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. Author manuscript; available in PMC: 2024 Jan 31.
Published in final edited form as: J Invest Dermatol. 2023 Jun 20;143(8):1412–1422. doi: 10.1016/j.jid.2023.04.005

Table 1.

Comparison of Investigational Approaches for Personalized Therapy Selection in Inflammatory Skin Disease

Tape Stripping Dermal Biomarker Patch (Mindera Health) Epidermal Curettage (Castle) RISH Staining scRNA-seq
Sampling technique 1–20 tape strips applied to the skin Dermal biomarker patch applied to the skin for 5 minutes 10 scrapes with curette Skin biopsy Skin biopsy
Layers of skin samples Stratum corneum Epidermis and upper dermis Not publicly disclosed Epidermis and dermis Epidermis and dermis
Cryopreservation necessary Yes. Must store tape strips at –80 °C No. Can be stored at 4 °C and processed within 72 hours Not publicly disclosed No Samples typically processed fresh
Likelihood of scar Low Not publicly disclosed Not publicly disclosed High High
Integration into clinical workflow1 Can be collected relatively rapidly; requires specific expertise, normalization, and possibly slow turnaround time. Can be collected relatively rapidly. Turnaround time and cost of commercial service not yet clear. Can be collected relatively rapidly. Turnaround time and cost of commercial service not yet clear. Integrates well with IHC workflow in dermatopathology laboratories with rapid turnaround for specific targets. Resource-intensive sample processing, sequencing, and data analysis.
Throughput/number of markers Full transcriptome (for RNA-based methods) Full transcriptome 28 transcripts One marker per staining; multiple markers can be batched Full transcriptome
Requires sequencing Yes Yes No No Yes
Data analysis Computational pipelines for microarray or RNA- sequencing data. Computational pipelines with proprietary algorithms. Comparison of count threshold values from qPCR. Manual or automated quantification of positive cells on microscopy slide. Computational pipelines for scRNA-seq data.
Histologic analysis inherent No No No Yes No

Abbreviations: RISH, RNA in situ hybridization; scRNA-seq, single-cell RNA sequencing.

1

Cost will also be an important factor in comparing the feasibility of workflow integration, but there are not enough data at this time to compare costs between methods.