We similarly identified these two cell populations and observed that the CXCL13 + CD8 + T subset tended to decrease in proportion post-treatment, while the CXCL13 + CD4 + T subset showed an increasing trend, although neither change reached statistical significance (Fig.
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Single-cell RNA sequencing analysis reveals a lack of CXCL13<sup>+</sup> T cell subsets associated with the recurrence of cervical squamous cell carcinoma following concurrent chemoradiotherapy.
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