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Published on: September 6, 2019
[Prognostic markers of progression to AIDS in infants vertically infected by human immunodeficiency virus type-1]
S Resino1, J M Bellón, D Gurbindo
1Servicio de Inmunología. Hospital General Universitario Gregorio Marañón. Madrid.
Insights
High viral load (VL) and low CD8+ T-cell percentages predict faster AIDS progression in vertically HIV-1 infected children. Monitoring these markers together improves risk assessment for disease progression.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Virology
Background:
- Assessing prognostic markers for AIDS progression in vertically HIV-1 infected children is crucial.
- CD4+, CD8+ T-cell percentages, and plasma viral load (VL) are potential indicators.
Purpose of the Study:
- To evaluate the prognostic value of CD4+, CD8+ T-cell percentages, and plasma VL in predicting AIDS progression.
- To determine the combined predictive value of these markers.
Main Methods:
- A cohort of 115 vertically HIV-1 infected children over 12 months old was studied.
- Plasma VL was quantified using standard molecular assays.
- CD4 and CD8 T-lymphocyte counts were determined by flow cytometry.
Main Results:
- Children with median VL > 4.5 log10 copies/ml and CD8+ percentage < 25% progressed faster to AIDS.
- Higher VL significantly increased the relative risk (RR) of AIDS progression (7-fold for VL > 4.5 log10, 3.5-fold per log10 increase).
- Lower CD8+ T-cell percentages were associated with increased RR of AIDS progression, indicating a protective effect.
Conclusions:
- Both baseline and follow-up CD8+ T-cell percentages and VL are valuable for assessing AIDS progression risk.
- Combining CD8+ T-cell percentage and VL offers enhanced predictive value for disease progression in HIV-1 infected children.
Background:
To study the prognostic AIDS progression value of the percentage of CD4+, CD8+, and plasma viral load (VL) (copies/ml) in HIV-1-vertically infected children.
Patients And Method:
We study a cohort of 115 HIV-1 infected children older than 12 months of age. The VL was quantified using standard molecular assay. CD4 and CD8 T lymphocytes were determined by flow cytometry.
Results:
The children with a median of VL > 4.5 log10 (p < 0.001) and percentage of CD8+ < 25% (p = 0.05) during follow-up, progressed faster to AIDS than children with a median of VL < 4.5 log10 and CD8 > 25%. The relative risk (RR) of AIDS progression was 7-fold higher in children with median VL above 4.5 log10. When considering VL as a continuous variable, risk of progression to AIDS is 3.5-fold higher for each increase of one log10 of VL. The percentage of CD8+ T-cells had a RR of AIDS progression of 0.95/% CD8+ at entry to the study and of 0. 19/% CD8+ during follow-up, indicating protection against progression to AIDS.
Conclusions:
Our results indicate that each basal values at entry in the study and during the follow-up of the percentage of CD8+ and VL helps to determine the risk of AIDS progression in HIV-1-infected children. More interestingly, the use of the two predictive markers together had higher predictive value.
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