ライフサイエンスコーパス: draining lymph node

1 by increasing local HA concentration in the draining lymph node.

2 tion of renal antigens to CD8 T cells in the draining lymph node.

3 ency of T cells and myeloid cells within the draining lymph node.

4 ent passive diffusion of the nanogels to the draining lymph node.

5 g parenchyma independently of priming in the draining lymph node.

6 ell (DC) Ag presentation in the local muscle-draining lymph node.

7 he MHC II(high) mature DCs were found in the draining lymph node.

8 iling of innate immune response genes in the draining lymph node.

9 he tumor suppresses T cell activation in the draining lymph node.

10 ce including blood, bone marrow, spleen, and draining lymph nodes.

11 prime parasite-specific CD8 T cells in liver-draining lymph nodes.

12 orm and improved immune cell infiltration in draining lymph nodes.

13 2L(hi)CD44(lo)Foxp3(+) central Treg cells in draining lymph nodes.

14 cific B cells were detected in local genital draining lymph nodes.

15 ad box P3) IFN-gamma(+) T cells in the heart-draining lymph nodes.

16 s was isolated from tonsils, gut mucosa, and draining lymph nodes.

17 he rationale for surgical resection of tumor-draining lymph nodes.

18 gnificant reduction in IL-17(+) cells in the draining lymph nodes.

19 the initiation of the immune response in the draining lymph nodes.

20 R T cells occurred only in the regional skin-draining lymph nodes.

21 nary MCs before leaving the inflamed skin to draining lymph nodes.

22 the vaccine injection site, but not vaccine-draining lymph nodes.

23 tivate antigen-specific CD8 T cells in renal draining lymph nodes.

24 upregulation of T cell activation markers in draining lymph nodes.

25 g trafficking of antigen-presenting cells to draining lymph nodes.

26 response on the malignancy and the affected draining lymph nodes.

27 , and BAFF(+) CD11b(hi) NK cells expanded in draining lymph nodes.

28 he kidney and T cell activation in the renal draining lymph nodes.

29 in tissue, and migrate through lymphatics to draining lymph nodes.

30 f specific B cells to the mesenteric but not draining lymph nodes.

31 IL-1beta expression by myeloid cells in the draining lymph nodes.

32 fibroblastic reticular cell networks in the draining lymph nodes.

33 o t 5, that targets the lung rather than the draining lymph nodes.

34 , and eosinophil infiltration in the stomach-draining lymph nodes.

35 e immune responses at the injection site and draining lymph nodes.

36 from whole nondiseased human lungs and lung-draining lymph nodes.

37 of organ-specific Treg cells in the prostate-draining lymph nodes.

38 significantly attenuated niT cell numbers in draining lymph nodes.

39 and kinetics, TFH and GC B cell responses in draining lymph nodes.

40 riven recruitment of T-cell oral tissues and draining lymph nodes.

41 ) T cell priming in both the spleen and skin-draining lymph nodes.

42 T cell subtype interacting with DCs in mouse draining lymph nodes.

43 CD4(+) T cells and plasmablasts in the joint-draining lymph nodes.

44 injection) trafficking of both cell types to draining lymph nodes.

45 s that carry the bacteria through successive draining lymph nodes.

46 gene expression in vivo, particularly within draining lymph nodes.

47 TB(4) receptors (R) in vitro and in inflamed draining lymph nodes.

48 nodes when compared with Tregs from the lung-draining lymph nodes.

49 -PD-1 augmented T cell infiltration in tumor-draining lymph nodes.

50 elevated Th1 and Th17 cell reactivity in the draining lymph nodes.

51 se in the effector CD4(+) T cell response in draining lymph nodes.

52 ion and impaired effector T-cell egress from draining lymph nodes.

53 vant distribution and prolonging activity in draining lymph nodes.

54 tory T cell response in the cornea and local draining lymph nodes.

55 ferentiation in the lung, independent of the draining lymph nodes.

