Dengue and Dengue Hemorrhagic Fever

The factors responsible for the dramatic resurgence and emergence of epidemic dengue and DHF, respectively, as a global public health problem in the past 17 years are complex and not fully understood. However, the resurgence appears to be closely associated with demographic and societal changes over the past 50 years (36, 41, 42, 48). Two major factors have been the unprecedented global population growth and the associated unplanned and uncontrolled urbanization, especially in tropical developing countries. The substandard housing, crowding, and deterioration in water, sewer, and waste management systems associated with unplanned urbanization have created ideal conditions for increased transmission of mosquito-borne diseases in tropical urban centers.

A third major factor has been the lack of effective mosquito control in areas where dengue is endemic (36, 38, 42, 48). The emphasis during the past 25 years has been on space spraying with insecticides to kill adult mosquitoes; this has not been effective (38, 107, 115) and, in fact, has been detrimental to prevention and control efforts by giving citizens of the community and government officials a “false sense of security” (38). Additionally, the geographic distribution and population densities of A. aegypti have increased, especially in urban areas of the tropics, because of increased numbers of mosquito larval habitats in the domestic environment. The latter include nonbiodegradable plastics and used automobile tires, both of which have increased dramatically in prevalence during this period.

A fourth factor responsible for the global emergence of dengue and DHF is increased air travel, which provides the ideal mechanism for the transport of dengue and other urban pathogens between population centers of the world (36, 40, 42, 48). For instance, in 1994, an estimated 40 million persons departed the United States by air, over 50% of whom traveled for business or holiday to tropical countries where dengue is endemic. Many travelers become infected while visiting tropical areas but become ill only after returning home, resulting in a constant movement of dengue viruses in infected humans to all areas of the world and ensuring repeated introductions of new dengue virus strains and serotypes into areas where the mosquito vectors occur (40, 119).

A fifth factor that has contributed to the resurgence of epidemic dengue has been the decay in public health infrastructures in most countries in the past 30 years. Lack of resources has led to a critical shortage of trained specialists who understand and can develop effective prevention and control programs for vector-borne diseases. Coincident with this has been a change in public health policy that placed emphasis on emergency response to epidemics by using high-technology mosquito control methods rather than on preventing those epidemics by using larval source reduction through environmental hygiene, the only method that has been shown to be effective (38).

In summary, demographic and societal changes, decreasing resources for vector-borne infectious disease prevention and control, and changes in public health policy have all contributed to increased epidemic dengue activity, the development of hyperendemicity, and the emergence of epidemic DHF.

Each year, dengue cases imported to the Continental United States are documented by the Centers for Disease Control and Prevention (CDC) (40, 119). These cases represent introductions of all four virus serotypes from all tropical regions of the world. Most cases of dengue introduced into the United States come from the American and Asian tropics, reflecting the increased number of persons traveling to and from those areas. Overall, from 1977 to 1995, a total of 2,706 suspected cases of imported dengue were reported to CDC (21, 40, 119). Although adequate blood samples were received from only some of these patients, 584 (22%) were confirmed in the laboratory as dengue.

These cases represent only the tip of the iceberg, because most physicians in the United States have a low index of suspicion for dengue, which is often not included in the differential diagnosis of acute febrile illness, even if the patient recently returned from a tropical country. As a result, the majority of imported dengue cases are never reported (21). It is important to increase awareness of dengue and DHF among physicians in temperate areas, however, because the disease can be life-threatening. For example, two cases of dengue shock syndrome (DSS) were recently described in Swedish tourists returning from holiday in Asia (152). In the United States, imported cases appear to be increasingly severe (21). From 1986 to 1993, for example, only 13 of 166 patients (8%) with laboratory-confirmed dengue were hospitalized. In 1994 and 1995, however, 6 of 46 patients (13%) and 11 of 86 patients (13%) with confirmed imported disease required hospitalization, respectively. Moreover, 3 (7%) of the patients in 1994 had severe, hemorrhagic disease (21). Therefore, it is important that physicians in the United States consider dengue in the differential diagnosis of a viral syndrome in all patients with a travel history to any tropical area.

The potential for epidemic dengue transmission in the United States still exists. After an absence of 35 years, autochthonous transmission, secondary to importation of the virus in humans, occurred on four occasions in the past 17 years (1980, 1986, 1995, and 1997) (21, 22). Although all of these outbreaks were small, they underscore the potential for dengue transmission in the United States, where two competent mosquito vectors are found (48) (Fig. 4). A. aegypti, the most important and efficient epidemic vector of dengue viruses, has been in the United States for over 200 years and was responsible for transmitting major epidemics in the southern states in the 19th and early 20th centuries (34). Currently, this species is found only in the Gulf Coast states from Texas to Florida, although small foci have recently been reported in Arizona (Fig. 4).Aedes albopictus, a secondary vector of dengue virus, was introduced into the continental United States from Asia in the early 1980s and has since become widespread in the eastern half of the country. This species currently is found in 866 counties in 26 of the continental states (22, 105); it has also been found in Hawaii for over 90 years, as well as in Guam and Saipan. Both A. aegypti and A. albopictus can transmit dengue viruses to humans, and their presence in the United States increases the risk of autochthonous dengue transmission, secondary to imported cases (37, 40).

