The Brazilian Journal of Infectious Diseases The Brazilian Journal of Infectious Diseases
Braz J Infect Dis 2013;17:622-3 - Vol. 17 Num.5 DOI: 10.1016/j.bjid.2013.05.003
Letter to the Editor
Categorization of dengue fever according to phase of illness—a suggestion for clinical studies using single diagnostic sample
Emmanuel Bhaskara,, , Raveendran Praveenab, Gopalan Sowmyaa, Swathy Moorthya
a Department of Medicine, Sri Ramachandra Medical College and Research Institute, Porur, Chennai, India
b Department of Microbiology, Sree Balaji Medical College and Hospital, Chrompet, Chennai, India
Received 01 April 2013, Accepted 02 May 2013
Dear Editor,

In 2008, World Health Organization (WHO) experts agreed that “dengue is one disease entity with different clinical presentations and often with unpredictable clinical evolution and outcome”.1 The development of a spectrum of laboratory methods to detect the first of seven non-structural proteins in dengue virus, NS1 (non-structural protein-1) leads us toward an opportunity to observe the features of dengue during viremic phase which corresponds to the first 3 days of illness.1 Prior to the availability of NS1 antigen assays for detection of dengue, the illness was confirmed only after the detection of IgM and (or) IgG antibodies. This also helps us infer that studies on dengue fever using positive serology as part of dengue case definition would have identified only features of dengue in the immune phase of the illness. Though inference based on paired sera is the ideal way to confirm dengue, our limited experience in dengue indicates that the concept of utilizing paired sera in dengue diagnosis is difficult to practice since obtaining a sample beyond the 10th day of illness in a patient who is free of symptoms raises consent related issues.2,3 WHO recommends classification of dengue as dengue fever±warning signs and severe dengue.1 We suggest a further laboratory based categorization for dengue illness (both WHO categories) using a single diagnostic sample incorporating aspects related to dengue pathogenesis.

A brief overview on the immunology of dengue may help in understanding our classification.1,4 Dengue fever is characterized by an initial viremic phase which corresponds to the first 3 days of illness followed by immune phase (also called critical phase) spanning from 3rd to 6th day of illness. The phase of dengue beyond 6th day of illness is called recovery phase (though a sizable number of patients take longer to recover). When the dengue virus infects a previously non-infected person, it is inferred as primary dengue infection [PDI]. A patient with PDI will demonstrate NS1 antigen till the 3rd day of illness (sometimes as long as the 9th day), IgM antibodies detectable beyond the 3rd day of illness and IgG beyond the 7th day of illness. Though IgM and IgG are detectable by the 7th day of PDI, the dominant antibody is IgM as demonstrated by IgM/IgG optical density ratio of more than the assay cut-off value (studies have used a cut-off value of >1.2 with patient sera in 1/100 dilution or >1.4 with patient sera in 1/20 dilution).5 When the dengue virus infects a person who had been previously infected by a different dengue serotype it is said to be secondary dengue infection [SDI]. The detection of NS1 in SDI is timed similar to PDI. However an anamnestic IgG response occurs at the onset of SDI earlier to the appearance of IgM antibodies making the onset of the immune phase concomitant with the viremic phase. The challenge in identifying SDI is complicated by two factors. First, a slow IgM rise (sometimes not detectable) during convalescence in SDI. Second, IgG is being the dominant antibody in SDI. These make IgM/IgG optical density ratio less than the assay dependent cut-off value as a laboratory hallmark of SDI. Though serial monitoring of IgG titers helps in SDI diagnosis, the concept is infrequently practised. Studying dengue illness after categorizing it as viremic phase, viremia-immune overlap phase, and immune phase (Table 1) will facilitate better understanding of occurrence and progression of clinical symptoms, signs and laboratory findings. Obtaining these information (especially course of thrombocytopenia and organ dysfunction) gains critical importance since it may help us predicting the course of the illness with current therapies for dengue fever.

Table 1.

Laboratory based staging for clinical studies using a single diagnostic sample.

Phase of illness  Primary infection  Secondary infection 
Viremic  NS1 positive  No isolated viremic phase since anamnestic IgG response often present at the onset of illness 
Viremia-immune overlapNS1 positive  NS1 positive 
Plus  Plus 
One of the following:  One of the following 
IgM positive (>40units) and IgG negative  IgG positive (>100units) and IgM negative 
IgM/IgG optical density ratio>cut-off value of assaya  IgM/IgG optical density ratio<cut-off value of assaya 
ImmuneIgM positive (>40units) and IgG negative  IgM/IgG optical density ratio<cut-off value of assaya 
OR   
IgM/IgG optical density ratio>cut-off value of assaya   

IgM and IgG detection by enzyme-linked immunosorbent assay (ELISA). NS1 detection by ELISA (further scientific inputs required).

a

Studies have used a cut-off value of 1.2 with patient sera in 1/100 dilution or 1.4 with patient sera in 1/20 dilution.5

The suggested classification may furthermore help identifying the effects of interventions (anti-viral therapy, corticosteroids, immunosuppresants) during viremic phase and viremia-immune overlap which could lessen the complications observed in the immune phase. The classification does have important limitations. First one is the diagnosis of SDI, a factor which is difficult to address taking into account the complex IgM and IgG antibody response observed in secondary infection. Second is the lack of standardization among NS1 assays, though an ELISA based protocol is generally preferred.6 WHO recommendation on methods of NS1 detection will add clarity to the classification. Third, diagnostic accuracy compared to paired sample. Adopting a cut-off value for IgM (>40units) and IgG (>100units) in the classification has partially addressed the non-inclusion of paired sera for dengue diagnosis.7

Conflict of interest

The authors declare no conflicts of interest.

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Corresponding author at: Sri Ramachandra Medical College and Research Institute, Porur, Chennai 600116, India. (Emmanuel Bhaskar drmeb1974@yahoo.co.in)
Copyright © 2013. Elsevier Editora Ltda.
Braz J Infect Dis 2013;17:622-3 - Vol. 17 Num.5 DOI: 10.1016/j.bjid.2013.05.003