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Expansion of human T cells using xenogeneic free and gamma irradiated human platelet lysate
Cancer Research Conference: American Association for Cancer Research Annual Meeting, ACCR ; 83(7 Supplement), 2023.
Article Dans Anglais | EMBASE | ID: covidwho-20232181
ABSTRACT
Commercially available human platelet lysate (hPL) is produced using expired human platelets obtained from accredited blood banks in the United States. These platelets were originally intended for use in patient transfusion. The safety of platelets used in transfusion is managed by the U.S. Food Drug Administration (FDA), as well as the American Association of Blood Banks (AABB). These organizations set standards, including testing for transmissible diseases. The United States record for blood safety is well established, with extremely low rates of disease transmission, making the platelet units used for hPL manufacture low risk. The Covid-19 pandemic has increased awareness of emerging infectious diseases, even though transmission of Covid-19 via blood transfusion has not been documented. For that reason, gamma irradiated hPL offers an additional safety measure in the clinic. Chimeric Antigen Receptor (CAR) expressing T-cells have demonstrated potent clinical efficacy in patients with hematological malignancies. In addition, there are several phase I clinical trials evaluating the use of CAR-T-cells for targeting of solid tumorassociated antigens. Some of the challenging issues found during production of CAR-T cells are the efficiency of T cell transduction to generate CAR-T cells, the expansion of T cells to clinically relevant numbers and the long-term survival in vivo of the therapeutic cells. The use of human platelet lysate has been demonstrated to improve these issues. Our data from experiments performed using human CD3+ from donors demonstrates that human platelet lysates offer an improved performance on T cell expansion versus serum derived products. hPL efficiently promotes T cell expansion, with higher cell yields and lower cell exhaustion rate. Additionally, we efficiently developed a protocol for suspension culture of T cells, which could facilitate the large-scale expansion of allogeneic CAR-T cells.
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Texte intégral: Disponible Collection: Bases de données des oragnisations internationales Base de données: EMBASE Type d'étude: Études expérimentales / Étude pronostique langue: Anglais Revue: Cancer Research Conference: American Association for Cancer Research Annual Meeting, ACCR Année: 2023 Type de document: Article

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Texte intégral: Disponible Collection: Bases de données des oragnisations internationales Base de données: EMBASE Type d'étude: Études expérimentales / Étude pronostique langue: Anglais Revue: Cancer Research Conference: American Association for Cancer Research Annual Meeting, ACCR Année: 2023 Type de document: Article