HIV-1 RNA Viral Load

Carlos E. Martinez

Molecular Diagnostic Student

Austin Community College

08/06/08

Objectives

The HVI-1 RNA PCR viral load is performed using the COBAS AmpliPrep TagMan HIV-1 Test is an in vitro nucleic acid amplification test for the quantitation of Human Immunodeficiency Virus Type 1 (HIV) RNA in human plasma using this instrument for automated processing and for automated amplification and detection.

Objectives…

The test is intended for use in conjunction with clinical presentation and other laboratory markers of disease progress for the clinical management of HIV-1 infected patient.

The test can be used to assess patient prognosis by measuring the base line HIV-1 RNA level or to monitor the effects of antiretroviral therapy by measuring changes in EDTA plasma HIV-1 RNA levels during the course of antiretroviral treatment.

Principle of the Procedure

The COBAS Ampliprep TagMan HIV-1 Test is a nucleic acid amplification test for the quantitation of Human Immunodeficiency Virus Type 1 (HIV-1) RNA in human plasma. Specimen preparation is automated using the Ampliprep Instrument with amplification and detection automated using the TagMan 48 analyzer.

The HIV-1 test is based on three major processes: specimen preparation to isolate HIV-1 RNA; reverse transcription of the target RNA to generate

complementary DNA (cDNA); Simultaneous PCR amplification of target cDNA and detection of

cleaved dual-labeled oligonucleotide probe specific to the target.

Store and handling requirements

Do not freeze reagents or controls. Store HIV-1 QC at 2-8 Celsius. Do no re-use any un-used Quality control,

once is used, discard using safety procedures as established by laboratory procedures and guidelines.

Quantitation Standard-QS-RNA The instrument TagMan HIV-1 test permits automated specimen preparation

followed by automated reverse transcription, PCR and detection of HIV-1 target RNA and HIV-1 Quantitation Standard (QS) Armored RNA.

The Master Mix reagent contains primers and probes specific for both HIV-1 RNA and HIV QS RNA. The Master Mix has been developed to ensure equivalent quantitation of group M subtypes of HIV-1. The detection of amplified DNA is performed using target-specific and QS-specific dual labeled oligonucleotide probe that permit independent identification of HIV-1 amplicon and HIV-1 QS amplicon.

The quantitation of HIV-1 viral RNA is performed using the HIV-1 QS. It compensates for effects of inhibition and controls the preparation and amplification process, allowing a more accurate quantitation of HIV-1 RNA in each specimen. The HIV-1 QS is a non-infectious Armored RNA construct that contains region that allows HIV-1 QS amplicon to be distinguished from the HIV-1 target amplicon.

The HIV-1 QS is added to each specimen at a known copy number and is carried through the specimen preparation, reverse transcription, PCR amplification and detection steps of cleaved dual-labeled oligonucleotide RNA concentration in the test specimen by comparing the HIV-1 signal to the HIV-1 QS signal for each specimen and control

Warning and precautions

For in vitro diagnostic use. This test is for use with human plasma collected in EDTA Do no pipette by mouth. Wear protective equipments at all times. Avoid microbial and ribonuclease contamination of reagents

when removing aliquots from control vials. Do not pool controls from different lots numbers. Do not mix reagent cassettes or control from different kits. Specimens and control should be handled as if infectious using

safe laboratory procedures.

Procedural precautions

1. As with any test procedure, good

laboratory technique is essential to

proper performance of this assay.

Procedural limitations

1. This test has been validated for use with only human plasma collected in EDTA anticoagulant. Testing of other specimen types may result in inaccurate results. 2. The performances of this test using the TagMan only applies for HIV-1. 3. Reliable results are dependent on adequate specimen collection, transport, storage and processing. Use of this product should be limited to personnel trained in the techniques of PCR.

Interfering substances

Elevated levels of triglycerides, bilirubin, albumin, hemoglobin and human DNA in specimens as well as the presence of autoimmune diseases such as Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA) and Antinuclear Antibody (ANA) has been shown NOT to interfere with the quantitation of HIV-1 RNA or impact the specificity of the TagMan for HIV-1 Test.

HIV Abstract

HIV infection is a disease caused by the human immunodeficiency virus (HIV). The condition gradually destroys the immune system, which makes it harder for the body to fight off infections

References REFERENCES:

Barre-Sinoussi, F., Chermann, J.C., Rey, F., Nugeyre, M.T.., Chamaret, S., Gruest, J., Dauguet, C. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired

immune deficiency syndrome (AIDS). Science 220:868-871. Popovic, M., Sarngahran, M.G., Read, E., Gallo, R. 1984. Detection, isolation, and continuos production of cytopathic retroviruses from patients with AIDS and pre- AIDS. Science 224:497-500. Gaines, H., von Sydow, M.A., von Stedingk, L.V. 1990. Immunological changes in primary HIV-1 infection. AIDS 4:995-999 Daar, E.S.,Moudgil, T, Meyer.R.D., H. O., D.D.1991 Transient levels of viremia in patient with primary human immunodeficiency virus type 1 infection. New England Journal of

Medecine 324:954 960. Piatak, M. Jr., Saag, M.S., Yang, L.C., Clark, S.J., Kappes, J.C.,Luk, K.C.,1993 High levels of HIV-1 in plasma during all stages of infection determined by competitive PCR.

Science 259:1749-1754. Mulder, J., Mckinney, N., Christopherson, C., Sninsky, Greenfield,L.,Kwok, S 1994. Rapid and simple PCR assay for quantitation of human immunodeficiency virus type 1 RNA in

plasma: Application to acute retroviral infection. Journal of Clinical Microbiology 32:292-300. van Gemen., B., Kievits, T., Schukkink, R., van Strijp, D., Malek, L.T., Sooknanan, R., Huisman, H.G., Lens, P. 1993. Quantification of HIV-1 RNA in plasma using NASBA during HIV-1 primary infection. Journal of Virological Methods 43:177-187. Holmes, H., Davis, C., C., Heath, A., Hewlett, I and N. 2001. An international collaborative study to establish the 1st international standard for HIV-1 RNA for use in nucleic

acid-based techniques. Journal of Virological Methods 92:141-150.