The NIAID Flow Cytometry Advisory Committee; the Guidelines Subcommittee



Similar documents
Stepcount. Product Description: Closed transparent tubes with a metal screen, including a white matrix at the bottom. Cat. Reference: STP-25T

BD FACSComp Software Tutorial

WHOLE BLOOD LYSING SOLUTION FOR FLOW CYTOMETRIC APPLICATIONS

Katharina Lückerath (AG Dr. Martin Zörnig) adapted from Dr. Jörg Hildmann BD Biosciences,Customer Service

Immunophenotyping Flow Cytometry Tutorial. Contents. Experimental Requirements...1. Data Storage...2. Voltage Adjustments...3. Compensation...

Application Note. Selecting Reagents for Multicolor Flow Cytometry. Holden Maecker and Joe Trotter BD Biosciences, San Jose

Application Note 10. Measurement of Cell Recovery. After Sorting with a Catcher-Tube-Based. Cell Sorter. Introduction

Laboratory Procedure Manual

Analyzing Samples for CD34 Enumeration Using the BD Stem Cell Enumeration Kit

Multicolor Flow Cytometry: Setup and Optimization on the BD Accuri C6 Flow Cytometer

APPLICATION INFORMATION

Flow Cytometry for Everyone Else Susan McQuiston, J.D., MLS(ASCP), C.Cy.

123count ebeads Catalog Number: Also known as: Absolute cell count beads GPR: General Purpose Reagents. For Laboratory Use.

Immunophenotyping peripheral blood cells

Spherotech, Inc Irma Lee Circle, Unit 101, Lake Forest, Illinois

Minimal residual disease detection in Acute Myeloid Leukaemia on a Becton Dickinson flow cytometer

CyAn : 11 Parameter Desktop Flow Cytometer

BD FACSCalibur. The flow cytometer for your routine cell analysis needs

ENUMERATION OF LYMPHOCYTE SUBSETS USING FLOW CYTOMETRY: EFFECT OF STORAGE BEFORE AND AFTER STAINING IN A DEVELOPING COUNTRY SETTING

Standard Operating Procedure

Using BD FACSDiva CST To. Evaluate Cytometer Performance, Create Custom Assay Settings. and

Fluorescence Compensation. Jennifer Wilshire, PhD

COMPENSATION MIT Flow Cytometry Core Facility

Introduction to Flow Cytometry

Compensation Controls Data Visualization Panel Development Gating Quantum Dots

Standardization, Calibration and Quality Control

Setting up and calibration of a flow cytometer for multicolor immunophenotyping

Three Rules for Compensation Controls

RPCI 004 v.002 Staining Procedure For all Directly Conjugated Reagents (Whole Blood Method)

Introduction to flow cytometry

Four Color Compensation

FCAP Array v3.0 Software: A New Tool to Analyze BD Cytometric Bead Array (CBA) Data. Monisha Sundarrajan, PhD BD Biosciences

Introduction to Flow Cytometry:

No-wash, no-lyse detection of leukocytes in human whole blood on the Attune NxT Flow Cytometer

DELPHI 27 V 2016 CYTOMETRY STRATEGIES IN THE DIAGNOSIS OF HEMATOLOGICAL DISEASES

Using the BD TM Cytometer Setup and Tracking (CS&T) System for Instrument Characterization and Performance Tracking

Compensation in Flow Cytometry

BD FACSDiva TUTORIAL TSRI FLOW CYTOMETRY CORE FACILITY

Technical Bulletin. Threshold and Analysis of Small Particles on the BD Accuri C6 Flow Cytometer

Multicolor Bead Flow Cytometry Standardization Heba Degheidy MD, PhD, QCYM DB/OSEL/CDRH/FDA Manager of MCM Flow Cytometry Facility

Technical Bulletin. Standardizing Application Setup Across Multiple Flow Cytometers Using BD FACSDiva Version 6 Software. Abstract

Boundary-breaking acoustic focusing cytometry

Flow Cytometric Diagnosis of Low Grade B-cell Leukemia/Lymphoma

BD Trucount Tubes IVD

International Beryllium Conference, Montreal, Canada March 10, 2005

Novel Use of the BD FACS TM SPA to Automate Custom Monoclonal Antibody Panel Preparations for Immunophenotyping

Introduction to Flow Cytometry

BD FACSCanto Flow Cytometer. Efficient Easy Powerful

FlowSight. Flow cytometry with vision

GETTING STARTED. 6. Click the New Specimen icon.

Instrument Characterization and Performance Tracking for Digital Flow Cytometers

BD FC Beads 8-Color Kit for BD OneFlow Assays

CyFlow SL. Healthcare Immunology. Portable FCM System for 3-colour Immunophenotyping

Technical Bulletin. An Introduction to Compensation for Multicolor Assays on Digital Flow Cytometers

Deep profiling of multitube flow cytometry data Supplemental information

The SickKids-UHN Flow Cytometry Facility at TMDT Instructions for Online Scheduling User Version 1.0

Flow cytometric analysis of stem cells derived from umbilical cord blood CD34+/CD45+ enumeration and viability

Notes on titering antibodies

Application Information Bulletin: Set-Up of the CytoFLEX Set-Up of the CytoFLEX* for Extracellular Vesicle Measurement

Below is a list of things you should be aware of before you schedule your sort.

