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Journal of Biomedicine and Biotechnology
Volume 2012 (2012), Article ID 151967, 12 pages
Commercial Dengue Rapid Diagnostic Tests for Point-of-Care Application: Recent Evaluations and Future Needs?
1Center for Tropical Medicine, Nuffield Department of Clinical Medicine, Churchill Hospital, University of Oxford, Oxford, UK
2Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, 420/6 Rajvithi Road, Bangkok, 10400, Thailand
Received 12 December 2011; Accepted 11 February 2012
Academic Editor: Roy A. Hall
Copyright © 2012 Stuart D. Blacksell. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Dengue fever, dengue haemorrhagic fever, and dengue shock syndrome (DF/DHF/DSS) are tropical diseases that cause significant humanitarian and economic hardship. It is estimated that more than 2.5 billion people are at risk of infection and more than 100 countries have endemic dengue virus transmission. Laboratory tests are essential to provide an accurate diagnosis of dengue virus infection so that appropriate treatment and patient management may be administered. In many dengue endemic settings, laboratory diagnostic resources are limited and simple rapid diagnostic tests (RDTs) provide opportunities for point-of-care diagnosis. This paper addresses current issues relating to the application of commercial dengue RDTs for the diagnosis of acute dengue virus infection, recent diagnostic evaluations, and identifies future needs.
1.1. The Burden of Dengue
Dengue fever, dengue haemorrhagic fever and dengue shock syndrome (DF/DHF/DSS) are a group of tropical disease states that cause significant humanitarian and economic hardship. DF/DHF/DSS are caused by the dengue virus, which belongs to the flavivirus genus of the family Flaviviridae. The flavivirus genus includes approximately 70 viruses of which there are 3 antigenic complexes; the Japanese encephalitis virus, tick-borne encephalitis, and the dengue virus complexes . There are four distinct serotypes of dengue virus (i.e., dengue virus serotypes 1–4) which all cause clinical disease. It is estimated that more than 2.5 billion people are at risk of infection and more than 100 countries have endemic dengue virus transmission. While exact numbers of dengue virus cases are not available, for the period 2000–2004, the annual average was 925,896 cases, which was almost double when compared to the 479,848 cases that were reported for the period 1990–1999 . About 250,000 to 500,000 cases of DHF are reported annually although the true incidence is not really known . In dengue endemic regions which include countries in Asia and the Americas, the burden of dengue is approximately 1,300 disability-adjusted life years (DALYs) per million population, which is similar to the disease burden of other childhood and tropical diseases, including tuberculosis, in these regions .
1.2. Why Do We Need Rapid Diagnostic Tests (RDTs) and Who Controls the Quality?
Laboratory tests are essential to provide an accurate diagnosis of acute dengue virus infection at patient presentation to a clinical setting so that appropriate treatment and patient management may be administered. In many dengue endemic settings, laboratory diagnostic resources are limited and simple rapid diagnostic tests (RDTs) provide opportunities for point-of-care diagnosis. The characteristics of the ideal diagnostic test are said to be defined by the ASSURED criteria: (1) Affordable by those at risk of infection; (2) Sensitive (few false-negatives); (3) Specific (few false-positives); (4) User-friendly (simple to perform and requiring minimal training); (5) Rapid (to enable treatment at first visit) and Robust (does not require refrigerated storage); (6) Equipment-free; (7) Delivered to those who need it .
The need for simple point-of-care diagnostic tests has led to the proliferation of antibody-based RDTs for tropical infections such as dengue, leptospirosis, melioidosis, and malaria using the immunochromatographic test (ICT) format. Unfortunately, many dengue antibody-based RDTs had substandard performance for the diagnosis of acute dengue at patient presentation which leads to the large-scale evaluations funded by independent international organisations such as World Health Organization (WHO) [5, 6] to determine which are the best of the commercial assays. Until these large-scale evaluations were performed, many “backyard” manufacturers marketed their products via the internet with little or no independent verification of the manufacturer’s performance claims. Results from these evaluations have provided independent performance details to consumers, and poor results challenged manufacturers to improve RDT performance. The RDT market still remains largely unregulated with the exception of the USA where in vitro devices require approval by the Food and Drug Administration (FDA) however, in the absence of national regulations, high-quality, independent assessments in peer-reviewed journals provide the best guide to quality.
