Host HLA B*Allele-Associated Multi-Clade Gag T-Cell Recognition Correlates with Slow HIV-1 Disease Progression in Antiretroviral Therapy-Naïve Ugandans
2009

HLA B*Allele and HIV Disease Progression in Ugandans

Sample size: 110 publication 10 minutes Evidence: moderate

Author Information

Author(s): Serwanga Jennifer, Shafer Leigh Anne, Pimego Edward, Auma Betty, Watera Christine, Rowland Samantha, Yirrell David, Pala Pietro, Grosskurth Heiner, Whitworth Jimmy, Gotch Frances, Kaleebu Pontiano

Primary Institution: MRC/UVRI Uganda Research Unit on AIDS

Hypothesis

Does the presence of specific HLA B alleles correlate with slower HIV-1 disease progression in antiretroviral therapy-naïve individuals?

Conclusion

The study found that slow HIV disease progression is associated with the presence of protective HLA B alleles and better virological control.

Supporting Evidence

  • Slow progressors had a higher frequency of protective HLA B alleles compared to rapid progressors.
  • Virological control was significantly better in slow progressors than in rapid progressors.
  • Multiclade Gag T-cell recognition was more common in slow progressors.

Takeaway

Some people with HIV can stay healthy for a long time without medicine, and this study found that certain genes help them do that.

Methodology

Multilevel regression modeling was used to classify HIV-infected individuals based on CD4 T cell slopes, and ELISpot assays quantified HIV-specific T-cell responses.

Potential Biases

Potential biases may arise from the retrospective nature of CD4 count data and participant selection.

Limitations

The study's sample size was limited, which may affect the reliability of the findings.

Participant Demographics

The cohort consisted of 110 HIV-infected individuals, predominantly female, with a median age of 37 years.

Statistical Information

P-Value

p=0.004

Confidence Interval

95% CI −28 to −14

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0004188

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