INTERPRETATION INFORMATION SHEET



Similar documents
Diagnosis of HIV-1 Infection. Estelle Piwowar-Manning HPTN Central Laboratory The Johns Hopkins University

Suggested Reporting Language for the HIV Laboratory Diagnostic Testing Algorithm

Blood Screening Assays. CTS lab locations where assays are performed are indicated by alpha codes D, P, and T.

Lyme (IgG and IgM) Antibody Confirmation

in hiv diagnostics the role of phls

Quality Assurance Guidelines for Testing Using Rapid HIV Antibody Tests Waived Under the Clinical Laboratory Improvement Amendments of 1988

LAB 14 ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA)

Coding and Billing for HIV Services in Healthcare Facilities

How Does a Doctor Test for AIDS?

Hepatitis and Retrovirus. LIAISON XL Accurate detection of HIV infection. HIV Ab/Ag FOR OUTSIDE THE US AND CANADA ONLY

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

LIAISON XL HCV Ab Accurate diagnosis of the early stage of HCV infection

LYME DISEASE. 2.5M specimen tests per year. 97% accuracy with Rockland tools

Appendix B: Provincial Case Definitions for Reportable Diseases

HIV DIAGNOSIS: A GUIDE FOR SELECTING RAPID DIAGNOSTIC TEST (RDT) KITS

Topic: Serological reactions: the purpose and a principle of reactions. Agglutination test. Precipitation test. CFT, IFT, ELISA, RIA.

Background Information

Molecular Diagnosis of Hepatitis B and Hepatitis D infections

(EMEA/CHMP/BWP/298390/2005)

510K Summary. This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of 21 CFR

Reconsideration Code Reconsideration Code Description Nuclear Matrix Protein 22 (NMP22), qualitative

U.S. Public Health Service Guidelines for Testing and Counseling Blood and Plasma Donors for Human Immunodeficiency Virus Type 1 Antigen

AIR FORCE REPORTABLE EVENTS GUIDELINES & CASE DEFINITIONS

Zika Virus. Fred A. Lopez, MD, MACP Richard Vial Professor Department of Medicine Section of Infectious Diseases

Evaluation of Blood Screening Nucleic Acid Tests (NAT) for Detection of Various HCV and HIV Genotypes

Guidelines for TB Blood Testing. Minnesota Department of Health TB Prevention and Control Program June 2011

Viral Safety of Plasma-Derived Products

Viral Hepatitis APHL survey report

APTIMA HIV-1 RNA Qualitative Assay

Syphilis Fast latex Agglutination Test: A Rapid Confirmatory Test for Syphilis

Viral Hepatitis Case Report

Chapter 6: Antigen-Antibody Interactions

GLOBAL FUND QUALITY ASSURANCE POLICY FOR DIAGNOSTICS PRODUCTS. (Issued on 14 December 2010, amended on 5 February 2014)

510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY

Virological Methods. Flint et al. Principles of Virology (ASM), Chapter 2

LIAISON XL HBsAg Quant

Viral Infection: Receptors

About Our Products. Blood Products. Purified Infectious/Inactivated Agents. Native & Recombinant Viral Proteins. DNA Controls and Primers for PCR

Direct Testing Systems and Serology

Essentials of Real Time PCR. About Sequence Detection Chemistries

ChIP TROUBLESHOOTING TIPS

HBV DNA < monitoring interferon Rx

HBV Quantitative Real Time PCR Kit

Serology: Fluorescent antibody tests and other tests employing conjugated antibodies

Algorithm for detecting Zika virus (ZIKV) 1

Patient Information Sheet

Viruses. Viral components: Capsid. Chapter 10: Viruses. Viral components: Nucleic Acid. Viral components: Envelope

RealLine HCV PCR Qualitative - Uni-Format

Understanding the Western Blot

HIV/AIDS: General Information & Testing in the Emergency Department

VLLM0421c Medical Microbiology I, practical sessions. Protocol to topic J10

Preface. TTY: (888) or Hepatitis C Counseling and Testing, contact: 800-CDC-INFO ( )

IKDT Laboratory. IKDT as Service Lab (CRO) for Molecular Diagnostics

ELISA BIO 110 Lab 1. Immunity and Disease

Molecular diagnostics is now used for a wide range of applications, including:

Distribution: General. English only

Coding guide for routine HIV testing in health care settings

Lancet Device Incident Investigation Report

ST. VINCENT'S. MEDICAL CENTER St. Vincent's Healthcare

BLOOD DONOR TESTING & LOOKBACK STUDIES Shan Yuan, MD Last Updated 2/8/ ABO Typing: Performed each time with each donation

Appendix 2 Molecular Biology Core Curriculum. Websites and Other Resources

SYBR Green Realtime PCR Master Mix -Plus-

4A. Types of Laboratory Tests Available and Specimens Required. Three main types of laboratory tests are used for diagnosing CHIK: virus

Course Curriculum for Master Degree in Medical Laboratory Sciences/Clinical Microbiology, Immunology and Serology

Data Analysis for Ion Torrent Sequencing

Results Demographic profile of these children is shown in Table I.

Standardization, Calibration and Quality Control

Testing for Tick Borne Diseases: How and When?

Biomedical Engineering for Global Health. Lecture Thirteen

DNA and Forensic Science

How To Get A Cell Print

WHO Prequalification of Diagnostics Programme PUBLIC REPORT. Product: Genscreen ULTRA HIV Ag-Ab Number: PQDx Abstract

How many of you have checked out the web site on protein-dna interactions?

Direct Antiglobulin Test (DAT)

1.5 Function of analyte For albumin, see separate entry. The immunoglobulins are components of the humoral arm of the immune system.

Tuberculosis and HIV/AIDS Co-Infection: Epidemiology and Public Health Challenges

Objectives. Immunologic Methods. Objectives. Immunology vs. Serology. Cross Reactivity. Sensitivity and Specificity. Definitions

OraQuick HCV Rapid Antibody Test Customer Letter

CAP Accreditation Checklists 2015 Edition

Hepatitis C 1) THE DISEASE AND ITS EPIDEMIOLOGY

Preamble: Explaining the Technical Aspects of HIV Testing

FBS06 P30 Antigen Test for the Presence of Seminal Fluid

RealStar HBV PCR Kit /2012

Reducing the Diagnostic Window for Acute HIV

Mobile Lab-Diagnostik

Prospects for Vaccines against Hepatitis C Viruses. T. Jake Liang. M.D. Liver Diseases Branch NIDDK, NIH, HHS

Assay Migration Studies for In Vitro Diagnostic Devices Guidance for Industry and FDA Staff

CHROMOSOMES Dr. Fern Tsien, Dept. of Genetics, LSUHSC, NO, LA

JOINT COMMISSION INTERNATIONAL ACCREDITATION STANDARDS FOR. 2nd Edition

Real-time PCR: Understanding C t

REAL TIME PCR USING SYBR GREEN

Diagnosing arbovirus infections (and Bill s holiday snaps) David W Smith Division of Microbiology and Infectious Diseases PathCentre

CANADIAN RULE BASED CLASSIFICATION SYSTEM (IVDD) Life Sciences British Columbia NRC-Industry Research Assistance Program

Dried Blood Spot Specimens for Serological Testing of Rodents

Transcription:

Creative Testing Solutions 2424 West Erie Dr. 2205 Highway 121 10100 Martin Luther King Jr. St. No. Tempe, AZ 85282 Bedford, TX 76021 St. Petersburg, FL 33716 INTERPRETATION INFORMATION SHEET Human Immunodeficiency Virus (HIV) Serology Anti-HIV-1/HIV-2 Plus O EIA: This enzyme-linked immunoassay (EIA) allows simultaneous detection of antibodies to HIV-1 and HIV-2, including HIV-1 Group O. It does not discriminate between HIV-1 and HIV-2 reactivity. An HIV-1, HIV-2 or dual infection can only be confirmed serologically by parallel testing against both antigens using specific EIA and confirmatory assays. Anti-HIV-2 EIA: This enzyme-linked immunoassay (EIA) detects antibodies to HIV-2. However, repeatedly reactive specimens may contain specific antibodies to HIV-2, cross-reacting antibodies to HIV-1, or be non-specifically reactive. Therefore, additional, more specific or supplemental tests for antibodies to both HIV-1 and HIV-2 should be performed. Anti-HIV-1 IFA: See separate sheet. Anti-HIV-1 or Anti-HIV-2 Western Blot: See separate sheet. Final interpretations of any serology assay should also consider the results from the nucleic acid amplification assay and additional medical history. A negative serology test does not exclude the possibility of infection with HIV-1.

