Bio

Professional Education


  • PhD, Radboud University, Medical Sciences (2017)
  • MSc, Radboud University, Molecular Mechanisms of Disease (2013)
  • BSc, Heinrich-Heine-University, Biochemistry (2011)

Publications

All Publications


  • Monitoring of dynamic changes in Keyhole Limpet Hemocyanin (KLH)-specific B cells in KLH-vaccinated cancer patients SCIENTIFIC REPORTS Wimmers, F., de Haas, N., Scholzen, A., Schreibelt, G., Simonetti, E., Eleveld, M. J., Brouwers, H. M., Beldhuis-Valkis, M., Joosten, I., de Jonge, M. I., Gerritsen, W. R., de Vries, I. J., Diavatopoulos, D. A., Jacobs, J. F. 2017; 7

    Abstract

    Keyhole limpet hemocyanin (KLH) is used as an immunogenic neo-antigen for various clinical applications and during vaccine development. For advanced monitoring of KLH-based interventions, we developed a flow cytometry-based assay for the ex vivo detection, phenotyping and isolation of KLH-specific B cells. As proof-of-principle, we analyzed 10 melanoma patients exposed to KLH during anti-cancer dendritic cell vaccination. Our assay demonstrated sensitive and specific detection of KLH-specific B cells in peripheral blood and KLH-specific B cell frequencies strongly correlated with anti-KLH serum antibody titers. Profiling of B cell subsets over the vaccination course revealed that KLH-specific B cells matured from nave to class-switched memory B cells, confirming the prototypic B cell response to a neo-antigen. We conclude that flow-cytometric detection and in-depth phenotyping of KLH-specific B cells is specific, sensitive, and scalable. Our findings provide novel opportunities to monitor KLH-specific immune responses and serve as a blueprint for the development of new flow-cytometric protocols.

    View details for DOI 10.1038/srep43486

    View details for Web of Science ID 000395636800001

    View details for PubMedID 28344338

    View details for PubMedCentralID PMC5361210

  • A membrane-anchored aptamer sensor for probing IFN? secretion by single cells. Chemical communications (Cambridge, England) Qiu, L., Wimmers, F., Weiden, J., Heus, H. A., Tel, J., Figdor, C. G. 2017; 53 (57): 8066?69

    Abstract

    Insight into the behavior of individual immune cells, in particular cytokine secretion, will contribute to a more fundamental understanding of the immune system. In this work, we have developed a cell membrane-anchored sensor for the detection of cytokines secreted by single cells using a combination of aptamer-based sensors and droplet microfluidics.

    View details for DOI 10.1039/c7cc03576d

    View details for PubMedID 28675396

  • Opportunities for immunotherapy in microsatellite instable colorectal cancer CANCER IMMUNOLOGY IMMUNOTHERAPY Westdorp, H., Fennemann, F. L., Weren, R. D., Bisseling, T. M., Ligtenberg, M. J., Figdor, C. G., Schreibelt, G., Hoogerbrugge, N., Wimmers, F., de Vries, I. J. 2016; 65 (10): 1249-1259

    Abstract

    Microsatellite instability (MSI), the somatic accumulation of length variations in repetitive DNA sequences called microsatellites, is frequently observed in both hereditary and sporadic colorectal cancer (CRC). It has been established that defects in the DNA mismatch repair (MMR) pathway underlie the development of MSI in CRC. After the inactivation of the DNA MMR pathway, misincorporations, insertions and deletions introduced by DNA polymerase slippage are not properly recognized and corrected. Specific genomic regions, including microsatellites, are more prone for DNA polymerase slippage and, therefore, more susceptible for the introduction of these mutations if the DNA MMR capacity is lost. Some of these susceptible genomic regions are located within the coding regions of genes. Insertions and deletions in these regions may alter their reading frame, potentially resulting in the transcription and translation of frameshift peptides with c-terminally altered amino acid sequences. These frameshift peptides are called neoantigens and are highly immunogenic, which explains the enhanced immunogenicity of MSI CRC. Neoantigens contribute to increased infiltration of tumor tissue with activated neoantigen-specific cytotoxic T lymphocytes, a hallmark of MSI tumors. Currently, neoantigen-based vaccination is being studied in a clinical trial for Lynch syndrome and in a trial for sporadic MSI CRC of advanced stage. In this Focussed Research Review, we summarize current knowledge on molecular mechanisms and address immunological features of tumors with MSI. Finally, we describe their implications for immunotherapeutic approaches and provide an outlook on next-generation immunotherapy involving neoantigens and combinatorial therapies in the setting of MSI CRC.

