Literature DB >> 19533255

Human glioma cell culture: two FCS-free media could be recommended for clinical use in immunotherapy.

Anne Clavreul1, Isabelle Jean, Laurence Preisser, Agnès Chassevent, Anne Sapin, Sophie Michalak, Philippe Menei.   

Abstract

Immunotherapy, particularly active vaccination, may be developed as an effective and safe treatment modality for malignant gliomas, which continue to have a poor prognosis, despite advances in surgical techniques and adjuvant chemotherapy and radiotherapy. Since no glioma-specific tumor-associated antigens (TAAs) have been discovered, autologous tumor cells or well-established glioma cell lines could be used in future vaccination protocols to induce antitumour immunity against unknown TAAs. One obstacle for clinical use of these tumour cell vaccines is related to foetal calf serum (FCS). Efforts are currently being directed toward developing FCS-free media and serum-free alternatives to culture these cell vaccines. In this study, a medium containing human serum and one serum-free medium (UltraCulture), supplemented or not with epidermal growth factor, were tested on morphology, survival, DNA content and TAA expression of human glioma cell lines and glioma biopsy primary cultures. Their effects were compared on FCS-containing medium. Results show that, whatever the medium used, no significant variations in morphology and survival were observed. Furthermore, human serum-containing medium or UltraCulture preserved at early passage cultures the cell population of interest present in the biopsies before culture. In addition, the expression profile of eight TAAs was similar between these media. These data indicate that human serum-containing medium and UltraCulture serum-free medium could be promising candidates to produce tumour-cell vaccines.

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Year:  2009        PMID: 19533255     DOI: 10.1007/s11626-009-9215-4

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol Anim        ISSN: 1071-2690            Impact factor:   2.416


  60 in total

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2.  Changes in glial fibrillary acidic protein and karyotype during culturing of two cell lines established from human glioblastoma multiforme.

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5.  Growth factor profile of irradiated human dermal fibroblasts using a serum-free method.

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6.  Identification of a novel HLA-A*0201-restricted, cytotoxic T lymphocyte epitope in a human glioma-associated antigen, interleukin 13 receptor alpha2 chain.

Authors:  Fumiyoshi Okano; Walter J Storkus; William H Chambers; Ian F Pollack; Hideho Okada
Journal:  Clin Cancer Res       Date:  2002-09       Impact factor: 12.531

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8.  Identification of a human leukocyte antigen-A24-restricted T-cell epitope derived from interleukin-13 receptor alpha2 chain, a glioma-associated antigen.

Authors:  Shinji Shimato; Atsushi Natsume; Toshihiko Wakabayashi; Kunio Tsujimura; Norimoto Nakahara; Jun Ishii; Motokazu Ito; Yoshiki Akatsuka; Kiyotaka Kuzushima; Jun Yoshida
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Review 9.  Cell- and peptide-based immunotherapeutic approaches for glioma.

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Journal:  Trends Mol Med       Date:  2008-04-09       Impact factor: 11.951

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  7 in total

1.  Aberrant immunostaining pattern of the CD24 glycoprotein in clinical samples and experimental models of pediatric medulloblastomas.

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2.  Isolation of a new cell population in the glioblastoma microenvironment.

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3.  Characterization of the distribution, retention, and efficacy of internal radiation of 188Re-lipid nanocapsules in an immunocompromised human glioblastoma model.

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4.  Identification of two glioblastoma-associated stromal cell subtypes with different carcinogenic properties in histologically normal surgical margins.

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5.  A standardized and reproducible protocol for serum-free monolayer culturing of primary paediatric brain tumours to be utilized for therapeutic assays.

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Review 6.  The dark side of foetal bovine serum in extracellular vesicle studies.

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7.  Porcine Neural Progenitor Cells Derived from Tissue at Different Gestational Ages Can Be Distinguished by Global Transcriptome.

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  7 in total

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