Cell Cycle Tutorial. Contents

PROTOCOL. Immunostaining for Flow Cytometry. Background. Materials and equipment required.

LOAD & GO and make flow cytometry simplicity itself. the full spectrum of Flow Cytometry

Selected Topics in Electrical Engineering: Flow Cytometry Data Analysis

BD FACSVerse. Simply brilliant

Corporate Medical Policy

BD CellQuest Pro Software Analysis Tutorial

Principles of Flowcytometry

HIGH PERFORMANCE FLOW CYTOMETER FOR EVERYONE

Chapter 6. Antigen-Antibody Properties 10/3/2012. Antigen-Antibody Interactions: Principles and Applications. Precipitin reactions

Welcome to More Choice BD Analyte Specific Reagent (ASR) Catalog

Compensation: An Instrumental Perspective

BD FACSCalibur Flow Cytometer

PRODUCT INFORMATION SHEET Monoclonal antibodies detecting human antigens

Titering Antibodies INTRODUCTION Materials Procedure for titering antibodies to extracellular antigens A. Directly conjugated antibodies

Instructions for Use. CyAn ADP. High-speed Analyzer. Summit G June Beckman Coulter, Inc N. Harbor Blvd. Fullerton, CA 92835

EdU Flow Cytometry Kit. User Manual

These particles have something in common

Application Note. Multiparametric Immunophenotyping of Human Hematopoietic Stem Cells and Progenitor Cells by Flow Cytometry.

Subtypes of AML follow branches of myeloid development, making the FAB classificaoon relaovely simple to understand.

Flow Cytometry. What is Flow Cytometry? What Can a Flow Cytometer Tell Us About a Cell? Particle Size. Flow = Fluid Cyto = Cell Metry = Measurement

NCL Method ITA-14. Analysis of Nanoparticle Effects on Maturation of Monocyte Derived Dendritic Cells In Vitro

Science is hard. Flow cytometry should be easy.

powerful. Intuitive. Customizable. The new star of benchtop flow cytometry

Whole Blood Flow Cytometry

BD StemFlow Human Pluripotent Stem Cell Sorting and Analysis Kit

Peripheral Blood Dendritic Cells Revealed by Flow Cytometry

Flow Cytometry. flow cytometer DNA apoptosis ph

MEASURABLE PARAMETERS: Flow cytometers are capable of measuring a variety of cellular characteristics such as:

Getting Started with BD FACSDiva Software

Hoechst HSC Staining and Stem Cell Purification Protocol (see Goodell, M., et al. (1996) J Exp Med 183, )

How to operate the BD FACSCanto flow cytometer

Transcription:

January, 1999 From: To: Subject: The NIAID Flow Cytometry Advisory Committee; the Guidelines Subcommittee NIAID DAIDS Flow Cytometry Laboratories Comparison study information for labs wishing to switch to measurement of percent CD3+CD4+ and CD3+CD8+ cells Laboratories measuring T cell subsets for studies have expressed an interest in using combinations of antibodies to arrive at percentage values for CD3+CD4+ and CD3+CD8+ cells. The Flow Cytometry Advisory Committee (FAC) agrees that using combinations may have certain advantages (see below). Therefore, laboratories with knowledge and experience in flow cytometry are allowed to switch to if an acceptable comparison study is performed. PLEASE DO NOT IMPLEMENT 4-COLOR PHENOTYPING FOR THE NIAID STUDIES UNTIL YOU HAVE RECEIVED APPROVAL FROM THE FLOW CYTOMETRY ADVISORY COMMITTEE. Comparison Study Whenever a laboratory is considering a change in procedures, there is a need to document the effect (or lack of effect) that change will make on reported laboratory values. Therefore, the FAC is requiring that a comparison study be conducted. At least 60 different sequential patient specimens with CD3+CD4+ 30% must be analyzed using your current or 3-color method and using your proposed method. Please do not submit your 60 "best" samples or your 60 "worst" samples. It is important that this data be reflective of the data generated in your laboratory and not a select subset of comparisons. PLEASE KEEP LIST MODE FILES FROM THIS STUDY IN CASE THERE IS A NEED TO LOOK AT THEM. Advantages of Immunophenotyping 1. Cost may be less than with a larger or 3-color panel 2. Time for specimen processing is less 3. There are fewer tubes to aliquot and handle 4. Isotype controls are not needed Disadvantages of Immunophenotyping 1. Spectral compensation for s is more complicated than for s or 3-colors 2. Added expertise is needed for instrument set-up, data collection, and data analysis 1