There are four dengue virus serotypes, called DEN-1, DEN-2, DEN-3, and DEN-4. They belong to the genus Flavivirus, family Flaviviridae (of which yellow fever virus is the type species), which contains approximately 70 viruses (150). The flaviviruses are relatively small (40–50 mm) and spherical with a lipid envelope. The flavivirus genome is approximately 11,000 bases long and is made up of three structural and seven nonstructural proteins. There are three major complexes within this family—tick-borne encephalitis virus, Japanese encephalitis virus, and dengue virus. All flaviviruses have common group epitopes on the envelope protein that result in extensive cross-reactions in serologic tests. These make unequivocal serologic diagnosis of flaviviruses difficult. This is especially true among the four dengue viruses. Infection with one dengue serotype provides lifelong immunity to that virus, but there is no cross-protective immunity to the other serotypes. Thus, persons living in an area of endemic dengue can be infected with three, and probably four, dengue serotypes during their lifetime (37).

The primitive enzootic transmission cycle of dengue viruses involves canopy-dwelling Aedes mosquitoes and lower primates in the rain forests of Asia and Africa (Fig.5) (37). Current evidence suggests that these viruses do not regularly move out of the forest to urban areas (116). An epidemic transmission cycle may occur in rural villages or islands, where the human population is small. Introduced viruses quickly infect the majority of susceptible individuals in these areas, and increasing herd immunity causes the virus to disappear from the population. A number of Aedes(Stegomyia) spp. may act as a vector in these situations, depending on the geographic area, including A. aegypti,A. albopictus, A. polynesiensis and other members of the A. scutellaris group (37). The most important transmission cycle from a public health standpoint is the urban endemic/epidemic cycle in large urban centers of the tropics (Fig. 5). The viruses are maintained in an A. aegypti-human-A. aegypti cycle with periodic epidemics. Often, multiple virus serotypes cocirculate in the same city (hyperendemicity).

Humans are infected with dengue viruses by the bite of an infective mosquito (37). A. aegypti, the principal vector, is a small, black-and-white, highly domesticated tropical mosquito that prefers to lay its eggs in artificial containers commonly found in and around homes, for example, flower vases, old automobile tires, buckets that collect rainwater, and trash in general. Containers used for water storage, such as 55-gallon drums, cement cisterns, and even septic tanks, are important in producing large numbers of adult mosquitoes in close proximity to human dwellings. The adult mosquitoes prefer to rest indoors, are unobtrusive, and prefer to feed on humans during daylight hours. There are two peaks of biting activity, early morning for 2 to 3 h after daybreak and in the afternoon for several hours before dark. However, these mosquitoes will feed all day indoors and on overcast days. The female mosquitoes are very nervous feeders, disrupting the feeding process at the slightest movement, only to return to the same or a different person to continue feeding moments later. Because of this behavior, A. aegypti females will often feed on several persons during a single blood meal and, if infective, may transmit dengue virus to multiple persons in a short time, even if they only probe without taking blood (46, 112, 114, 135). It is not uncommon to see several members of the same household become ill with dengue fever within a 24- to 36-h time frame, suggesting that all of them were infected by a single infective mosquito (43). It is this behavior that makes A. aegypti such an efficient epidemic vector. Inhabitants of dwellings in the tropics are rarely aware of the presence of this mosquito, making its control difficult.

After a person is bitten by an infective mosquito, the virus undergoes an incubation period of 3 to 14 days (average, 4 to 7 days), after which the person may experience acute onset of fever accompanied by a variety of nonspecific signs and symptoms (136). During this acute febrile period, which may be as short as 2 days and as long as 10 days, dengue viruses may circulate in the peripheral blood (51). If other A. aegypti mosquitoes bite the ill person during this febrile viremic stage, those mosquitoes may become infected and subsequently transmit the virus to other uninfected persons, after an extrinsic incubation period of 8 to 12 days (37, 46).

Classic dengue fever is primarily a disease of older children and adults. It is characterized by the sudden onset of fever and a variety of nonspecific signs and symptoms, including frontal headache, retro-orbital pain, body aches, nausea and vomiting, joint pains, weakness, and rash (1, 71, 131, 136, 149). Patients may be anorexic, have altered taste sensation, and have a mild sore throat. Constipation is occasionally reported; diarrhea and respiratory symptoms are infrequently reported and may be due to concurrent infections.

