Protective and Enhancing HLA Alleles, HLA-DRB1*0901 and HLA-A*24, for Severe Forms of Dengue Virus Infection, Dengue Hemorrhagic Fever and Dengue Shock Syndrome
2008

HLA Alleles and Severe Dengue Infection

Sample size: 1079 publication 10 minutes Evidence: moderate

Author Information

Author(s): Lan Nguyen Thi Phuong, Kikuchi Mihoko, Huong Vu Thi Que, Ha Do Quang, Thuy Tran Thi, Tham Vo Dinh, Tuan Ha Manh, Tuong Vo Van, Nga Cao Thi Phi, Van Dat Tran, Oyama Toshifumi, Morita Kouichi, Yasunami Michio, Hirayama Kenji

Primary Institution: Institute of Tropical Medicine (NEKKEN), Nagasaki University, Japan

Hypothesis

The study investigates the association of specific HLA alleles with the severity of dengue virus infection.

Conclusion

The study found that HLA-A*24 is associated with increased risk of severe dengue, while HLA-DRB1*0901 is protective against dengue shock syndrome.

Supporting Evidence

  • HLA-A*24 was found to increase the risk of severe dengue infection.
  • HLA-DRB1*0901 was associated with a decreased risk of dengue shock syndrome.
  • The study included a large sample size of patients from multiple hospitals.
  • The findings support previous research on the role of HLA in dengue severity.

Takeaway

Some people have special genes that make them more likely to get really sick from dengue fever, while others have genes that help protect them.

Methodology

A hospital-based case-control study was conducted analyzing HLA alleles in patients with dengue hemorrhagic fever and dengue shock syndrome.

Potential Biases

Potential biases may arise from the selection of control groups and the reliance on clinical diagnosis.

Limitations

The study is limited to a specific ethnic group and geographic area, which may affect the generalizability of the findings.

Participant Demographics

Participants were Vietnamese children aged 6 months to 15 years, primarily of Kinh ethnicity.

Statistical Information

P-Value

0.008

Confidence Interval

1.02–2.58

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pntd.0000304

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