Our group has:
- Designed, constructed and characterized vaccines based on virus-like particles (VLPs) carrying specific tumor antigens. We have engineered chimeric hepatitis B surface antigen (HBsAg) VLPs, which harbor human Papillomavirus (HPV) T cell epitopes and cytokine domains while still preserve their capability to self-assemble into VLPs. The oncogenic HPV types 16 and 18 are associated with precancerous lesions in the uterine cervix (cervical intraepithelial neoplasia, CIN) that eventually progress to cervical cancer. They are also associated with anogenital and oropharingeal cancers. Individuals infected by these viruses cannot take advantage of the prophylactic HPV vaccines and are at risk of developing HPV-related cancer. However, these patients could benefit from vaccines that activate T cell effector cells against HPV-infected tumor cells.
We have shown that codon optimization of the viral genes facilitates the production of protein vaccines (Cid-Arregui and zur Hausen, Modified HPV E6 and E7 genes and proteins useful for vaccination, US Patent 7,201,908 B2, 2007). Yet, overexpression of E7 in human cells results in significant cytotoxicity. Immunization of HLA-A2 transgenic mice either with plasmids or recombinant adenoviruses engineered to express HPV-16 E7-HBsAg chimeric particles evoke strong B and T cell responses (figure 1). Addition of the chemokine CCL19 and interleukin 2 (IL-2) to the HBsAg-E7 particles significantly enhanced the anti-E7 T cell responses in the absence of adjuvant (Cid-Arregui, A. and zur Hausen, Fusion polypeptides and their use for prevention and treatment of cancer, patent EP2335730 A1, 2011).
In addition, we have generated HBsAg fusion proteins harboring endogenous tumor antigens. Frequently, the genome of cancer cells carry multiple mutations that inactivate the cytostatic function of certain proteins and activate the growth-promoting functions of others, thereby creating non-self neo-antigens. The induction of T cell responses against neo-antigens could facilitate the elimination of tumor cells. In addition of VLPs we are testing soluble chimeric proteins made of fragments of HPV-16 E7 and CCL19/IL-2, as well as single chain trimers (SCTs) carrying the previously described E711-19 T cell epitope.
- Explored diagnostic and prognostic markers for CIN and cervical cancer. Progression from CIN to cervical cancer is associated with altered circulating levels of cytokines. We have designed a prospective cohort study to determine the levels in serum of a large number of cytokines. A cohort of patients with cervical pathology (CIN I, CIN II, CIN III and invasive squamous cell carcinoma) as well as healthy donors has been enrolled for this study at the National Center for Tumor Diseases and the Gynecology Department of the University Hospital in Heidelberg in collaboration with Prof Dr. Frederik Marmé. Measurement of the serum concentration of cytokines is being performed using a bead-based sandwich immunoassay, the LEGENDplex™ Human Th Cytokine and Human Inflammation Panels (BioLegend), which include the following cytokines: IL-2, IL-4, IL-5, IL-9, IL-13, IL-21 and IL-22; and IL-1b, IL-6, IL-8, IL-10, IL-12p70, IL-17A, IL-18, IL-23, IFN-g, TNF-a and MCP-1, respectively. Preliminary results have shown that progression from low to high grade CIN and cervical cancer is associated with altered levels of Th1/Th2 and proinflammatory cytokines, indicating the potential balance that cytokines can exert in the immunologic control of cervical cancer and that circulating levels of some of the above cytokines could be useful in identifying women at higher risk of developing cervical invasive cancer when altered levels are detected at the CIN I/CIN II stages. In addition, we analyze the frequencies and phenotypes of CD4+ and CD8+ cells in the blood of CIN and cervical cancer patients compared with healthy donors (Figure 2). Based on immunosequencing, we also have started a systematic study of the immune receptor (TCR) profiles of tumor infiltrating lymphocytes (TILs) and peripheral blood T cells isolated from CIN and cervical cancer patients. This approach should reveal the numbers and diversity of T cell clonotypes in the CIN and cervical cancer-infiltrating lymphocytes, which will be compared with the circulating TCR clonal expansion profiles. Immunoprofiling will reveal differentially expanded clones throughout the different stages of the disease, providing the basis for new immune diagnostic and prognostic tools. Additionally, immunoprofiling will identify dominant TCR clones, which will be characterized and evaluated for their therapeutical application.
- Investigated innate immune responses in cervical cancer patients. The innate immune response is considered to be the first line of defense at mucosal surfaces. NK cells represent an important arm of the innate immune system specialized in killing virus-infected and tumor cells through the NKG2D activating receptor. NKG2D can promote the lysis of target cells by binding to ligands encoded by the MHC class I chain-related (MIC) genes. The MIC family includes MICA, MICB and ULBP1-6. NKG2D ligands are overexpressed in a number of epithelial tumors. NKG2D engagement by its ligands induces proliferation, survival, and, cytotoxic activity in NK cells. However, the shedding of MICA from the cell surface has been demonstrated in a variety of malignant epithelial tumors, including cervical cancer. Shedding leads to accumulation of soluble MICA (sMICA) in serum leading to NKG2D down-modulation by facilitating its internalization and lysosomal degradation. This has been proposed to be a mechanism used by cancer cells to evade NK-mediated tumor surveillance. We have shown an increase of soluble MICA (sMICA) levels in serum during progression of HPV-induced premalignant lesions to cervical cancer (figure 3 a). Thus, shedding of sMICA might be a critical immune evasion event in the natural history of cervical cancer. Moreover, we also investigate the expression of B7H6, a ligand for the NK cell activating receptor NKp30, in CIN and cervical cancer tissues (figure 3 b).
- Developed liposomal/VLP-based drug delivery systems. Chemotherapeutic agents are far from ideal because they have been selected for their activity against proliferating cells, and they do not discriminate between tumor cells and normal cells undergoing rapid division. In addition, many potentially useful chemotherapeutic agents show poor water solubility and hence are difficult to deliver through traditional methods. Therefore, attempts are being made to develop delivery systems to improve both targeting and efficacy of drug delivery. However, there are considerable problems with many of the current in vivo delivery systems for therapeutic drugs. We have developed hollow nanoparticles in the form of membrane-enclosed vesicles comprising a truncated form of an HBsAg(S) protein lacking one or two of its amino-terminal transmembrane domains and a targeting domain, such as an integrin binding peptide or a pre-S1 binding domain (Cid-Arregui, Hollow nanoparticles and uses therefor, patent EP2262489 A2, US20110052496 A1, 2011). These particles (figure 4) can be loaded with chemotherapeutic agents to be delivered to tumor cells. In addition, we are approaching the targeting of liposomal nanoparticles to tumor cells and antigen presenting cells using various types of molecules, such as peptides, aptamers and single chain antibodies.