Uncovering the Hidden Burden of Occult Hepatitis B Infection

Hepatitis B virus (HBV) is a major global health concern, affecting more than 250 million people worldwide. Beyond the well-known, surface antigen–positive infection lies a more elusive challenge: occult HBV infection (OBI) — a condition where HBV DNA persists in the body even when hepatitis B surface antigen (HBsAg) tests negative.
This silent infection can remain undetected for years, allowing HBV to spread within communities, evade early treatment, and reactivate under conditions of immunosuppression, sometimes with severe consequences such as liver failure or hepatocellular carcinoma.
A recent study published in BMC Research Notes1 examined this phenomenon in northern Uganda, a region with high HBV endemicity. The findings shed light on how OBI can silently sustain HBV transmission within the community and pose a risk of viral reactivation, even in individuals with no overt clinical symptoms.
What the Study Found
Researchers screened 387 HBsAg-negative individuals and found that 5.43% had detectable HBV DNA, confirming occult infection (OBI). Most OBI cases were observed in participants under 30 years old, and the majority were positive for anti-HBc (hepatitis B core antibody), indicating prior exposure or resolved infection. Interestingly, liver enzyme levels (ALT and AST) were largely within normal ranges, highlighting the clinically silent nature of OBI.
Despite the absence of detectable HBsAg, these individuals still carried HBV DNA, meaning they could potentially transmit the virus through blood and were at risk of viral reactivation, particularly under immunosuppressive conditions.
The researchers emphasized the urgent need for more sensitive and accessible diagnostic strategies to identify OBI, especially in regions where routine nucleic acid testing (NAT) is limited or unavailable.
Why Occult HBV Matters
Occult infections carry several important risks:
- Blood safety: OBI can escape standard screening, leading to potential transmission via transfusion or transplantation.
- Reactivation: In patients undergoing chemotherapy, HIV treatment, or organ transplantation, latent HBV can reactivate with serious outcomes.
- Public health surveillance: Traditional screening programs may underestimate true HBV prevalence if OBI is overlooked.
While this study focused on Uganda, the findings have global relevance, particularly in regions where HBV is endemic and testing infrastructure is limited.
Moving Toward Better Screening
Detecting OBI requires a combination of serological and molecular approaches. While NAT remains the gold standard, serological markers such as anti-HBc can help identify individuals who may require further molecular testing.
Point-of-care (POC) diagnostic tools can play an important role in broadening early screening, particularly when lab-based PCR testing is inaccessible. Rapid screening platforms — including Healgen’s HBsAg and HBcAb tests — provide accessible first-line tools to identify at-risk individuals and guide confirmatory testing strategies.
By combining reliable serological screening with targeted molecular follow-up, healthcare programs can more effectively capture the “hidden” cases that sustain HBV persistence.
Looking Ahead
The study reinforces that HBV control requires more than vaccination and treatment. Addressing the silent reservoir of OBI is essential to reduce transmission, prevent reactivation, and protect vulnerable populations. Expanding access to high-quality diagnostic tools and raising awareness of OBI can strengthen screening programs and public health efforts.
For laboratories and community health programs looking to strengthen HBV screening frameworks, tools like Healgen’s rapid tests can complement national strategies, bridging the gap between initial detection and molecular confirmation.
References
1 Kafeero, H.M., Ocama, P., Ndagire, D. et al. The status of occult HBV infection in a high endemic region: risk of community HBV transmission and reactivation. BMC Res Notes 18, 255 (2025). https://doi.org/10.1186/s13104-025-07337-6
Disclaimer: This article highlights findings from a peer-reviewed study published in BMC Research Notes (2025). Original study: Kafeero, H.M., Ocama, P., Ndagire, D. et al. “The status of occult HBV infection in a high endemic region: risk of community HBV transmission and reactivation.” https://doi.org/10.1186/s13104-025-07337-6
The Healgen® COVID-19/Flu A&B Test Kit Named One of 2024’s Top 5 Medical Breakthroughs by ABC News

Healgen® is proud to be acknowledged as part of this select group of groundbreaking discoveries and is deeply committed to delivering innovative and accessible healthcare solutions that truly make a difference in people’s lives. Read the full story from ABC News.
The Healgen® COVID-19/Flu A&B Antigen Test Kit is the first over-the-counter, at-home diagnostic tool to receive De Novo authorization from the U.S. Food and Drug Administration (FDA) for detecting both SARS-CoV-2 and Influenza A/B. Learn more about this news. This milestone is a testament to our dedication to advancing in vitro diagnostics for improved public health.
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- Dual Detection: Simultaneously identifies COVID-19, Influenza A, and Influenza B, helping users quickly determine the cause of their symptoms.
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- COVID-19 Sensitivity: 99.1%
- Influenza A Sensitivity: 99.9%
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Thank You for Your Support! We extend our deepest gratitude to our partners and distributors for your continued trust and support. Together, we are revolutionizing diagnostics and making healthcare more accessible worldwide.
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Readily Available and Accurate, the Healgen® Rapid Check® COVID-19/Flu A&B Antigen Test is Now Available Online.
Healgen Scientific announces the expansion of online availability for the Healgen® Rapid Check® COVID-19/Flu A&B Antigen Test. This momentous milestone enhances accessibility, enabling individuals to easily purchase and perform at-home rapid tests for COVID-19, Flu A, and Flu B.
This combination test is the first test to be granted FDA De Novo for over-the-counter (OTC) use by the FDA, making this test the first of its kind in combination diagnostic testing for COVID-19, Flu A, and Flu B.
“…our ability to detect these pathogens effectively and efficiently can be impactful on our daily lives. Today’s authorization expands the options for individuals with respiratory symptoms to receive information about their health from the comfort of their home.” – Michelle Tarver, M.D., Ph.D., acting director of the FDA’s Center for Devices and Radiological Health (Click here for FDA Release)
As cases of all three viruses rise and fall yearly, the accessibility of this at-home rapid test plays a significant role in public health. ABC News provided coverage for the authorization of the first over-the-counter combination COVID-19 and flu test outside of emergency use, and also named this test one of the five biggest medical breakthroughs in 2024. The NY Times has also covered this exciting innovation in at-home testing in their article, New Covid Tests Are Here. They Test for Flu, Too.
With this test being the first of its kind to be granted traditional marketing authorization by the FDA, USA Today covered the high demand for this test in their article, and CBS News spoke on the accuracy of this test compared to the emergency use tests in their article. As the need for accurate combination tests increases, so will the production of the tests, as covered in 360Dx’s article, Following FDA De Novo Clearance, Healgen Ramping up Manufacturing of OTC Combo COVID-19/Flu Test. With similar symptoms, this combination test provides clarity for the virus(es)causing the illness, as covered in CNET’s article, Is It COVID or the Flu? Take This FDA-Approved, At-Home Test to Find Out.
This simple nasal swab test allows individuals to quickly determine whether their symptoms are due to COVID-19, Influenza A or Influenza B, eliminating the need for multiple tests and reducing the burden on the healthcare system. The Healgen® Rapid Check® COVID-19/Flu A&B Antigen Test is authorized for individuals aged 14 years or older, or for aged 2 years or older when administered by an adult, who are experiencing symptoms within the first five days.
This test has been designed to meet the highest performance standards, including accuracy, reliability, and ease of use, ensuring individuals can trust the results they receive. With rigorous development and validation processes employed to bring the Healgen® Rapid Check® COVID-19/Flu A&B Antigen Test to market, the commitment from Healgen Scientific to quality and innovation for improving patient health is evident.

