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1 and regress multiple solid tumors following adoptive cell transfer.
2 ine delivery or optimal T cell expansion for adoptive cell transfer.
3 tive target for TCR-based gene therapy using adoptive cell transfer.
4 r tumor rejection or inhibit treatment after adoptive cell transfer.
5 e of circulating antitumor T cells following adoptive cell transfer.
6 N-gamma-/- mice, were used as recipients for adoptive cell transfer.
7 tive vaccines and strategies for therapeutic adoptive cell transfer.
8 lymphocytes from melanoma patients following adoptive cell transfer.
9 pulations were rejected within 18 days after adoptive cell transfer.
10 ns and reducing the therapeutic potential of adoptive cell transfers.
11 such as administration of the cytokine IL-2, adoptive cell transfer (ACT) and the recent success of b
15 umor microenvironment (TME), the efficacy of adoptive cell transfer (ACT) is much curtailed in treati
16 the potential for immunotherapy based on the adoptive cell transfer (ACT) of engineered T lymphocytes
23 dy that describes a potential new target for adoptive cell transfer (ACT), in this case CD44 splice v
24 esponse is enhanced through a combination of adoptive cell transfer (ACT), specific vaccination and c
27 f successful cancer immunotherapies, such as adoptive cell transfer and antibody-based immunotherapeu
29 its functional loss reduces the efficacy of adoptive cell transfer and checkpoint blockade immunothe
31 r, did not require total body irradiation or adoptive cell transfer and resulted in induction of anti
32 ls, with potential clinical implications for adoptive cell transfer and vaccine-based immunotherapies
34 ts for successful tumor rejection through an adoptive cell transfer approach reveals that the presenc
36 ere dissected using bone marrow chimeras and adoptive cell transfer approaches to profile clonal expa
38 eric antigen receptor (CAR) for T-cell-based adoptive cell transfer are among these developments that
41 upport suggests that IL-12 could be added to adoptive cell transfer clinical strategies in cancer pat
46 Furthermore, use of gene-deficient mice and adoptive cell transfer experiments revealed that ILC2s w
47 ent tumor models suppressed CTL responses in adoptive cell transfer experiments unless GM-CSF was pro
48 tumor-sensitized T cells is demonstrated by adoptive cell transfer experiments using purified spleen
52 the main challenge to the development of TIL adoptive cell transfer for metastatic GI cancers may not
53 -1/PD-L1 and CTLA-4 checkpoints blockade and adoptive cell transfer) have remarkably improved the res
54 ith porcine skin grafts and administered, by adoptive cell transfer, human cells stimulated in vitro
56 corporating tumor-reactive CD4(+) T cells in adoptive cell transfer immunotherapies against ovarian c
59 cell compartment in immunodeficient mice by adoptive cell transfer leads to a wasting syndrome and i
60 for administering high levels of IL-2 during adoptive cell transfer-mediated antitumor responses.
63 re analyzed using cytokine reporter mice, an adoptive cell transfer model, and gene knockout mice.
67 us immunotherapies under development such as adoptive cell transfer of TCR-engineered CD8(+) T cells,
69 clonotypes that persisted in vivo following adoptive cell transfer possessed telomeres that were lon
71 -engineered T cells are a novel approach for adoptive cell transfer, providing flexible platform for
77 e significant progress in the development of adoptive cell-transfer therapies (ACTs) using gene-engin
81 hways (i.e. PD-1, CTLA-4, and IDO); and (iv) adoptive cell transfer therapy with T cells engineered t
82 e yielded only limited clinical success, but adoptive cell transfer therapy, particularly following a
85 ession of CTLs that is often observed during adoptive cell transfer tumor immunotherapy and identify
87 mice missing different leukocyte subsets and adoptive cell transfers, we demonstrated the involvement
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