56 pe 2 conventional dendritic cells (cDC2s) in draining lymph nodes.

57 es which also depend upon T cell egress from draining lymph nodes.

58 lariae migrated through lymphatic vessels to draining lymph nodes.

59 uce migration of Th2-skewing CD301b(+) DC to draining lymph nodes.

60 eficient Th2 cells were retained in the lung-draining lymph nodes.

61 ed inflammatory Th1 populations in allograft draining lymph nodes.

62 to persistence at the injection site and in draining lymph nodes.

63 of dendritic cells and T-cell priming in the draining lymph nodes.

64 monocytes and then delivered to mediastinal draining lymph nodes.

65 oid organs with the exception of the thyroid-draining lymph nodes.

66 DC differentiation in the brain and in tumor-draining lymph nodes.

67 cell function within the TME but not in the draining lymph nodes.

68 en-primed dendritic cell numbers in the skin-draining lymph nodes.

69 ruitment of activated dendritic cells to the draining lymph nodes.

70 odes, which are known to accumulate in joint-draining lymph nodes.

71 the CNS and meninges to the peripheral (CNS-draining) lymph nodes.

72 ype 1 dendritic cell IL-27 production in the draining lymph node 12 h after s.c. vaccination directly

73 AM did not prevent lymphocyte recruitment to draining lymph nodes 24 h after transfer, but it was req

74 lts indicate that tumor growth reduces tumor-draining lymph node accumulation and alters the distribu

75 g nanoparticles that are rapidly conveyed to draining lymph nodes after administration in peripheral

76 of IL-4-producing TFH cells and TH2 cells in draining lymph nodes after airway exposure to IL-1 famil

77 However, colonization of neither draining lymph nodes after IN infection nor the spleen a

78 8+ cells are likewise elevated in the tumour draining lymph node and activated to a greater extent th

79 B cells and follicular helper T cells in the draining lymph node and Ag-specific Th1 and Th17 cells i

80 s to a delay in CD8 T cell activation in the draining lymph node and hinders the timely appearance of

81 IL-1beta production by myeloid cells in the draining lymph node and served as a strong stimulus for

82 of IFNgamma-producing CD8(+) T cells in the draining lymph node and spleen.

83 istant tumors, while sparing the intervening draining lymph node and spleen.

84 bserved Th1/Th17 effector cells in the tumor draining lymph node and tumors.

85 erized by an early burst transit through the draining lymph nodes and a relatively limited overall sy

86 er, lymphocytes were isolated from allograft draining lymph nodes and analysed by flow cytometry.

87 oid dendritic cells migrating to mediastinal draining lymph nodes and bearing migratory and immunoreg

88 a necessary step for virus dissemination via draining lymph nodes and blood.

89 ntional DCs that transport tumor antigens to draining lymph nodes and cross-present antigen to activa

90 of programmed-death-ligand-1) in spinal cord-draining lymph nodes and decreases the number of T helpe

91 engulfed MCGs are actively shuttled to skin-draining lymph nodes and finally degraded inside DCs wit

92 nhibited fever-induced T cell trafficking to draining lymph nodes and impaired the clearance of bacte

93 on significantly increased Foxp3(+) Tregs in draining lymph nodes and in the spleen but failed to red

94 en caused homing of tumor-infiltrating DC to draining lymph nodes and increased infiltration of T cel

95 complex class II molecules, migrated to the draining lymph nodes and induced an increase in Treg cel

96 ine needle aspiration to serially sample the draining lymph nodes and investigate the dynamics and sp

97 ls and subsequent dissemination to the tumor-draining lymph nodes and lungs.

98 ired the emigration of XCR1(+) dermal DCs to draining lymph nodes and occurred irrespective of TLR si

99 gulatory T cells at the graft site and graft-draining lymph nodes and preventing T-cell infiltration.

