稀少な免疫細胞を用いた新たながんワクチンを開発(Mount Sinai Researchers Engineer Rare Immune Cells to Create Powerful New Cancer Vaccine)

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2025-07-21 マウントサイナイ医療システム(MSHS)

米マウントサイナイ医科大学の研究チームは、希少な免疫細胞「cDC1(1型樹状細胞)」を大規模かつ高機能で生成する技術を開発し、がんワクチンの新たな道を切り開いた。臍帯血由来の造血幹細胞100万個から約30億個のcDC1を無血清培養で作製可能で、抗原提示能やT細胞活性化能も保持。ヒト化マウスモデルでの実験では、強力な抗腫瘍免疫応答を誘導した。cDC1はがん患者では数・機能が低下しており、本技術は「既製型がん細胞ワクチン」としての応用が期待される。今後、多様ながん種への展開や、免疫チェックポイント阻害薬との併用による効果増強も視野に入る。

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がん免疫療法に応用するためのヒトI型樹状細胞の生成と機能性を強化するためのノッチシグナルの利用 Harnessing Notch Signaling to Enhance the Generation and Functionality of Human Conventional Type I Dendritic Cells for Cancer Immunotherapy Applications

Sreekumar Balan;Liam O’Brien;Ante Peros;Xuedi Wang;Ingrid Leal-Rojas;Christopher Mcclain;Kristen J. Radford;Nina Bhardwaj
Cancer Immunology Research  Published:July 02 2025
DOI:https://doi.org/10.1158/2326-6066.CIR-25-0034

Abstract

Dendritic cell (DC) based-vaccines remain the sole approved cancer vaccine. Despite their established safety and efficacy in numerous trials against cancers and infections, long-term clinical benefits have been modest. Most trials have employed DCs derived from blood monocytes (MoDC), but emerging evidence underscores the unique role of cDC1 in triggering potent antitumor immune responses and their intratumoral infiltration with favorable prognoses in many cancers. However, the scarcity of cDC1 in peripheral blood and the challenges in generating them in vitro have hindered a deeper understanding of their biology and their widespread application as cellular vaccines. Here, we present a novel serum-free culture system capable of generating billions of human cDC1s from CD34+ progenitors derived from cord or peripheral blood. The system leverages the requirement of Notch signaling for cDC1 differentiation and generates DCs that closely resemble in vivo cDC1s, exhibiting superior functions, including cellular antigen cross-presentation. This robust protocol enables the scalable production of cDC1s for both fundamental biological research and therapeutic applications.

細胞遺伝子工学
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