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Synapse
February 14, 2026Retrovirology0 citationsOpen Access

Versatile HIV Rev-dependent reporter cell system for stringent and sensitive quantification of viral reservoirs, neutralizing antibodies, and restriction factors

MSMark SpearJCJoseph ChoiBHBrian Hetrick

Key Points

  • The aim is to develop and validate HIV Rev-dependent reporter cell systems for quantifying viral reservoirs and neutralizing antibodies.
  • Developed various T-lymphoblast and HeLa-derived HIV reporter cell lines.
  • Compared cell lines for responsiveness to different tropic viruses.
  • Conducted viral dilution assays using primary HIV-1 clade C swarms.
  • Validated systems for quantifying antibody neutralization and restriction factors.
  • Confirmed reporter expression is responsive to HIV Tat and Rev.
  • Demonstrated sensitivity of the systems in quantifying viral reservoirs.
  • Validated applications in neutralizing antibody assays and identifying new restriction factors.

Abstract

Detecting and measuring HIV reservoirs, neutralizing antibodies, and restriction factors are important for HIV cure research and the development of new therapeutics and vaccines. Here we describe the development and validation of several HIV Rev-dependent indicator cell lines for these purposes. These reporter cells derive from different T-lymphoblast cell lines, including Molt4-CCR5, SupT1-CCR5, CEM-SS, A3R5, and from the adherent TZM cell platform based on HeLa clone JC53. These cells express CD4, CXCR4, and various levels of CCR5. We compared these cell lines for responsiveness to both X4 and R5-tropic viruses, and confirmed that reporter expression in these cells is not affected by stimulation from mitogens but is responsive to HIV Tat and Rev, reducing non-specific reporter induction from the leaky LTR promoter. To validate the sensitivity of the Rev-dependent reporter cell systems, we conducted a viral dilution assay with three primary HIV-1 clade C swarms from an adult in Malawi. We also validated the systems for quantifying antibody neutralization and screening restriction factors; these systems are also sensitive for viral outgrowth assays for quantifying viral reservoirs in clinical and basic research settings. Given that the systems can measure HIV accurately in complex environments with mitogens or other substances, they can be used for versatile applications, such as quantifying latent reservoirs, testing inhibitory compounds, conducting neutralizing antibody assays, and identifying new restriction factors.

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Cite This Study

Spear et al. (2026) studied this question.

synapsesocial.com/papers/699010382ccff479cfe56c9bhttps://doi.org/10.1186/s12977-026-00675-8
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