HPVがんワクチンが腫瘍成長抑制と生存期間延長を確認(HPV Cancer Vaccine Slows Tumor Growth, Extends Survival in Preclinical Model)

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2026-02-11 ノースウェスタン大学

ノースウェスタン大学の研究チームは、HPV関連がんを標的とする治療用ワクチンが前臨床モデルで腫瘍増殖を抑制し、生存期間を延長することを示した。ワクチンはHPV由来のがん特異的抗原に対する免疫応答を強化し、T細胞を活性化して腫瘍細胞を攻撃する仕組み。動物モデルでは腫瘍縮小と生存率改善が確認された。既存治療との併用による相乗効果も示唆され、HPV関連がんに対する新たな免疫療法戦略として臨床応用が期待される。

HPVがんワクチンが腫瘍成長抑制と生存期間延長を確認(HPV Cancer Vaccine Slows Tumor Growth, Extends Survival in Preclinical Model)
An artistic interpretation of a spherical nucleic acid (SNA) nanoparticle carrying HPV antigen. Image by Connor Forsyth and Jake Cohen from the Mirkin Research Group

<関連情報>

E7 11-19の配置と方向は、構造的に定義された球状核酸ワクチンにおけるCD8+ T細胞応答を決定する E711-19 placement and orientation dictate CD8+ T cell response in structurally defined spherical nucleic acid vaccines

Jeongmin Hwang, Tonatiuh A. Ocampo, Vinzenz Mayer, Janice Kang, […] , and Chad A. Mirkin
Science Advances  Published:11 Feb 2026
DOI:https://doi.org/10.1126/sciadv.aec3876

Abstract

To develop effective nanostructured immunotherapeutics, identifying structural parameters that maximize immune response is essential. Spherical nucleic acids (SNAs) provide a modular platform for coordinated antigen-adjuvant delivery, where subtle structural differences can markedly influence potency. Herein, three SNAs were designed with HLA-A2–restricted HPV16 E711-19 peptide and CpG adjuvant, nearly identical in composition but differing in antigen presentation. All enhanced dendritic cell activation and CD8+ T cell cytotoxicity in primary human cells compared to peptide-CpG admixture; however, one variant, N-HSNA, elicited the strongest response, inducing ~8-fold higher interferon-γ secretion and ~2.5-fold greater cytotoxicity. In tumor-bearing AAD mice, N-HSNA reduced tumor burden by ~3.5-fold, prolonged survival, and expanded CD8+ T cells. Transcriptomic profiling revealed up-regulation of activation genes and suppression of exhaustion markers. In patient-derived HPV+ head and neck cancer spheroids, N-HSNA enhanced cytotoxicity ~2.5-fold, establishing antigen placement and orientation as key parameters for translational cancer immunotherapy.

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