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Characterization of Buffy Coat-Derived Granulocytes for Clinical
UvA-DARE (Digital Academic Repository) Neutrophil defects and deficiencies van de Geer, A. Publication date 2020 Document Version Other version License Other Link to publication Citation for published version (APA): van de Geer, A. (2020). Neutrophil defects and deficiencies. General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:01 Oct 2021 Chapter 6 1 Characterization of buffy-coat-derived granulocytes for clinical use: a 2 comparison with granulocyte-colony stimulating factor/dexamethasone- pretreated donor-derived products. 3 Annemarie van de Geer1, Roel P. Gazendam1, Anton T.J. Tool1, John L. van Hamme1, Dirk de Korte1,2, Timo K. van den Berg1, Sacha S. Zeerleder3,4 and Taco W. Kuijpers1,5. 4 1. Dept. of Blood Cell Research, Sanquin Research, Amsterdam, The Netherlands 2. -
(2019). Manufacturing Variables and Hemostatic Function of Cold Stored Platelets: a Systematic Review of the Literature
Scorer, T., Williams, A., Reddoch-Cardenas, K., & Mumford, A. (2019). Manufacturing Variables and Hemostatic Function of Cold Stored Platelets: A Systematic review of the Literature. Transfusion, 59(8), 2722 - 2732. https://doi.org/10.1111/trf.15396 Peer reviewed version Link to published version (if available): 10.1111/trf.15396 Link to publication record in Explore Bristol Research PDF-document This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Wiley at 10.1111/trf.15396 . Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/red/research-policy/pure/user-guides/ebr-terms/ Manufacturing Variables and Hemostatic Function of Cold Stored Platelets: A Systematic review of the Literature Thomas Scorer1,2,3 Ashleigh Williams4 Kristin Reddoch-Cardenas3 Andrew Mumford1 1. School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK 2. Centre of Defence Pathology, RCDM, Birmingham, UK 3. Coagulation and Blood Research, U.S. Army Institute of Surgical Research, JBSA Ft Sam Houston, Texas, USA. 4. Department of Anaesthesia, Derriford Hospital, Plymouth Word count: 4352 Abstract word count - 250 Number of figures and tables: 3 figures and 5 tables References: 54 Corresponding author: Dr Tom Scorer, Research Floor Level 7, University of Bristol, Bristol Royal Infirmary, Bristol, BS2 8HW United Kingdom. Email: [email protected] The authors have no relevant conflicts of interest to declare. -
761070Orig1s000
CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 761070Orig1s000 NON-CLINICAL REVIEW(S) Tertiary Pharmacology/Toxicology Review Date: November 1, 2017 From: Timothy J. McGovern, PhD, ODE Associate Director for Pharmacology and Toxicology, OND IO BLA: 761070 Agency receipt date: November 16, 2016 Drug: FASENRA (benralizumab) injection, for subcutaneous use Sponsor: AstraZeneca Pharmaceuticals LP Indication: Add-on maintenance treatment of patients with severe asthma aged 12 years and older, and with an eosinophilic phenotype. Reviewing Division: Division of Pulmonary, Allergy, and Rheumatology Products The primary pharmacology/toxicology reviewer and team leader concluded that the nonclinical data for FASENRA (benralizumab) solution for subcutaneous injection support approval for the indication listed above. Benralizumab is a humanized, afucosylated IgG1 kappa monoclonal antibody that targets interleukin-5 receptor alpha. The recommended dose of benralizumab is 30 mg administered once every 4 weeks for the first 3 doses, and then once every 8 weeks thereafter. The Established Pharmacologic Class (EPC) for benralizumab is “interleukin- 5 receptor alpha-directed cytolytic monoclonal antibody”. Pivotal nonclinical studies were conducted in Cynomolgus monkeys. In toxicology studies up to 39 weeks duration, NOAELs of 10 mg/kg IV and 30 mg/kg SC were identified. The primary finding at a dose of 25 mg/kg IV was a post-dose reaction in one high-dose female that included bruising in the areas of the eyes, face, chest and lower abdomen, a decrease in platelet counts, and abnormal erythrocytes after the fourth dose. The NOAEL doses were associated with systemic exposures (AUC) that provided 153- to 271-fold exposure margins compared to the recommended clinical dose. -