The initial temperature may rise to 102 to 105°F, and fever may last for 2 to 7 days. The fever may drop after a few days, only to rebound 12 to 24 h later (saddleback). A relative bradycardia may be noted despite the fever. The conjunctivae may be injected, and the pharynx may be inflamed. Lymphadenopathy is common. Rash is variable but occurs in up to 50% of patients as either early or late eruptions. Facial flushing or erythematous mottling may occur coincident with or slightly before onset of fever and disappears 1 to 2 days after onset of symptoms. A second rash, varying in form from scarlatiniform to maculopapular, may appear between days 2 and 6 of illness. The rash usually begins on the trunk and spreads to the face and extremities. In some cases, an intense erythematous pattern with islands of normal skin is observed. The average duration of the second rash is 2 to 3 days. Toward the end of the febrile phase of illness or after the temperature falls to or below normal, petechiae may appear; these may be scattered or confluent. Intense pruritus followed by desquamation on the palms of the hands and soles of the feet may occur.

Hemorrhagic manifestations in dengue fever patients are not uncommon and range from mild to severe. Skin hemorrhages, including petechiae and purpura, are the most common, along with gum bleeding, epistaxis, menorrhagia, and gastrointestinal (GI) hemorrhage. Hematuria occurs infrequently, and jaundice is rare.

Clinical laboratory findings associated with dengue fever include a neutropenia followed by a lymphocytosis, often marked by atypical lymphocytes. Liver enzyme levels in the serum may be elevated; the elevation is usually mild, but in some patients, alanine aminotransferase and aspartate aminotransferase levels reach 500 to 1,000 U/liter. In one epidemic of DEN-4, 54% of confirmed patients with data reported on liver enzymes had elevated levels (32). Thrombocytopenia is also common in dengue fever; in the above epidemic, 34% of patients with confirmed dengue fever who were tested had platelet counts of less than 100,000/mm³(32).

Dengue fever is generally self-limiting and is rarely fatal. The acute phase of illness lasts for 3 to 7 days, but the convalescent phase may be prolonged for weeks and may be associated with weakness and depression, especially in adults. No permanent sequelae are known to be associated with this infection.

DHF is primarily a disease of children under the age of 15 years, although it may also occur in adults (1, 32). It is characterized by sudden onset of fever, which usually lasts for 2 to 7 days, and a variety of nonspecific signs and symptoms. During the acute phase of illness, it is difficult to distinguish DHF from dengue fever and other illnesses found in tropical areas. The differential diagnoses during the acute phase of illness should include measles, rubella, influenza, typhoid, leptospirosis, malaria, other viral hemorrhagic fevers, and any other disease that may present in the acute phase as a nonspecific viral syndrome. Children frequently have concurrent infections with other viruses and bacteria causing upper respiratory symptoms. There is no pathognomonic sign or symptom for DHF during the acute stage; on the other hand, as fever remits, characteristic manifestations of plasma leakage appear, making accurate clinical diagnosis possible in many cases (1).

The critical stage in DHF is at the time of defervescence, but signs of circulatory failure or hemorrhagic manifestations may occur from about 24 h before to 24 h after the temperature falls to normal or below (1). Blood tests usually show that the patient has thrombocytopenia (platelet count, ≤100,000/mm³) and hemoconcentration relative to baseline as evidence of a vascular leak syndrome. Common hemorrhagic manifestations include skin hemorrhages such as petechiae, purpuric lesions, and ecchymoses. Epistaxis, bleeding gums, GI hemorrhage, and hematuria occur less frequently. The tourniquet test, which indicates that the patient has increased capillary fragility, may be diagnostically helpful to the physician.

Scattered petechiae are the most common hemorrhagic manifestation observed; they appear most often on the extremities but are also found on the trunk, other parts of the body, and on the face in patients with severe dengue shock syndrome (DSS). Purpuric lesions may appear on various parts of the body but are most common at the site of venipuncture. In some patients, large ecchymotic lesions develop on the trunk and extremities; other patients bleed actively at the site of venipuncture, some profusely. More severely ill patients have GI hemorrhage. Classic hematemesis with coffee-ground vomitus and melena usually occur after prolonged shock, but patients may develop massive, frank upper GI hemorrhage as well, often before the onset of shock. Without early diagnosis and proper management, some patients experience shock from blood loss, which may be mild or severe (35, 138, 139). More commonly, shock is caused by plasma leakage; it may be mild and transient or progress to profound shock with undetectable pulse and blood pressure (1). Children with profound shock are often somnolent, exhibit petechiae on the face, and have perioral cyanosis.

In patients with severe DHF or DSS, fever and nonspecific constitutional signs and symptoms of a few days duration are followed by the sudden deterioration of the patient’s condition (1). During or shortly before or after the fall in temperature, the patient’s skin may become cool, blotchy, and congested; circumoral cyanosis is frequently observed, and the pulse becomes rapid and weak. Although some patients appear lethargic at first, they become restless and then rapidly pass into a critical stage of shock. They frequently experience acute abdominal pain shortly before the onset of shock (1, 138, 139).

In patients with mild DHF, all signs and symptoms abate shortly after the fever subsides. Subsidence of fever, however, may be accompanied by profuse sweating and mild changes in pulse rate and blood pressure, together with coolness of the extremities and skin congestion. These changes reflect mild and transient circulatory disturbances as a result of plasma leakage. Patients usually recover spontaneously or after fluid and electrolyte therapy (1). Patients in shock are in danger of dying unless appropriately managed. The duration of shock is usually short; the patient may die within 8 to 24 h, but recovery is usually rapid following antishock therapy. Convalescence for patients with DHF, with or without shock, is usually short and uneventful. Once the shock is overcome, even patients with undetectable pulse and blood pressure will usually recover within 2 to 3 days (1).

