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Updated: May 2, 2026

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
Published on: September 14, 2014
Capacity for infectious HIV-1 virion capture differs by envelope antibody specificity
Pinghuang Liu1, Latonya D Williams, Xiaoying Shen
1Duke Human Vaccine Institute, Duke University, Durham, North Carolina, USA.
Antibodies can distinguish between infectious and non-infectious viruses. Broadly neutralizing antibodies (bNAbs) selectively capture infectious virions, offering potential for improved vaccine-induced antibody responses.
Area of Science:
- Virology
- Immunology
- Vaccinology
Background:
- Antibody recognition of infectious virions is crucial for antiviral defense.
- Understanding antibody specificity is key to developing effective vaccines.
Purpose of the Study:
- To quantify the ability of different antibodies to capture infectious virions.
- To assess the potential of antibody combinations for enhanced viral recognition.
Main Methods:
- Determination of the infectious virion capture index (IVCI) for various antibody specificities.
- Analysis of antibody capture of both infectious and non-infectious virions.
Main Results:
- Broadly neutralizing antibodies (bNAbs) primarily captured infectious virions.
- Non-bNAbs and human immunodeficiency virus type 1 (HIV-1)-positive IgG captured both infectious and non-infectious virions.
- Infectious virion capture was additive when using antibody mixtures.
Conclusions:
- Antibody specificity dictates the selective capture of infectious virions.
- Additive capture by antibody mixtures demonstrates potential for vaccine-induced responses with improved infectious virion recognition.
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