Measuring CD8 Immune States in Four Tissue Specimens

Matched RNA, protein, and spatial measurements revealed differences in cytotoxic-signature expression within the CD8 compartment.

Immune-state differences across samples

We compared four selected wells from a 14-well Singular G4X analysis. The fraction of CD8 cells expressing a cytotoxic RNA signature ranged from 24.6% to 63.8%. Reporting the fraction within the CD8 compartment distinguishes this measure from total immune-cell abundance.

CD8 cytotoxic-signature results by sample
SampleTissue metadataCD8 cellsSignature-positive cellsFraction of CD8 cells
H01Lung82552663.8%
G04Other21910347.0%
E01Lung721926.4%
C01Lung3388324.6%

These differences define a measurable immune-state feature for follow-up alongside spatial organization and cell abundance. Testing an association with treatment response requires documented outcomes and a separate patient-level evaluation.

Measurement and study scope

The G4X measurements combined a 341-gene RNA panel with 16 protein markers measured in the same cells. Cell typing used the standard 425-class MiraTyper model with tissue constraints and protein-informed decoding. A CD8 cell was flagged as cytotoxic-signature positive when at least one transcript was detected from GZMB, GZMA, GZMK, GZMH, PRF1, GNLY, or NKG7.

This is a descriptive comparison of four selected wells, with three recorded as lung and one as “Other.” The signature measures transcriptional state; it does not directly measure cell killing. These results do not establish treatment-response prediction, and the four wells do not constitute an independent validation cohort.

Source: MiraOmics Elephas / Singular G4X follow-up analysis, July 16, 2026. Counts and fractions are taken from the current per-well results table; percentages are rounded to one decimal place.

Related publication: von Euw et al., Cancer Research 86(7 Supplement), abstract 1389 (AACR 2026). This publication reports a separate cytokine-profiling study; the four-sample CD8 results above come from the MiraOmics follow-up analysis.