Abstract

IntroductionIn previous study the streptavidin interleukin-2 (SA-IL-2)-modified MB49 vaccine was effective against bladder cancer in a mouse model. However, a small portion of tumors regrew because the vaccine could not eliminate MB49 bladder cancer stem cells (MCSCs). Accordingly, we developed a SA-IL-2-modified MCSCs vaccine and evaluated its antitumor effects.MethodsMCSCs were isolated and identified in cancer stem cells (CSCs) characters, with high expression of CSCs markers, higher resistance to chemotherapy, greater migration in vitro, and stronger tumorigenicity in vivo. The SA-IL-2 MCSCs vaccine was prepared and its bioactivity was evaluated. The protective, therapeutic, specific and memory immune response in animal experiments were designed to identify whether the vaccine elicited antitumor immunity and acted against metastatic bladder cancer.ResultsMCSCs had higher level of CD133 and CD44, less susceptibility to chemotherapy, more pronounced migration and greater tumorigenic ability. The successfully prepared SA-IL-2 MCSCs vaccine inhibited the tumor volume and prolonged mice survival in animal experiments. The expression of IgG, the population of dendritic cells, CD8+ and CD4+ T cells were highest in the experimental group than in the four control groups.ConclusionsThe SA-IL-2 MCSCs vaccine induced an antitumor immune response and was used to eliminate MCSCs to prevent tumor regrowth.

Highlights

  • In previous study the streptavidin interleukin-2 (SA-IL-2)-modified MB49 vaccine was effective against bladder cancer in a mouse model

  • The Western blotting (WB) analysis indicated that the CD133 and CD44 proteins were abundantly expressed in MB49 bladder cancer stem cells (MCSCs), but much less in MB49 cells (Fig. 1b)

  • The Quantitative polymerase chain reaction (qPCR) analysis showed that the relative levels of CD133 and CD44 mRNAs in MCSCs were 2.7 and 4.7 times higher, respectively, than those observed in MB49 cells (Fig. 1c)

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Summary

Introduction

In previous study the streptavidin interleukin-2 (SA-IL-2)-modified MB49 vaccine was effective against bladder cancer in a mouse model. A small portion of tumors regrew because the vaccine could not eliminate MB49 bladder cancer stem cells (MCSCs). We developed a SA-IL-2-modified MCSCs vaccine and evaluated its antitumor effects. The standard treatment is radical cystectomy with pelvic lymphadenectomy. More than 50 % of patients who undergo treatment will develop local or metastatic recurrence [2]. The human interleukin-2 (IL-2) surface modified MB49 bladder cancer cells vaccine induced specific antitumor immunity and was effective against. Zhu et al Stem Cell Research & Therapy (2015) 6:224 streptavidin mouse interleukin-2 (SA-IL-2)-modified MCSCs vaccine, and evaluated the antitumor effects of this vaccine in a MCSCs metastatic mouse model

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