{"id":4698,"date":"2021-09-16T15:22:05","date_gmt":"2021-09-16T07:22:05","guid":{"rendered":"http:\/\/43.135.177.8\/?p=4698"},"modified":"2021-09-16T15:56:58","modified_gmt":"2021-09-16T07:56:58","slug":"microfluidic-enrichment-of-plasma-cells-improves-treatment-of-multiple-myeloma","status":"publish","type":"post","link":"https:\/\/whmicro.com\/?p=4698","title":{"rendered":"Microfluidic enrichment of plasma cells improves treatment of multiple myeloma"},"content":{"rendered":"<h2 id=\"d9509641\" class=\"article-section__header section__title main abstractlang_en main cyxy-trs-source cyxy-trs-source-ted\">Abstract<\/h2>\n<div class=\"article-section__content en main\">\n<p class=\"cyxy-trs-source cyxy-trs-source-ted\">Cytogenetic alterations form the basis for risk stratification for multiple myeloma (MM) and guide the selection of therapy; however, current pathology assays performed on bone marrow samples can produce false-negatives due to the unpredictable distribution and rarity of MM cells. Here, we report on a microfluidic device used to facilitate CD45 depletion to enhance the detection of cytogenetic alterations in plasma cells (PCs). Bone marrow samples from 48 patients with MM were each divided into two aliquots. One aliquot was subjected to classic flow cytometry and fluorescent\u00a0<i>in\u00a0situ<\/i>\u00a0hybridization (FISH). The other first went through CD45<sup>+<\/sup>\u00a0cell depletion, further enriched by microfluidic size selection. The enriched samples were then analyzed using flow cytometry and FISH and compared to those analyzed using the classic method only. Unlike the traditional method, the microfluidic device removed the CD45<sup>+<\/sup>\u00a0leukocytes and specifically selected PCs from the remaining white blood cells. Therefore, the microfluidic method (MF-CD45-TACs) significantly increased the percentage of CD38<sup>+<\/sup>\/CD138<sup>+<\/sup>\u00a0cells to 37.7\u00a0\u00b1\u00a020.4% (<i>P<\/i>\u00a0&lt;\u00a00.001) from 10.3\u00a0\u00b1 8.5% in bone marrow. After the MF-CD45-TAC enrichment, the detection rate of IgH rearrangement, del(13q14), del(17p), and 1q21 gains, rose to 56.3% (<i>P<\/i>\u00a0&lt;\u00a00.001), 37.5% (<i>P<\/i>\u00a0&lt;\u00a00.001), 22.9% (<i>P<\/i>\u00a0&lt;\u00a00.001), and 41.7% (<i>P<\/i>\u00a0=\u00a00.001), respectively; all rates of detection were significantly increased compared to the classically analyzed samples. In this clinical trial, this microfluidic-assisted assay provided a precise detection of cytogenetic alterations in PCs and improved clinical outcomes.<\/p>\n<\/div>\n<p>&nbsp;<\/p>\n<h2 id=\"mol212201-sec-0001-title\" class=\"article-section__title section__title section1 cyxy-trs-source cyxy-trs-source-ted\">1 Introduction<\/h2>\n<p class=\"cyxy-trs-source cyxy-trs-source-ted\">Multiple myeloma (MM) is an incurable neoplasm of plasma cells (PCs) that affects more than 20\u00a0000 people annually in the United States. Risk stratification, primarily based on cytogenetic abnormalities, has emerged as essential for its management (Mikhael\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0014R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0014\" data-tab=\"pane-pcw-references\">2013<\/a>). Thalidomide, lenalidomide, and pomalidomide, which represent the first to third generations of immunomodulatory drugs, respectively, are used for MM maintenance therapy. Cytogenetic alterations form the basis of MM risk stratification and selection of immunomodulatory drugs for therapy (Nathwani\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0015R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0015\" data-tab=\"pane-pcw-references\">2016<\/a>). PCs undergo clonal evolution: In earlier and smoldering disease, CD45-positive cells predominate, whereas CD45-negative PCs are more prevalent in patients with advanced disease (both new and relapsed) (Kumar\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0009R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0009\" data-tab=\"pane-pcw-references\">2005<\/a>). Thus, both CD45<sup><b>\u2212<\/b><\/sup>\u00a0and CD45<sup><b>+<\/b><\/sup>\u00a0can serve as prognostic biomarkers for MM (Gonsalves\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0005R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0005\" data-tab=\"pane-pcw-references\">2016<\/a>) but with distinct prognoses. The tumor load in patients with CD45<sup>\u2212<\/sup>\u00a0cells is higher than those with CD45<sup>+<\/sup>\u00a0cells, which could be explained by the lower proliferation rate of the latter population (Asosingh\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0001R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0001\" data-tab=\"pane-pcw-references\">2001<\/a>). Malignant PCs manifest as CD45<sup>\u2212<\/sup>\u00a0cells with co-expression of CD38\/CD138 plus CD19 and CD56, implying the clinical significance of CD45<sup>\u2212<\/sup>\u00a0cells in risk stratification of MM (Langer\u00a0<i>et\u00a0al<\/i>.,\u00a0<a id=\"mol212201-bib-0010R\" class=\"bibLink tab-link\" href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-bib-0010\" data-tab=\"pane-pcw-references\">2016<\/a>). Therefore, depletion of CD45<sup>+<\/sup>\u00a0cells in bone marrow could enrich PCs for this purpose.