1.3. Rapid Test Formats
Immunochromatographic tests for the detection of dengue virus nonstructural protein 1 (NS1) antigen, IgM, IgG, and IgA antibodies have been developed by a number of commercial companies and have found wide application because of their ease of use and rapidity of results. These dengue RDTs are presented in the form of a lateral flow cassette that allows the flow of sample in a horizontal plane or a wick-style test that is performed in a tube and draws sample vertically by capillary action. Dengue virus RDTs use a cocktail of dried antigens and colloidal gold-labelled monoclonal antibodies (specific for dengue NS1 antigen, IgM, IgG, or IgA antibodies) on a pad at the head of a nitrocellulose strip which is impregnated with either antidengue NS1 antigen, IgM, IgG, or IgA antibody lines. Test sample and running buffer are added to the pad which releases the colloidal gold from the pad and facilitates the mixing of the patient sample with the gold complex and facilitates the migration of the reagents and sample by capillary action along the nitrocellulose strip towards the anti-human IgM, IgG, or IgA antibody lines. The presence of dengue virus NS1 antigen or IgM, IgG, or IgA antibodies is signified by the development of maroon lines in the location of the antibody lines. The dengue RDTs have the advantage that they can be performed in approximately 10–15 minutes and requires no specialized equipment or training, making them ideal for low-technology environments; however, this format has the weakness of subjective reading by the operator.
1.4. Rapid Test Evaluation Methodologies
Diagnostic assays are usually evaluated in terms of sensitivity and specificity that is calculated using a 2 × 2 cross-tabulation where a “gold standard” result (the peer-acknowledged, most accurate test) or reference standard result (normally, the test most widely used) is compared with the rapid test to determine diagnostic accuracy. A test that is 100% sensitive and specific is deemed to be a perfect test. The choice of gold standard assay, final patient result, or comparison with nonreference assay as the reference comparator can have a large influence on the final diagnostic accuracy results. Unfortunately, there is a lack of conformity in the evaluation methodologies and choice of reference assays for dengue RDT diagnostic assessments; however, it should be noted that this issue is not confined only to dengue diagnostics. Guidelines for the evaluations of dengue diagnostic assays have recently been published  which is hoped will provide a framework for a uniform approach to diagnostic assessments.
1.5. Dynamics of Dengue Virus Infection: Implications for Diagnosis
The dynamics of dengue virus infection have a potentially large influence on the interpretation of RDTs (Figures 1 and 2). Following the initial infection, the dengue virus replicates to high titers in the blood before patients are unwell enough to present to a physician, with viraemia peaking at the time or shortly after the onset of symptoms. Virus remains detectable in the blood for up to 2 to 12 days after the onset of symptoms and may reach titers of up to 1 × 108 50% infectious doses (ID50) per mL or 108.5 50% mosquito infectious doses (MID50) [8, 9]. During the viraemic phase of dengue infection, NS1 antigen is produced concomitantly during the virus replication process. NS1 antigen is a 46- to 50-kilodalton glycoprotein highly conserved by all dengue serotypes and is expressed in either membrane-associated or secreted forms [10, 11]. Soluble NS1 circulates in the serum of patients during the viraemic phase of infection of dengue virus infections and hence is an excellent diagnostic target for acute dengue diagnosis. Difference in the persistence of soluble NS1 antigen in serum between primary (5-6 days post-onset of illness) and secondary dengue infections (6–12 days) has been, noted and it is hypothesised that the presence of anti-NS1 antibodies, that are more frequently detected in dengue secondary infection , modulates the formation of antibody-antigen complexes which impede the ability of the test to detect free NS1 antigen [13, 14].
