<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Immunoproteomics | Schmidt Science</title><link>https://schmidt-science-7d3097.gitlab.io/tag/immunoproteomics/</link><atom:link href="https://schmidt-science-7d3097.gitlab.io/tag/immunoproteomics/index.xml" rel="self" type="application/rss+xml"/><description>Immunoproteomics</description><generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Thu, 21 May 2026 00:00:00 +0000</lastBuildDate><image><url>https://schmidt-science-7d3097.gitlab.io/media/icon_hu14918251628535694572.png</url><title>Immunoproteomics</title><link>https://schmidt-science-7d3097.gitlab.io/tag/immunoproteomics/</link></image><item><title>New Science Advances publication explores immune-protein pathways underlying multimorbidity</title><link>https://schmidt-science-7d3097.gitlab.io/post/2026-05-21-immunoproteome-sci-adv/</link><pubDate>Thu, 21 May 2026 00:00:00 +0000</pubDate><guid>https://schmidt-science-7d3097.gitlab.io/post/2026-05-21-immunoproteome-sci-adv/</guid><description>&lt;p>We have published a new study in Science Advances investigating how immune-related proteins may contribute to
multimorbidity — the presence of multiple chronic diseases in the same individual.&lt;/p>
&lt;p>We are pleased to share our new publication in Science Advances, &amp;lsquo;The immunoproteome and multimorbidity:
a Mendelian randomisation study&amp;rsquo;.&lt;/p>
&lt;p>In this study, we used large-scale human genetic and proteomic data to investigate 151 immune-related proteins across
64 diseases and biomarkers. Our findings showed that several immune proteins were linked to multiple conditions spanning
cardiometabolic, inflammatory, and neurodegenerative diseases, highlighting shared biological pathways that may contribute
to multimorbidity.&lt;/p>
&lt;p>We identified replicated associations involving proteins including IL6R, APOE, and CD163, alongside several druggable
proteins, including targets of existing therapies. These findings highlight potential opportunities for drug repurposing
and indication expansion across multiple diseases.&lt;/p>
&lt;p>Overall, our study provides new insight into the molecular basis of multimorbidity and demonstrates
how human genetics can identify shared putative therapeutic targets across common chronic diseases.&lt;/p></description></item></channel></rss>