Roche launches Elecsys Epstein-Barr Virus (EBV) immunoassay panel to improve EBV infection staging

Rhea-AI Summary

Roche has launched the Elecsys® EBV panel in CE Mark-accepting countries, designed for accurate EBV infection staging from a single blood sample. This development aims to reduce confirmatory testing and facilitate quicker diagnoses for patients, particularly transplant recipients. The panel includes three immunoassays that detect specific antibodies and enhances laboratory efficiency while saving time and resources. Roche plans to file for FDA approval in the future, furthering its commitment to improving healthcare through targeted diagnostics.

Positive

• Accurate identification of EBV infection stage from a single blood sample reduces confirmatory testing.
• Faster diagnosis for transplant patients can lead to quicker treatment decisions.
• The panel's efficiency may save time and resources in laboratories.

Negative

• None.

• The Elecsys EBV panel accurately identifies the EBV infection stage from a single blood sample, which means less confirmatory testing and, potentially, faster diagnosis for patients
• Clear and quick diagnosis of acute infection allows physicians to decide faster on treatment for transplant patients
• The EBV panel can be used to rule out other acute infections, such as missed HIV infections
  
  

Basel, 31 March 2021 - Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the Elecsys® EBV panel has launched in countries accepting the CE Mark. Roche will file for approval with the FDA in the future. The Elecsys® EBV panel consists of three immunoassays: Elecsys EBV IgM, Elecsys EBV VCA IgG, and Elecsys EBV EBNA IgG, that detect antibodies specific to the Epstein-Barr virus (EBV), at different stages of infection. When used in combination, the three tests can help to define how far the infection has progressed in a patient.

Epstein-Barr Virus is one of the most common viruses in humans, infecting more than 90% of the global population by adulthood.^1-2 It is mainly transmitted by saliva, or via organ or cell transplants. After the first infection, EBV remains in a dormant state for life. Clinical symptoms vary according to the immune status of the patients and people with weakened immune systems may develop more severe symptoms.

“The launch of the Elecsys EBV panel is an important step for the diagnosis of infections in transplant patients as it gives clear and accurate results from a single sample”, said Thomas Schinecker, CEO Roche Diagnostics. “The tests help to provide the information clinicians need to diagnose and treat their patients quickly, effectively reducing the need for further confirmatory testing.”

EBV testing with immunoassays, from a blood sample, has a number of clinical uses. EBV is used to confirm the diagnosis of glandular fever in people with clinical signs and symptoms and to rule out other acute diseases with a similar clinical picture, such as certain infections in pregnant women that may cause congenital disorders. Knowing the EBV status of donors and recipients of organ and cell transplants is important, as recipients typically have a weaker immune system and may be at risk of complications.^3-5

Routine EBV testing and result interpretation can be challenging, and additional testing is required for EBV infection stages in as many as 5-10% of normal samples, where the stage of infections is not clear.^6-10 The Elecsys EBV panel correctly classifies a high percentage of routine samples, when determining the stage of EBV infection. This means that less confirmatory testing is required, saving time and resources for the laboratory, as well as potentially leading to more effective patient management.

About Epstein-Barr Virus (EBV) Testing
While there is no international serological standard or consensus algorithm defined for EBV serology testing, there are different ways of conducting the EBV blood tests. Often the three immunoassays used to determine the stage of EBV infection are run in parallel. However, in an immunocompetent, adult population, the number of tests per sample can be reduced up to 50%, by using the “EBNA-first” sequential algorithm. Approximately, 70-80% of routine samples for EBV testing indicate past infections, and only 2.4% are acute infections.³ Therefore, by determining the Epstein-Barr nuclear antigen 1 (EBNA-1) results first, a positive result will rule out all past infections, meaning that only EBNA-1 negative samples will have to be further tested for the presence of IgM and VCA IgG antibodies to determine the final EBV infection stage. This further reduces costs and increases the efficiency of the laboratory testing. The high specificity and sensitivity of the Elecsys EBV EBNA IgG, in combination with clearly defined results, makes this assay very well suited for the implementation of the “EBNA-first” algorithm and thus brings greater value to laboratories and patients through more cost effective and efficient testing.¹¹

About the Elecsys EBV immunoassay panel
The Elecsys® EBV panel consists of three immunoassays to detect antibodies specific to the Epstein-Barr virus (EBV). The three assays, Elecsys® EBV IgM, Elecsys® EBV VCA IgG, and Elecsys® EBV EBNA IgG are used in combination to accurately determine the patient's EBV infection stage. The immunoassays have excellent clinical sensitivity and specificity, and a short time to result of only 18 minutes. The tests require a small sample volume of between 6 μL to 35 μL, depending on the assay and analyzer. The addition of the EBV panel isd an important addition to the routine infectious diseases testing panel for Roche’s immunoassay portfolio.

This further addition to the Roche EBV testing portfolio follows on from the announcement of the CE Mark and FDA authorisation for the first Epstein-Barr virus quantitative test on the cobas 6800/8800 Systems to improve care for transplant patients.

About Roche
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible.

Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management.

Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. More than thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Moreover, for the twelfth consecutive year, Roche has been recognised as one of the most sustainable companies in the Pharmaceuticals Industry by the Dow Jones Sustainability Indices (DJSI).

The Roche Group, headquartered in Basel, Switzerland, is active in over 100 countries and in 2020 employed more than 100,000 people worldwide. In 2020, Roche invested CHF 12.2 billion in R&D and posted sales of CHF 58.3 billion. Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan. For more information, please visit www.roche.com.

All trademarks used or mentioned in this release are protected by law.

References
[1] Balfour HH, Jr, et al..  J Infec Dis. 2013;208(8):1286-93.
[2] Dudley et al. Nephron Clin Prac (2011) 118 Suppl 1:c209-24 , 
[3] EDQM. 7th edition.
[4] Padalko et al, Cell Tissue Bank (2018;)19(4):681-95,
[5] Nowalk A and Green M.. Microbiol Spectr. 2016;4(3).
[6] De Paschale and Clerici World J Virol. 2012;1(1):31-43,
[7] Niller HH and Bauer G. Methods in Molecular Biology; 2017.
[8] Klutts et al. J ClinMicrobiol , 2009 :81(2):325-331.
[9 De Paschale et al. J Med Virol 2009;81(2):325-331.
[10] Vetter et al. Clin Diagn Virol 1994;2(1):29-40.
[11] Sickinger et al. Diagn. Microbiol. Infect. Dis. 2014, 79, 310-316.


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Attachment

• 31032021_MR_Elecsys Epstein-Barr Virus immunoassay_en

FAQ

What is the Elecsys EBV panel launched by Roche?

The Elecsys EBV panel consists of three immunoassays that detect antibodies for Epstein-Barr virus (EBV) infection, allowing for accurate infection staging from a single blood sample.

How does the Elecsys EBV panel improve diagnosis for transplant patients?

The Elecsys EBV panel enables quick and clear diagnosis of acute EBV infections, allowing physicians to make faster treatment decisions for transplant patients.

When will Roche file for FDA approval for the Elecsys EBV panel?

Roche has indicated plans to file for FDA approval for the Elecsys EBV panel in the future, following its launch in countries accepting the CE Mark.

What is the significance of the Elecsys EBV panel in clinical settings?

The Elecsys EBV panel helps clinicians accurately determine the infection stage of EBV with minimal confirmatory testing, improving patient management and laboratory efficiency.