2021
DOI: 10.1002/1878-0261.12904
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Adoptive transfer of immature myeloid cells lacking NF‐κB p50 (p50‐IMC) impedes the growth of MHC‐matched high‐risk neuroblastoma

Abstract: High-risk neuroblastomas harbor abundant myeloid cells that suppress anti-tumor immunity and support tumor growth. Macrophages lacking the inhibitory NF-κB p50 subunit adopt a pro-

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Cited by 2 publications
(3 citation statements)
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References 38 publications
(63 reference statements)
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“…The following mechanism seems to govern the potentiation of tumor growth inhibitory activity of the checkpoint inhibitor PD-1 [18]. The PD-1 antibody binding to PD-1 on T-cells prevents T-cells from receiving an inhibitory signal from PD-1 ligands (PDL1 and PDK2) expressed on cancer and on myeloid such as macrophages present in the tumor.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The following mechanism seems to govern the potentiation of tumor growth inhibitory activity of the checkpoint inhibitor PD-1 [18]. The PD-1 antibody binding to PD-1 on T-cells prevents T-cells from receiving an inhibitory signal from PD-1 ligands (PDL1 and PDK2) expressed on cancer and on myeloid such as macrophages present in the tumor.…”
Section: Discussionmentioning
confidence: 99%
“…Immune checkpoint inhibitors such as PD-1 that active exhausted antitumor T cells are used alone or with chemotherapy for the treatment of a wide range of cancers [16] [17] [18] [19]. To our knowledge, immune checkpoint inhibitors have not previously been evaluated in combination with anticancer functional foods such as the bioprocessed black rice bran.…”
Section: Introductionmentioning
confidence: 99%
“…We were surprised and disappointed that RT + anti-GD2 immunocytokine (IC) + anti-CTLA-4 did not slow the progressive growth of this tumor any more than the minimal slowing seen with 12 Gy RT alone. Several other immunotherapy (and other novel) regimens have been used on mice bearing this "cold" 9464D-GD2 neuroblastoma, and for the most, part tumor growth could be slowed in vivo, but rarely could mice be cured of measurable 9464D-GD2 tumors due to a variety of proposed mechanisms of resistance [14][15][16][17][18][19][20][21][22][23]. This refractory behavior was consistent with the low tumor mutation burden of this NBL (1/10 that of the B78 melanoma) [13], and consistent with the observation of potentially inhibitory macrophages and myeloid elements in this (and other) NBLs [24].…”
Section: Introductionmentioning
confidence: 99%