As with dengue fever, leukopenia is common; thrombocytopenia and hemoconcentration are constant findings in DHF and DSS. A platelet count of ≤100,000/mm³ is usually found between the days 3 and 8 of illness. Hemoconcentration, indicating plasma leakage, is almost always present in classic DHF but is more severe in patients with shock. Hepatomegaly is a common but not constant finding (35, 138, 139). In some countries, most patients with confirmed DHF and DSS have enlarged livers. In other countries, however, hepatomegaly varies from one epidemic to another, suggesting that the strain and/or serotype of virus may influence liver involvement (35). Elevated liver enzyme levels are common.

The primary pathophysiologic abnormality seen in DHF and DSS is an acute increase in vascular permeability that leads to leakage of plasma into the extravascular compartment, resulting in hemoconcentration and decreased blood pressure (1, 77). Plasma volume studies have shown a reduction of more than 20% in severe cases. Supporting evidence of plasma leakage includes serous effusion found postmortem, pleural effusion on X-ray, hemoconcentration, and hypoproteinemia. Early diagnosis and aggressive fluid replacement therapy with good nursing care can decrease fatality rates to 1% or less. Normal saline or lactated Ringer’s solution can be used in patients with mild DHF and DSS, but plasma or plasma expanders may be necessary in those with severe cases. Details of effective management of DHF and DSS have been published previously (1). There are no apparent destructive vascular lesions, suggesting that the transient functional vascular changes are due to a short-acting mediator (1). Once the patient is stabilized and begins recovery, the extravasated fluid is rapidly reabsorbed, causing a drop in the hematocrit.

Hemostatic changes in DHF and DSS involve three factors: vascular changes, thrombocytopenia, and coagulation disorders (1). Almost all DHF patients have increased vascular fragility and thrombocytopenia, and many have abnormal coagulograms, suggesting disseminated intravascular coagulation, which is also evidenced by concomitant thrombocytopenia, a prolonged partial thromboplastin time, a decreased fibrinogen level, and increased levels of fibrinogen degradation products. GI hemorrhage is found at autopsy in the majority of patients who die.

The pathology of DHF and DSS has been well studied (6, 7, 9), but that of dengue infections has not. Gross and microscopic pathologic studies of tissues taken at autopsy in Thailand have shown diffuse petechial hemorrhages of most organs, as well as serous effusions in the pericardial, pleural, and peritoneal cavities. Microscopically, perivascular edema and loss of integrity of endothelial junctions are found. Dengue antigen can be demonstrated in endothelial cells, but there is no apparent damage to the blood vessels or endothelial cells.

In the liver, midzonal necrosis is common and is often indistinguishable from the pathologic changes caused by the closely related yellow fever virus; Councilman bodies are common. In the brain, edema and hemorrhage have been observed but pathologic changes associated with encephalitis have not. However, recent isolations of dengue virus from the brain and cerebrospinal fluid and intrathecal antibody production in the latter suggest that on occasion, the dengue virus crosses the blood-brain barrier. There is increased proliferation of reticuloendothelial cells in the bone marrow, spleen, lymph nodes, and lungs.

Unfortunately, there are no good animal models for DHF and DSS, making studies on pathogenesis difficult to interpret. Primates are natural hosts for dengue virus, but those that have been studied generally show no signs of disease; these animals become infected and develop viremia, although at a lower titer than humans (126). However, the results obtained with these animals are conflicting. One of the few studies cited as evidence that ADE occurs in vivo showed that rhesus monkeys that experienced a secondary DEN-2 infection or had been infused with dengue immune serum had higher viremias than did monkeys with primary infections (60, 64, 65). All monkeys were infected parenterally by needle inoculation. These results could not be repeated in macaque monkeys infected naturally by a mosquito bite or in chimpanzees infected parenterally; primary and secondary infections of all serotypes and combinations routinely showed that monkeys with primary infection had viremia of the same or higher titer and longer duration (126, 134). Clinical and laboratory studies on humans have shown the same results (35, 47, 49, 51, 87).

In humans, viremias range in titer from barely detectable (10³), measured as 50% mosquito infection doses (MID₅₀) (125) to over 10^8.5MID₅₀ (51). Viremia usually peaks at the time of or shortly after the onset of illness and may remain detectable for various periods ranging from 2 to 12 days, depending on the strain of virus and the immune status of the individual (35, 43, 47, 49, 51, 87, 147). It has been suggested that the severity of the disease associated with dengue infection is determined by the number of cells infected with the virus and that the number of cells infected is related to ADE infection of peripheral blood leukocytes in secondary infections (77). It follows that viremias should be higher in secondary infections, but this is not borne out by experimental infection of lower primates or by clinical studies on humans (35, 49, 51, 87, 126, 134). In fact, the opposite has usually been observed; that is, viremias are usually higher in primary infections.