100 rentially retained at the injection site and draining lymph nodes and produced fewer systemic inflamm

101 follicular helper (Tfh) cells in their lung draining lymph nodes and produced IgE Abs to peanuts.

102 immune responses was analyzed by collecting draining lymph nodes and sera and by challenging the ani

103 nt CD11b(+) DCs, which enhances migration to draining lymph nodes and Th2 priming capacity.

104 ion by plasmacytoid DC (pDC) from skin/tumor draining lymph nodes and the cross-priming of Ag-specifi

105 of CCR6(+) Treg cells was also found in the draining lymph nodes and tumor-infiltrating lymphocytes

106 T(FH) were first observed in the lung-draining lymph nodes and with further exposure were also

107 e identified in the porcine-NICC xenografts, draining lymph node, and spleen.

108 they are rare, including adipose, lung, skin-draining lymph nodes, and a previously undescribed popul

109 ent in ApoE(-/-)Irf5(-/-) mice in the aorta, draining lymph nodes, and bone marrow cell cultures, ind

110 antigen presenting cell (APC) trafficking to draining lymph nodes, and enhances antigen cross-present

111 tracting chemokines, migration of DCs to the draining lymph nodes, and priming of allergen-specific T

112 +)CD80(-) GC B cells in proximal- and distal-draining lymph nodes, and promoted the persistence of GC

113 Treg cells remained unchanged in the lungs, draining lymph nodes, and spleens of infected mice.

114 enous and exogenous DCs, migration of DCs to draining lymph nodes, and tumor infiltration of CD4(+) a

115 oducing CD4(+) T cells in muscle tissues and draining lymph nodes as well as reduced parasite burden

116 +) and CD103(+) dendritic cells, in the lung-draining lymph node, as well as increased expression of

117 alloantigen-induced immune responses in the draining lymph node at lower doses and reduced administr

118 reduced CD40 expression in DCs isolated from draining lymph nodes at 2 days post infection (dpi).

119 Here we report that macrophages in the draining lymph node, but not in the tissue at the site o

120 cific CD4(+) T cells proliferated in the eye draining lymph nodes, but did not induce uveitis.

121 cer cells tend to metastasize first to tumor-draining lymph nodes, but the mechanisms mediating cance

122 ited T(H) cell TGF-beta signalling in tumour-draining lymph nodes, causing reorganization of tumour v

123 Within the draining lymph node CD4(+) T-cell population, 30% expres

124 Gene set enrichment analysis of draining lymph node cells from day 1 after immunization

125 In addition, draining lymph node cells from FHL2-KO mice show reduced

126 reduced IFN-gamma and IL-17 were detected in draining lymph node cells from P2rx7(-/-) mice.

127 re found in bronchoalveolar lavage fluid and draining lymph node cells of Nur77-KO mice, as well as i

128 led to a similar bias in CD4(+) T cells from draining lymph node cells toward IL-17A and away from IF

129 sue, bronchoalveolar lavage fluid (BALF) and draining lymph node cells were analysed for inflammation

130 served both full-length and cleaved SIRT1 in draining lymph node cells.

131 antigen-specific CD8(+) T cells in the skin draining lymph nodes compared to a conventional intrader

132 stimulator (ICOS), in the skin allograft and draining lymph nodes compared to endogenous and polyclon

133 y extensive Treg proliferation in the uterus-draining lymph nodes, comprising 70% neuropilin 1(+) tTr

134 increased emm1 GAS dissemination locally to draining lymph nodes (controls median 183 CFU per node [

135 ) T cells were also suppressed in pancreatic draining lymph node, demonstrating bystander tolerance a

136 Bacteria then traffic to the draining lymph node (dLN) where they replicate to large

137 on to, and localization with, T cells in the draining lymph node (dLN).

138 nce requires effector T-cell egress from the draining lymph node (dLN).

139 ment of inflammatory monocytes (iMos) to the draining lymph node (dLN).

140 induce the migration of CD301b(+) DCs to the draining lymph node (dLN).

