Dengue fever in immunocompromised patients: A systematic review and meta-analysis

Int J Infect Dis. 2024 Dec:149:107272. doi: 10.1016/j.ijid.2024.107272. Epub 2024 Oct 28.

Abstract

Objectives: Given the complex role of immunity in dengue severity, we aimed to review the clinical course of dengue infection in immunocompromised patients.

Methods: We conducted a systematic review of studies reporting outcomes among immunocompromised patients with laboratory-confirmed dengue infection. Meta-analysis using the Mantel-Haenszel method (fixed effects) was performed for studies with control groups. We registered the study with PROSPERO (No. CRD42021258930).

Results: We included 115 studies. Among these, 30 studies compared immunocompromised (cases) and nonimmunocompromised (control) patients, focusing mainly on children (n = 22 studies) with malnutrition (n=18). Immunocompromised patients had a higher likelihood of dengue complications (OR 1.87; 95% CI: 1.04-3.35]) but a lower likelihood of severe dengue (OR 0.83; 95% CI: 0.69-1.00]. No significant difference in mortality was observed. In the 85 studies focused solely on immunocompromised patients, severe dengue and mortality rates were 9% and 4%, respectively, mostly among adult solid organ transplant recipients and those with inflammatory diseases. Immunosuppressive treatment alterations and temporary graft dysfunction were reported.

Conclusion: Immunocompromised patients have an increased risk of dengue-related complications. However, definitive conclusions about the comparative severity of dengue across different immunocompromised patient groups are limited by a lack of robust data, highlighting the need for well-designed future studies.

Keywords: Arboviral disease; Arbovirus; Clinical outcomes; Immunosuppressed host; Immunosuppression; Imported infections; Infectious disease; Meta-analysis; Tropical infections; Vector borne disease.

Publication types

  • Systematic Review
  • Meta-Analysis

MeSH terms

  • Adult
  • Child
  • Dengue* / complications
  • Dengue* / immunology
  • Humans
  • Immunocompromised Host*