INTERPRETATION INFORMATION SHEET Human Immunodeficiency Virus Type 1 (HIV-1) Nucleic Acid Testing (NAT) Procleix Ultrio HIV-1/HCV/HBV Assay: This assay utilizes target amplification nucleic acid probe technology for the detection of HIV-1 and HCV RNA and HBV DNA. The screen assay is referred to as Ultrio testing which does not discriminate between HIV-1 and HCV RNA and/or HBV DNA. Specimens found to be reactive upon Ultrio testing are then tested in HIV-1, HCV and HBV Discriminatory Assays (dhiv, dhcv, dhbv assays) to determine if they are reactive for HIV, HCV, and/or HBV. It is possible for all three discriminatory tests to be non-reactive. This may indicate a false positive Ultrio screen test. All assays have a chemiluminescent signal produced by a hybridized probe, which is measured by a luminometer and reported as Relative Light Units (RLU). dhiv-1 Assay: This assay utilizes HIV-1 specific probe reagent directed against specific conserved regions in the viral genome to determine the presence of HIV-1 Virus by Transcription Mediated Amplification (TMA). Roche AmpliScreen HIV-1 Assay: This assay utilizes Polymerase Chain Reaction (PCR) technology for the detection of HIV-1 RNA. This assay detects probe-bound amplified product by colorimetric determination. Final interpretations of any serology assay should also consider the results from the nucleic acid amplification assay and additional medical history.

INTERPRETATION OF ANTI-HIV-1 IFA RESULTS The HIV-1 immunofluorescence assay (IFA) is a qualitative test for detection of antibodies to HIV-1 and is intended to be used as an additional, more specific test in specimens found to be repeatedly reactive by screening procedures such as EIA. In this assay, specific HIV-1 antibodies present in a specimen bind to HIV-1 infected human T cells which are fixed to a microscope slide. Uninfected cells are included on the microscope slide for comparison purposes. Bound HIV-1 antibodies are detected with anti-human immunoglobulin conjugated to fluorescein isothiocyanate, which fluoresces when exposed to UV light. Interpretation of the degree and pattern of fluorescence of the infected cells compared to uninfected cells determines the HIV-1 status of a sample. HIV-1 IFA results are interpreted as Positive, Negative or Indeterminate. POSITIVE: A specimen is interpreted as positive when there is a specific cytoplasmic staining pattern in the HIV- 1 infected cells and there is a significant difference in the intensity of fluorescent staining and the pattern of fluorescence between the HIV-1 infected and uninfected cells. Although a positive IFA for antibodies to HIV-1 usually indicates infection with the virus, a diagnosis of Acquired Immunodeficiency Syndrome, AIDS, can only be established on clinical grounds, provided that an individual meets the case definition of AIDS established by the Centers for Disease Control. ACTION REQUIRED: It is imperative an inquiry be made regarding blood donation history and pertinent information forwarded to the Medical Director or Technical Director of the local blood bank, regardless of where the donation may have taken place. The patient must be assured confidentiality will be maintained. NEGATIVE: A specimen is interpreted as negative when there is no specific fluorescent staining of the infected cells and there is no significant difference between the HIV-1 infected and uninfected cells. INDETERMINATE: A specimen is interpreted as indeterminate when there is fluorescent staining present in both the HIV- 1 infected and uninfected cells OR when it is not possible to clearly differentiate the intensity of fluorescent staining and the pattern of fluorescence between the HIV-1 infected and uninfected cells OR when duplicates are discordant. NOTE: A sample with an initial indeterminate result is retested in duplicate before a final interpretation is made. Indeterminate IFA interpretation does not imply that HIV-1 antibodies are, or are not, present in the specimen. It means that the HIV-1 status cannot be resolved and results must not be considered positive or negative. In most cases, indeterminate IFA results are due to the presence of nonspecific staining. Non-specific staining can occur as a result of a variety of conditions and may mask the presence of specific HIV-1 staining. The correct evaluation in such situations must be based on subsequent testing and clinical evaluation. REFERENCES: Sanochemia Pharmazeutika AG Fluorognost TM HIV-1 IFA (product insert) April 2005.