In secondary infections, the virus may be complexed with antibody, making it undetectable by most current virus isolation techniques. However, studies in humans during an outbreak of DEN-2 on an island in the Pacific (Tonga) showed great variation in both the magnitude and duration of viremia in primary infections (49). Some patients were identified on the day of onset of mild illness and monitored for as long as 8 days. Blood samples were taken daily for viremia studies, and uninfected mosquitoes were allowed to feed on some patients. The majority of patients, confirmed as DEN-2 infection by seroconversion, had undetectable viremia both by virus isolation and by isodiagnosis (feeding mosquitoes on patients) (49). When virus was detectable, viremia was at a low titer (≤10⁶MID₅₀) and of short duration (1 to 3 days). The same DEN-2 virus had caused explosive epidemics associated with severe disease in neighboring islands in the previous 3 years, but in Tonga it circulated for nearly a year without being detected in a human population that was fully susceptible to DEN-2 virus (silent transmission) (49). Two species of vector mosquitoes (A. aegypti and Aedes tabu) were present in large numbers. The data suggested that the virus had changed from an epidemic strain to one that circulated in nature silently, causing mild or inapparent disease. Similar observations have been made with DEN-3 and DEN-1 viruses (41).

Molecular studies have demonstrated that dengue viruses vary genetically in nature; unfortunately, phenotypic changes that have been observed in the field have not yet been associated with genetic changes in the virus (26, 99, 100, 116, 117, 143). Collectively, however, the data suggest that viral factors play a significant role in the pathogenesis of severe dengue disease.

There is a large body of evidence, mostly obtained in vitro, suggesting that heterotypic, nonneutralizing antibody binds with dengue virus, facilitating the entry of the virus into cells of the monocytic line and hence facilitating infection (15, 61, 62, 67, 68, 83). These data, along with epidemiologic observations that the majority of patients with reported DHF cases are experiencing a secondary infection, form the basis for the hypothesis that preexisting heterotypic dengue antibody is a risk factor for DHF (18, 57, 61, 62, 83, 133). The lack of a good animal model for human disease and limitations of human clinical studies have made it difficult to confirm this hypothesis. In recent years, however, detailed, well-designed studies that support the concept of immunopathogenesis of dengue infection in humans have been conducted. The results of these studies have been comprehensively reviewed in a recent article (92).

Briefly, the data show that dengue virus-specific memory CD4⁺ CD8⁻ and CD4⁻CD8⁺ lymphocytes are detectable in humans after natural dengue infections. Infection with a single dengue serotype induces both serotype-specific and serotype-cross-reactive CD4⁺ memory T cells, while CD8⁺ T lymphocytes have virus-specific cytotoxic activity.

The pathogenetic mechanism responsible for the increased vascular permeability observed in DHF and DSS is not known, but it has been suggested that cytokines and chemical mediators such as tumor necrosis factor (TNF), interleukin-1 (IL-1), IL-2, IL-6, platelet-activating factor (PAF), complement activation products C3a and C5a, and histamine may play a role.

CD4⁺ T lymphocytes produce a number of cytokines, including gamma interferon (IFN-γ), IL-2, IL-4, IL-5, IL-6, IL-10, and lymphotoxin. Moreover, monocytes/macrophages which are infected by dengue viruses produce TNF, IL-1, IL-1B, IL-6, and PAF. Finally, cytokine and chemical mediator production is induced by other cytokines. Thus, once cytokines are produced, a complex network of induction may further increase the levels of cytokines and chemical mediators, resulting in even higher levels with synergistic effects on vascular permeability (92).

Kurane and Ennis have proposed a model of immunopathogenesis based on these observations (92). Briefly, it is hypothesized that dengue virus infections of monocytes/macrophages is enhanced by ADE. This enhancement is facilitated by the fact that the dengue virus-specific CD4⁺ T lymphocytes produce IFN-γ, which in turn up-regulates the expression of FC-γ receptors. The increased number of dengue virus-infected monocytes/macrophages results in increased T-cell activation, which results in the release of increased levels of cytokines and chemical mediators. Kurane and Ennis (92) hypothesized that the rapid increase in the levels and the synergistic effects of mediators such as TNF, IL-2, IL-6, IFN-γ, PAF, C3a, C5a, and histamine induce increased vascular permeability, plasma leakage, shock, and malfunction of the coagulation system, which may lead to hemorrhage.

In summary, available evidence suggests that both viral and host immune factors are involved in the pathogenesis of severe dengue disease. Unfortunately, the role of each is not fully understood and the lack of an animal model makes this a difficult area to study. It would appear that different clinical pathologic manifestations of the disease may be caused by different pathogenetic mechanisms (37). For example, it has been suggested that hepatic injury may relate more to viral factors whereas vascular permeability may be mediated predominantly by the immune response (92, 127). Clearly, the strain of virus is important since ADE apparently occurs only with selected virus strains when tested in vitro. Also, the rate of virus replication and infectivity in various tissues varies with the strain of virus. Collectively, the data suggest that only certain strains of dengue virus are associated with major epidemics and severe disease, and it is most likely that these are the viruses that infect cells of the monocytic line via ADE (12, 37, 49, 116, 117).