141 T cell migration from the dermis to the skin draining lymph node (dLN).

142 required CCR2 expression to traffic between draining lymph nodes (dLN) and the tumor.

143 ent of neutrophils to the ear dermis and ear draining lymph nodes (dLN) as early as 6-18 h after immu

144 n vitro but failed to home from the graft to draining lymph nodes (dLN) as efficiently as wild type.

145 antigen capture and subsequent migration to draining lymph nodes (DLN).

146 cells and T cells to lymphatics and then to draining lymph nodes (dLN).

147 ed s.c. shows minimal uptake into lymphatics/draining lymph nodes (dLNs) and instead is rapidly distr

148 d with a lack of iNKT cell activation in the draining lymph nodes (dLNs) and prevented the protective

149 nfection, CD4(+) T cells are expanded in the draining lymph nodes (DLNs) and restimulated in the infe

150 cation of intravaginally administered DCs to draining lymph nodes (dLNs) and stimulate in vivo prolif

151 raction of the vaccine dose localized in the draining lymph nodes (dLNs) and the spleen 6h after i.p.

152 n of multiple T cell subsets to the skin and draining lymph nodes (DLNs) during dengue virus (DENV) i

153 ice and for lifelong parasite persistence in draining lymph nodes (dLNs) of healed mice.

154 igated virus-host interactions in the rectal draining lymph nodes (dLNs) of rhesus macaques at differ

155 terestingly, the environmental milieu of the draining lymph nodes (DLNs) of the mice implanted with t

156 flammatory factors in the grafted cornea and draining lymph nodes (dLNs) were evaluated with slit-lam

157 gens that are regionally drained and through draining lymph nodes (DLNs).

158 ic CD4 T cells in the CNS during disease and draining lymph node during priming.

159 antigen specific T cell proliferation in the draining lymph nodes during EAE.

160 mune disease by regulating SIRT1 cleavage in draining lymph node effector cells.

161 CD11b(-) cDCs from the gut-draining lymph nodes efficiently induced pT(reg) cells a

162 cells found in the infected liver and liver-draining lymph nodes exhibited transcriptionally and phe

163 and alloantigen-induced T cell expansion in draining lymph node experiments.

164 o showed suppressed T cell activation in the draining lymph nodes following challenge.

165 of CD4(+) central-memory T cells within the draining lymph nodes following induction of contact hype

166 ed to support a role of macrophage efflux to draining lymph nodes following treatment with infliximab

167 within the interfollicular areas of mucosal draining lymph nodes, forming a distinct microenvironmen

168 Cells in draining lymph nodes from BALB/c-CXCR3(Tg) mice showed e

169 Neutrophils sorted from vaccine-draining lymph nodes from rhesus macaques also showed ex

170 The gut-draining lymph nodes (gLNs) are key sites for orchestrat

171 r, the severe loss of dendritic cells in the draining lymph node had no impact on viral replication i

172 on of dermal mast cells from the skin to the draining lymph nodes has a prominent role in activating

173 -L1 inhibition specifically within the tumor-draining lymph node, identifying a potential role for PD

174 tion of dendritic cells and T cells into the draining lymph node immediately following infection and

175 causes retention of effector T cells in the draining lymph node in a neuroinflammatory autoimmunity

176 robust activation of dendritic cells in the draining lymph node in vivo.

177 IFN-gamma and IL-2-producing T cells in skin draining lymph nodes in a cell-intrinsic fashion.

178 T cells into the lung lumen, parenchyma, and draining lymph nodes in HDM-sensitized mice.

179 ro and in vivo, trafficking through lymph to draining lymph nodes in mice.

180 te a massive B cell response in the abomasal draining lymph nodes in Ostertagia ostertagi (OO)-infect

181 dies have highlighted the importance of lung-draining lymph nodes in the respiratory allergic immune

182 Tregs were examined in the uterus and uterus-draining lymph nodes in virgin estrus mice and 3.5 d pos

183 n by Ag-specific T cells upon stimulation of draining lymph nodes in vitro.

