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STAT5 Activation Enhances Adoptive Therapy Combined with Peptide Vaccination by Preventing PD-1 Inhibition

delete2024-12-11
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PRE
AI
A
Aaron E. Fan *
H
Hussein Sultan
T
Takumi Kumai
V
Valentyna I. Fesenkova
J
Juan Wu
J
John D. Klement
J
Joshua D. Bernstock
G
Gregory K. Friedman
E
Esteban Celis
DOI:10.1158/1535-7163.MCT-24-0505delete
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Abstract

Abstract

En 中文
Adoptive cell therapy (ACT) using retrovirally transduced T cells represents a promising strategy for enhancing antitumor responses. When used with TriVax, a peptide vaccination strategy, this approach synergistically expands antigen-specific cell populations. STAT5 plays a vital role as a transcription factor in regulating T-cell proliferation and their differentiation into effector and memory T cells. We aimed to explore the combination therapy using CD8 T cells engineered to express constitutively active STAT5 (CA-STAT5) with vaccines. CD8 T cells were transduced with a retrovirus (RV) encoding the mouse gp100 T-cell receptor (TCR). In certain treatment groups, cells were also co-transduced with RV encoding CA-STAT5. We assessed transduction efficiency and functional activity through flow cytometry and various functional assays. B16F10 tumor-bearing mice were treated with ACT using RV-transduced CD8 T cells and subsequently vaccinated with TriVax. We demonstrate that TriVax selectively enhanced the expansion of ACT cell populations bearing gp100-specific TCRs. T cells engineered to express CA-STAT5 showed not only increased expansion and polyfunctionality but also reduced PD-1 expression, leading to decreased cellular exhaustion. In a B16F10 melanoma mouse model, our approach yielded a potent antitumor effect, with CA-STAT5 further amplifying this response. We found that CA-STAT5 improved antitumor activities, in part, by attenuating the PD-1/PD-L1 inhibitory pathway. These findings indicate that TCR-transduced CD8 T cells can undergo antigen-dependent expansion when exposed to TriVax. Additionally, the expression of CA-STAT5 enhances T-cell proliferation and persistence, partly by promoting resistance to PD-1/PD-L1-mediated inhibition in antitumor T cells.
Keywords:
CD8 T-CELLS
GENE-THERAPY
CANCER REGRESSION
EFFECTOR
EXPRESSION
MEMORY
IMMUNOTHERAPY
RECEPTORS
AFFINITY

Journal

Molecular Cancer Therapeutics cover
Molecular Cancer Therapeutics
IF:
5.5
Papers:
9.0K
Citations:
2.0W

Organization

A
Augusta University
Scholars:
5.9K
Papers: 4.6K
Citations: 8.2K
U
utmd anderson cancer center
Scholars:
3.0W
Papers: 2.4W
Citations: 27
N
national institutes of health (nih) - usa
Scholars:
10.2W
Papers: 8.2W
Citations: 111
U
university of texas system
Scholars:
18.3W
Papers: 15.5W
Citations: 210
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