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Enhanced anti-tumor efficacy of tumor-infiltrating lymphocytes by GITR agonist in ovarian cancer.

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Frontiers in immunology 📖 저널 OA 100% 2021: 2/2 OA 2022: 13/13 OA 2023: 10/10 OA 2024: 62/62 OA 2025: 810/810 OA 2026: 522/522 OA 2021~2026 2025 Vol.16() p. 1670841
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유사 논문
P · Population 대상 환자/모집단
환자: ovarian cancer (OC), their therapeutic efficacy remains limited
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
we demonstrated that the addition of an agonistic GITR antibody during the early phase of TIL culture increased the CD8 T cell to Treg cell ratio and enhanced anti-tumor T cell immunity.

Jung D, Goh AR, Kim KY, Lee JM, Lee EJ, Hwang S, Kang H, Park H, An HJ

📝 환자 설명용 한 줄

[BACKGROUND] Adoptive cell therapy (ACT) using autologous tumor-infiltrating lymphocytes (TILs) is a personalized immunotherapy that has shown promising clinical results in various tumor types.

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↓ .bib ↓ .ris
APA Jung D, Goh AR, et al. (2025). Enhanced anti-tumor efficacy of tumor-infiltrating lymphocytes by GITR agonist in ovarian cancer.. Frontiers in immunology, 16, 1670841. https://doi.org/10.3389/fimmu.2025.1670841
MLA Jung D, et al.. "Enhanced anti-tumor efficacy of tumor-infiltrating lymphocytes by GITR agonist in ovarian cancer.." Frontiers in immunology, vol. 16, 2025, pp. 1670841.
PMID 41280919 ↗

Abstract

[BACKGROUND] Adoptive cell therapy (ACT) using autologous tumor-infiltrating lymphocytes (TILs) is a personalized immunotherapy that has shown promising clinical results in various tumor types. Although TILs are associated with improved survival in patients with ovarian cancer (OC), their therapeutic efficacy remains limited. Therefore, novel strategies to enhance the anti-tumor activity of TILs are needed to improve outcomes in OC treatment.

[METHODS] Single cells were isolated from tumor tissues of patients with high-grade serous carcinoma (HGSC) and expanded for 14 days in the presence of IL-2 under four different conditions: (1) control (W), (2) PD-1 antagonist (WI), (3) PD-1 antagonist + IL-15 + IL-21 (WIO), and (4) PD-1 antagonist + IL-15 + IL-21 + GITR-agonist (WIOG). Following validation of TIL purity and activation phenotypes by flow cytometry, RNA sequencing was performed to elucidate the underlying mechanisms. efficacy was assessed using a 7-AAD/Far-Red cytotoxicity assay against autologous tumor cells, and efficacy was evaluated in NSG mice bearing subcutaneous patient-derived tumor cell xenografts (PDCX).

[RESULTS] On day 14, the WIOG group showed a 1.3-fold increase in expansion compared to the control group, along with a high CD8/Treg ratio (454.6). Furthermore, both CD8 and CD4 T cells in the WIOG group exhibited elevated Granzyme B expression. RNA sequencing identified 279 upregulated genes associated with T cell activation (), cytotoxicity (), and anti-apoptosis (). Compared to the controls, the WIOG group demonstrated a 1.9-fold increase in cytolytic activity and a 56% reduction in tumor growth in the patient-derived tumor cell xenograft (PDCX) model.

[CONCLUSIONS] Taken together, we demonstrated that the addition of an agonistic GITR antibody during the early phase of TIL culture increased the CD8 T cell to Treg cell ratio and enhanced anti-tumor T cell immunity. Enhancing TILs with a GITR agonist may be beneficial for improving the clinical outcomes of TIL-based ACT in OC.

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