    View details for DOI 10.1007/s00262-016-1832-7

    View details for Web of Science ID 000386515000011

    View details for PubMedID 27060000

    View details for PubMedCentralID PMC5035655

  • Effective Clinical Responses in Metastatic Melanoma Patients after Vaccination with Primary Myeloid Dendritic Cells CLINICAL CANCER RESEARCH Schreibelt, G., Bol, K. F., Westdorp, H., Wimmers, F., Aarntzen, E. H., Duiveman-de Boer, T., van de Rakt, M. W., Scharenborg, N. M., de Boer, A. J., Pots, J. M., Nordkamp, M. A., van Oorschot, T. G., Tel, J., Winkels, G., Petry, K., Blokx, W. A., van Rossum, M. M., Welzen, M. E., Mus, R. D., Croockewit, S. A., Koornstra, R. H., Jacobs, J. F., Kelderman, S., Blank, C. U., Gerritsen, W. R., Punt, C. J., Figdor, C. G., de Vries, I. J. 2016; 22 (9): 2155-2166

    Abstract

    Thus far, dendritic cell (DC)-based immunotherapy of cancer was primarily based on in vitro-generated monocyte-derived DCs, which require extensive in vitro manipulation. Here, we report on a clinical study exploiting primary CD1c(+) myeloid DCs, naturally circulating in the blood.Fourteen stage IV melanoma patients, without previous systemic treatment for metastatic disease, received autologous CD1c(+) myeloid DCs, activated by only brief (16 hours) ex vivo culture and loaded with tumor-associated antigens of tyrosinase and gp100.Our results show that therapeutic vaccination against melanoma with small amounts (3-10 10(6)) of myeloid DCs is feasible and without substantial toxicity. Four of 14 patients showed long-term progression-free survival (12-35 months), which directly correlated with the development of multifunctional CD8(+) T-cell responses in three of these patients. In particular, high CD107a expression, indicative for cytolytic activity, and IFN? as well as TNF? and CCL4 production was observed. Apparently, these T-cell responses are essential to induce tumor regression and promote long-term survival by stalling tumor growth.We show that vaccination of metastatic melanoma patients with primary myeloid DCs is feasible and safe and results in induction of effective antitumor immune responses that coincide with improved progression-free survival. Clin Cancer Res; 22(9); 2155-66. 2015 AACR.

    View details for DOI 10.1158/1078-0432.CCR-15-2205

    View details for Web of Science ID 000375329100011

    View details for PubMedID 26712687

  • T cell responses in end-stage melanoma patients can be induced by dendritic cell vaccination. Oncoimmunology Wimmers, F., Aarntzen, E. H., Duiveman-deBoer, T., Figdor, C. G., Jacobs, J. F., Tel, J., De Vries, I. J. 2016; 5 (1)

    Abstract

    Cytotoxic T cells are considered crucial for antitumor immunity and their induction is the aim of various immunotherapeutic strategies. High frequencies of tumor-specific CD8+ T cells alone, however, are no guarantee for long-term tumor control. Here, we analyzed the functionality of tumor-specific CD8+ T cells in melanoma patients upon dendritic cell vaccination by measuring multiple T cell effector functions considered crucial for anticancer immunity, including the expression of pro-inflammatory cytokines, chemokines and cytotoxic markers (IFN?, TNF?, IL-2, CCL4, CD107a). We identified small numbers of multifunctional (polyfunctional) tumor-specific CD8+ T cells in several patients and dendritic cell therapy was able to improve the functionality of these pre-existing tumor-specific CD8+ T cells. Generated multifunctional CD8+ T cell responses could persist for up to ten years and within the same patient functionality could vary greatly for the different vaccination antigens. Importantly, after one cycle of DC vaccination highly functional CD8+ T cells were only detected in patients displaying prolonged overall survival. Our results shed light on the dynamics of multifunctional tumor-specific CD8+ T cells during metastatic melanoma and reveal a new feature of dendritic cell vaccination in vivo.