An understanding of the features of the host humoral immune response to dengue virus infection also is important for the interpretation of dengue RDTs. Dengue IgM antibodies are a reliable marker of recent infection but not necessarily acute infection. In primary dengue virus infections, IgM antibodies develop following the decline of viraemia between days 3–5 after the onset of infection using very sensitive detection methods [15, 16] and reache peak levels approximately 2 weeks later . Persistence of IgM antibodies following primary infection using linear regression method has been estimated at 179 days (95% confidence interval, 155 to 215 days) . In dengue endemic settings where in secondary infections dominate, IgM antibodies may be detectable by RDTs as soon as after 2-3 days of infection [19–21] and peak IgM antibody levels are usually lower than in primary infections [8, 22]. Persistence of IgM antibodies following secondary infection is estimated to be shorter than that of primary infections at 139 days (95% confidence interval, 119 to 167 days) , and other published estimates of IgM antibody persistence range from 2 months to 6 months [8, 23]. The IgG antibody response develops a few days after the onset of the IgM antibody response and is serotype specific and may persist for many years following a single infection. Secondary dengue virus infections generate an anamnestic IgG antibody response that is characterised by a rapid rise in IgG antibodies detectable at days 4-5 of illness  which is much sooner than the normal IgG antibody response of a primary infection. Dengue IgA antibodies have been reported in serum of dengue fever patients only between days 8 and 11 after onset of fever . However, in the more severe forms of the disease, IgA antibodies were reportedly undetectable in DHF patients in the acute phase of illness (days 2 to 4) but increased in the following early convalescent phase (days 5 to 14) and, in DSS patients, increased to the highest levels on days 8 to 11 and slightly decreased 15 days after onset of fever . In primary dengue infection, the onset of detectable levels of IgA antibodies has been reported on average at 5.5 days after onset of fever, and, in secondary infection, IgA antibodies increased slowly during the first days of the study . The rates of positivity for IgA antibodies in serum were reportedly significantly higher in secondary infections than in primary infections (100 versus 84.6%) .
2. Diagnostic Evaluations
2.1. Performance of Antibody-Based Diagnostics
Dengue IgM and IgG antibody-based RDTs have been in existence for approximately 15 years in various forms by different manufacturers (see Table 1 for description of contemporary commercial dengue IgM and IgG-based RDTs). Multiple diagnostic evaluations were performed from the late 1990s to the mid-2000s [25–29]; however, significant heterogeneity in evaluation methodologies makes direct comparison of diagnostic accuracy problematic . In 2005, WHO Western Pacific Regional Office (WPRO) commissioned an independent evaluation of dengue IgM RDT performance for acute diagnosis as well as an evaluation of storage conditions using stored samples from Thailand  and prospectively recruited patient samples from Lao PDR . The results for the majority of the evaluated dengue IgM antibody RDTs demonstrated a lack of sensitivity for acute dengue infection diagnosis that ranged from 6.4% to 65.3% and specificities ranged from 69.1% to 100% (selected results are presented in Table 2). Subsequently, WHO sponsored a multicentre evaluation of dengue IgM antibody RDTs where test sensitivities ranged from 21% to 99% and specificities ranged from 77% to 98% when compared with reference ELISAs . Subsequent evaluations of the Panbio Duo IgM RDT reported sensitivities ranging from 65.3 to 81.8% and specificities ranging from 75.0 to 97.6% (Table 2). Recent assessments of the Standard Diagnostics (SD) IgM RDT demonstrated improved sensitivity compared to the very poor 1st generation device results from the WHO study  (21.8%), with 2nd generation device having reported sensitivities of 53.5%  and 79.2% . The improvement in the 2nd generation SD IgM RDT is evidence of the positive feedback of diagnostic evaluations to the manufacturers.
