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Antigen-specific T cells fully conserve antitumour function following cryopreservation.


ABSTRACT: Immunotherapies based on the autologous adoptive transfer of ex vivo-manipulated T cells are rapidly evolving for the treatment of both metastatic and primary malignancies. However, extended ex vivo culturing reduces the functionality of isolated T cells. Cryopreservation of rapidly expanded T cells for subsequent use throughout an immunotherapeutic regimen is a highly desirable recourse, thus far encumbered by a lack of studies investigating its effects on effector T-cell functionality. Here we directly compare murine tumour-reactive CD8(+) T cells cryopreserved during ex vivo expansion to freshly isolated populations. We show that cryopreservation fully conserves the differentiation potential of effector T cells, secretion of pro-inflammatory cytokines, cytotoxic function and does not impair the three-dimensional scanning motility of T cells or their capacity to infiltrate and reject tumours.

SUBMITTER: Galeano Nino JL 

PROVIDER: S-EPMC4840239 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Antigen-specific T cells fully conserve antitumour function following cryopreservation.

Galeano Niño Jorge L JL   Kwan Rain Y Q RY   Weninger Wolfgang W   Biro Maté M  

Immunology and cell biology 20160112 4


Immunotherapies based on the autologous adoptive transfer of ex vivo-manipulated T cells are rapidly evolving for the treatment of both metastatic and primary malignancies. However, extended ex vivo culturing reduces the functionality of isolated T cells. Cryopreservation of rapidly expanded T cells for subsequent use throughout an immunotherapeutic regimen is a highly desirable recourse, thus far encumbered by a lack of studies investigating its effects on effector T-cell functionality. Here we  ...[more]

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