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- W2728447325 abstract "Disease recurrence following chemotherapy and allogeneic hematopoietic cell transplantation is the major unmet clinical need of acute leukemia. Adoptive cell therapy (ACT) with allogeneic T lymphocytes can control recurrences at the cost of inducing detrimental GVHD. Targeting T cell recognition on leukemia cells is therefore needed to overcome the problem and ensure safe and durable disease remission. In this review, we discuss adoptive cells therapy based on CD1-restricted T cells specific for tumor associated self-lipid antigens. CD1 molecules are identical in every individual and expressed essentially on mature hematopoietic cells and leukemia blasts, but not by parenchymatous cells, while lipid antigens are enriched in malignant cells and unlike to mutate upon immune-mediated selective pressure. Redirecting T cells against self-lipids presented by CD1 molecules can thus provide an appealing cell therapy strategy for acute leukemia that is patient-unrestricted and can minimize risks for GVHD, implying potential prognostic improvement for this cancer." @default.
- W2728447325 created "2017-07-14" @default.
- W2728447325 creator A5016574603 @default.
- W2728447325 creator A5020167318 @default.
- W2728447325 creator A5078970596 @default.
- W2728447325 creator A5083089027 @default.
- W2728447325 date "2017-08-01" @default.
- W2728447325 modified "2023-09-27" @default.
- W2728447325 title "Harnessing the CD1 restricted T cell response for leukemia adoptive immunotherapy" @default.
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- W2728447325 doi "https://doi.org/10.1016/j.cytogfr.2017.06.007" @default.
- W2728447325 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28712863" @default.
- W2728447325 hasPublicationYear "2017" @default.
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