184 +) pulmonary dendritic cells in the lung and draining lymph nodes in wild-type BALB/c mice after RSV

185 n increase in donor cells in the mediastinal draining lymph nodes; increased lymphatic vessel area; a

186 igen transfer into and presentation in tumor-draining lymph nodes induce activation of tumor-specific

187 gest that the presence of TPO in the thyroid draining lymph nodes induces the activation of T(eff) an

188 infection, we find that while CD169 promoted draining lymph node infection, it limited systemic sprea

189 s circulating between parenchymal organs and draining lymph nodes; injection of known amounts of mole

190 cited a Th1 response that was primed in skin-draining lymph nodes involving Ag presentation by migrat

191 Tumor metastasis to the draining lymph nodes is critical in patient prognosis an

192 ry changes either in the lung or in the lung draining lymph nodes (LDLN), pretreatment of blood eosin

193 mour antigens to antigen-presenting cells in draining lymph nodes, leading to increased surface prese

194 by myeloid-derived suppressor cells in tumor-draining lymph nodes, leading to T cell responses skewed

195 ing of these antigen-presenting cells to the draining lymph node (LN), it was shown that the iron oxi

196 ans cells are APCs that migrate from skin to draining lymph nodes (LN) to drive peripheral tolerance

197 as well as a decreased number of LC in skin-draining lymph nodes (LN).

198 pecific cells underwent several divisions in draining lymph nodes (LN; DLNs) while maintaining expres

199 ls in mouse skin and colon, their respective draining lymph nodes (LNs) and spleen.

200 d presentation of antigen to T cells in skin draining lymph nodes (LNs) both 3 and 10days after admin

201 ent increase in size and cellularity of skin-draining lymph nodes (LNs) in mice.

202 rease in Treg percentages in aorta and aorta-draining lymph nodes (LNs) of these mice compared with a

203 cells and germinal center (GC) B cells from draining lymph nodes (LNs) than the parent virus rLBNSE.

204 f natural and peripheral Tregs in spleen and draining lymph nodes (LNs), elevated IL-10 and TGF-beta

205 e generation of cellular immune responses in draining lymph nodes (LNs).

206 45(+) leukocytes present in tumor tissue and draining lymph nodes (LNs).

207 duce IL-17 in the skin and expand rapidly in draining lymph nodes (LNs).

208 une responses at peripheral sites and within draining lymph nodes (LNs).

209 However, we show that draining lymph node macrophages, but not macrophages at

210 lated from tumor-infiltrating lymphocytes or draining lymph nodes maintained similar phenotypic and s

211 t of SIV from penile mucosal surfaces to the draining lymph nodes may allow an HIV vaccine that produ

212 Interestingly, tumor-infiltrating and tumor-draining lymph node NK cells displayed an upregulated ex

213 lungs (including the major blood vessels and draining lymph nodes) obtained en bloc from 72 individua

214 rment at entering or distributing within the draining lymph node of ectromelia virus (ECTV)-infected

215 gus macaques, of the trafficking dynamics to draining lymph nodes of a model messenger RNA vaccine la

216 r helper T (Tfh) cells were also detected in draining lymph nodes of allergic mice.

217 ntional effector T cells were collected from draining lymph nodes of allogeneic or syngeneic corneal

218 onstrate that although lymphocytes from skin-draining lymph nodes of autoimmune-prone MRL/MpJ-Fas(lpr

219 solated CD4(+) T cells from the upper airway draining lymph nodes of both OVA323-339- and MPO409-428-

220 B cells were induced at higher levels in the draining lymph nodes of CD47KO mice compared to those in

221 m cells leads to maturation and migration to draining lymph nodes of cross-presenting dermal DCs.

