","embeddable":true,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profile_category?post=5165"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}