Abstract 725: <i>In-vivo</i> fluorescence lifetime tomography for detection and quantification of programmed death ligand-1.

Abstract Programmed death ligand-1 (PD-L1) is the only clinically approved predictive biomarker for cancer immunotherapy; however, its expression is highly heterogeneous and routinely assessed by ex vivo immunohistochemistry. To enable spatially resolved, noninvasive PD-L1 quantification, we employed fluorescence lifetime (FLT) tomography with a normalization strategy designed to account for nonspecific probe uptake. C57BL/6 mice bearing orthotopic RIL-175 liver tumors (n=10) were injected with αPDL1-800 (anti-PD-L1 antibody conjugated to IRDye 800CW). 48 hours post-injection, we performed in vivo time-domain FLT imaging with co-registered CT, followed by in situ FLT imaging and western blotting to validate PD-L1 expression. Bi-exponential fitting of the time-resolved fluorescence data yielded spatial maps of FLT (τ) and amplitude (a). The top 10% of FLTs within the tumor were averaged to define the bound lifetime component (τ_b), while the mean FLT in the normal liver was considered as the FLT of the unbound component (τ_u). Amplitudes of bound (a_b) and unbound (a_u) probes were extracted and segmented into tumor (a_b,T; a_u,T) and normal (a_b,N; a_u,N) ROIs. Among four normalization strategies tested, one correcting for background cross-talk (a_b,T - a_u,T) and normalizing by total uptake (a_b,N - a_u,N) showed the strongest correlation with PD-L1 expression (R2 = 0.77). 3D reconstructions using asymptotic time-domain analysis confirmed accurate tumor localization and size. FLT tomography distinguished bound from unbound αPDL1-800 and enabled quantitative assessment of PD-L1 expression in deep-seated tumors. The normalization method enabled accurate quantification of PD-L1 expression across tumors, supporting the utility of FLT imaging for preclinical immunotherapy evaluation and biomarker-guided therapy monitoring. Citation Format: Rahul Pal, Murali Krishnamoorthy, Xin Liu, Satoru Morita, Atsuyo Morita, Hak Soo Choi, Dan Duda, Anand T. Kumar. In-vivo fluorescence lifetime tomography for detection and quantification of programmed death ligand-1 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 725.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-725
Primary Topic
Advanced Fluorescence Microscopy Techniques
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article
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article

Abstract 725: In-vivo fluorescence lifetime tomography for detection and quantification of programmed death ligand-1.

Murali Krishnamoorthy, Atsuyo Morita, Satoru Morita, Hak Soo Choi et al.
Cancer Research
Advanced Fluorescence Microscopy Techniques
article

Abstract 725: In-vivo fluorescence lifetime tomography for detection and quantification of programmed death ligand-1.

Murali Krishnamoorthy, Atsuyo Morita, Satoru Morita, Hak Soo Choi, Xin Liu, Dan Duda, Rahul Pal
article en

Abstract

Abstract Programmed death ligand-1 (PD-L1) is the only clinically approved predictive biomarker for cancer immunotherapy; however, its expression is highly heterogeneous and routinely assessed by ex vivo immunohistochemistry. To enable spatially resolved, noninvasive PD-L1 quantification, we employed fluorescence lifetime (FLT) tomography with a normalization strategy designed to account for nonspecific probe uptake. C57BL/6 mice bearing orthotopic RIL-175 liver tumors (n=10) were injected with αPDL1-800 (anti-PD-L1 antibody conjugated to IRDye 800CW). 48 hours post-injection, we performed in vivo time-domain FLT imaging with co-registered CT, followed by in situ FLT imaging and western blotting to validate PD-L1 expression. Bi-exponential fitting of the time-resolved fluorescence data yielded spatial maps of FLT (τ) and amplitude (a). The top 10% of FLTs within the tumor were averaged to define the bound lifetime component (τ_b), while the mean FLT in the normal liver was considered as the FLT of the unbound component (τ_u). Amplitudes of bound (a_b) and unbound (a_u) probes were extracted and segmented into tumor (a_b,T; a_u,T) and normal (a_b,N; a_u,N) ROIs. Among four normalization strategies tested, one correcting for background cross-talk (a_b,T - a_u,T) and normalizing by total uptake (a_b,N - a_u,N) showed the strongest correlation with PD-L1 expression (R2 = 0.77). 3D reconstructions using asymptotic time-domain analysis confirmed accurate tumor localization and size. FLT tomography distinguished bound from unbound αPDL1-800 and enabled quantitative assessment of PD-L1 expression in deep-seated tumors. The normalization method enabled accurate quantification of PD-L1 expression across tumors, supporting the utility of FLT imaging for preclinical immunotherapy evaluation and biomarker-guided therapy monitoring. Citation Format: Rahul Pal, Murali Krishnamoorthy, Xin Liu, Satoru Morita, Atsuyo Morita, Hak Soo Choi, Dan Duda, Anand T. Kumar. In-vivo fluorescence lifetime tomography for detection and quantification of programmed death ligand-1 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 725.

Cancer ResearchVol. 86(7_Supplement)
Massachusetts Eye and Ear Infirmary (US), MGH Institute of Health Professions (US), University of Madras (IN), Indian Institute of Technology Madras (IN), Massachusetts General Hospital (US)
Good health and well-being
Openalex Percentile: Top 25%
Advanced Fluorescence Microscopy Techniques
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