Genetic Engineering & Biotechnology News

AUG 2017

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28 | AUGUST 2017 | GENengnews.com | Genetic Engineering & Biotechnology News and immunotherapy. Multiplexing in immuno-oncology is increasing. This trend, however, imposes new requirements. For example, novel markers and marker signatures will be useful in the stratification of drug responders vs. nonresponders only if they provide sufficient accuracy. Also, combination therapies and less-invasive biopsy procedures will require more effi- cient analytical tools to extract more content-rich informa- tion from fewer and smaller samples. Preserving Spatial Information Multiple cell subpopulations define the tumor microen- vironment, such as tumor cells, tumor-infiltrating lympho- cytes, and stromal cells. Specific biomarkers are used to de- tect these cell populations and their spatial relationships to understand the biological mechanisms underlying response to immunotherapy; numerous biomarkers may need to be imaged on single tumor-biopsy sections. Commonly used, spectral-multiplexing methods are based on successive iterations of antigen retrieval, staining, and amplification steps. Multiplexing often results in long cycle times per sample and likely causes irreversible damage to the tissue sample's integrity and antigenicity. According to Louis Levy, director, corporate and busi- ness development, Ultivue InSituPlex is a flexible immuno- fluorescence platform used for the multiplex detection and analysis of protein markers in tissue using stable DNA–DNA interactions. Measurements are order independent and allow high multiplexing levels with fast cycles without tissue or an- tigenic damage. Complementary strands of DNA are associated with either an antibody (to bind to a target) or a fluorophore (to image). Multiple targets are stained simultaneously in a single staining step using antibody-DNA conjugates, where each conjugate contains a target-specific DNA strand serving as a barcode. The barcodes are extended through a single DNA-based am- plification step to bind to complementary fluorophore-labeled DNA strands and image a target of low- to high-level abun- dance. The DNA strands can be dehybridized to completely remove the fluorescence signal from the sample, if desired. InSituPlex Discovery relies on sequential multiplexing to image double-digit numbers of protein markers. Multiple cy- cles of hybridization, imaging, and dehybridization are car- ried out on single formalin-fixed paraffin-embedded (FFPE) sections. After completion of image acquisition, the resulting images are digitally overlaid to visualize the targets of interest using available software packages (i.e., HALO, Visiopharm, and ImageJ). Quantitative RNA ISH Immunohistochemistry (IHC) and RNA hybridization (ISH) are widely used to analyze biomarkers at the tissue or single-cell level while preserving the morphological context. These techniques have been incorporated into RNAscope, an ISH assay developed by Advanced Cell Diagnostics for the detection of target RNA within FFPE or fresh frozen tissues. The assay has a proprietary probe design to amplify tar- get-specific signals, but not background noise, from nonspe- cific hybridization; two independent probes (double-Z) need to hybridize to the target sequence in tandem for signal am- plification to occur. Because it is highly unlikely that two independent probes will hybridize to a nonspecific target right next to each other, this design ensures selective amplification of target-specific signals. For each target RNA species, 3–20 double-Z probe pairs are designed to specifically hybridize to the target mol- ecule region. "The absence of universally accepted standards and guidelines for antibody characterization, including target sensitivity and specificity, limits the confidence of IHC data and supports the need for alternative biomarker validation methods," says Rob Monroe, M.D., Ph.D., CMO, Advanced Cell Diagnostics. "With fast development timelines, RNA ISH is an excel- lent method for validation of biomarkers discovered through a variety of genomic approaches, such as DNA-seq, RNA- seq, digital PCR, and microarray, as well as for the validation of antibodies used for detection of biomarkers with IHC," adds Dr. Monroe. "The RNAscope technology's unique probe design strategy, which simultaneously amplifies signal while suppressing background, allows for routine and reli- able in situ detection at single-molecule sensitivity." RNAscope is available in fluorescence as well as chromogen- ic singleplex and multiplex assay formats. Automated on both the Leica Biosystems Bond platform and the Ventana Medical Systems Discovery platform, the half-day turnkey assay pro- vides consistent, easy-to-interpret, and quantifiable results. Approximately 15,000 off-the-shelf probe targets are available; new targets can be developed within two weeks. Pharma assay services are also offered for target validation, target safety assessment, and biomarker discovery to support preclinical research, clinical biomarker, and companion diag- nostic assay development. Ultra-Sensitive Protein Measurement Simoa, another new technology, uses single-molecule mea- surements to assess previously undetectable proteins, or those only observed in acute responses, in blood across a variety of therapeutic areas, such as neurology, oncology, cardiology, infectious disease, and inflammation. The technology isolates individual immunocomplexes on paramagnetic beads using standard ELISA reagents. Mol- ecules are trapped in femtoliter-sized wells, allowing a "digi- tal" readout of each individual bead to determine whether or not it is bound to the target analyte. "The digital feature allows a 1,000× sensitivity increase with coefficients of variation of less than 10%. The device is so sensitive that it can find a grain of sand in 2,000 Olympic swimming pools and find a single blade of grass in a field as big as the state of Alaska," explains Kevin Hrusovsky, execu- tive chairman and CEO, Quanterix. For example, Simoa assays can detect neurodegeneration markers in serum and plasma that were previously only de- tectable in cerebrospinal fluid samples, and can directly de- tect critical biomarkers for measurement of latent replication competent viral reservoirs, such as interferon-α in serum and HIV p24 protein from single cells. "Precision biomarker measurement is crucial to realizing the potential of precision medicine. Monitoring biomarker baseline levels is becoming a key element of early detection and treatment approaches. It is our hope that one day clini- cians will use technology like ours and a simple blood test as part of annual physicals, to create a baseline patient-specific protein profile," continues Mr. Hrusovsky. Recently, the company introduced the Simoa Neurology 4-Plex A assay (N4PA), the first comprehensive multiplex panel to study traumatic brain injury and other neurogenerative condi- tions. N4PA simultaneously measures four protein biomarkers from either cerebrospinal fluid or directly from blood samples. A planned benchtop Simoa instrument will support in- creased levels of multiplexing and provide the ability to mea- sure circulating protein and nucleic acid biomarkers on the same platform. In addition, the Quanterix Accelerator Lab provides dedicated laboratory resources to facilitate new bio- marker research, customer assay development, and clinical sample testing. Monitoring Cell Proliferation Many biomarkers, such as protein or genetic signatures, indicate the likelihood that a malignancy will respond to a therapy, but do not provide information as to how fast the malignancy is growing, also known as the proliferation rate. Similarly, many traditional serum biomarkers, such as CEA, PSA, and CA15-3, provide information regarding tumor mass and past growth but not the current or the future ex- pected growth rate. The AroCell TK 210 ELISA is a novel, sensitive, and spe- cific assay for serum thymidine kinase 1 (TK1), a key enzyme Biomarker Platforms Advance Immuno-Oncology Ultivue has developed InSituPlex, a platform that uses stable DNA-DNA interactions to sequentially image targets. Multiple cycles of hybridization, imaging, and dehybridization are carried out to achieve high multiplexing in situ. In these images, which show human tonsil tissue, the Ultivue-2 two-plex kit for super- resolution microscopy has been used to accomplish six consecutive cycles of addition and removal of fluorophore- labeled DNA strands. The gentle removal of fluorescence in the Ultivue-2 workflow helps maintain tissue integrity. Translational Medicine Feature Continued from page 1

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