P- Reviewer: Arsenijevic N, Gherlan GS, Romeo R, Silva LD S- Editor: Ji FF L- Editor: A E- Editor: Wu HL
Published online Mar 27, 2015. doi: 10.4254/wjh.v7.i3.600
Peer-review started: August 24, 2014
First decision: November 3, 2014
Revised: November 29, 2014
Accepted: December 16, 2014
Article in press: December 16, 2014
Published online: March 27, 2015
Transfusion-transmitted infections including hepatitis B virus (HBV) have been a major concern in transfusion medicine. Implementation of HBV nucleic acid testing (NAT) has revealed occult HBV infection (OBI) in blood donors. In the mid-1980s, hepatitis B core antibody (HBc) testing was introduced to screen blood donors in HBV non-endemic countries to prevent transmission of non-A and non-B hepatitis. That test remains in use for preventing of potential transmission of HBV from hepatitis B surface antigen (HBsAg)-negative blood donors, even though anti-hepatitis C virus tests have been introduced. Studies of anti-HBc-positive donors have revealed an HBV DNA positivity rate of 0%-15%. As of 2012, 30 countries have implemented HBV NAT. The prevalence of OBI in blood donors was estimated to be 8.55 per 1 million donations, according to a 2008 international survey. OBI is transmissible by blood transfusion. The clinical outcome of occult HBV transmission primarily depends on recipient immune status and the number of HBV DNA copies present in the blood products. The presence of donor anti-HBs reduces the risk of HBV infection by approximately five-fold. The risk of HBV transmission may be lower in endemic areas than in non-endemic areas, because most recipients have already been exposed to HBV. Blood safety for HBV, including OBI, has substantially improved, but the possibility for OBI transmission remains.
Core tip: Hepatitis B surface antigen negative but hepatitis B virus (HBV) DNA positive blood products can evoke hepatitis in blood recipients. Anti-hepatitis B core and HBV nucleic acid testing screening tests are necessary to prevent occult HBV infection transmission by transfusion. Anti-HBs antibody in donors and recipients can protect against hepatitis B infection.
- Citation: Seo DH, Whang DH, Song EY, Han KS. Occult hepatitis B virus infection and blood transfusion. World J Hepatol 2015; 7(3): 600-606
- URL: https://www.wjgnet.com/1948-5182/full/v7/i3/600.htm
- DOI: http://dx.doi.org/10.4254/wjh.v7.i3.600
Hepatitis B virus (HBV) infection via blood transfusion is a major concern in transfusion medicine[1-4]. Screening tests for hepatitis B surface antigens (HBsAg) and anti-hepatitis B core (HBc) antibodies detect HBV transmissible blood and prevent recipient HBV infection. After the introduction of HBV nucleic acid tests (NAT) in blood donor screening, the residual risk of HBV infection by transfusion decreased[5,6]. Implementation of this test revealed occult hepatitis B virus infection (OBI) in blood donors. OBI is defined as the presence of HBV DNA in the liver (with detectable or undetectable HBV DNA in the serum) of individuals who tested negative for HBsAg. The amount of viral DNA in the serum is typically very low in cases of true OBI. Because testing liver tissue is not always practical or possible, OBI is often diagnosed through serum HBV DNA and viral marker tests[8,9].
A positive OBI test may be found in blood donors as a result of various clinical conditions, including: (1) the incubation period of acute infections; (2) the tail-end stage of chronic hepatitis B; (3) low-level viral replication after recovery from hepatitis; and (4) escape mutants not detected by current HBsAg tests[10,11]. HBV transmission by blood transfusion from an OBI donor was first reported in 1978. An increasing number of studies on OBI infectivity of blood products have recently been published[13,14]. In this review, we summarize the role of blood screening tests for HBV infections and update the known risks of OBI transfusion transmission.
Hepatitis B core antigen (HBcAg) appears in hepatocytes within 2 wk after HBV infection; infectious viremia including HBsAg and polymerase are present in the blood after 3 wk. Anti-HBc IgG forms during the recovery phase of infection and is persistent for life, thus, the presence of this antibody in blood indicates past HBV infection. The analytic sensitivity of HBsAg tests in the 1980s was lower than that of current assays. In 1983, Nath et al found that 1 of 16 samples with anti-HBc in the absence of anti-HBs was found to have HBsAg when tested with a more sensitive test. Therefore, additional screening for HBV and surrogate tests for non-A, non-B hepatitis were necessary in the 1980s until the anti-hepatitis C virus (HCV) antibody test became available. The anti-HBc test was introduced in the mid-1980s for screening of blood donors in HBV non-endemic countries, such as the United States. Even after the introduction of the anti-HCV test in the early 1990s, the anti-HBc test continues to be used for donor screening in many countries to prevent potential transmission of HBV from HBsAg-negative donors[18,19]. Several studies have reported effective screening of blood for anti-HBc[20,21]. However, HBV endemic countries were unable to implement anti-HBc screening because many blood products would be discarded due to positive screening tests even though most of the blood would be safe for transfusion. Cases of posttransfusion hepatitis B from positive carrier blood and posttransfusion fulminant hepatitis B from blood containing precore-defective HBV mutants have been reported in Norway and Japan, respectively, countries that did not screen donors for anti-HBc[22,23]. In 1989, Japan introduced anti-HBc testing with a modified algorithm in which anti-HBc-reactive blood with titers < 1:32 or ≥ 1:32 with anti-HBs ≥ 200 mIU/mL were used for transfusion.
