TY  - JOUR
TI  - Dendritic cell-based immunotherapy modulates the systemic inflammatory profile in a 4T1 breast cancer model
AU  - Dias, Tauana Christina
AU  - Vieira, Jéssica Ferreira
AU  - Tostes, Katiane
AU  - Silva, Polyana Barbosa
AU  - Lopes, Angela Maria Moed
AU  - Rebolho, Gabriela Karam
AU  - Murta, Eddie Fernando Candido
AU  - Arantes, Lidia Maria Rebolho Batista
AU  - Michelin, Márcia Antoniazi
PY  - 2026
JO  - Exploration of Targeted Anti-tumor Therapy
VL  - 7
SP  - 1002393
DO  - 10.37349/etat.2026.1002393
UR  - https://www.explorationpub.com/Journals/etat/Article/1002393
AB  - Aim: Breast cancer remains a major cause of cancer-related mortality in women, particularly in advanced stages where therapeutic options are limited. While immune checkpoint inhibitors (ICIs) have improved outcomes in a subset of patients, many do not respond, highlighting the need for alternative immunotherapeutic strategies. This study evaluated the effect of dendritic cell (DC)-based immunotherapy on tumor growth and on the inflammatory profile of peritoneal myeloid cells in a 4T1 murine breast cancer model. Methods: BALB/c mice bearing 4T1 breast tumors were treated with bone marrow-derived DC-based immunotherapy. Tumor volume was monitored over time, and CD14+ cells obtained from peritoneal lavage were analyzed by flow cytometry for the cytokines IL-12, IL-17, and TNF-α and the transcription factors RORγT and GATA3. Results: DC-based immunotherapy was associated with a non-significant trend toward reduced tumor volume and a marked suppression of key proinflammatory cytokines: IL-12 (P < 0.0005), IL-17 (P < 0.0001), and TNF-α (P < 0.0001). Expression of the transcription factors RORγT and GATA3, associated with Th17 and Th2 differentiation, was also downregulated (P < 0.0001). These immunological effects were observed in CD14+ myeloid cells from the peritoneal compartment. Conclusions: DC-based immunotherapy modulates the systemic/peritoneal inflammatory profile and attenuates tumor-promoting inflammation. This strategy may offer therapeutic benefit for patients with breast cancer who are unresponsive to conventional or ICI-based treatments and supports its further evaluation in translational studies.
ER  -