    View details for PubMedID 26942087

    View details for PubMedCentralID PMC4760336

  • Paradigm shift in dendritic cell-based immunotherapy: from in vitro generated monocyte-derived DCs to naturally circulating DC subsets FRONTIERS IN IMMUNOLOGY Wimmers, F. F., Schreibelt, G., Skold, A. E., Figdor, C. G., de Vries, I. J. 2014; 5

    Abstract

    Dendritic cell (DC)-based immunotherapy employs the patients' immune system to fight neoplastic lesions spread over the entire body. This makes it an important therapy option for patients suffering from metastatic melanoma, which is often resistant to chemotherapy. However, conventional cellular vaccination approaches, based on monocyte-derived DCs (moDCs), only achieved modest response rates despite continued optimization of various vaccination parameters. In addition, the generation of moDCs requires extensive ex vivo culturing conceivably hampering the immunogenicity of the vaccine. Recent studies, thus, focused on vaccines that make use of primary DCs. Though rare in the blood, these naturally circulating DCs can be readily isolated and activated thereby circumventing lengthy ex vivo culture periods. The first clinical trials not only showed increased survival rates but also the induction of diversified anti-cancer immune responses. Upcoming treatment paradigms aim to include several primary DC subsets in a single vaccine as pre-clinical studies identified synergistic effects between various antigen-presenting cells.

    View details for DOI 10.3389/fimmu.2014.00165

    View details for Web of Science ID 000354068100001

    View details for PubMedID 24782868

    View details for PubMedCentralID PMC3990057

  • Early predictive value of multifunctional skin-infiltrating lymphocytes in anticancer immunotherapy ONCOIMMUNOLOGY Wimmers, F., Aarntzen, E. H., Schreibelt, G., Jacobs, J. F., Punt, C. J., Figdor, C. G., de Vries, I. J. 2014; 3 (1)

    Abstract

    Bioassays that predict clinical outcome are essential to optimize cellular anticancer immunotherapy. We have recently developed a robust and simple skin test to evaluate the capacity of tumor-specific T cells to migrate, recognize their targets and exert effector functions. This bioassay detects T cells with an elevated antineoplastic potential and hence rapidly identifies patients responding to immunotherapy.

    View details for DOI 10.4161/onci.27219

    View details for Web of Science ID 000339952700004

    View details for PubMedID 24653961

    View details for PubMedCentralID PMC3960298

  • Dendritic Cell Cross Talk with Innate and Innate-like Effector Cells in Antitumor Immunity: Implications for DC Vaccination CRITICAL REVIEWS IN IMMUNOLOGY van Beek, J. J., Wimmers, F., Hato, S. V., de Vries, I. J., Skold, A. E. 2014; 34 (6): 517-536

    Abstract

    Dendritic cells (DCs) are key players in the induction of immune responses. Adoptive transfer of autologous mature DCs loaded with tumor-associated antigens is a promising therapy for the treatment of immunogenic tumors. For a long time, its therapeutic activity was thought to depend solely on the induction of tumor-specific CD8+ and CD4+ T cell responses. More recently, DCs were shown to bidirectionally interact with innate and innate-like immune cells, including natural killer (NK), invariant natural killer T (iNKT), and ?? T cells. These effector cells can amplify responses induced by DCs via several mechanisms, including induction of DC maturation and conventional T cell priming. In addition, NK, iNKT, and ?? T cells possess cytolytic activity and can act directly on tumor cells. Therapeutic strategies targeting these innate and innate-like immune cells hence hold potential to improve current DC vaccination protocols.

    View details for DOI 10.1615/CritRevImmunol.2014012204

    View details for Web of Science ID 000348413900006

    View details for PubMedID 25597314

  • Probing cellular heterogeneity in cytokine-secreting immune cells using droplet-based microfluidics LAB ON A CHIP Chokkalingam, V., Tel, J., Wimmers, F., Liu, X., Semenov, S., Thiele, J., Figdor, C. G., Huck, W. T. 2013; 13 (24): 4740-4744

    Abstract

    Here, we present a platform to detect cytokine (IL-2, IFN-?, TNF-?) secretion of single, activated T-cells in droplets over time. We use a novel droplet-based microfluidic approach to encapsulate cells in monodisperse agarose droplets together with functionalized cytokine-capture beads for subsequent binding and detection of secreted cytokines from single cells. This method allows high-throughput detection of cellular heterogeneity and maps subsets within cell populations with specific functions.

    View details for DOI 10.1039/c3lc50945a

    View details for Web of Science ID 000326982900003

    View details for PubMedID 24185478

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