Principles of Blood Separation and Apheresis Instrumentation
Principles of Blood Separation and Apheresis Instrumentation Dobri Kiprov, M.D., H.P. Chief, Division of Immunotherapy, California Pacific Medical Center, San Francisco, CA Medical Director, Apheresis Care Group Apheresis History Apheresis History Apheresis History Apheresis From the Greek - “to take away” Blood separation Donor apheresis Therapeutic apheresis Principles of Blood Separation Filtration Centrifugation Combined centrifugation and filtration Membrane Separation Blood is pumped through a membrane with pores allowing plasma to pass through whilst retaining blood cells. Available as a hollow fiber membrane (older devices used parallel-plate membranes) Pore diameter for plasma separation: 0.2 to 0.6μm. A number of parameters need to be closely controlled Detail of Membrane Separation Courtesy of CaridianBCT Membrane Blood Separation Trans Membrane Pressure (TMP) Too High = Hemolysis TMP Too Low = No Separation Optimal TMP = Good Separation Membrane Apheresis in the US - PrismaFlex (Gambro – Baxter) - NxStage - BBraun Filtration vs. Centrifugation Apheresis Filtration Centrifugation Minimal availability The standard in the in the USA USA • Poor industry support • Very good industry support Limited to plasma Multiple procedures (cytapheresis) exchange • Opportunity to provide • Low efficiency cellular therapies Centrifugation vs. Filtration Apheresis Centrifugation Apheresis Filtration Apheresis Blood Flow 10 – 100 ml/min 150 ml/min Efficiency of Plasma 60 – 65% 30% Removal Apheresis in Clinical Practice and Blood Banking Sickle Cell Disease Falciparum Malaria Thrombocytosis RBC WBC PLT Plasma Leukemias TTP-HUS Cell Therapies Guillain Barre Syndrome Myasthenia Gravis CIDP Autoimmune Renal Disease Hyperviscosity Syndromes Centrifugal Separation Based on the different specific gravity of the blood components. In some instruments, also based on the cellular size (Elutriation). -
Joint UKBTS Professional Advisory Committee (1)
Joint UKBTS Professional Advisory Committee (1) Position Statement Granulocyte Therapy November 2017 Revised by: Edwin Massey, Simon Stanworth, Suzy Morton, & Rebecca Cardigan at the request of the Standing Advisory Committee on Blood Components November 2017 - The contents of this document are believed to be current. Please continue to refer to the website for in-date versions. Introduction Granulocyte transfusions continue to be requested by clinicians for use in patients with refractory infection or at high risk of developing severe infection (Strauss 2003). Most patients prescribed granulocyte transfusions are those with cancer related neutropenia, who are receiving myeloablative chemotherapy with or without haemopoietic stem cell rescue. Interest in the use of granulocytes remains high (Van Burik & Weisdorf, 2002; Price 2006), and requests for granulocyte components for transfusion were steadily increasing in the UK until 2015 but since then requests have been more stable or even reduced. This pattern has been driven by publications describing transfusion in neutropenic patients both for therapeutic indications, when they have an infection refractory to antimicrobials (Hubel et al. 2002) and for secondary prophylaxis, in patients who have had severe bacterial or fungal infections previously but who require a further cycle of chemotherapy or haemopoietic stem cell rescue (Kerr et al. 2003, Oza et al., 2006). A number of studies with variable or promising, but overall inconclusive, results have been reported both in adults (Oza et al. 2006, Seidel et al, 2008) and children (Sachs et al., 2006). More recently, a further trial in North America was published: The Resolving Infection in Neutropenia with Granulocytes (RING) study (Price et al, 2015); this is discussed in more detail below. -
Efficient Buffy Coat Extraction
