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10057 - CD31+CD34, Kidney Cancer

INTRODUCTION

Advanced kidney cancer is treated by targeted therapies with antiangiogenic agents. However, not all patients will benefit from this treatment and therefore patients can be divided into two groups: responders and non-responders.
It is of interest to define the differences between these two groups. One of the differences that are examined is the degree of maturity of the microvessels. For this purpose the vessel markers CD31 and CD34 are used. Since CD31 is a marker for mature vessels, CD34 positivity in the absence of CD31 can be used to identify more immature vessels.

The purpose of this APP is to quantify the CD31 positive areas, CD34 positive areas, and overlapping positive areas to investigate if the ratio of mature to immature vessels is one of the differences between the responder and non-responder groups.

From a TMA block, sequential slides were obtained and each slide was stained with either CD31 or CD34 [See EXAMPLES: figure 1]. Using the patented Autodisector technology, the two sequential slides can be overlaid [See EXAMPLES: figure 2] and each TMA core-pair is automatically aligned at a high magnification, cell-to-cell level, to facilitate the detection of overlapping positive stain between the two slides [See EXAMPLES: figure 7].

Note: To obtain satisfying results from this technology it is crucial that the sequential slides are taken with as small a distance between them as possible. This technology can be applied to both TMAs and whole tissue sections. When used with TMAs or other small tissue sections, tissue folds and other artifacts must be kept at an absolute minimum to obtain good alignment results.

KEYWORDS

CD31, CD34, Kidney Cancer, responders, non-responders, vessel maturity, immunohistochemistry, image analysis

METHODS

The images that are obtained from the alignment procedure are two-layered TIFF files. In each image, the first layer is the CD31 stained core and the second layer is the CD34 stained core. The layers are referred to as frame 1 and frame 2 in the software.

Based on a DAB color deconvolution, [See EXAMPLES: figure 5], the positive stain areas are identified as areas where the stain density is higher than a certain threshold. This leads to a segmentation of the image using three labels:

Overlap Pos Stain: Areas where the stain density is high enough for both CD31 and CD34.
CD31 Positive: Areas where only CD31 positivity is present.
CD34 Positive: Areas where only CD34 positivity is present.

These three categories are labeled in green, blue, and red respectively, [See EXAMPLES: figure 6].

If there are artifacts on the slides, such as black spots or shadows these must be manually removed from the ROI to ensure that they are not included as positive stain.

QUANTITATIVE OUTPUT VARIABLES

- Immature vessel Area (CD34 alone), [µm2]: CD31 positive area

- Overlap Positive stain (A), [µm2]: Area of overlapping positive CD31 and CD34 stain

- Mature vessel area, [µm2]: CD31 Positive (A) + Overlap Positive stain (A)

- Mature to immature vessel ratio (A): (Mature vessel area)/(Immature vessel Area)


AUXILIARY APPS (included)

Auxiliary APPs are used for additional process steps, e.g. finding Region of Interest (ROI).

Alignment

This auxiliary APP is used to for the semi-automatic alignment of tissue pairs and must be launched from the Sectionassembler (Tissuealign) module. The alignment APP includes settings for TMA tissue detection, auto alignment parameters, detection of tissue before sampling and sample settings so that the user does not have to decide on any settings, but only has to go through the workflow.

Alignment of serial sections:

Step 1: Load the Auxiliary APP in the Sectionassembler (Tissuealign) module.

Step 2: Import virtual slides and follow the workflow steps in the module:

a. Detect tissue and manually correct if necessary

b. Link cores. Skip cores that are too damaged (excess amount of tissue folds, holes, or similar) or where it is obvious that there is not a good correlation between the two sections, e.g. if one tissue core has been severely stretched or otherwise deformed.

c. Align sections - press the Align All button.

d. Detect sampling area (can be skipped). Used to refine the outline that was made in a).

e. Sample. Press the ‘Sample in All’ button. Cores are extracted and aligned at high magnification.

f. Review the high magnification alignment.

g. Adjust the high magnification alignment if required, otherwise close the Tissuealign module and go to the Image Analysis module.



STAINING PROTOCOL

There is no staining protocol available


ADDITIONAL INFORMATION

The APP utilizes the EngineTM and Viewer software modules, where EngineTM offers an execution platform to expand processing capability and speed of image analysis. Viewer gives a fast review together with several types of image adjustment properties ex. outlining of regions, annotations and direct measures of distance, curve length, radius, etc.
By adding the AuthorTM module the APP can be customized to fit other purposes. AuthorTM offers a comprehensive and dedicated set of tools for creating new fit-for-purpose analysis APPs, and no programming experience is required.

The APP also utilizes the modules TissuearrayTM and TissuealignTM, where TissuearrayTM offers an automated Tissue Micro Array (TMA) analysis and TissuealignTM offers manual or automated alignment with either VirtualDoubleStainingTM or VirtualMultiplexingTM in the TMA workflow.

WORKFLOW

Quantification of mature to immature vessel ratio:

Step 1: Load the APP

Step 2: The ROI from the alignment was saved with the extracted cores. Manually exclude areas of artifacts.

Step 3: Run the APP in batch mode or on single images.


REFERENCES

USER

Development of this APP was in collaboration with Dr James Thompson, Karolinska Healthcare Research Biobank (KHRBB) - Karolinska University Hospital, Stockholm, Sweden, and Dr Carina Strell, Cancer Center Karolinska, Dept of Oncology & Pathology, Karolinska Institutet, Stockhom, Sweden.

RUO
FIGURE 1
FIGURE 1
Each TMA slide is stained with either CD31 or CD34.
FIGURE 2
FIGURE 2
Using the Tissuealign module, the sequential core pair is overlaid. Here they are shown with a 50 % transparency to illustrate the initial misalignment.
FIGURE 3
FIGURE 3
In the next step the two tissue cores are automatically aligned, as shown here with a 50% transparency (as in the previous example). Notice the curved edge of the top layer which illustrates that it has been stretched/deformed to get the best possible match between the two layers.
FIGURE 4
FIGURE 4
High magnification (20X) view of the same vessel stained with CD31 (left) and CD34 (right).
FIGURE 5
FIGURE 5
DAB color deconvolution of the CD31 layer. This is the feature on which the detection of CD31 positive areas is based.
FIGURE 6
FIGURE 6
Final segmentation showing the overlapping positive stain (green label), CD31 positive areas (blue) and CD34 positive areas (red). In many cases the vessel outline will look (slightly) different in the two sequential sections and will not match 100% when aligned. Therefore, there will be areas where only CD31 positive stain is present.
FIGURE 7
FIGURE 7
Example of the quality of alignment, using a slide where there is very little CD31 positivity. Two red crosses are used as fix points to illustrate how well they have been aligned.
FIGURE 8
FIGURE 8
Quantification of the overlaid images shown in Figure 7. Since there are very few CD31 positive areas, the area of green label (representing overlapping positive stain) and blue label (representing CD31 positive stain) is almost zero.