Five basic serologic tests have been routinely used for diagnosis of dengue infection; hemagglutination-inhibition (HI), complement fixation (CF), neutralization test (NT), immunoglobulin M (IgM) capture enzyme-linked immunosorbent assay (MAC-ELISA), and indirect immunoglobulin G ELISA (47, 55, 148). Regardless of the test used, unequivocal serologic diagnosis depends upon a significant (fourfold or greater) rise in the titer of specific antibodies between acute- and convalescent-phase serum samples. The antigen battery for most of these serologic tests should include all four dengue virus serotypes, another flavivirus (such as yellow fever virus, Japanese encephalitis virus, or St. Louis encephalitis virus), a nonflavivirus (such as Chikungunya virus or eastern equine encephalitis virus), and ideally, an uninfected tissue control antigen (47).

Of the above tests, HI has been the most frequently used; it is sensitive, is easy to perform, requires only minimal equipment, and is very reliable if properly done (28). Because HI antibodies persist for long periods (up to 48 years and probably longer) (58), the test is ideal for seroepidemiologic studies. HI antibody usually begins to appear at detectable levels (titer of 10) by day 5 or 6 of illness, and antibody titers in convalescent-phase serum specimens are generally at or below 640 in primary infections, although there are exceptions (4, 47). By contrast, there is an immediate anamnestic response in secondary and tertiary dengue infections, and reciprocal antibody titers increase rapidly during the first few days of illness, often reaching 5,120 to 10,240 or more. Thus, a titer of ≥1,280 in an acute-phase or early convalescent-phase serum sample is considered presumptive evidence of a current dengue infection. Such high levels of HI antibody persist for 2 to 3 months in some patients, but antibody titers generally begin to wane by 30 to 40 days and fall below 1,280 in most patients (47). The major disadvantage of the HI test is its lack of specificity, which generally makes it unreliable for identifying the infecting virus serotype. However, some patients with primary infections show a relatively monotypic HI response that generally correlates with the virus isolated (47).

The CF test is not widely used for routine dengue diagnostic serologic testing. It is more difficult to perform, requires highly trained personnel, and therefore is not used in most dengue laboratories. It is based on the principle that complement is consumed during antigen-antibody reactions (20). CF antibodies generally appear later than HI antibodies, are more specific in primary infections, and usually persist for short periods, although low levels of antibodies persist in some persons (47). It is a valuable test to have in a diagnostic laboratory because of the late appearance of CF antibodies; some patients thus show a diagnostic rise in antibody titers by CF but have only stable antibody titers by HI or ELISA (47). The greater specificity of the CF test in primary infections is demonstrated by the monotypic CF responses when HI responses are broadly heterotypic; it is not specific in secondary infections. The CF test is useful for patients with current infections but is of limited value for seroepidemiologic studies, where detection of persistent antibodies is important.

The NT is the most specific and sensitive serologic test for dengue viruses (33, 129). The most common protocol used in dengue laboratories is the serum dilution plaque reduction NT. In general, neutralizing-antibody titers rise at about the same time or slightly more slowly than HI and ELISA antibody titers but more quickly than CF antibody titers and persist for at least 48 years (58). Because the NT is more sensitive, neutralizing antibodies are present in the absence of detectable HI antibodies in some persons with past dengue infection.

Because relatively monotypic neutralizing-antibody responses are observed in properly timed convalescent-phase serum, the NT can be used to identify the infecting virus in primary dengue infections (4, 47, 129, 148). As noted above, the HI and CF tests may also give monotypic responses to dengue infection that generally agree with NT results. In cases when the responses are monotypic, the interpretation of all these tests is generally reliable. In secondary and tertiary infections, determining the infecting virus serotype by NT or any other serologic test is not reliable (90). Because of the long persistence of neutralizing antibodies, the test may also be used for seroepidemiologic studies. The major disadvantages are the expense, time required to perform the test, and technical difficulty. It is therefore not used routinely by most laboratories.

MAC-ELISA has become the most widely used serologic test for dengue diagnosis in the past few years. It is a simple, rapid test that requires very little sophisticated equipment (17, 47, 78, 89, 97). Anti-dengue IgM antibody develops a little faster than IgG antibody. By day 5 of illness, most patients (80%) in Puerto Rico whose cases were subsequently confirmed by HI on paired serum samples or by virus isolation had detectable IgM antibody in the acute-phase serum in this assay (47). Nearly all patients (93%) developed detectable IgM antibody 6 to 10 days after onset, and 99% of patients tested between 10 and 20 days had detectable IgM antibody. The rapidity with which IgM develops varies considerably among patients. Although the dates of onset are not always recorded accurately, some patients have detectable IgM on days 2 to 4 after the onset of illness whereas others may not develop IgM for 7 to 8 days after onset (47). This variation is also reflected in the amount of IgM produced and the length of time detectable IgM persists after infection. IgM antibody is produced by patients with both primary and secondary dengue infections and probably by persons with tertiary infections, although the response in some secondary and probably most tertiary infections is low level and transient (89). IgM antibody titers in primary infections are significantly higher than in secondary infections, although it is not uncommon to obtain IgM titers of 320 in the latter cases (47). In some primary infections, detectable IgM persists for more than 90 days, but in most patients, it has waned to an undetectable level by 60 days. A small percentage of patients with secondary infections have no detectable IgM antibody (89).

