# Oropouche Virus (OROV) Vaccine Development for Vulnerable Populations: Epidemiological Context, Challenges and Future Directions

**Authors:** Wenrui Wu, Yiu-Wing Kam

PMC · DOI: 10.3390/vaccines14030267 · Vaccines · 2026-03-16

## TL;DR

This paper reviews the challenges in developing a vaccine for Oropouche virus, emphasizing the need for population-specific strategies and improved public health measures.

## Contribution

The paper proposes prioritizing population-specific vaccine development and integrating it with better surveillance and diagnostics.

## Key findings

- OROV transmission is more widespread than surveillance data indicates.
- Factors like age, pregnancy, and healthcare access significantly influence OROV disease risk.
- Current vaccine development is hindered by limited immunological data and poor animal models.

## Abstract

Oropouche virus (OROV) is an emerging arthropod-borne virus in the Americas that has evolved from a pathogen historically restricted to forest environments into an increasingly important regional and international public health concern. Despite decades of documented circulation, the true burden of OROV infection remains substantially underestimated, largely because of frequent misdiagnosis and the high proportion of asymptomatic or subclinical infections. This review synthesizes current evidence on the historical emergence, epidemiology, transmission dynamics, and clinical features of OROV, with a particular focus on populations at increased risk due to biological susceptibility, environmental exposure, and limited access to healthcare. Drawing on seroepidemiological data, we demonstrate that OROV transmission is far more widespread than routine surveillance suggests and examine how factors such as age, pregnancy, immune status, underlying health conditions, occupational exposure, and healthcare accessibility interact to influence disease risk and detection. Although multiple vaccine platforms have shown promise in preclinical studies, progress toward clinical development remains constrained by limited immunological evidence, shortcomings of available animal models, diagnostic uncertainty, and structural barriers in endemic regions. We propose that future OROV vaccine development prioritize population-specific needs rather than focusing solely on technological platforms, and that effective prevention will require integrating vaccination with strengthened surveillance, improved diagnostics, and equitable delivery systems.

## Full-text entities

- **Genes:** IFNAR1 (interferon alpha and beta receptor subunit 1) [NCBI Gene 3454] {aka AVP, CRF2-1, IFN-R-1, IFN-alpha-REC, IFNAR, IFNBR}
- **Diseases:** yellow fever (MESH:D015004), Zika (MESH:D000071243), Myalgia (MESH:D063806), aseptic meningitis (MESH:D008582), neglected tropical disease (MESH:D058069), Gastrointestinal symptoms (MESH:D012817), arthralgia (MESH:D018771), inflammation (MESH:D007249), congenital anomalies (MESH:D000013), vomiting (MESH:D014839), fetal death (MESH:D005313), dengue (MESH:D003715), anorexia (MESH:D000855), metabolic or cardiovascular conditions (MESH:D024821), liver failure (MESH:D017093), OROV (MESH:D002044), Fever (MESH:D005334), immune impairment (MESH:D020274), maternal illness (MESH:D000079262), photophobia (MESH:D020795), malaria (MESH:D008288), clinical disease (MESH:D004194), Infection (MESH:D007239), abdominal pain (MESH:D015746), encephalitis (MESH:D004660), arboviral diseases (MESH:D004671), nausea (MESH:D009325), injury to (MESH:D014947), dizziness (MESH:D004244), HIV (MESH:D015658), pruritus (MESH:D011537), hypercytokinemia (MESH:D000080424), febrile (MESH:D000071072), neurological complications (MESH:D002493), placental (MESH:D010922), neurological sequelae (MESH:D009422), headache (MESH:D006261), immunodeficiency (MESH:D007153), miscarriage (MESH:D000022), viremia (MESH:D014766), rash (MESH:D005076), acute (MESH:D000208), retro-orbital pain (MESH:D010146), chikungunya (MESH:D065632)
- **Chemicals:** ribonucleoside (MESH:D012263), quercetin (MESH:D011794), acridone (MESH:C041300), 4'-FlU (MESH:C000717487), BeAn19991 (-), lipid (MESH:D008055), favipiravir (MESH:C462182)
- **Species:** Oropouche virus (no rank) [taxon 118655], Culicoides paraensis (species) [taxon 1027879], Zika virus (no rank) [taxon 64320], Culex quinquefasciatus (southern house mosquito, species) [taxon 7176], Orthobunyavirus (genus) [taxon 11572], Vesicular stomatitis virus (species) [taxon 11276], Mus musculus (house mouse, species) [taxon 10090], Couepia paraensis (species) [taxon 1856779], Bradypus tridactylus (Pale-throated sloth, species) [taxon 9354], Chironomus thummi (midge, species) [taxon 7154], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13030507/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030507/full.md

## References

102 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030507/full.md

---
Source: https://tomesphere.com/paper/PMC13030507