Saenz Francisco R, Velasquez Brett, Waldrop Trey, Aguilar Edgardo, Cox Kathryn R, Delahoussaye Abagail, Laberiano-Fernandez Caddie, Clemente Leticia Campos, Connell Luke, Mims Nefetiti, Neill Denae, Parra Edwin R, Clise-Dwyer Karen, Schüler Emil, Spiotto Michael T
bioRxiv. 2025 Apr 11:2025.04.07.647544. doi: 10.1101/2025.04.07.647544.
Radiotherapy (RT) delivered at conventional dose rates (CONV) can both stimulate antitumor immune responses and inhibit these immune responses by depleting circulating lymphocytes. Given the observed normal tissue sparing associated with ultra-high dose rate (FLASH) RT, we hypothesized that FLASH RT may protect lymphocytes while increasing the immunogenicity of cancer cells. We irradiated cancer cell lines with FLASH RT or CONV RT and assessed immunogenic mRNA and protein expression. Both HPV-positive cell lines MEER and TC-1 showed upregulation of , and cGAS-STING family members after FLASH RT but not after CONV RT . To assess changes in lymphocyte populations, we irradiated murine mEER tumors in syngeneic C57BL/6 mice with 27 Gy in 3 fractions of FLASH RT or CONV RT. In mice bearing FLASH irradiated tumors, tumor-draining lymph nodes contained greater numbers of CD8 T cells (FLASH 1.7×10 vs 0.8×10 CONV; <0.001) and CD4 T cells (FLASH 2.3×10 vs CONV 1.2×10 ; <0.001) after irradiation. FLASH RT was associated with increased numbers of activated CD44 CD62L CD8 and CD4 lymphocytes. In irradiated tumors, FLASH RT was associated with increased CD8 tumor-infiltrating lymphocytes, increased PD1 expression on these lymphocytes and increased PDL1 expression on macrophages. Compared with CONV RT, FLASH RT spared activated T cells in tumor-draining lymph nodes and in tumors but increased checkpoint inhibitor expression in tumors. These results suggest that FLASH RT may enhance antitumor immune responses by maintaining the immunogenic effects of RT while preserving lymphocyte numbers, which may be augmented with immune checkpoint blockade.
Radiation-induced lymphopenia is associated with poorer survival outcomes. New treatment approaches, like FLASH radiation therapy (FLASH RT), which reduce lymphopenia and enhance the antitumor response, could potentially lead to better outcomes for cancer patients.
常规剂量率(CONV)的放射治疗(RT)既能刺激抗肿瘤免疫反应,又能通过消耗循环淋巴细胞来抑制这些免疫反应。鉴于观察到与超高剂量率(FLASH)RT相关的正常组织 sparing,我们假设FLASH RT可能在增加癌细胞免疫原性的同时保护淋巴细胞。我们用FLASH RT或CONV RT照射癌细胞系,并评估免疫原性mRNA和蛋白质表达。HPV阳性细胞系MEER和TC-1在FLASH RT后均显示出 以及cGAS-STING家族成员的上调,但在CONV RT后未出现上调。为了评估淋巴细胞群体的变化,我们用27 Gy的FLASH RT或CONV RT分3次照射同基因C57BL/6小鼠中的鼠mEER肿瘤。在携带FLASH照射肿瘤的小鼠中,照射后肿瘤引流淋巴结中含有更多数量的CD8 T细胞(FLASH 1.7×10 对CONV 0.8×10 ; <0.001)和CD4 T细胞(FLASH 2.3×10 对CONV 1.2×10 ; <0.001)。FLASH RT与活化的CD44 CD62L CD8 和CD4 淋巴细胞数量增加有关。在照射的肿瘤中,FLASH RT与CD8 肿瘤浸润淋巴细胞增加、这些淋巴细胞上PD1表达增加以及巨噬细胞上PDL1表达增加有关。与CONV RT相比,FLASH RT在肿瘤引流淋巴结和肿瘤中保留了活化的T细胞,但增加了肿瘤中的检查点抑制剂表达。这些结果表明,FLASH RT可能通过维持RT的免疫原性作用同时保留淋巴细胞数量来增强抗肿瘤免疫反应,这可能会因免疫检查点阻断而增强。
辐射诱导的淋巴细胞减少与较差的生存结果相关。新的治疗方法,如FLASH放射治疗(FLASH RT),可减少淋巴细胞减少并增强抗肿瘤反应,可能会为癌症患者带来更好的结果。