14 results match your criteria: "The Medawar Centre[Affiliation]"

The attenuated vaccinia virus, modified vaccinia Ankara, has been engineered to deliver the tumor antigen 5T4 (TroVax®). Here, we report results from a randomized open-label phase II trial in castration-resistant prostate cancer patients in which TroVax was administered in combination with docetaxel and compared against docetaxel alone. The aim was to recruit 80 patients (40 per arm), but the study was terminated early due to recruitment challenges.

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Personalized medicine is playing an increasingly important role in the treatment of patients living with cancer. This landmark shift has been driven in part by statistics emerging from the "one size fits all" approach to the treatment of cancer patients. Some reports suggest that only a minority of individuals actually benefit from treatment and adverse effects of medications remain a major cause of hospitalization, morbidities and deaths.

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Cancer vaccines such as MVA-5T4 (TroVax(®)) must induce an efficacious immune response to deliver therapeutic benefit. The identification of biomarkers that impact on the clinical and/or immunological efficacy of cancer vaccines is required in order to select patients who are most likely to benefit from this treatment modality. Here, we sought to identify a predictor of treatment benefit for renal cancer patients treated with MVA-5T4.

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Article Synopsis
  • * In a phase III trial, patients with renal cancer received either MVA-5T4 or a placebo alongside other treatments, revealing that a strong immune response (5T4 antibody levels) corresponded to longer survival rates in those treated with MVA-5T4.
  • * An immune response surrogate (IRS) was created to predict treatment benefit and was validated not only in the main study but also in additional datasets for patients with other types of cancer, indicating its potential usefulness for future research and vaccine development.
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The attenuated vaccinia virus MVA has been engineered to deliver the tumor antigen 5T4 (MVA-5T4; TroVax), a surface glycoprotein expressed by most solid tumors. MVA-5T4 has been tested in 2 phase I/II and 7 phase II clinical trials in colorectal (4 trials), renal (4 trials), and prostate (1 trial) advanced cancer patients. Data have been collated from all 9 studies and used to investigate the magnitude and kinetics of 5T4-specific antibody responses after vaccination and to identify potential associations between the immune response and patient survival.

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Modified vaccinia Ankara (MVA) encoding the tumor antigen 5T4 (TroVax) has been evaluated in an open label phase II study in metastatic colorectal cancer patients. The primary objective was to assess the safety and immunogenicity of TroVax injected before, during and after treatment with 5-fluorouracil, leukovorin and irinotecan. TroVax was administered to 19 patients with metastatic colorectal cancer.

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Purpose: The attenuated strain of vaccinia virus, modified vaccinia Ankara (MVA) encoding the tumor antigen 5T4 (TroVax), has been evaluated in an open-label phase II study in metastatic colorectal cancer patients. The primary objective was to assess the safety and immunogenicity of TroVax injected before, during, and after treatment with cycles of 5-fluorouracil, folinic acid, and oxaliplatin.

Experimental Design: TroVax was administered to 17 patients with metastatic colorectal cancer.

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Article Synopsis
  • Pseudotyping viral vectors with VSV-G allows for efficient transduction across various cell types and species.
  • Two key factors influencing lentiviral vector transduction potential are the glycosylation status of VSV-G and the amount of glycoprotein on the virions.
  • VSV-G isoforms (VSV-G1 and VSV-G2) show differences in effectiveness, particularly impacting primate cells, with glycosylation enhancing expression in HEK293T cells, while the required amounts of VSV-G vary significantly across different cell types.
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Purpose: The highly attenuated strain of vaccinia virus, modified vaccinia Ankara (MVA), encoding the tumor antigen 5T4 (termed TroVax), has been evaluated in an open-label phase I/II study in colorectal cancer patients. The primary objectives were to assess the safety and immunogenicity of ascending doses of TroVax and to determine the biodistribution of the vector.

Experimental Design: TroVax was given to 22 patients with metastatic colorectal cancer.

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Gene therapy holds great promise for the treatment of a wide range of inherited and acquired disorders. The development of viral vector systems to mediate safe and long-lasting expression of therapeutic transgenes in specific target cell populations is continually advancing. Gene therapy for the nervous system is particularly challenging due to the post-mitotic nature of neuronal cells and the restricted accessibility of the brain itself.

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5T4 is a tumor associated antigen that is expressed on the surface of a wide spectrum of human adenocarcinomas. The highly attenuated virus, modified vaccinia Ankara, has been engineered to express human 5T4 (h5T4). In a pre-clinical murine model, the recombinant virus (TroVax) induces protection against challenge with CT26-h5T4 (a syngeneic tumor line expressing h5T4).

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Effects of stoichiometry of retroviral components on virus production.

J Gen Virol

September 2000

Oxford BioMedica (UK) Ltd, The Medawar Centre, The Oxford Science Park, Oxford OX4 4GA, UK2.

A study was conducted to investigate the effects of increasing the amount of each retroviral component on vector production. It was found that, while the components of both amphotropic and ecotropic vectors were expressed independently of each other in a transient transfection system, increasing the amount of the gag/gag-pol component resulted in a decrease in virus titres for the amphotropic particles but not ecotropic particles. Analyses of the virus stocks produced indicated that the negative effect on titres was closely linked to the availability of envelope proteins for virion incorporation.

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WEBMAP: radiation hybrid mapping on the WWW.

Bioinformatics

June 1999

Oxford Molecular Ltd, The Medawar Centre, Oxford Science Park, Oxford OX4 4GA, UK.

Summary: A Java interface to radiation hybrid (RH) mapping software is described which enables users to build and interactively refine RH maps over the web.

Availability: The Java applets described here are available on the internet at http://www.oxmol.

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A method of estimating distances between pairs of genetic markers is described that directly uses their observed joint frequency distribution in a panel of radiation hybrids (RHs). The distance measure is based on the strength of association between marker pairs, which is high for close markers and decays with distance. These distances are then submitted to a previous method that generates linear coordinates for the markers directly from the intermarker distance matrix.

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