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Updated: Aug 25, 2026

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
Published on: September 14, 2014
[HIV Antigens as complement fixing circulating immune complexes]
P Filippini1, M Guarino, C Lapenta
1Clinica Malattie Tropicali e Subtropicali, Seconda Universita di Napoli, Italy.
Insights
This study introduces a novel ELISA to detect HIV antigens within immune complexes (ICs). The assay identifies HIV antigens in ICs up to 8 months earlier than standard HIV tests.
Area of Science:
- Immunology
- Virology
- Biochemistry
Context:
- Immune complexes (ICs) play a role in various immune responses and diseases.
- Early detection of HIV infection is crucial for effective management and treatment.
- Current diagnostic methods for HIV have limitations in early detection.
Purpose:
- To develop and validate an Enzyme-Linked Immunosorbent Assay (ELISA) for detecting HIV antigens in circulating complement fixing immune complexes (ICs).
- To evaluate the efficacy of this novel ELISA in identifying HIV infection earlier than conventional methods.
Summary:
- An ELISA was developed using F(ab)2 anti-C3b and monoclonal antibodies against HIV gp120 and p24 to detect HIV antigens in ICs.
- The assay was tested on HIV-positive subjects, at-risk HIV-negative subjects, and healthy controls, as well as seroconversion panels.
- HIV antigens in ICs were detected in seroconversion panels, 25.5% of HIV-positive subjects, and 28.6% of at-risk subjects, with one subject in the at-risk group seroconverting during the study.
Impact:
- This novel ELISA can detect HIV antigens in ICs up to 8 months prior to the detection of anti-HIV antibodies and antigens by commercial ELISAs.
- The findings suggest a potential for earlier HIV diagnosis, enabling timely intervention and improved patient outcomes.
- The assay's ability to detect HIV antigens in ICs in at-risk individuals may aid in identifying recent infections.
Abstract:
To detect HIV antigens in circulating complement fixing immune complexes (ICs) we assessed an ELISA using wells of microtitre plates coated with F(ab)2 anti-C3b and monoclonal antibodies anti-HIV gp120 and anti-HIV p24. We tested 24 anti-HIV positive subjects (Group A), 10 anti-HIV negative subjects at risk of acquiring HIV infection (Group B), 20 normal controls (Group C) and 2 seroconversion panels. We found HIV antigens in ICs in all sera from seroconversion panels, in 25.5% of sera from subjects in Group A, in 28.6% of sera from subjects in Group B and in no serum from subjects in Group C. A subject in Group B acquired HIV infection during the observation. HIV antigens in ICs by our assay were detected 8 months before Anti-HIV and Ag by commercial ELISA.
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