MAC-ELISA with a single acute-phase serum sample is slightly less sensitive than the HI test with paired serum samples for diagnosing dengue infection (47). However, it has the advantage of frequently requiring only a single, properly timed blood sample. In one series of 288 patients during the 1986 epidemic in Puerto Rico, paired blood samples were tested by HI and the single acute-phase sample from the same pairs were tested by MAC-ELISA. The HI test on the pairs indicated that 228 (79%) were considered positive, while MAC-ELISA on the single samples indicated that 203 (70%) were positive. Five samples (1.7%) showed a false-positive response and 30 samples (10%) showed a false-negative response by MAC-ELISA (47). When one considers the difficulty in obtaining second blood samples and the long delay in obtaining conclusive results from the HI test, this low error rate would be acceptable in most surveillance systems. It must be emphasized, however, that because of the persistence of IgM antibody for 1 to 3 months, MAC-ELISA-positive results obtained with single serum samples are only provisional and do not necessarily mean that the dengue infection was current (47, 148). These results do mean that it is reasonably certain that the person had a dengue infection sometime in the previous 2 to 3 months. Similarly, a negative result with an acute-phase sample may be a false-negative result because the sample was taken before detectable IgM appeared. Unfortunately, many dengue diagnostic laboratories have adopted MAC-ELISA as a confirmatory test and do not conduct follow-up tests to confirm the presumptive IgM results. As noted above, this may be acceptable for surveillance reports, but it is unacceptable in a clinical setting. If this test is used to make patient management decisions, it could result in a higher case fatality rate among patients with false-negative results.

The specificity of MAC-ELISA is similar to that of HI. In both primary and secondary dengue infections, some monotypic responses may be observed, but in general, the response is broadly reactive among both dengue virus and other flavivirus antigens. With serum samples from patients with other flavivirus infections such as Japanese encephalitis, St. Louis encephalitis, and yellow fever, however, the response is generally more specific; while there may be some cross-reaction with dengue antigens, most specimens show relatively monotypic IgM responses to the infecting flavivirus (47). In dengue infections, monotypic IgM responses frequently do not correlate with the virus serotype isolated from a patient. Therefore, MAC-ELISA cannot be reliably used to identify the infecting virus serotype.

MAC-ELISA has become an invaluable tool for surveillance of dengue, DHF, and DSS. In areas where dengue is not endemic, it can be used in clinical surveillance for viral illness or for random, population-based serosurveys, with the certainty that any positive results detected indicate recent infections (within the last 2 to 3 months). A properly timed serosurvey by MAC-ELISA during an epidemic can determine very quickly how widespread transmission has become. In areas where dengue is endemic, MAC-ELISA can be used as an inexpensive way to screen large numbers of serum specimens with relatively little effort. It is especially useful for hospitalized patients, who are generally admitted late in the illness after detectable IgM is present in the blood (47), but it must be emphasized again that this test should not be used to make patient management decisions.

An indirect IgG-ELISA has been developed that is comparable to the HI test and can also be used to differentiate primary and secondary dengue infections (27). The test is simple and easy to perform and is thus useful for high-volume testing. The IgG-ELISA is very nonspecific and exhibits the same broad cross-reactivity among flaviviruses as the HI test does; therefore, it cannot be used to identify the infecting dengue virus serotype. However, it has a slightly higher sensitivity than the HI test. As more data are accumulated on the IgG-ELISA, it is expected to replace the HI test as the most commonly used IgG test in dengue laboratories.

A number of commercial test kits for anti-dengue IgM and IgG antibodies have become available in the past few years. Unfortunately, the accuracy of most of these tests is unknown because proper validation studies have not been done. Some evaluations have been published (91, 96, 146, 153), but the sample sizes have been too small to accurately measure sensitivity and specificity. Moreover, the samples generally used have represented only strong positives and negatives, with few samples representing optical densities or positive-negative values in the equivocal range. One exception to this were kits that were independently evaluated at CDC; both IgM and IgG test kits had a high rate of false-positive results compared to standard tests, especially with samples with optical densities in the equivocal range (91). Other studies, however, have given results comparable to those of standard tests (96, 146, 153). It is anticipated that these test kits can be reformulated to make them more accurate, making global laboratory-based surveillance for dengue and DHF an attainable goal in the near future.

Four isolation systems have routinely been used for dengue viruses; intracerebral inoculation of 1- to 3-day-old baby mice, the use of mammalian cell cultures (primarily LLC-MK₂ cells), intrathoracic inoculation of adult mosquitoes, and the use of mosquito cell cultures (47, 55, 148).