222 xtended monitoring of IDO(+) DC in the tumor-draining lymph nodes of IL-12 plus GM-CSF-treated tumor-

223 CXCL13 levels correlated with GC activity in draining lymph nodes of immunized mice, immunized macaqu

224 Furthermore, skin-draining lymph nodes of LC-ablated MRL-lpr mice had sign

225 Upon analysis of microRNA (miR) profile in draining lymph nodes of mice with DTH, treatment with I3

226 clinical-grade adjuvants in whole blood and draining lymph nodes of mice.

227 -secreting virus-specific CD4 T cells in the draining lymph nodes of NK1R(-/-) mice was much higher t

228 MC-derived IL-13 acted on DCs from draining lymph nodes of OVA-sensitized skin to selective

229 In uterus-draining lymph nodes of pregnant dams, the frequencies o

230 ion of MOG35-55-specific T cells in the skin draining lymph nodes of primed mice, but it is not requi

231 cal animal models, ss-CyFaP is visualized in draining lymph nodes of rats through 3.1 cm of overlaid

232 ion, dendritic cells (DCs) purified from the draining lymph nodes of tape-stripped and ovalbumin (OVA

233 CD103(+) DC from the skin/tumor draining lymph nodes of the immunized mice appeared resp

234 pPD-1(+) T cells were also detected in tumor-draining lymph nodes of tumor bearing mice and in biopsi

235 and maintenance and maturation of GCs in the draining lymph nodes of vaccinated mice.

236 ation on T cells population in the wound and draining lymph nodes; on day 14, these mice also display

237 tion, and migration of immune cells to local draining lymph node or to an anatomically distant tumor.

238 s (P = .086 and .006, respectively), and the draining lymph nodes (P = .02).

239 otein expression were higher in T cells from draining lymph nodes (P = 0.03 and P = 0.04, respectivel

240 es of CD4(+)Foxp3(+) T cells in the pancreas-draining lymph nodes, pancreas, and peripheral blood of

241 promotes DC maturation and migration to skin-draining lymph nodes, partially through MC-derived TNF,

242 und in histopathologically negative prostate draining lymph nodes (PDLN) in mice harboring oncogene-d

243 RNA vaccine at the injection site and in the draining lymph nodes, performed cellular analyses of the

244 mal mast cell migration from the skin to the draining lymph nodes plays a prominent role in activatin

245 om peripheral blood (PB) and from pancreatic draining lymph nodes (PLN) of T1D patients and non-diabe

246 antly, we found that the signal in the tumor-draining lymph nodes provides key information about resp

247 g RPM we find that high endothelial cells in draining lymph nodes rapidly increase translation in the

248 gher frequencies of memory Th17 cells in the draining lymph nodes relative to young mice.

249 oscopic examination of the primary tumor and draining lymph nodes) require the infrastructure and exp

250 sed migration of lung dendritic cells to the draining lymph nodes, resulting in greater numbers of vi

251 g kinetics in IL-12-treated tumors and tumor-draining lymph nodes revealed a transient loss followed

252 is of CD11c(+)MHC-II(hi) DCs in the lung and draining lymph nodes revealed that allergen exposure inc

253 ualization of the potential metastatic tumor-draining lymph node(s) for their needed surgical biopsy

254 4+ T cell hyporesponsiveness within the skin-draining lymph nodes (sdLN), manifested as reduced CD4+

255 s, resulting in reduced LC migration to skin-draining lymph nodes (sdLNs) and defective skin toleranc

256 OTAP results in an IFN-dependent increase in draining lymph node size and a concomitant increase in C

257 under steady-state conditions, ILCs in skin-draining lymph nodes (sLNs) were continuously activated

258 e TR1 cells and their recruitment to the CNS-draining lymph nodes, sparing their liver-draining count

259 ased numbers of migratory dendritic cells in draining lymph nodes, specifically dendritic cells with

260 ficant reductions in bacterial burden in the draining lymph nodes, spleen, and liver were observed.

