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Published on: August 31, 2014
Anti-HIV-1 antibody avidity is correlated with clinical status in infected children
1Department of Pediatrics, University of Turin, Italy.
Insights
Antibody avidity to HIV-1 is lower in children with advanced disease. Lower antibody avidity and CD4 cell count predict disease progression earlier than CD4 count alone.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Antibody avidity is a measure of antibody-antigen binding strength.
- Assessing antibody avidity may offer insights into HIV-1 disease progression.
- Perinatally HIV-1 infected children represent a unique population for disease progression studies.
Purpose of the Study:
- To evaluate the relationship between anti-HIV-1 antibody avidity and disease status in perinatally infected children.
- To determine if antibody avidity can serve as an early predictor of HIV-1 disease progression.
Main Methods:
- Assessed antibody avidity to gp41 and p24, CD4 cell count, and p24 antigen levels in 37 HIV-1 infected children.
- Categorized children into groups based on clinical severity (CDC categories N, A, B, and C).
- Conducted longitudinal analysis in four children with varying disease outcomes.
Main Results:
- Significantly higher antibody avidity and CD4 cell counts were observed in children with less severe disease (Group 1) compared to those with severe manifestations (Group 2).
- No significant differences in free or dissociated p24 antigen levels were found between groups.
- Combined antibody avidity and CD4 cell count showed the strongest correlation with clinical status (r = 0.57, p = 0.001).
Conclusions:
- Reduced antibody avidity to HIV-1 is associated with advanced disease in children.
- Declining antibody avidity appears to be an earlier predictor of disease progression than CD4 cell count.
- Antibody avidity may be a valuable biomarker for monitoring HIV-1 progression in pediatric populations.
Abstract:
Avidity of antibodies to gp41 and p24, CD4 cell count, and free and dissociated p24 antigen were assessed in 37 HIV-1-infected children, in order to evaluate whether the avidity of anti-HIV-1 antibodies is related to the disease status in perinatally infected children. The HIV-infected children were divided into two groups. Group 1 included 25 children: 2 not symptomatic (CDC category N), 12 mildly (A) and 11 moderately (B) symptomatic; group 2 included 12 children with severe clinical manifestations (C). The same parameters were assayed longitudinally in four children: two with long-term nonprogressive disease and two with fatal outcome. Antibody avidity was significantly higher in group 1 than in group 2 children (7272 +/- 4788 vs. 2624 +/- 1344 D50, p < 0.01), as was the CD4 cell count (1295 +/- 1122 vs. 348 +/- 488 cells/mm3, p < 0.01). No differences between the two groups were observed in either free or dissociated p24 antigen. Combined measures of antibody avidity and CD4 cell count showed the best correlation with the clinical status (r = 0.57, p = 0.001). In the two children with nonprogressive disease the antibody avidity remained high throughout the follow-up, whereas in those with clinical deterioration its decline preceded, by at least 8 months, the drop in CD4 cells and, by at least 23 months, the appearance of AIDS. In conclusion the avidity of anti-HIV-1 antibodies is reduced in HIV-infected children with advanced disease state and seems an earlier predictor of disease progression than CD4 cell count.
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