Deliver objective and reproducible transplant biopsy assessments
In the post-transplant setting, data derived from the molecular profile of a biopsy can signal ongoing and often subclinical immune-mediated injury, as well as identify acute T cell-mediated rejection, even in samples without histological evidence of inflammation.1 This approach helps to overcome the limitations of conventional biopsy diagnosis, which often relies on histopathology scores that are empirically derived, subjective, and opinion-based.
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MMDx-Heart and MMDx-Kidney complement conventional biopsy processing to improve the assessment of rejection and injury in transplanted organs. These Laboratory Developed Tests use a GeneChip™ Custom Microarray to measure mRNA transcript levels in biopsies along with extensive big data derived from individuals and populations. The MMDx-Heart and MMDx-Lung systems combine these technologies to deliver objective and reproducible transplant biopsy assessments on a molecular level.
“Using an objective scientific approach instead of by eye, we can look at the molecular signature of a biopsy to make a more accurate diagnosis” 1
Andrew Fisher, PhD
Institute of Transplantation at Freeman Hospital
Newcastle Upon Tyne, United Kingdom
Obtaining results starts with requesting a free Specimen Collection Kit.
The illustration below shows how the sample is analyzed and the biopsy report is generated and made available to clinicians.
Kashi Clinical Laboratories, Inc., a CLIA licensed CAP-accredited laboratory located in Portland, Oregon, adopted the MMDx technology. This laboratory-based service will be offered by Kashi in collaboration with Transcriptome Sciences Inc. (TSI) for processing of sample biopsies in the US. Kashi Clinical Laboratories is licensed in all states, including New York, California and Florida.
Molecular Microscope and MMDx are registered trademarks of Transcriptome Sciences Inc.
MMDx is a Laboratory Developed Test offered by Kashi Clinical. MMDx is not intended to provide information for the diagnosis, prevention or treatment of disease or to aid in the clinical decision-making process. This system is not cleared or approved for clinical use by the FDA or approved in the EU as an in vitro diagnostic test, nor is it CE marked.