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March 21, 2026Travel Medicine and Infectious Disease4 citationsOpen Access

Towards National Guidance on Dengue and Chikungunya Vaccination in Travellers: Lessons from Global Recommendations

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ABAnna BogackaMDMałgorzata DanielAWAgnieszka Wroczyńska

Key Points

  • This review aims to evaluate current national vaccination recommendations for dengue and chikungunya targeting travellers.
  • Reviewed vaccination guidelines from WHO, ECDC, CDC, and various national advisory bodies.
  • Analyzed the implementation challenges associated with dengue and chikungunya vaccination.
  • Proposed tailored recommendations for Poland based on the findings.
  • Identified substantial heterogeneity in vaccination recommendations across countries.
  • Highlighted restrictions on Qdenga usage to individuals with prior dengue infection.
  • Noted safety concerns leading to curtailment of IXCHIQ in several countries.

Abstract

Dengue and chikungunya are mosquito-borne viral diseases with expanding geographical ranges driven by climate change, urbanisation, and globalisation. In 2024, dengue cases exceeded 14.6 million globally, with more than 12,000 deaths, while chikungunya cases surpassed 410,000 in the Americas. Increasing international mobility has resulted in a growing burden among travellers from non-endemic regions, including 126 imported dengue cases and four imported chikungunya cases in Poland in 2024. Recent approvals of Qdenga (TAK-003) for dengue and IXCHIQ (VLA1553) for chikungunya have expanded preventive options. However, implementation remains challenging because of variable efficacy, evolving safety concerns, and the absence of standardised national guidance. This review analyses vaccination recommendations issued by the WHO, ECDC, CDC, and national advisory bodies in Germany, the United Kingdom, Switzerland, France, Belgium, Canada, and the U.S. Substantial heterogeneity was identified. Most authorities recommend restricting Qdenga use in travellers to individuals with laboratory-confirmed prior dengue infection, despite broader regulatory authorisation in some jurisdictions. Use of IXCHIQ has been curtailed in several countries following reports of severe adverse events, including encephalitis and one fatal case; in August 2025 the U.S. Food and Drug Administration suspended the biologics license for IXCHIQ pending further safety evaluation. Diagnostic limitations, including flavivirus cross-reactivity and restricted access to neutralisation assays, complicate vaccination decision-making. Based on this analysis, we propose tailored recommendations for Poland, prioritising vaccination of travellers with documented prior dengue infection and high exposure risk, alongside strengthened personal protective measures and pre-travel counselling. The analytical framework presented may also support policy development in other non-endemic countries.

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Cite This Study

Bogacka et al. (2026) studied this question.

synapsesocial.com/papers/69be37726e48c4981c67722bhttps://doi.org/10.1016/j.tmaid.2026.102972
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Chikungunya Vaccines in Travel Medicine: From Regulatory Approval to Real-World Challenges2026
  2. 2Shared evidence, different recommendations: a comparative analysis of Qdenga (TAK-003) dengue vaccine guidance for travellers across countries2026
  3. 3Dengue and chikungunya vaccines past, present and future: implications for travelers2026 · 1 citations
  4. 4Travel-Related Challenges of Chikungunya Virus and Vaccination Options2026 · 2 citations
  5. 5Travel health advice for chikungunya viral disease2025