Application Note Efficient buffy coat extraction Reliable extraction of buffy coat from human blood on a Freedom EVO® platform Introduction The recent advances in personalized diagnostics continue to A valuable body fluid for diagnostic purposes is the buffy coat, inspire a wealth of personalized treatments, resulting in a layer of leukocytes and platelets that forms between the state-of-the-art personalized heathcare. The Integrated erythrocyte layer and the plasma when unclotted blood is Biobank of Luxembourg (IBBL), a newly founded independent, centrifuged or allowed to stand. Typically, the isolation of the not-for-profit biobank, designed for a new era of research and buffy coat from whole blood has been a tedious and lengthy the next generation of healthcare, is at the forefront of these manual process. Researchers at the Integrated Biobank of medical advances. Research into personalized medicine Luxembourg have tested and evaluated the feasibility and requires high quality samples (including tissue and body efficiency of extracting the buffy coat using an automated fluids, such as blood, blood fractions and saliva) and clinical process on Tecan’s Freedom EVO platform. data from large numbers of patients, collected by biobanks, to translate today’s discoveries into future personalized medical The automation of buffy coat extraction is challenging. In care innovations. As a world class EU biobank, the IBBL addition to the blood volumes in the individual blood collection provides a wide variety of the highest quality samples, tubes varying, important inter-individual variations in the alongside cutting-edge technology, to accelerate clinical quantity, viscosity and texture of the buffy coat layer itself, for research and improve public health. -
Original Article HAEMATOPOIETIC THROMBOCYTE PRECURSORS
Bulgarian Journal of Veterinary Medicine, 2021, 24, No 1, 2231 ISSN 1311-1477; DOI: 10.15547/bjvm.2019-0063 Original article HAEMATOPOIETIC THROMBOCYTE PRECURSORS IN RAT FEMORAL AND STERNAL BONE MARROW D. SULJEVIĆ1, A. HAMZIĆ1, E. ISLAMAGIĆ1, E. FEJZIĆ2 & A. ALIJAGIĆ1 1Department of Biology, Faculty of Science, University of Sarajevo, Sarajevo, Bosnia and Herzegovina; 2Institute for Transfusion Medicine of FBiH, Sarajevo, Bosnia and Herzegovina Summary Suljević, D., A. Hamzić, E. Islamagić, E. Fejzić & A. Alijagić, 2021. Haematopoietic thrombocyte precursors in rat femoral and sternal bone marrow. Bulg. J. Vet. Med., 24, No 1, 2231. This research presents the first findings on thrombopoiesis for Wistar rats. Haemopoietic cells from the femur and the sternum were analysed by light microscopy in combination with infrared and near- ultraviolet light for fine cytoplasmic structure analysis. Five main types of thrombocyte precursor cells were identified in the bone marrow samples: megakaryoblast, promegakaryocyte and megakaryocyte (basophilic, acidophilic and thrombocytogenic). More intensive thrombopoiesis and morphologically differentiated cells were found in sternum samples. Key words: bone marrow, megakaryocyte, platelets, thrombopoiesis, Wistar rat INTRODUCTION Bone marrow smears from rats usually is diminished as platelets production is contain a large number of megakaryocytes shifted from the spleen to some other accounting for 0.40–0.77% of total organ, like bone marrow (Bolliger, 2004). nucleated cells in rat bone marrow (Saad Large megakaryocytes could be a et al., 2000). Density and distribution of product of an early thrombopoietic phase megakaryocytes vary with technique and occurring in the first days of pregnancy as among smears; however, there are no observed in the mammalian order of published results regarding the precise rodents (Rodentia) (Pacheco et al., 2002). -
Platelet and Erythrocyte Functional Defects Caused by Mutations of Transcription Factor GFI1B