Anti-HBc prevalence is related to regional hepatitis B prevalence, and both are typically proportional to one another. The prevalence rates of anti-HBc in blood donors in the United States are 0.23%; United Kingdom, 0.56%; Denmark, 0.70%; Japan, 1.1%; Germany, 1.88%; Italy, 4.85%; India, 10.82%; South Korea, 13.5%; Egypt, 14.2%; Greece, 14.9%; and Pakistan, 17.28% (Figure 1). O’Brien et al reported 5585 (1.13%) anti-HBc repeat-reactive blood donors among 493344 blood donors in Canada, of which 29 (0.52%) were HBsAg-negative but HBV DNA-positive. The anti-HBc test lacks specificity and reactivity of the test reagents varies by manufacturer. Therefore, comparison of anti-HBc positivity should be conducted with caution; it is better to describe general features rather than directly comparing studies. Efforts to improve test specificity have included the addition of reductants such as dithiothreitol and cysteine. High donor HBsAg antibody (anti-HBs) levels (> 100 mIU/mL) are assumed to be putatively protective against the transfusion transmission of HBV. Anti-HBc only or isolated anti-HBc are defined as anti-HBc positive without HBsAg and anti-HBs. An HBV DNA positivity of 0%-15% among those donors positive for anti-HBc only was reported in studies performed in Greece, China, Japan, and Germany. Therefore, the presence of anti-HBc only does not necessarily indicate active viral replication and transmission potential.
Improved molecular methods for the detection of viral nucleic acids made it possible to introduce NAT for donor screening in the late 1990s. By 1997, several countries in Europe had initiated voluntary screening of pooled plasma donations using NAT, and a directive was issued by the EU requiring HCV RNA testing for all plasma intended for fractionation in Europe by July 1, 1999. Routine NAT for HBV was first introduced in German blood transfusion services in January of 1997. The United States began screening source plasma pools for HCV and human immunodeficiency virus (HIV)-1 RNA in early 1998 under the Food and Drug Administration’s Investigational New Drug (IND) program. Currently, more than 90% of whole blood and nearly all source plasma are screened for HCV and HIV by NAT. NAT for blood screening is typically conducted using a multiplex polymerase chain reaction method that simultaneously detects the presence of HIV, HCV and HBV. And a multiplex reaction positive case requires discrimination testing. NAT can be performed on pooled samples to reduce running costs. In pooling test system, primary NAT positive cases require a secondary confirmation procedure for identification of positivity of individual donation samples. The American Red Cross implemented automated triplex NAT for HIV, HCV, and HBV in June of 2009. Japan implemented NAT in November 1997 and all donations have been screened since October 1999. Japanese Red Cross Blood Centers serologically screened 500 samples that were pooled and tested for HBV, HCV and HIV-1. To increase HBV detection sensitivity in Japan, the sample pooling size was reduced to 50 in 2000, and 20 in 2004.
As of 2012, 30 countries have implemented HBV NAT[44,45], as shown in Table 1. According to international survey results, there were a total of 170 HBV NAT-only positive donors among 19887649 blood donations in 2008, and the prevalence of OBI among blood donors was an estimated 8.55 per 1 million donations. In Taiwan, 8 (0.13%) HBV NAT-only positive donors were identified among 5,973 random donor samples. In China, 22 among 165371 HBsAg-negative plasma samples were identified as OBI-positive; their alanine aminotransferase levels were normal and their viral loads low, with a median of 14 IU/mL. In Iran, 4% of 1000 healthy blood donors were anti-HBc- and OBI-positive, and 8.23% of 11,240 volunteer donors were anti-HBc positive and OBI-positive in Mexico[48,49]. To detect OBI, the HBV DNA test is substantial, and minipool NAT can be used to reduce the cost of testing in developing countries. However, in HBV endemic areas, minipool NAT can result in many primary positive cases, which means that many blood products must be retained until the positivity of individual sample is resolved through a secondary confirmation test. Therefore, it is better to implement NAT for individual–donations rather than minipools for NAT in HBV endemic areas[50-53]. HBV replicates more slowly than HIV or HCV, and its doubling time during the ramp-up phase was estimated to be 2.56 d by Biswas et al. Therefore, minipool NAT for HBV detection is less effective than for HIV or HCV detection. Each country should develop its own blood screening strategy based on HBV prevalence, yields of infectious units by different screening methods and cost-effectiveness of testing methods.