2.2. Performance of NS1 Antigen-Based Diagnostics
The most important development in dengue diagnostics in recent years is the advent of the specific detection of dengue virus NS1 antigen (see Table 1 for description of contemporary commercial dengue NS1 antigen RDTs). Dengue RDTs that detect NS1 antigen employ a number of serotype-specific anti-NS1 monoclonal antibodies to capture and detect soluble NS1 antigen in serum, plasma, or blood. The first commercial assays for dengue NS1 antigen detection used the ELISA format [14, 36] and demonstrated excellent sensitivity and specificity in the early phase of infection that diminished with falling viraemia levels. The major commercial diagnostics manufacturers, Panbio, Biorad, and SD, have all developed RDT-based NS1 antigen tests, and all have equivalent ELISA-based assays. The diagnostic performance of NS1-based RDTs from the abovementioned manufacturers has been evaluated in numerous geographical locations with the results from 21 diagnostic evaluations presented in Table 3. Twelve studies evaluated the Biorad STRIP RDT for the diagnosis of acute dengue infection using admission samples, and the results demonstrated considerable variation in sensitivity (49.8%–98.7%) but the specificities reported were more consistent with all being >90%. For 25% (3/12) of the studies, the sensitivity was >89%; however, all of these studies used a skewed comparator of either virus isolation, RT-PCR, or NS1-ELISA and did not examine the possibility of false-negative results by testing paired serum samples to examine for dynamic rise in serological assays such as IgM (MAC) or IgG (GAC) capture ELISAs. Studies that used a more representative combination of virus or antigen detection and serology as reference comparators gave sensitivities for the Biorad STRIP RDT of between 49.4%  and 78.9% . The SD Bioline Dengue Duo RDT NS1 antigen detection strip was evaluated for acute dengue diagnosis in four studies (Table 3) with consistently high specificity estimates (96.7–100%) and sensitivities that ranged from 48.5%  to 65.4%  with the studies either using a combination of virus detection and serology [21, 39, 40] as comparators or serology alone . The Panbio Early Rapid RDT NS1 antigen detection strip was evaluated in two studies using samples from three locations (Vietnam, Malaysia, and Sri Lanka) with high specificity estimates (92.5–96.7%) and sensitivities that ranged from 58.6%  to 69.2%  for admission samples. A few studies have compared the diagnostic accuracy of NS1 antigen RDTs in primary and secondary dengue infections. Generally, NS1-antigen RDTs demonstrated higher sensitivities in primary infections when compared to secondary infections [39, 41–43]; however, other studies have reported the opposite . As mentioned earlier, it has been suggested that this phenomenon of lowered NS1-antigen detection in dengue secondary infections is caused by NS1 antigen complexing with anti-NS1 antibodies [12–14]. This observation results in an inability of the NS1-antigen RDT to detect complexed NS1 antigen and should not be interpreted insensitivity on the part of the diagnostic assay.
2.3. Combination of NS1 Antigen and IgM Antibody Results
To take advantage of the entire temporal spectrum of patient presentation during the acute phase of dengue infection (usually from 1 to 7 days after onset of fever), NS1 antigen and IgM antibody results have been combined in a Boolean manner using AND/OR operators. NS1 antigen is present in the serum in the early phase of infection; however, patients that present late in the course of infection may have undetectable levels of NS1 antigen. Dengue IgM antibodies are usually present following 2–5 days of infection, and, by combining the results of dengue NS1 antigen and IgM antibody testing, accurate diagnosis during acute presentation is afforded. This approach was initially described  by combining the results of the Panbio NS1 antigen and IgM antibody ELISAs in Lao PDR. Subsequently, studies [19–21] have combined NS1 antigen and antibody results to exploit the temporal diagnostic characteristics of each analyte (Table 4). Combining the SD Bioline Dengue Duo RDT NS1 antigen and IgM antibody results for acute diagnosis, the sensitivity ranged from 75.5%  to 92.9%  and the specificity from 88.8%  to 100% . Combining the Panbio Early Rapid RDT NS1 antigen and IgM antibody results, the sensitivity ranged from 89.0% to 89.9%; the only specificity reported was 75.0% .
3. Future Needs for Dengue Rapid Tests
Despite recent improvements in the RDTs, there are a number of issues that require further investigation.
3.1. Standardisation of Diagnostic Assessments
The aforementioned lack of conformity in the evaluation of dengue RDTs remains a problem and a standardised approach must be considered when performing diagnostic assessments so that there is comparability between studies. The recently published guidelines for the evaluations of dengue diagnostic assays  should be followed whenever possible.