261 to secondary sites of infection, mainly the draining lymph nodes, spleen, gastrointestinal tract, an

262 e maturation of dendritic cells in the tumor-draining lymph nodes, subsequently initiating T cell-med

263 ime dependent changes in RNA profiles of the draining lymph node, suggesting a change in cell profile

264 mice, ARG1-containing EVs are transported to draining lymph nodes, taken up by dendritic cells and in

265 Although STING also induced IDO in tumor-draining lymph nodes (TDLN) during EL4 thymoma growth, t

266 nsively characterized myeloid cells in tumor draining lymph nodes (tdLN) of mice and identified two s

267 sophils expressing IL4 are enriched in tumor-draining lymph nodes (TDLN) of PDAC patients.

268 g responses, which quickly manifest in tumor-draining lymph nodes (TDLNs) after tumor inoculation and

269 ar sinus (SCS) CD169(+) macrophages in tumor-draining lymph nodes (tdLNs) in mice and humans.

270 In draining lymph nodes, tdTomato-positive (tdTomato(+)) AS

271 skin infection by restoring DC migration to draining lymph nodes, Th17 differentiation, and increase

272 gammadelta T cells in the infected foot and draining lymph node that was associated with the product

273 differential distribution of exosomes in the draining lymph nodes that is dependent on the lymphatic

274 th appropriate Ag specificity are present in draining lymph nodes, they are conspicuously absent from

275 cumulation, although Bmem outnumbered ASC in draining lymph nodes throughout infection.

276 xogenous tumor Ags, and migrate to the tumor draining lymph node to initiate cross-priming of tumor-r

277 r phenotype that allows trafficking from the draining lymph node to the lungs and, thereby, prevented

278 lung during inflammation and migrated to the draining lymph nodes to boost TH2-mediated effector resp

279 mechanistic studies at site of injection and draining lymph nodes to directly address the question of

280 ouse MB49 bladder tumors, spleens, and tumor-draining lymph nodes to identify patterns of anti-tumor

281 dendritic cells (DCs) mature and migrate to draining lymph nodes to induce immune responses.

282 nd migrate out of the skin and mucosa to the draining lymph nodes to present antigens to T and B cell

283 tor T cell responses, from activation in the draining lymph node, to the execution of effector functi

284 Thus, ILC populations traffic to draining lymph nodes using different mechanisms.

285 ith pBCG or rBCG, and gene expression in the draining lymph nodes was analyzed by microarray at day 1

286 liposome and protein retention at the local draining lymph nodes was demonstrated with the liposome-

287 Furthermore, HIV-1 dissemination to draining lymph nodes was detected only in HSV-2-coinfect

288 wing TNF inhibition, positing that efflux to draining lymph nodes was involved.

289 lymphocytes expressing RANKL in the cervical draining lymph nodes were higher in IL-33-treated P. gin

290 nced suppressive capacity of Tregs from skin-draining lymph nodes when compared with Tregs from the l

291 Both VLPs efficiently reached the same draining lymph node where they were taken up and process

292 s) are professional APCs that traffic to the draining lymph nodes where they present processed antige

293 also induce germinal centre reactions in the draining lymph nodes, where diversification and maturati

294 he interfollicular regions of the intestinal draining lymph nodes, where they act to limit TfH respon

295 gene-expressing melanocytes localize to skin-draining lymph nodes, where they induce T-cell prolifera

296 s in the paws and in Th17 lymphocytes in the draining lymph nodes, whereas T-regulatory cells were da

297 leukocytes found in primary tumors or tumor-draining lymph nodes, which included mainly CD14(+) mono

298 eased lymphatic flow from the donor graft to draining lymph nodes, which may be a factor in promoting

299 focused the in vivo immune activation on the draining lymph nodes while dramatically reducing systemi

300 inhibited Th1 and Th17 and amplified Treg in draining lymph nodes, while reducing dry eye pathogenesi