Platelet and erythrocyte functional defects caused by mutations of transcription factor GFI1B Lucinda Beutler A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Faculty of Medicine University of Sydney December 2018 I praise you because…… I am fearfully and wonderfully made; Your works are wonderful - I know that full well. Psalm 139:14 (NIV) TABLE OF CONTENTS STATEMENT OF ORIGINALITY ...................................................................................................... vi ACKNOWLEDGEMENTS .............................................................................................................. vii ABSTRACT ................................................................................................................................... ix PUBLICATIONS AND PRESENTATIONS ........................................................................................... x LIST OF FIGURES .......................................................................................................................... xi LIST OF TABLES........................................................................................................................... xv ABBREVIATIONS ........................................................................................................................ xvii 1. Literature review ...................................................................................................................... 2 1.1 Introduction ...................................................................................................................... -
Comparing the Buffy Coat and Traditional Blood Smears in the Microscopic Diagnosis of Malaria
International Journal of Malaria Research and Reviews www.resjournals.org/IJMR ISSN: 2346-7266 Vol. 2(2): 7-12, November, 2014 Comparing the Buffy Coat and Traditional Blood Smears in the Microscopic Diagnosis of Malaria Anna Longdoh Njunda1, Dickson Shey Nsagha2, Jules Clement Nguedia Assob1,3, Tayong Dizzle Bita Kwenti4, Nfor Loveline Giwe1 and Tebit Emmanuel Kwenti1,4* 1Department of Medical Laboratory Sciences, Faculty of Health Sciences, University of Buea, P.B. 63, Buea, Cameroon 2Department of Public Health and Hygiene, Faculty of Health Sciences, University of Buea, P.B. 63, Buea, Cameroon 3Department of Biomedical Sciences, Faculty of Health Sciences, University of Buea, P.B. 63, Buea, Cameroon 4Department of Microbiology and Parasitology, Faculty of Sciences, University of Buea, P.B. 63, Buea, Cameroon *Email for Correspondence: [email protected]; Tel:+(237)97979776 #All Authors contributed equally ABSTRACT The purpose of this study was to compare buffy coat smear (BCS) and traditional blood smear (TBS) in the microscopic diagnosis of malaria using Giemsa-stained blood films. Blood samples were collected from 130 patients clinically suspected of malaria. Thin and thick blood films were prepared using whole blood and buffy coat for each sample. The Giemsa-stained slides were examined to determine the number of parasites per high power field (HPF). Data were analysed using the student T test, Chi-square and correlation analysis. Eleven (8.5 %; CI: 3.7 – 13.3) specimen were positive for the TBS and 16 (12.3 %; CI: 6.7 – 18) were positive for the BCS including all the specimens that were positive with the TBS. -
Donor Granulocyte Transfusions in Patients with Hematologic Malignancies and in Recipients of Hematopoietic Stem Cell Transplantation
Review Article iMedPub Journals Journal of Stem Cell Biology and Transplantation 2019 www.imedpub.com ISSN 2575-7725 Vol.3 No.1:1 DOI: 10.21767/2575-7725.100022 Donor Granulocyte Transfusions in Patients Al-Jasser AM1 and Al-Anazi 2* with Hematologic Malignancies and in KA Recipients of Hematopoietic Stem Cell 1 Riyadh Regional Laboratory, Ministry of Transplantation Health, Saudi Arabia 2 Department of Adult Hematology and Hematopoietic Stem Cell Transplantation, Oncology Center, King Abstract Fahad Specialist Hospital, Saudi Arabia Despite the progress achieved in antimicrobial therapies and supportive care, infections remain a major cause of morbidity and mortality in patients with hematologic malignancies and in recipients of hematopoietic stem cell *Corresponding author: Khalid A. Al-Anazi transplantation. In the 1990s, there was renewed interest in donor granulocyte transfusions due to the availability of granulocyte-colony stimulating factor and advanced apheresis technology. The results of several clinical trials did not show [email protected] clear advantage of adding granolucyte concentrates to antimicrobial therapies due to significant defects that affected the final results of these trials. Department of Adult Hematology and With the recent increase in incidence of multidrug resistant bacteria and invasive Hematopoietic Stem Cell Transplantation, fungal infections in neutropenic patients and the reduced efficacy of the recently Oncology Center, King Fahad Specialist introduced antimicrobial agents, the need for transfusing donor granulocytes Hospital, Saudi Arabia. to these patients is renewed again. However, well designed, multicenter randomized controlled trials that include large numbers of patients are needed to Tel: 966-03-8431111 determine the effectiveness of donor granulocyte transfusions in these severely Fax: 966-03-8427420 immunocompromised patients. -
