Zhaoyi Ye, Congkuan Song, Yueyun Weng, Sheng Liu, Du Wang, Liye Mei, Cheng Lei
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引用次数: 0
Abstract
Immune checkpoint inhibitors have emerged as frontline
therapies
for lung cancer, yet the lack of reliable biomarkers for predicting
the treatment response remains a critical challenge. While single-cell
analysis offers a potent approach to probing physiological states,
conventional techniques suffer from limited throughput and insufficient
multimodal profiling capability. To address the aforementioned issues,
we propose a novel framework for lung cancer immunotherapy diagnosis.
Specifically, we develop multimodal optical time-stretch imaging flow
cytometry (OTS-IFC) that simultaneously acquires label-free bright-field
(BF) and quantitative phase (QP) images at a throughput of 10,000
cells/s. In response to the influence of phase unwrapping artifacts,
we propose CellDiffuser, an intermediate domain transformation diffusion
model that aligns BF and QP images in a shared latent space at a preselected
time step, thus generating high-fidelity synthesized QP images. CellDiffuser
achieves an SSIM of 0.747 in the leukocyte immunotherapy response
prediction data set and an SSIM of 0.708 in the A549 cell death state
identification data set. Finally, our framework demonstrates its practical
utility in lung cancer immunotherapy diagnosis in the above two clinically
relevant data sets. This work establishes a cost-effective, high-throughput
framework for single-cell phenotyping, offering a new paradigm to
guide lung cancer personalized immunotherapy diagnosis. The code is
available at: https://github.com/yzygit1230/CellDiffuser.
期刊介绍:
Published as soon as accepted and summarized in monthly issues, ACS Photonics will publish Research Articles, Letters, Perspectives, and Reviews, to encompass the full scope of published research in this field.