Abstract

While highly active anti-retroviral therapy has greatly improved the lives of HIV infected individuals, these treatments are unable to eradicate the virus. Current approaches to reactivate the virus have been limited by toxicity, lack of an orally available therapy, and limited responses in primary CD4+ T cells and in clinical trials. The PKC agonist ingenol, purified from Euphorbia plants, is a potent T cell activator and reactivates latent HIV. Euphorbia kansui itself has been used for centuries in traditional Chinese medicine to treat ascites, fluid retention, and cancer. We demonstrate that an extract of this plant, Euphorbia kansui, is capable of recapitulating T cell activation induced by the purified ingenol. Indeed, Euphorbia kansui induced expression of the early T cell activation marker CD69 and P-TEFb in a dose-dependent manner. Furthermore, Euphorbia kansui reactivated latent HIV in a CD4+ T cell model of latency and in HIV+ HAART suppressed PBMC. When combined with the other latency reversing agents, the effective dose of Euphorbia kansui required to reactive HIV was reduced 10-fold and resulted in synergistic reactivation of latent HIV. We conclude that Euphorbia Euphorbia kansui reactivates latent HIV and activates CD4+ T cells. When used in combination with a latency reversing agent, the effective dose of Euphorbia kansui is reduced; which suggests its application as a combination strategy to reactivate latent HIV while limiting the toxicity due to global T cell activation. As a natural product, which has been used in traditional medicine for thousands of years, Euphorbia kansui is attractive as a potential treatment strategy, particularly in resource poor countries with limited treatment options. Further clinical testing will be required to determine its safety with current anti-retroviral therapies.

Highlights

  • Active anti-retroviral therapy (HAART) has changed the face of the HIV/AIDS epidemic, allowing infected individuals to live relatively normal lives [1]

  • We demonstrate that an extract of this plant, Euphorbia kansui, is capable of recapitulating T cell activation induced by the purified ingenol

  • Resting CD4 + T cells express very low levels of cyclin T1 (CycT1), an important component of positive transcription elongation factor b (P-TEFb) [44]. This deficiency prevents reactivation of resting T cells by HDACi or BETi alone [21,22]. Both CycT1 and cyclin dependent kinase 9 (CDK9) expression increased in cells treated with 500 μg/ml Euphorbia kansui (Fig 2C, lane 4), similar to the increase observed in cells treated with Phorbol myristate acetate (PMA)/PHA and 50 ng/ml ingenol dibenzoate (IngDB) (Fig 2C, lanes 2 and 3)

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Summary

Introduction

Active anti-retroviral therapy (HAART) has changed the face of the HIV/AIDS epidemic, allowing infected individuals to live relatively normal lives [1]. While these LRA are able to release P-TEFb from its inactive complex, they do not affect cellular levels of CycT1 and CDK9 or translocate NF-κB into the nucleus [21,22] This finding explains why these compounds were effective in cell line models of latency, but failed to reactivate latent HIV in primary CD4+ T cells and in clinical trials [28,29]. Ingenol B (IngB), a semi-synthetic ingenol, has been safely administered as an oral dose to non-human primates [34] These ingenols reactivate latent HIV in cell lines and primary T cell models of latency and in cells from HAART suppressed patients [14,32,35,36]. When used in combination with an HDACi (SAHA) or BETi (JQ1), the effective concentration of Euphorbia kansui is greatly reduced and results in synergistic reactivation of latent HIV at doses which had been administered to humans

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