3.2. Determining Geographical Variation and Practical Aspects of Test Use
To further strengthen the current diagnostic accuracy estimates, prospective recruitment studies are required in different dengue-endemic locations where there are variations in dengue infection status (primary versus secondary), days of illness, and prior to presentation. Further studies are also required to examine some of the more practical aspects of dengue RDT performance that includes the influence of operator training, interoperator variation, and ease of use of the assays. Where case-control studies are to be performed using characterised archived samples, consideration should also be given to the appropriateness of the composition of dengue patient (serotypes, days of illness) and non-dengue patient (other dengue-like fevers) cohorts.
3.3. Differentiation of Primary versus Secondary Dengue Infections
Patients with secondary or later dengue infections are considered to have an increased risk of the more severe forms of the disease, and therefore the accurate detection of primary and secondary at presentation to a clinical facility may become a promising patient management tool. Some manufacturers of antibody-based RDTs claim their assays are able to differentiate primary and secondary dengue virus infections using the following criteria: (1) acute primary dengue virus infection defined as an IgM-positive and IgG-negative (IgM+/IgG−) result and (2) acute secondary dengue virus infection defined as IgM-positive and IgG-positive (IgM+/IgG+) or IgM-negative and IgG-positive (IgM−/IgG+) results. Examination of the voracity of the manufacturer’s claims is limited to a few studies [6, 19, 31] and is often conducted in dengue endemic settings where there a dominance of secondary dengue infections. Such studies have demonstrated that RDTs cannot reliably differentiate the different dengue infection states.
3.4. Sample Type and the Effect of Anticoagulants and Preservatives
Many manufacturers allow the use of serum, plasma, or whole blood (Table 1) for use in dengue RDTs in both antigen and antibody formats. Interestingly, the Panbio Duo antibody RDTs only permits the use of serum. Unfortunately, there is little quantitative evidence that all sample types perform equally and it is incumbent of manufacturers to provide these performance details. The effect of sample anticoagulants and whole blood on RDT performance and ease of reading also require examination in a field setting.
3.5. Storage Considerations
Dengue endemic regions are normally located in tropical regions that have high temperature and high humidity climates. Many of the contemporary dengue rapid tests require refrigeration (i.e., 2–8°C) (see Table 1); however, some manufacturers specify storage at 2–30°C; however, ambient tropical temperatures often exceed 30°C. There is an urgent need to examine the effect of storage temperature on contemporary dengue RDTs as the only previous investigation concentrated on earlier-generation antibody-based tests .
3.6. Prognostic Markers of Disease Severity
While the acute diagnosis of dengue infection is clinically useful, in a dengue endemic setting where the majority of infections are seen in outpatient settings, there is a clear need to also have prognostic details of disease severity. The more severe forms of dengue infection (DHF and DSS) require patient admission to hospital and critical care facilities, and prognostic indicators of clinical severity would provide direction for patient management. Quantifying secreted NS1 antigen has been hypothesised as a marker of disease severity , and subsequent studies have shown that dengue NS1 antigen levels correlate with severity disease where plasma levels of secreted NS1 correlated with viraemia levels and were higher in patients with DHF than in those with the clinically less-severe dengue fever [13, 49].
Despite improvements in the accuracy of IgM-based RDTs, this format is not sufficiently sensitive for acute dengue diagnosis alone. Acute dengue diagnosis using IgG-based RDTs is not recommended due to the lifelong persistence of dengue IgG antibodies and hence the possibility of misdiagnosis by false-positive detection. NS1-antigen-based diagnostics are an important component of modern point of care diagnostics; however, they are only sensitive in the early phase of infection and therefore are not suitable for sole use in dengue-endemic settings where late clinical presentations may occur. To take advantage of the results of testing modalities across the entire temporal spectrum of patient presentation, dengue NS1 antigen, and IgM antibody, RDT results must be combined; however, there is a need to educate clinicians and scientists of this fact. The challenge for manufacturers and researchers is to address the gaps in the more practical aspects of dengue RDT performance including samples types, RDT storage, disease severity, and conduct of future diagnostic assessments.
Stuart D. Blacksell is supported by the Wellcome Trust of Great Britain.
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