Abstract

Viral infection is associated with many types of tumorigenesis, including human papillomavirus (HPV)-induced cervical cancer. The induction of a specific T-cell response against virus-infected cells is desired to develop an efficient therapeutic approach for virus-associated cancer. Chinese herbal medicine (CHM) has a long history in the treatment of cancer patients in Asian countries. Hedyotis diffusa Willd (Bai Hua She She Cao, BHSSC) is frequently used clinically and has been shown to inhibit tumor growth in vitro. However, in vivo data demonstrating the antitumor efficacy of BHSSC are still lacking. We showed that BHSSC induces murine and human antigen-presenting cell (APC) activation via the MAPK signaling pathway and enhances antigen presentation in bone marrow-derived dendritic cells (BMDCs) in vitro. Furthermore, we identified that treatment with BHSSC leads to improved specific effector and memory T-cell responses in vivo. Variant peptide-based vaccines combined with BHSSC improved antitumor activity in preventive, therapeutic, and recurrent HPV-related tumor models. Furthermore, we showed that rutin, one of the ingredients in BHSSC, induces a strong specific immune response against HPV-related tumors in vivo. In summary, we demonstrated that BHSSC extract and its active compound, rutin, can be used as adjuvants in peptide-based vaccines to increase immunogenicity and to bypass the requirement of a conditional adjuvant.

Highlights

  • Human papillomavirus (HPV) infections may account for the development of several cancers, and a link between HPV infection and squamous cell cancer of the cervix has been identified [1]

  • We found that only BHSSC and not Scutellaria barbata (Ban Zhi Lian) and Salvia miltiorrhiza (Dan Shen) could induce TNF-α secretion from bone marrow-derived dendritic cells (BMDCs) (Figure S2)

  • We examined the effect of BHSSC extract on the activation of human Monocyte-Derived DCs (MoDCs)

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Summary

Introduction

Human papillomavirus (HPV) infections may account for the development of several cancers, and a link between HPV infection and squamous cell cancer of the cervix has been identified [1]. Commercial HPV vaccines contain the HPV capsid protein (L1), which can induce neutralizing antibodies that block HPV type 16/18 viral infection but do not act against virus-infected or cancerous cells [3]. The development of efficient therapeutic approaches for HPVassociated cancer is still needed. Oncogenes E6 and E7 are major HPV genes involved in neoplastic transformation, and the main targets of these viral proteins are the cellular tumor suppressor proteins p53 and pRB [5]. The E7 protein is suitable for use as a tumorspecific target for therapeutic vaccine development to treat HPVassociated cancer. Due to the emphasis on safety, a new approach for vaccine development involves using highly purified peptides or recombinant proteins as the target antigen; these vaccines often have poor immunogenicity

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