{"id":5025,"date":"2026-05-13T15:10:05","date_gmt":"2026-05-13T19:10:05","guid":{"rendered":"https:\/\/oge.mit.edu\/msrp\/?post_type=profiles&#038;p=5025"},"modified":"2026-08-10T11:32:50","modified_gmt":"2026-08-10T15:32:50","slug":"nia-blunt","status":"publish","type":"profiles","link":"https:\/\/oge.mit.edu\/msrp\/profiles\/nia-blunt\/","title":{"rendered":"Nia Blunt"},"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\/Blunt-Nia.jpg\" alt=\"by Corban Swain\" class=\"wp-image-5579\" style=\"aspect-ratio:1;object-fit:cover;width:200px;height:auto\" srcset=\"https:\/\/oge.mit.edu\/msrp\/wp-content\/uploads\/sites\/2\/2026\/05\/Blunt-Nia.jpg 400w, https:\/\/oge.mit.edu\/msrp\/wp-content\/uploads\/sites\/2\/2026\/05\/Blunt-Nia-200x300.jpg 200w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><figcaption class=\"wp-element-caption\">by Corban Swain<\/figcaption><\/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>Albany State University<\/strong><br>Faculty Advisor: Prof. Forest White<br>Research Surpervisor: Sergio Quispe Sanchez<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\">Nia Blunt is a rising senior at Albany State University, majoring in Forensic Science<br>on the pre-med track. She plans to pursue an MD or MD\/PhD and is especially interested in<br>oncology and research that can improve healthcare outcomes in her community. Her research<br>experience includes projects in dermatological science, electrochemistry, and immunology.<br>On campus, Nia serves as Honors Council President, is on the executive board of Women in<br>Pre-Med, and works as a student mentor in the Honors Program. She also volunteers at the<br>food bank and in other campus service activities. Nia enjoys learning new things, entering new<br>research environments, and gaining skills that will help her grow as both a future physician<br>and a researcher. Through medicine and research, she hopes to make a meaningful impact on<br>healthcare, especially in underserved communities.<\/p>\n\n\n\n<p class=\"has-text-align-center wp-block-paragraph\"><br><strong>Uncovering treatment-specific antigens in NRASmut melanom<\/strong>a<br>Nia Blunt1,2, Sergio Quispe Sanchez2, and Forest White2<br>1Department of Natural Sciences, Albany State University<br>2Department of Biological Engineering, Massachusetts Institute of Technology<br>Melanoma is a type of skin cancer initiated by proliferating melanocytes which are the cells that<br>give the skin its pigmentation. NRAS-mutant melanoma, which is driven by constitutively active<br>MAPK signaling, affects roughly 15-20% of melanoma patients. This subtype is associated with<br>a a more aggressive clinical phenotype, including thicker lesions and higher rates of lymph node<br>metastasis, leaving patients at the advanced stage with few treatment options. The standard of care<br>for advanced NRAS-mutant melanoma primarily relies on immune checkpoint inhibitors, which<br>are ineffective in about 50% of cases due to acquired resistance. Recent efforts to profile changes<br>in the antigen repertoire of NRAS-mutant melanoma have identified antigens induced by targeted<br>therapy. However, traditional DDA-based workflows may miss a rich source of lower-abundance<br>or poorly fragmented antigen targets. Combining an untargeted DDA analysis with a targeted PRM<br>workflow will be able to uncover \u201chidden\u201d treatment-induced antigens. We used standard cell<br>culture techniques, immunoprecipitation to isolate pMHC complexes, a dual mass-spectrometry<br>approach, and R\/Python scripts to identify treatment-specific precursors and build an inclusion<br>list for PRM analysis. This work will add a new set of candidate antigens for cancer vaccines and<br>T-cell directed immunotherapies.<\/p>\n","protected":false},"featured_media":5391,"template":"","profile_category":[25],"class_list":["post-5025","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\/5025","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":4,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles\/5025\/revisions"}],"predecessor-version":[{"id":5677,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profiles\/5025\/revisions\/5677"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/media\/5391"}],"wp:attachment":[{"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/media?parent=5025"}],"wp:term":[{"taxonomy":"profile_category","embeddable":true,"href":"https:\/\/oge.mit.edu\/msrp\/wp-json\/wp\/v2\/profile_category?post=5025"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}