American Journal of Epidemiology Vol. 152, No. 9 : 804
Copyright © 2000 by The Johns Hopkins University School of Hygiene and Public Health
ORIGINAL CONTRIBUTIONS |
Dr. Guzmán et al. Respond to Dr. Vaughn
1 Institute of Tropical Medicine "Pedro Kouri," Havana, Cuba.
2 Provincial Public Health and Epidemiology Center, Santiago de Cuba, Cuba.
3 Department Molecular Microbiology and Immunology, Johns Hopkins School of Hygiene and Public Health, Baltimore, MD.
| ABSTRACT |
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Abbreviations: DEN-1, dengue virus type 1; DEN-2, dengue virus type 2; DHS/DSS, dengue hemorrhagic fever/dengue shock syndrome.
| INTRODUCTION |
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Vaughn (1
Vaughn has identified the alarming implications of naturally attenuated dengue viral strains that produce overt disease in heterotypically immune individuals. What about purposely attenuated viruses? The safety of dengue vaccines must be judged and tested in dengue-immune subjects.
Because population-based studies of dengue infection and disease are rare, it is good to underscore the power of neutralizing antibodies to quantify past dengue infections. As our report (2
) and the commentary by Vaughn (1
) make clear, studies directed at hospitalized cases can be expected to miss many important attributes of a dengue epidemic. Yet, hospitalized cases have been the principal focus of dengue research during the dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS) era. Looking for correlates of "virulence," many researchers compare the genomic or phenotypic properties of viruses that have been isolated from overt disease that varies in severity. This approach, however, ignores the only available measure of viral virulence, the incidence rate of disease to total infections. For secondary infection dengue, this means the ratio of clinical disease due to a specific viral strain to total secondary dengue infections with that strain. Virulence is recognized when ratios with genotypically or phenotypically distinct viruses are not the same. Just this phenomenon was recognized during the 1980 population-based study in Rayong, Thailand (3
). There, the numerous dengue virus type 1 (DEN-1) infections that occurred in children immune to DEN-2 resulted in no cases of DHF/DSS, while as many as 20 percent of the children infected with DEN-1 and then DEN-2 developed DHF/DSS. A similar approach in Iquitos, Peru, in 1995 provided the first hard evidence that the American genotype of DEN-2 lacks virulence, i.e., no DHF/DSS accompanied the thousands of DEN-2 infections in subjects immune to DEN-1 (4
). It appears that in 1980 a similar phenomenon was described for DEN-1. To date, appropriate genotyping studies on DEN-1 strains have not been reported. That such data may be difficult to attain should not deter the field from balancing gene sequencing with a greater or equal emphasis on carefully designed seroepidemiologic studies.
| NOTES |
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Reprint requests to Dr. Scott B. Halstead, 5824 Edson Lane, N. Bethesda, MD 20852 (e-mail: halsteads{at}erols.com).
| REFERENCES |
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Vaughn D. Invited commentary: Dengue lessons from Cuba. Am J Epidemiol 2000;152:8003.
[Abstract/Free Full Text] -
Guzmán MG, Kouri G, Valdes G, et al. Epidemiologic studies on dengue in Santiago de Cuba, 1997. Am J Epidemiol 2000:152:7939.
[Abstract/Free Full Text] -
Sangkawibha N, Rojanasuphot S, Ahandrik S, et al. Risk factors in dengue shock syndrome: a prospective epidemiological study in Rayong, Thailand. 1. The 1980 outbreak. Am J Epidemiol 1984;120:65369.
[Abstract/Free Full Text] - Watts DM, Porter K, Putvatana R, et al. Failure of secondary infections with American genotype dengue 2 viruses to cause dengue haemorrhagic fever. Lancet 1999;354:14314.[Web of Science][Medline]
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