Biomarker Lens

Biomarkers · Chemical

Absolute CD8 Cells

What it measures

Also listed as
Absolute CD8+ Cells
Tests in the graph that measure it
4

A plain-language description with its source has not been added for this biomarker yet. What the laboratories say about the tests that measure it is below.

Tests that measure Absolute CD8 Cells

Lymphocyte Subset Panel 2

Laboratory
Quest Diagnostics
Test code
36420
Specimen
Blood
Fasting
Not stated as required

What the laboratory says this test is for

T-lymphocyte count assists in evaluating cellular immunocompetency.

Quest Diagnostics test directory, test code 36420

Lymphocyte Subset Panel 1

Laboratory
Quest Diagnostics
Test code
7197
Specimen
Blood
Fasting
Not stated as required

What the laboratory says this test is for

Immunophenotypic analysis may assist in evaluating cellular immunocompetency in suspected cases of primary and secondary immunodeficiency states.

Quest Diagnostics test directory, test code 7197

Lymphocyte Subset Panel 3

Laboratory
Quest Diagnostics
Test code
7195
Specimen
Blood
Fasting
Not stated as required

What the laboratory says this test is for

T-lymphocyte count assists in evaluating cellular immunocompetency.

Quest Diagnostics test directory, test code 7195

Lymphocyte Subset Panel 4

Laboratory
Quest Diagnostics
Test code
7924
Specimen
Blood
Fasting
Not stated as required

What the laboratory says this test is for

This panel separately reports CD4+ T cells (CD4) and CD8+ T cells (CD8) in the blood, as well as a calculated CD4/CD8 ratio. This panel may provide information of the immune status of individuals living with HIV. It can be used to help establish baseline values and track antiretroviral (ARV)-related treatment progress. It can also be used to evaluate helper and suppressor cell immune status in individuals with other immunodeficiency diseases. The CD4 count is the most valuable indicator of immune status in HIV-infected individuals. It can help determine the need for prophylaxis for opportunistic infections and the urgency of ARV initiation. The CD8 count reflects the level of immune activation in response to HIV. In the early stages of infection, CD4 levels and the CD4/CD8 ratio typically decline after seroconversion occurs. However, after seroconversion, CD8 cells increase in an attempt to mount a response against HIV. In ARV-treated patients with controlled viral load, CD8 counts. Post-therapy, persistently elevated CD8 counts have been linked to increased risk of non--AIDS-defining diseases, independent of CD4 count, including cardiovascular, renal, respiratory, metabolic diseases, and cancer [1-3]. This panel can be used to establish baseline CD4 and CD8 levels, as well as percentages and ratios, which help determine how long the virus has been present in the blood and the overall prognosis. During ARV treatment, this panel can help assess CD4 recovery and CD8 response to treatment [1,2]. During the first 2 years of ARV therapy, The National Institutes of Health recommends testing CD4 every 3 to 6 months. Patients who develop viremia while on therapy or whose CD4 count stays below 300 cells/µL. should also have their CD4 levels tested every 3 to 6 months. After 2 years of ARV therapy, with consistently suppressed viral load and a CD4 count of 300 to 500 cells/µL, CD4 counts should be tested every 12 months. CD4 testing should also be conducted if therapy fails. Note that CD4 testing is optional when CD4 counts are >500 cells/µL [1]. References 1. Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the use of antiretroviral agents in HIV-1-infected adults and adolescents. Department of Health and Human Services. https://aidsinfo.nih.gov/contentfiles/lvguidelines/adultandadolescentgl.pdf. Updated July 10, 2019. Accessed November 10, 2019. 2. Warren JA, et al. Front Immunol. 2019;10:291. Published February 26, 2019. doi:10.3389/fimmu.2019.00291 3. Cao W, et al. J Int AIDS Soc. 2016;19:20697. Published March 3, 2016. doi: 10.7448/IAS.19.1.20697

Quest Diagnostics test directory, test code 7924

About this page

Everything above is drawn from the named sources and shown as they published it. Reference ranges belong to the laboratory that issued them and the population it named; they are not a universal normal. This page describes the biomarker in general and does not interpret anyone's result. For your own numbers, talk to a clinician, or use Aumnivida, which reads the same graph next to your records.

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