PlexEBV™
Epstein-Barr virus (EBV) is a common virus. Half of all adults have been infected by EBV at some point. Most infections do not cause symptoms. EBV persists in a latent state after the initial infection and can reactivate in individuals whose immune systems are compromised by immunosuppressive drugs, viral infections, or genetic changes. This reactivation can progress from a virus that is only detected in the blood (viremia), to the involvement of tissues and organs (disease), which can result in major illness. In transplant recipients, EBV can cause post-transplant lymphoma-like disease.
Reactivation of EBV is accompanied by loss of cell-based immunity to the virus. Currently available antiviral drugs are not very effective. In transplant patients, reactivation leads physicians to lower immunosuppression. The reduction of immunosuppression can lead to rejection in some patients. In transplant patients, a first-time EBV infection or reactivation of the virus can lead to the persistence of the virus in the blood. The persistence of a high viral load in the blood can lead to tissue invasive EBV disease or post-transplant lymphoma. Knowing whether cell-based immunity to EBV is intact or decreased can further guide how to best manage immunosuppression.
PlexEBV™ is a lab-developed blood test that measures the level of cellular immunity to the Epstein-Barr virus (EBV). Decreased anti-EBV immunity increases the risk of EBV infection*.
Knowledge about immunity to EBV and therefore the risk of EBV infection can be combined with available clinical data to plan additional treatment for your patient.
Establishing the level of anti-EBV immunity at baseline and during periods of high dose immunosuppression permits the level of anti-EBV immunity to be assessed in each patient allowing for adequate treatment planifcation.
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CATEGORY
DETAILS
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Assay Category
Lab-developed test, antigen-specific T-cell function.
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Intended Use
To measure the likelihood of Acute cellular rejection after Renal Transplantation.
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Methodology
Stimulation of peripheral blood leukocytes with donor and non-donor cells, flow cytometry.
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Test Report
Available within 30 hours of receiving a blood sample.
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Test Readout
Index of Rejection (IR), the IR is the ratio of the recipient T-cytotoxic memory cell activity toward donor or donor-like cells and reference cells.
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Reference Range
The IR is an absolute number with a range of less than 1.15 to 1.15 or greater.
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Test Interpretation
An IR of 1.15 or more indicates an increased likelihood of acute cellular rejection.
Purpose
Knowledge about immunity to EBV and therefore the risk of EBV infection can be combined with available clinical data to plan additional treatment for your patient.
Rationale
First-time or primary infections with EBV or reactivation of EBV is accompanied by loss of cell-based immunity to the virus. Currently available antiviral drugs are not very effective. In transplant patients, EBV infection leads physicians to lower immunosuppression. The reduction of immunosuppression can lead to rejection in some patients. In transplant patients, EBV infection can lead to the persistence of the virus in the blood. The persistence of high viral load in the blood can lead to tissue-invasive EBV disease. Post-transplant lymphoma is a severe form of EBV disease. Recovery of cell-based immunity helps fight an EBV infection. Knowing whether cell-based immunity to EBV is intact or decreased can further guide how to best manage immunosuppression.
Intended Use
To measure the level of cellular immunity to Epstein-Barr virus (EBV). Decreased anti-EBV immunity increases the risk of EBV infection*.
Procedure
Performance
Benefits
Establishing the level of anti-EBV immunity at baseline and during periods of high dose immunosuppression allows the level of anti-EBV immunity to be assessed in each patient. This can help formulate personalized preventive measures or treatment.
Sample & Handling
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CATEGORY
DETAILS
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Sample Type
Whole blood collected in a sodium heparin (green-top) tube.
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Volume
3 mL for children and 5 mL for adults.
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Transport Conditions
Ship priority overnight, at room temperature. Sample must get to Plexision within 30 hours of phlebotomy.
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Specimen Stability
30 hours at room temperature from the time of phlebotomy.
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Sample Discard Criteria
How To Order
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CATEGORY
DETAILS
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Test Brochure
View and download the product brochure here.
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Ordering Tests
Please complete this form, print, and fax to 412-224-2776.
What is PlexEBV™?
PlexEBV™ is a blood test that helps your healthcare provider determine your level of protection from EBV infection after transplantation.
Who can benefit?
Transplant recipients of any age, individuals that have low general immunity, and those who are at risk for EBV infection can benefit from the PlexEBV™ test.
What is involved in the PlexEBV™ test?
The PlexEBV™ test must be ordered by your healthcare provider. The test requires a sample of blood of half to one teaspoon. This sample is shipped overnight to Plexision’s laboratory for analysis. Results are sent to your healthcare provider within 24 hours of your sample arriving at the laboratory. Your healthcare provider will help you understand the results.
How long does it take to get results of the PlexEBV™ test?
Test results are available 24 hours after the laboratory receives the blood sample.
How does the PlexEBV™ test work?
The PlexEBV™ test determines whether the recipient has low levels of cell-mediated immunity for EBV infection or not. This immunity is measured by a type of white blood cell called the T-lymphocyte. Low levels immunity to EBV are associated with increased risk of EBV infection. When combined with other clinical and laboratory information, the results of this test can help your healthcare provider decide whether to use more or less immunosuppressive medications or other stronger medications.
How do I interpret the test results?
The results are reported as the frequency of EBV-specific T-cells. EBV-specific T-cell frequencies of 5.5% or less are associated with increased risk of EBV infection in transplant recipients.
What are the benefits of the PlexEBV™ test?
Determining when to increase or lower immunosuppression during EBV infection can help resolve EBV infection or avoid transplant rejection. Knowledge about the level of cell-based immunity to EBV can be combined with other clinical data by your healthcare provider to make such clinical decisions.
How do I order the PlexEBV™ test?
The PlexEBV™ test must be ordered by your healthcare provider. The test requisition form is provided here. The completed form can be faxed to 412-224-2776. If there are any questions, please contact (855) PLE.XISION (753.9474) or 412-224-2504.
Is PlexEBV™ covered by insurance?
Plexision will bill your healthcare facility or your insurance plan as indicated on the requisition form. Plexision’s patient assistance plans will assist with the cost of PlexEBV™ if there is no insurance coverage.
US Patent 9606109
*PlexEBV™ is not FDA-approved