Abstract

Dengue is a arboviral infection that represents a major global health burden. There is an unmet need for effective dengue therapeutics to reduce symptoms, duration of illness and incidence of severe complications. Here, we consider the merits of a dengue human infection model (DHIM) for drug development. A DHIM could allow experimentally controlled studies of candidate therapeutics in preselected susceptible volunteers, potentially using smaller sample sizes than trials that recruited patients with dengue in an endemic country. In addition, the DHIM would assist the conduct of intensive pharmacokinetic and basic research investigations and aid in determining optimal drug dosage. Furthermore, a DHIM could help establish proof of concept that chemoprophylaxis against dengue is feasible. The key challenge in developing the DHIM for drug development is to ensure the model reliably replicates the typical clinical and laboratory features of naturally acquired, symptomatic dengue.

Highlights

  • The 4 serotypes of dengue virus (DENV-1 to DENV-4) are the most important arboviral pathogens of humans

  • Dengue is an acute systemic febrile illness that manifests with abrupt onset as an undifferentiated fever that is difficult to distinguish from other infections without laboratory diagnostic tests [1]

  • In a subset of cases, a transient vascular leakage syndrome develops after 3–4 days of illness, which, when severe, can lead to life-threatening hypovolemic shock and/or hemorrhage [1, 5]

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Summary

Dengue Human Infection Models Supporting Drug Development

Dengue is a arboviral infection that represents a major global health burden. We consider the merits of a dengue human infection model (DHIM) for drug development. The key challenge in developing the DHIM for drug development is to ensure the model reliably replicates the typical clinical and laboratory features of naturally acquired, symptomatic dengue. Dengue; human infection model; clinical trial; drug development. In a subset of cases, a transient vascular leakage syndrome develops after 3–4 days of illness, which, when severe, can lead to life-threatening hypovolemic shock (called dengue shock syndrome) and/or hemorrhage [1, 5]. Supportive care and the careful titration of minimum volumes of parenteral crystalloid fluids to maintain stable cardiac output during the 1–3-day period of vascular permeability are critical elements in dengue case management [5]. S66 JID 2014:209 (Suppl 2) Whitehorn et al overwhelmed with patients with dengue who require ongoing observation as outpatients or are admitted for inpatient observation

THE CASES FOR DENGUE THERAPEUTIC AND PROPHYLACTIC AGENTS
POTENTIAL ROLES FOR A HUMAN INFECTION MODEL IN DENGUE DRUG DEVELOPMENT
Extensive clinical experience and expertise in endemic settings
CRITICAL HURDLES FOR A DHIM
STRENGTHS AND WEAKNESSES OF A DHIM FOR DRUG DEVELOPMENT
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