4-Color Panel Recommendation The Flow Cytometry Advisory Committee recommends the following panel. There are currently no recommendations for use of particular fluorochromes for the monoclonal antibodies. CD3/CD4/CD8/CD45 Advantages: 1. Easy to distinguish lymphocytes based on CD45 and SSC 2. Isotype control is not needed 3. "Bright" CD45 as a gating parameter in the tube helps to ensure inclusion of only lymphocytes, thus eliminating the need to correct for gate purity Disadvantages: 1. Sometimes gating is not clear-cut as there are dim CD45+ cells that have low side scatter 2. Use of only one tube does not allow for QC check with CD3 3. Added expertise is needed versus 2 or 3 color methods Please note that CD19 (to enumerate total B cells) must be included in the panel for all pediatric patients. (Please include CD45 in the combination). 2

TWO-COLOR VS FOUR-COLOR COMPARISON STUDY FOR APPROVAL TO SWITCH TO FOUR-COLOR FLOW CYTOMETRY Institution: Department: Name of Person Completing Form: Title: Phone Number: Date Form Completed: Please complete the following information Model of flow cytometer used : Model of flow cytometer used : 01-EPICS-C 02-EPICS Profile I 04-FACS Analyzer 05-FACScan 09-Other, Specify (if not listed below) 10-EPICS Profile II 11-EPICS Elite 12 EPICS XL 13 FACStar 14-FACStar Plus 15 Ortho Cytoron Absolute 16-FACSCalibur 17-FACSort 18-FACS Vantage 19-EPICS Altra Method of cell preparation used : Method of cell preparation used : 1-Whole Blood Lysis using Ammonium Chloride 2-Whole Blood Lysis using FACS Lysing Solution (BD) 3-Whole Blood Lysis using Immuno-lyse (Coulter) 4-Whole Blood Lysis using Immuno-Prep (Q-Prep, Coulter) 5-Whole Blood Lysis using Lyse and Fix (GenTrak) 6-Whole Blood Lysis using Ortho-mune Lysing Reagent (Ortho) 7-Whole Blood Lysis using OptiLyse B Lysing Solution (AMAC) 8-Whole Blood Lysis using OptiLyse C Lysing Solution (AMAC) 9-Other, Specify 10-Whole Blood Lysis using FACS Lysing Solution (BD) NO WASH 3

Institution Using the list of codes for antibody manufacturers (MAb Mfg) and conjugates on the next page, please fill in the following information Two-Color Tubes Used to Collect and Please enter the antibody manufacturer (MAb Mfg) in row two, fluorochrome for each marker in row three, and whether a premix was used (Y or N) in row 4. If the antibody manufacturer or fluorochrome codes are not listed on the next page, please use code 99 then fill in the information on the line below the appropriate box. TUBE 1 TUBE 2 1) CD 3 CD 4 CD 3 CD 8 2) MAb MAb Mfg Mfg 3) Fluorochrome Fluorochrome 4) Premix Premix (Y or N) (Y or N) Four-Color Tube Used to Collect and Please enter the markers for the tube in row one, antibody manufacturer (MAb Mfg) in row two, and fluorochrome for each marker in row three. If the antibody manufacturer or fluorochrome codes are not listed on the next page, please use code 99 then fill in the information on the line below the appropriate box. TUBE 1 1) CD CD CD CD 2) MAb Mfg 3) Fluorochrome 4) Premix (Y or N) 4

Codes for antibody manufacturers (MAb Mfg): AA BD BI CT CL DK EX GT IM Antigenix America Becton Dickinson Biodesign International Caltag Coulter Dako Exalpha GenTrak Immunotech IS Immunosource IN In-house LN Leinco OR Ortho PM PharMingen SG Sigma SR Serotec 99 Other, specify Codes for fluorochromes: 1-FITC (Green) 2-PE (Yellow) 3-RD1 (Yellow) 5-PerCP (Far Red) 6-ECD (Red) 7-Cy-Chrome (Far-Red) 9-RPE (Yellow) 10-Cy3 (Yellow) 11-PE-Cy5 (Far Red) 12-Alpha Red (Red) 13-Quantum Red (Red) 14-Tricolor (TC) (Far Red) 15-PC5 (Far Red) 16-APC (Far Red) 99-Other, specify 5

TWO-COLOR VS FOUR-COLOR COMPARISON STUDY FOR APPROVAL TO SWITCH TO FOUR-COLOR FLOW CYTOMETRY BE SURE ALL SAMPLES HAVE A TWO-COLOR 30% PLEASE USE 60 SEQUENTIAL SAMPLES MEETING THIS REQUIREMENT Institution: Sample Number Date 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 6

Institution: Sample Number Date 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 7

Institution: Sample Number Date 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 PLEASE SEND COMPLETED FORMS TO CINDY WILKENING, STATISTICAL AND DATA ANALYSIS CENTER, HARVARD SCHOOL OF PUBLIC HEALTH FXB 549-A, 651 HUNTINGTON AVE, BOSTON, MA 02115-6017 OR FAX THE FORMS 617-432-3163 QUESTIONS? CALL CINDY WILKENING AT 617-432-2809 8