The method of choice for dengue virus identification is IFA with serotype-specific monoclonal antibodies produced in tissue culture or mouse ascitic fluids and an anti-mouse immunoglobulin G-fluorescein isothiocyanate conjugate (47, 52, 55, 72). This test can be easily performed with infected cell cultures, mosquito brain or tissue squashes, mouse brain squashes, or even on formalin-fixed tissues embedded in paraffin and sectioned for histopathologic testing (56). It is simple and reliable and is the most rapid method. Moreover, it allows the detection of multiple viruses in patients with concurrent infections with more than one serotype (53, 94).

The success of isolating dengue virus from human serum depends on several factors (47). First, the manner in which the specimen has been handled and stored is important. Virus activity can be inhibited by heat, pH, and several chemicals; therefore, improper handling is often an important cause of unsuccessful virus isolation. Second, the level of viremia may vary greatly depending on the time after onset, the antibody titers, and/or the strain of the infecting virus. Viremia usually peaks at or shortly before the onset of illness and may be detectable for an average of 4 to 5 days (43, 47, 51, 147). The success of virus isolation decreases rapidly with the appearance of IgM antibody (47, 148). With some virus strains, however, viremia may remain below the level of detectability throughout the illness (47, 49). Finally, the virus isolation system used influences the success of isolation, as discussed above.

In recent years, several new methods of diagnosis have been developed and have proven very useful in dengue diagnosis. This topic has recently been reviewed extensively (29). The various methods are discussed briefly below.

The first candidate dengue vaccines were developed shortly after the viruses were first isolated by Japanese and American scientists (81, 132). Despite considerable work over the years, an effective safe vaccine was never developed (3, 59, 69, 130, 151). The World Health Organization designated the development of a tetravalent dengue vaccine a priority for the most cost-effective approach to dengue prevention (13, 14). Effective vaccination to prevent DHF will most probably require a tetravalent vaccine, because epidemiologic studies have shown that preexisting heterotypic dengue antibody is a risk factor for DHF (18, 57, 61, 62, 133). With the support of the World Health Organization, considerable progress in developing a vaccine for dengue and DHF has been made in recent years (8, 10, 11, 145, 154). Promising candidate attenuated vaccine viruses have been developed and have been evaluated in phase I and II trials in Thailand as monovalent, bivalent, trivalent, and tetravalent formulations (8). A commercialization contract has been signed, and the tetravalent vaccine formulation is currently undergoing repeat phase I trials in the United States. Current progress on the live attenuated dengue vaccine has been recently reviewed (8).

Promising progress in the development of alternative vaccine strategies using new molecular technology has also been made in recent years. Recent approaches include the use of inactivated whole-virion vaccines (23), synthetic peptides (5, 121, 122), subunit vaccines (31, 101, 140), vector expression, recombinant live vector systems (23, 102), infectious cDNA clone-derived vaccines (16, 25, 79, 80, 82, 93, 113), and naked DNA (24, 84). The last two approaches appear to be the most promising. An infectious clone of the DEN-2, PDK-53 vaccine candidate virus from Thailand (11) has been constructed, and work is in progress to construct chimeric viruses by inserting the capsid, premembrane, and envelope genes of DEN-1, DEN-3 and DEN-4, into the DEN-2 PDK-53 backbone (82). Through genetic manipulation, these recombinants may be made to grow better and to be more immunogenic and safer than the original live attenuated virus vaccine candidates. In addition, chimeras are being constructed by inserting the structural proteins of dengue viruses into the infections clones of the 17D yellow fever and the SA14-14-2 Japanese encephalitis vaccine viruses (103a). The development of naked DNA vaccines is in its infancy but shows great promise (24). This area has been recently reviewed (23, 144).

Despite the promising progress, it is unlikely that an effective, safe, and economical dengue vaccine will be available in the near future. A major problem has been and continues to be lack of financial support for dengue vaccine research. Thus, other approaches to disease prevention must be developed by using the program components outlined above.

There is no completely effective method of preventing dengue infection in travelers visiting tropical areas. The risk of infection can be significantly decreased, however, by understanding the basic behavior and feeding habits of the mosquito vector and by taking a few simple precautions to decrease exposure to infective mosquito bites. Female A. aegypti mosquitoes prefer to feed indoors, with peak biting activity occurring for 2 to 3 hours after daybreak and for 3 to 4 hours before nightfall. Although the risk may be higher at these times, it is important to remember that the mosquito may feed indoors at anytime during the day as well as outdoors, especially on overcast days. Precautions, therefore, include staying in screened or air-conditioned rooms, spraying these rooms with aerosol bomb insecticides to kill adult mosquitoes indoors (especially in bedrooms), using a repellent containing dimethyl-metatoluamide (DEET) on exposed skin, and wearing protective clothing treated with a similar repellant. The risk of exposure may be lower in modern, air-conditioned hotels with well-kept grounds and in rural areas.