Simultaneous detection of lymphocytes and tumor cells in vivo in response to STING-TLR9 immunotherapy with Raman active multiplexed gold nanostars

TL;DR

This study uses gold nanostars to track immune and tumor cells in real time during immunotherapy, helping predict treatment response in mice.

Contribution

The novel use of multiplexed gold nanostars with SERS imaging enables simultaneous tracking of immune and tumor cells during immunotherapy.

Findings

MGNs detected dynamic changes in CD8+ T cells and VEGFR2+ tumor cells during STING-TLR9 immunotherapy.

SERS imaging distinguished responders and nonresponders to immunotherapy in murine breast cancer models.

High-resolution SERS maps showed spatial distribution of biomarkers correlating with ex vivo immunofluorescence results.

Abstract

Immunotherapies show heterogeneous response in patients and identifying those likely to benefit from these therapies remains challenging. This is in part because histopathology, the current clinical standard, cannot accurately predict response. Dynamic changes occur in both tumor cells and immune cells in vivo during and after treatment which are not captured by histopathology or by single biomarker imaging. To address this urgent need, this study leverages multiplexed profiling of both CD8+ T cells and VEGFR2+ expressing tumor cells in 4T1 murine breast cancer tumors with surface-enhanced Raman spectroscopy (SERS) using multiplexed gold nanostars (MGNs). MGNs are conjugated with antibodies targeting each cell type and Raman labels to enable multiplexing. Real time SERS in vivo imaging enables detection of dynamic longitudinal changes in CD8 and VEGFR2 in response to STING + TLR9 (stimulator of interferon genes + toll like receptor 9) immunotherapies, a treatment that increases tumor immunogenicity through a type I interferon response. MGNs also distinguished nonresponders of immunotherapies where 4T1 tumors were treated with antiOX40 antibodies. In vivo endpoints were validated ex vivo with flow cytometry analysis of immune cell population, cytokine analysis, STING activation, and immunofluorescence (IF) imaging of key markers (CD8, VEGFR, CD31, Ki67, and STING). Further, high resolution SERS maps provided a spatial context of CD8 and VEGFR2 distribution that showed the molecular makeup of tumors in responder and nonresponder mice. Biomarker distribution in ex vivo SERS aligned with in vivo findings and showed moderate to strong correlations via a Pearson's correlation to quantification of IF markers in tumors.

Multiplexed gold nanostars enable in vivo and ex vivo SERS imaging of CD8+ T cells and VEGFR2+ tumor cells capturing dynamic T cell recruitment and vascular changes in the tumor to enable treatment response to immunotherapy.

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