|2005||Poland, France (OT + army), South Africa|
|2006||Greece, Italy, Portugal, Thailand|
|2007||Hong Kong, Kuwait, Malaysia, New Zealand, Slovenia, Switzerland|
|2008||Finland, Israel, Latvia, Netherlands, Taiwan|
|2009||United States, Denmark, Ireland, United Kingdom (England and Wales)|
|2010||Australia, United Kingdom (Scotland), Canada|
Occult HBV is transmissible by blood transfusion, although the transmission rate is considered to be very low. The clinical outcome of OBI transmission mainly depends on the immune status and copies of HBV DNA in blood products of the recipient. A look-back program by the Japanese Red Cross showed that window period-derived blood components evoked 50% (11/22) seroconversion in recipients, but tail-end chronic hepatitis B infections caused only 3% (1/33) seroconversion in recipients. Satake et al concluded that the blood infectivity rate during the window period was 10-fold higher than the transmission rates from occult carriers with low-titer anti-HBc. In Canada, a look-back study identified 9.7% anti-HBc-positive recipients and 4 HBV DNA-positive, HBsAg-negative, anti-HBc-positive donors. However, hepatitis cases were reported to have occurred as the result of transfusion of anti-HBc-positive, anti-HBs-positive (12 IU/L), HBV DNA-positive (180 IU/mL) blood product.
A study on blood component infectivity by Allain et al reported that the presence of anti-HBs in donors reduces the risk of HBV infection by approximately five-fold, while therapeutic fresh frozen plasma over platelet concentrate increases the risk by approximately three-fold by logistic regression analysis. A case of OBI transmission by plasma has been reported, but not by red blood cells[57,58]. Because the amount of plasma containing viral particles is very small in RBCs, they are considered to be less infective than plasma products. In a look-back study in Taiwan, Su et al identified 12 (0.11%) OBI-positive donors among 10824 repository samples; they also identified no post-transfusion hepatitis cases among the recipients. They suggested that the risk of HBV transmission is lower in hyperendemic areas such as Taiwan than in non-endemic areas, because most recipients have already experienced an HBV infection. In a look-back study in Hyogo-prefecture, one of 12 recipients was diagnosed with post-transfusion hepatitis B. Of the remaining 11 recipients, 7 were lost to follow-up, and 4 were negative for HBV.
The life-saving role of blood transfusion makes it an essential component of modern medical practice. However, blood used for transfusion is not always free of transmissible diseases. According to the 2008 World Health Organization Global Database on Blood Safety, approximately 92 million blood donations are collected worldwide each year. Of these donations, 48% are collected in high-income countries. Blood products from these countries are screened for HBV, HCV, and HIV. However, 39 countries do not routinely test blood donations for transfusion-transmissible infections. HBsAg-positive blood products, including OBI, could be transfused to patients in these counties more frequently than in the countries that screen blood. Although the prevalence of OBI in blood donors differs by country, a 2008 international survey estimated it to be 8.55 per 1 million donations. To reduce the risk of HBV transmission, HBsAg testing was introduced, followed by anti-HBc and HBV NAT in countries where additional testing was feasible. These approaches were also effective for the prevention of transfusion-transmission of OBI. A modified algorithm for anti-HBc screening of blood donors was implemented in intermediate HBV endemic areas, such as Japan, where the test alone could not be introduced because of the resultant high blood discard rates. Unlike anti-HBc screening, HBV NAT can detect infections during window periods. Therefore, despite higher costs, HBV NAT is more suitable for screening in areas with endemic HBV.
Although OBI infectivity depends on recipient immunity and blood product type, it is transmissible by transfusion. One study observed higher genetic diversity in occult HBV genotype B and C strains from South East Asian blood donors. Epigenetic factors have also been identified in HBV cccDNA molecules, and studies to understand OBI immunopathogenesis are currently underway[63-68]. Even with HBV NAT screening, there is a risk of false-negative results. NAT using sample pooling systems in particular cannot detect low-level viremia. Pathogen inactivation technologies that destroy viral DNA or RNA in blood products using chemical agents and ultraviolet illumination have been introduced as alternatives in blood services[69,70]. HBV vaccination of potential recipients is also an important preventive measure. In conclusion, following the implementation of anti-HBc and HBV NAT screening, blood safety for HBV including OBI has improved substantially, but the potential for OBI transmission remains.
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