INTERPRETATION OF ANTI-HIV-1* OR ANTI-HIV-2** WESTERN BLOT RESULTS Western blot results are interpreted as Positive, Negative or Indeterminate, depending upon the presence or absence of reactivity to the various HIV gene products: GAG proteins: POL proteins: ENV proteins: HIV-1 = p18, p24, p40, p55 HIV-2 = p15, p26 HIV-1 = p31, p51, p65 HIV-2 = p31, p68/58/55 HIV-1 = gp41, gp120, gp160 HIV-2 = gp36, gp36 trimer (gp105), gp120, gp140 POSITIVE - HIV-1: Reactivity to at least two of the major bands: gp120/gp160, gp41 or p24. HIV-2: Reactivity to two env bands or p26 and one env band. Antibody reactivity indicates possible infection and alone is not diagnostic of AIDS. Although a persistently positive immunoblot for antibodies to HIV-1 indicates infection with the virus, a diagnosis of Acquired Immunodeficiency Syndrome or AIDS can only be made on clinical grounds if an individual meets the case definitions of AIDS established by the Centers for Disease Control. Specimens with reactivity for ENV (envelope) proteins only (gp41 and gp120/gp160 for HIV-1 or gp36, gp105, gp120 and gp140 for HIV-2) may meet the criteria for positive even though reactivity to only one gene product is demonstrable. Individuals with this pattern of reactivity who have no risk factors for infection or whose risk history is undetermined must be carefully evaluated using four to six week followup testing and/or additional more sensitive or specific tests such as Nucleic Acid Amplification Testing (NAT) prior to determination of true HIV status. ACTION REQUIRED: It is imperative an inquiry be made regarding blood donation history and pertinent information forwarded to the Medical Director or Technical Director of the local blood bank, regardless of where the donation may have taken place. The patient must be assured confidentiality will be maintained. NEGATIVE - No reactivity is present. INDETERMINATE - Reactivity which does not meet the criteria for positive. Persons who have recently seroconverted may display incomplete patterns but will develop increased reactivity when followed for a period of one to six months. Persons with HIV infection may also have incomplete patterns due to the natural course of the infection or other immunodeficiencies. In addition, individuals infected with HIV-2 may have indeterminate banding patterns using an HIV-1 Western blot. Conversely, persons at low risk for infection may have nonspecific reactions, which may persist but not evolve into more extensive patterns over time. Studies show that non-viral bands are stable and have not been associated with HIV infection. NOTE: Indeterminate results should not be considered either positive OR negative due to variation in test performance and uncertainty associated with indeterminate immunoblots. Additional testing and clinical evaluation must be utilized to correctly evaluate an indeterminate result. *Genetic Systems anti-hiv-1 Western blot **California State Health Department in-house Western blot California State Health Department reports HIV-2 Western blot as inconclusive

UNREADABLE When the background is as dark or darker than the control band used to determine a +/- level of reactivity, the laboratory cannot determine or distinguish if there might be viral bands present under the background of reactivity. When this happens, the band location is graded as U to indicate that at that location, the background interferes with the ability to read viral banding. The final interpretation of the blot is unreadable if there are no other bands identified. The blot is interpreted as indeterminate if there are other bands identified that do not meet the criteria of positive. In most cases, a follow-up sample is requested for clarification especially if any of the major viral bands used for the interpretation of a positive blot are unreadable. REFERENCES: Genetic Systems HIV-1Western Blot (Product Insert) October 1998. Transfusion 1996: Vol. 36, p37-44 (Frequency of HIV Infection Among Contemporary anti-hiv-1 and anti-hiv 1/2 Supplemental Test Indeterminate Blood Donors by M. Busch, et.al.). Transfusion 1995: Vol. 35, p98-102 (Long Term Follow-up of Blood Donors with Indeterminate Human Immunodeficiency Virus Type 1 Results on Western Blot by JB Jackson, et. al.). Morbidity and Mortality Weekly Report - October 11, 1991: Vol 40, No 40, p692-695. Morbidity and Mortality Weekly Report - July 21, 1989: Vol 38, No S-7. Journal of the American Medical Association - August 5, 1988: Vol 260, No. 5, p674-679. Journal of Clinical Immunology - Fall 1988: Vol 11, No. 3, p 107-114. HIV-INT (Rev. 12)