CD137-guided isolation and expansion of antigen-specific CD8 cells for potential use in adoptive immunotherapy

K Watanabe, S Suzuki, M Kamei, S Toji… - International journal of …, 2008 - Springer
K Watanabe, S Suzuki, M Kamei, S Toji, T Kawase, T Takahashi, K Kuzushima, Y Akatsuka
International journal of hematology, 2008Springer
The efficient isolation and ex vivo expansion of antigen-specific T cells are crucial for
successful adoptive immunotherapy against uncontrollable infections and cancers. Several
methods have been reported for this purpose, for example, employing MHC-multimeric
complexes, interferon-gamma secretion, and antibodies specific for molecules expressed on
T-cell surfaces, including CD25, CD69, CD107a, CD137, and CD154. Of the latter, CD137
has been shown to be one of the most promising targets since it is only expressed on CD8+ …
Abstract
The efficient isolation and ex vivo expansion of antigen-specific T cells are crucial for successful adoptive immunotherapy against uncontrollable infections and cancers. Several methods have been reported for this purpose, for example, employing MHC-multimeric complexes, interferon-gamma secretion, and antibodies specific for molecules expressed on T-cell surfaces, including CD25, CD69, CD107a, CD137, and CD154. Of the latter, CD137 has been shown to be one of the most promising targets since it is only expressed on CD8+ T cells early after encountering antigen, while being almost undetectable on resting cells. However, detailed comparisons between CD137-based and other methods have not yet been conducted. In this study, we therefore compared three approaches (with CD137, CD107a, and tetramers) using HLA-A24-restricted CMV pp65 and EBV BRLF1 epitopes as model antigens. We found that the CD137-based isolation of antigen-stimulated CD8+ T cells was comparable to tetramer-based sorting in terms of purity and superior to the other two methods in terms of subsequent cell expansion. The method was less applicable to CD4+ T cells since their CD137 upregulation is not sufficiently high. Collectively, this approach is most likely to be optimal among the methods tested for the isolation and expansion of antigen-specific CD8+ cells.
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