Cardiovascular System
Cardiovascular System BLOOD PART 2 Leukocytes Make up <1% of total blood volume Defend Diapedesis Formed elements Plasma • 55% of whole blood • Least dense component Buffy coat • Leukocytes and platelets • <1% of whole blood Erythrocytes 1 Withdraw 2 Centrifuge the • 45% of whole blood blood and place blood sample. • Most dense in tube. component Copyright © 2010 Pearson Education, Inc. Figure 17.1 Differential WBC count (All total 4800 – 10,800/l) Five types Formed of WBC’s elements Platelets Granulocytes Neutrophils (50 – 70%) Leukocytes Eosinophils (2 – 4%) Basophils (0.5 – 1%) Erythrocytes Agranulocytes Lymphocytes (25 – 45%) Monocytes (3 – 8%) Figure 17.9 Leukocytes Granulocytes Neutrophils, eosinophils and basophils Cytoplasmic granules Larger and shorter-lived than RBCs Lobed nuclei All phagocytic to some degree (a) Neutrophil; (b) Eosinophil; (c) Basophil; multilobed bilobed nucleus, bilobed nucleus, nucleus red cytoplasmic purplish-black granules cytoplasmic granules Figure 17.10 (a-c) Neutrophils AKA: Polymorphonuclear leukocytes (PMNs) Most numerous WBC Diapedesis Granules contain hydrolytic enzymes Bacteria slayers #’s increase during acute infection Eosinophils Diapedesis Granules Antihistamines Lysozyme like substances Parasites Allergic response Basophils Rare WBC Diapedesis Large, purplish-black granules Histamine Inflammatory chemical vasodilation Attracts other WBC’s to inflamed sites Heparin Prevents clotting (a) Neutrophil; (b) Eosinophil; (c) Basophil; multilobed bilobed nucleus, bilobed -
DNA Buffy Coat 400 V6 DSP Protocol
QIAsymphony SP Protocol Sheet DNA_Buffy_Coat_400_V6_DSP protocol General information For in vitro diagnostic use. This protocol is for purification of total genomic and mitochondrial DNA from fresh or frozen buffy coat using the QIAsymphony® SP and the QIAsymphony DSP DNA Midi Kit. Kit QIAsymphony DSP DNA Midi Kit (cat. no. 937255) Sample material Buffy coat (EDTA, citrate, or heparin anti-coagulated) Protocol name DNA_BC_400_V6_DSP Default Assay Control Set ACS_BC_400_V6_DSP Editable Elution volume: 200 µl, 400 µl Required software version Version 4.0 September 2012 Sample & Assay Technologies “Sample” drawer Sample type Buffy coat (EDTA, citrate, or heparin anti-coagulated) Sample volume Depends on type of sample tube used; for more information see www.qiagen.com/goto/dsphandbooks. Primary sample tubes n/a Secondary sample tubes For more information see www.qiagen.com/goto/dsphandbooks. Inserts Depends on type of sample tube used; for more information see www.qiagen.com/goto/dsphandbooks. n/a = not applicable. “Reagents and Consumables” drawer Position A1 and/or A2 Reagent cartridge Position B1 n/a Tip rack holder 1–17 Disposable filter-tips, 200 µl or 1500 µl Unit box holder 1–4 Unit boxes containing sample prep cartridges or 8-Rod Covers n/a = not applicable. “Waste” drawer Unit box holder 1–4 Empty unit boxes Waste bag holder Waste bag Liquid waste bottle holder Empty liquid waste bottle “Eluate” drawer Elution rack (we For more information see recommend using slot 1, www.qiagen.com/goto/dsphandbooks. cooling position) QIAsymphony SP Protocol Sheet: DNA_Buffy_Coat_400_V6_DSP page 2 of 4 Required plasticware Three One batch, Two batches, batches, Four batches, 24 samples* 48 samples* 72 samples* 96 samples* Disposable 4 4 4 8 filter-tips, 200 µl†‡ Disposable 110 212 314 424 filter-tips, 1500 µl†‡ Sample prep 18 36 54 72 cartridges§ 8-Rod Covers¶ 3 6 9 12 * Use of less than 24 samples per batch decreases the number of disposable filter-tips required per run.