<\/p>\n<h3 id=\"mol212201-sec-0004-title\" class=\"article-section__sub-title section2 cyxy-trs-source cyxy-trs-source-ted\">Microfluidic device fabrication<\/h3>\n<p>Microfluidic DLD devices were fabricated with standard photolithography and soft lithography techniques. Negative photoresist SU8-3025 (Microchem, Westborough, MA, USA) was used to fabricate the master mold on a silicon wafer with a photomask. The patterned silicon wafers were silanized with chlorotrimethylsilane (Aldrich, Burlington, MA, USA) to facilitate particle desorption mass spectrometry mold release. Polydimethylsiloxane (PDMS, RTV615; General Electric, USA) mixed with curing agent (5\u00a0:\u00a01 w\/w ratio) was poured into the silicon mold and cured at 80\u00a0\u00b0C for 1\u00a0h. Holes were punched for inlet and outlets, and the PDMS mold was bonded to glass slides after oxygen plasma treatment. The design of the DLD device is shown in Fig.\u00a0<a href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-fig-0002\">2<\/a>.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-4699\" src=\"http:\/\/43.135.177.8\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-300x161.jpeg\" alt=\"\" width=\"300\" height=\"161\" srcset=\"https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-300x161.jpeg 300w, https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-1024x550.jpeg 1024w, https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-768x412.jpeg 768w, https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-1536x824.jpeg 1536w, https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m-2048x1099.jpeg 2048w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>&nbsp;<\/p>\n<h3 id=\"mol212201-sec-0005-title\" class=\"article-section__sub-title section2 cyxy-trs-source cyxy-trs-source-ted\">Microfluidic enrichment of plasma cells (MF-CD45-TACs)<\/h3>\n<p class=\"cyxy-trs-source cyxy-trs-source-ted\">The microfluidic DLD design consisted of an inlet, three outlets, and a central flow chamber with micropost array, as shown in Fig.\u00a0<a href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201#mol212201-fig-0002\">2<\/a>. The flow chamber was 35\u00a0mm long, 3.5\u00a0mm wide, and 30\u00a0\u03bcm high. The micropost array was tilted at an angle of 3.2\u00b0 relative to the fluid flow direction. For each patient, a 1.0\u00a0mL sample of bone marrow fluid and 500\u00a0\u03bcL CD45 TACs were mixed at room temperature for 30\u00a0min. The mixture was slowly added into 2.0\u00a0mL Ficoll in a test tube. Low-speed\/low-temperature centrifugation was performed at 450\u00a0<b><i>g<\/i><\/b>\u00a0for 15\u00a0min. The white film layer at the interface of the plasma and the Ficoll solution was transferred to a fresh tube. Then, the white film layer (50\u2013100\u00a0\u03bcL, 1\u00a0\u00d7\u00a010<sup>6<\/sup>\u00a0cells) was loaded into DLD chip for PC enrichment. The DLD critical deflection diameter is designed such that large cells (PCs) flow in a bumping mode and thus are concentrated in the center of chamber, while small cells (erythrocytes and most of leukocytes) follow the mainstream direction. We optimized the design in the outlet portion to maximize the PC enrichment. The outlet portion of the device consists of a row of microposts with gradually decreasing gaps. With this design, although part of the erythrocytes and leukocytes escaped through the gaps at the outlet, the PCs can be fully collected once they were concentrated in the DLD chip. The resulting DLD-enriched PCs were then subjected to FACS detection.<\/p>\n<p>Read the original articles:<\/p>\n<p><a href=\"https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201\">https:\/\/febs.onlinelibrary.wiley.com\/doi\/10.1002\/1878-0261.12201<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Cytogenetic alterations form the basis for risk stratification for multiple myeloma (MM) and guide the selection of therapy; however, current pathology assays performed on bone marrow samples can produce false-negatives due to the unpredictable distribution and rarity of MM cells. Here, we report on a microfluidic device used to facilitate CD45 depletion to enhance the detection of cytogenetic alterations in plasma cells (PCs).<\/p>\n","protected":false},"author":1,"featured_media":4699,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[100,101],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v18.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Microfluidic enrichment of plasma cells<\/title>\n<meta name=\"description\" content=\"Cytogenetic alterations form the basis for risk stratification for multiple myeloma (MM) and guide the selection of therapy\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/whmicro.com\/?p=4698\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Microfluidic enrichment of plasma cells\" \/>\n<meta property=\"og:description\" content=\"Cytogenetic alterations form the basis for risk stratification for multiple myeloma (MM) and guide the selection of therapy\" \/>\n<meta property=\"og:url\" content=\"https:\/\/whmicro.com\/?p=4698\" \/>\n<meta property=\"og:site_name\" content=\"WenHao\" \/>\n<meta property=\"article:published_time\" content=\"2021-09-16T07:22:05+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2021-09-16T07:56:58+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/whmicro.com\/wp-content\/uploads\/2021\/09\/mol212201-fig-0002-m.jpeg\" \/>\n\t<meta property=\"og:image:width\" content=\"2128\" \/>\n\t<meta property=\"og:image:height\" content=\"1142\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Happy\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebSite\",\"@id\":\"https:\/\/whmicro.com\/#website\",\"url\":\"https:\/\/whmicro.com\/\",\"name\":\"WenHao\",\"description\":\"Microfluidic Chip &amp; 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