Active Infection & Immunity Pregnancy, Children & Inherited Conditions

Profiling the clinico-epidemiological, genomic, and immunological markers of dengue and Zika infections and co-infections in Kerala, India via longitudinal studies

In plain English

AI plain-English summary

Over 17,000 patients in Kerala will be tracked from their first fever to recovery in a five-year study of dengue and Zika viruses, which co-circulate in the region and can cause similar symptoms. This matters because current diagnostic and treatment guidelines treat dengue and Zika as separate problems, yet co-infections and sequential infections are common in Kerala. The study will screen patients within five days of symptom onset, monitor household contacts in geographic clusters, and follow pregnant women and their infants for congenital anomalies linked to Zika. Researchers will also sequence viral genomes from patients and test local mosquitoes for infection rates. If successful, the project will produce a database linking viral genetic variation to disease severity, and map immune responses—antibody and T cell—across mono-infections, co-infections, and sequential infections. These findings could sharpen diagnostic algorithms, improve hospital triage and patient management, and guide future vaccine or immunotherapy design for both viruses. The work is applied: it directly targets clinical and public health decisions in a region where both viruses circulate year-round.

View original technical description
Dengue and Zika are major health threats in Kerala, with co-circulation of both viruses complicating the region's health landscape. This five-year longitudinal study, in partnership with the Kerala health system, aims to evaluate the burden, and distribution of ZIKV and DENV infections. The study will recruit >17000 probable dengue or zika patients within five days of symptom onset from healthcare facilities of all levels. Patients will be screened for infections and antibody status to determine primary or secondary infections. Active surveillance of contacts in geographical clusters will be conducted. Additionally, an antenatal cohort will be recruited and monitored for these infections. They will undergo serology testing post-delivery to assess new infections and infants will be followed for congenital anomalies in positive cases. Immune responses in asymptomatic and symptomatic individuals will be analyzed, focusing on antibody and T cell responses in mono- infections, co-infections, and sequential infections. Vectors will be examined for infection rates. A database of genomic heterogeneity will be established through next-generation sequencing to correlate with disease outcomes. The study aims to understand transmission dynamics and significant genomic and immunological readouts will help sharpen our responses to diagnostic, prognostic and management policies and potentially guiding future immunotherapeutic and vaccine developments.

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Researchers

JITHESH VEETILAKATH (EPMC Awardee)Manju Rahi (EPMC Awardee)Prasanta Saini (EPMC Awardee)Rohit Sharma (EPMC Awardee)

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Original classification

Understanding dengue and Zika spread, immunity and clinical outcomes

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