Accurately characterizing the tumor micro-environment when tissue sample access is restricted generally is a key challenge within the immuno-oncology field. The balance and tumor infiltration of T–cell subpopulations are of significant interest. On this interview, NewsMedical speaks to Cerba Research on the use and value of T-regulatory immunochemsitry multiplex for solid tumor analytical validation.
What are T-Cells and why are they vital?
T-cells are typically categorized as helper (Th), cytotoxic (Tcyto), memory or regulatory (Treg) cells. T-cells are considered vital immune effector cells, making them preferred targets for immuno-modulation. Tcyto cells deliver optimal immune responses and protect against invading microbes and tumor antigens. Under homeostatic conditions, Tregs encourage peripheral tolerance. Nonetheless, where tumors are concerned, Tregs may suppress Tcyto cell functions.
What’s the multiplex protocol and the way was it developed?
Cerba Research developed the multiplex protocol, Histoprofile®- T-reg light panel, using the Discovery ULTRA (Ventana) platform, which was designed to stain sub-populations of specific T-cells on a single slide. This prevented the necessity for serial sections from a patient’s precious formalin-fixed paraffin-embedded (FFPE) samples in clinical trials while still offering a comprehensive evaluation of the tumor microenvironment.
The multiplex protocol was optimized and pre-validated on a non-small cell lung cancer FFPE sample. The analytical validation included specificity, sensitivity, precision, and antigen stability tests on healthy tonsils (control) and pathological breast, lung, head and neck and colon FFPE samples sourced from the Cerba Research Montpellier Biobank.
Are you able to describe a particular application involving the Histoprofile®- T-reg light panel multiplex protocol?
To judge Histoprofile®-T-reg light protocol specificity, the multiplex protocol was used to analyze healthy human tonsil samples (negative/positive controls). An FDA-approved healthy multi-tissue TMA comprised 33 different tissues from three donors. On this application, a pathologist validated the specificity of the three biomarkers on all tested tissues.
The Histoprofile®-Tregs light protocol was tested on a spread of solid tumor FFPE samples, including non-small cell lung cancer (NSCLC), triple-negative breast cancer (TNBC), head and neck squamous cell carcinoma (HNSCC), and colorectal cancer (CRC).
A multi-organ cancer TMA complemented tissue blocks to guage a sufficient variety of samples for every indication. A pathologist then scored slides to offer a semi-quantitative evaluation of the targets and make sure specificity.
How is the analytical precision of the Histoprofile®- T-reg light panel assessed?
To evaluate the analytical precision of the Histoprofile®-T-reg light protocol, we performed intra-run and inter-run reproducibility on two samples of breast, lung, colorectal, and head and neck cancers. On this evaluation, slides were analyzed with Halo for cell density. The mean CV of all samples was then calculated for every tissue type and solid tumors.
When using positive cell densities for CD3, CD8, and FoxP3 because the readout for the protocol, it is feasible to satisfy the acceptance criteria (CV<20%) for solid tumors. For CD3, the CV is 21%, but at Cerba Research, we consider this sufficient resulting from a low positive cell density (<5% of total cells).
How do you go about testing antigen stability?
To evaluate the steadiness of the targets within the Histoprofile®-T-reg light protocol, a kinetics experiment is crucial to investigate the identical sample aged over a time frame (from fresh up to a few months). This test is often performed using two samples per indication, with various ranges of signal expression.
Over time, the resulting images of an NSCLC sample were assessed with Halo image evaluation software. The slides included in the steadiness test were analyzed with Halo software to determine each goal’s cell density of the multiplex.
What are the important thing biomarkers that indicate effective treatment?
T-cell infiltration into the tumor is a key biomarker to estimate the response to checkpoint immune therapies. In a single particular study, five colorectal cancer (CRC) samples were stained with the Histoprofile®-T-reg light panel after which analyzed with Halo to find out the densities of CD8 T-cells and Treg cells within the tumor and stroma compartments, and the densities of the cell populations on the tumor/stroma border.
On this particular case, there have been significantly more Tregs within the stroma than within the tumor (p = 0.026). Similarly, more T-cells were present within the stromal compartment than within the tumor but to not a major level (p = 0.096). An accumulation of the T-cells and Tregs cells on the stromal side of the interface was observed.
What makes the Histoprofile®- T-reg light panel multiplex protocol a standout tool for the study of T-Cell populations?
After demonstrating clear specificity and sensitivity, the analytical performance of the Histoprofile®-T-reg light protocol using anti-CD8, anti-CD3 and anti-FoxP3 indicated the power to detect Tcyto and Treg cells in a spread of solid tumors, including, but not limited to, lung, head and neck, breast, and colorectal cancer FFPE tissues. The protocol met the acceptance criteria in relation to repeatability and inter-assay reproducibility.
Antigen stability shows that it is feasible to detect antigens at a level much like fresh sections after three months. At Cerba Research, the Histoprofile®-T-reg light protocol has been validated on solid tumors at an experimental endpoint level.
Spatial evaluation of the protocol provides an in-depth evaluation of the tumor microenvironment, allowing appreciation of immune cell infiltration into the tumor. We consider that the Histoprofile®- T-reg light panel is a practical tool that facilitates the investigation of T-cell populations in various human solid tumors in clinical trials.
Figure 1. Comparison of cell density between simplex and multiplex slides. Image Credit: Cerba Research
Figure 2. Specificity assessment on Healthy Tonsil FFPE samples. Representative images of two tonsil samples stained with the Histoprofile®-Tregs light panel. CD3 (Red), CD8 (Orange) and FoxP3 (Green). Scale bar: 50 μm. Image Credit: Cerba Research
Figure 3. Heat Map of specificity results obtained on Healthy Tonsil Blocks and Healthy Multi-organ TMA. Count represents the variety of stained samples for every tissue and every goal in each percentage of positive cells range. Image Credit: Cerba Research
Figure 4. Heat Map of sensitivity results obtained on Blocks and Multi-organ TMA. Count represents the variety of stained samples for every tissue and every goal in each percentage of positive cells range. Image Credit: Cerba Research
Figure 5. Representative images from precision assessment of the Histoprofile®-T-reg light protocol on NSCLC, TNBC, HNSCC and CRC. CD3 (Red), CD8 (Orange) and FoxP3 (Green). Scale bar = 100 μm. Image Credit: Cerba Research
Figure 6. Distribution Graph of reproducibility test slides. CD3 (top row), CD8 (middle row) and FoxP3 (lower row) cell densities in function of sample and indications. Image Credit: Cerba Research
Figure 7. CD3/CD8/FoxP3 stability assessment on NSCLC.From top to bottom: merge, CD3 (red), CD8 (orange), FoxP3 (green). Scale bar = 100 μm. Image Credit: Cerba Research
Figure 8. Representative images from spatial evaluation using HaLo (Green line represents the Tumor/Stroma interface. Left image: Histoprofile®-Tregs light panel CD3 (red), CD8 (orange), FoxP3 (green). Middle image: Halo masks for T cells (top) and Tregs (bottom). Right image: Halo representation of the areas evaluated throughout the interface evaluation. Each color represents a distance of 10 μm. Scale bar = 100 μm. Image Credit: Cerba Research
Figure 9. Box Plot for Tregs (top) and T cells (bottom) density within the Stroma (blue) and Tumor (red) for five CRC samples. Image Credit: Cerba Research
Figure 10. Area Plot showing Tregs (red) and T cells (blue) infiltration within the Tumor (left) from the Stroma (right) for five CRC samples. Image Credit: Cerba Research
About Cerba Research
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