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Cited by 310

The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.

Targeting the tumor-draining lymph node with adjuvanted nanoparticles reshapes the anti-tumor immune response

Open access
Thomas, Susan N., Vokali, Efthymia, Lund, Amanda W., Hubbell, Jeffrey A., Swartz, Melody A.·2014·Biomaterials

Abstract

Accumulating evidence implicates the tumor-draining lymph node (TDLN) in tumor-induced immune escape, as it drains regulatory molecules and leukocytes from the tumor microenvironment. We asked whether targeted delivery of adjuvant to the TDLN, presumably already bathed in tumor antigens, could promote anti-tumor immunity and hinder tumor growth. To this end, we used 30 nm polymeric nanoparticles (NPs) that effectively target dendritic cells (DCs, CD11c(+)) within the lymph node (LN) after intradermal administration. These NPs accumulated within the TDLN when administered in the limb ipsilateral (i.l.) to the tumor or in the non-TDLN when administered in the contralateral (c.l.) limb. Incorporating the adjuvants CpG or paclitaxel into the NPs (CpG-NP and PXL-NP) induced DC maturation in vitro. When administered daily i.l. and thus targeting the TDLN of a B16-F10 melanoma, adjuvanted NPs induced DC maturation within the TDLN and reshaped the CD4(+) T cell distribution within the tumor towards a Th1 (CXCR3(+)) phenotype. Importantly, this also led to an increase in the frequency of antigen-specific CD8(+) T cells within the tumor. This correlated with slowed tumor growth, in contrast to unhindered tumor growth after c.l. delivery of adjuvanted NPs (targeting a non-TDLN) or i.l. delivery of free adjuvant. CpG-NP treatment in the i.l. limb also was associated with an increase in CD8(+)/CD4(+) T cell ratios and frequencies of activated (CD25(+)) CD8(+) T cells within the TDLN whereas PXL-NP treatment reduced the frequency of regulatory T (FoxP3(+) CD4(+)) cells in the TDLN. Together, these data implicate the TDLN as a delivery target for adjuvant therapy of solid tumors.

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Metadata

Authors
Thomas, S. N., Vokali, E., Lund, A. W., Hubbell, J. A., & Swartz, M. A.
Venue
Biomaterials
Publisher
Elsevier BV
Published
2014-01
Volume
35
Issue
2
Pages
814-824
ISSN
0142-9612 (ISSN-L)
OpenAlex
W1987416012
Cited by
310
References
55
FWCI
9.91
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Targeting the tumor-draining lymph node with adjuvanted nanoparticles reshapes the anti-tumor immune response. https://app.cochat.ai/papers/10.1016/j.biomaterials.2013.10.003
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Thomas, S. N., Vokali, E., Lund, A. W., Hubbell, J. A., & Swartz, M. A. (2014). Targeting the tumor-draining lymph node with adjuvanted nanoparticles reshapes the anti-tumor immune response. Biomaterials. https://doi.org/10.1016/j.biomaterials.2013.10.003

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