ライフサイエンスコーパス: draining lymph node

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

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

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

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

5 id drainage of the vaccine components to the draining lymph node.

6 er cells were also readily detectable in the draining lymph node.

7 tract induces strong Th2 priming in the lung draining lymph node.

8 ow precursors, and CCR7 for migration to the draining lymph node.

9 cating viral RNA into dendritic cells in the draining lymph node.

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

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

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

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

14 significantly attenuated niT cell numbers in draining lymph nodes.

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

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

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

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

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

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

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

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

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

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

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

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

27 vant distribution and prolonging activity in draining lymph nodes.

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

29 erum and proportion of Th1 and Th17 cells in draining lymph nodes.

30 activated CD4(+) T-cell populations in lung draining lymph nodes.

31 he skin, and IFN-gamma, IL-1beta, and UBD in draining lymph nodes.

32 isseminated from local sites of infection to draining lymph nodes.

33 delivery to antigen presenting cells in the draining lymph nodes.

34 D4(+)(CD25(+))FoxP3(+) T cells in pancreatic draining lymph nodes.

35 gen clearance from the inflamed colon to the draining lymph nodes.

36 endogenous T cells in the uterus and uterine-draining lymph nodes.

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

38 e TSLP-induced DC migration potential to the draining lymph nodes.

39 ssociated with reduced neutrophil numbers in draining lymph nodes.

40 serum IgE levels, and by flow cytometry from draining lymph nodes.

41 +) Tcm) cells including retention within the draining lymph nodes.

42 d is constitutively presented in the stomach-draining lymph nodes.

43 s significant numbers of bystander DC in the draining lymph nodes.

44 CD4+ T cell priming does not occur in liver-draining lymph nodes.

45 from peripheral tissues to the paracortex of draining lymph nodes.

46 th reduced IL-17 and IFN-gamma expression in draining lymph nodes.

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

48 ype (WT) OT-I cells that accumulated in skin-draining lymph nodes.

49 nces, especially mycobacteria, in their skin-draining lymph nodes.

50 IL-17(+) gammadelta T cells and DETCs in the draining lymph nodes.

51 uration and migration of resident DCs to the draining lymph nodes.

52 ng by altering the composition of DCs in the draining lymph nodes.

53 autoreactive donor T cells in the pancreatic draining lymph nodes.

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

55 d malignant L-selectin-negative cells to the draining lymph nodes.

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

57 s as well as Th2-polarized CD4(+) T cells in draining lymph nodes.

58 cell response in the cornea as well as local draining lymph nodes.

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

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

61 2L(hi)CD44(lo)Foxp3(+) central Treg cells in draining lymph nodes.

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

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

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

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

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

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

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

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

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

71 fibroblastic reticular cell networks in the draining lymph nodes.

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

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

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

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

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

77 utrophil recruitment in the footpads and the draining lymph nodes 1 d following infection.

78 activated immune cells, were detected in the draining lymph node 2 days after WNV infection.

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

80 s taken up by two distinct DC populations in draining lymph nodes: a mostly CD11c(int)MHC class II (M

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

82 the capacity to robustly expand in the lung-draining lymph node after live influenza virus infection

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

84 In the draining lymph node, after 24 h, the numbers of activate

85 erentially transport Ag from the lung to the draining lymph node and are crucial for the initiation o

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

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

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

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

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

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

92 rain predominately by neutrophils in vaccine-draining lymph nodes and by smaller numbers of dendritic

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

94 DCs triggers CCR7-dependent migration to the draining lymph nodes and enhances their capacity to init

95 yD88(-/-)CD4(+) T cells to accumulate in the draining lymph nodes and genital tract when exposed to t

96 fect of reducing bacterial sequences in skin-draining lymph nodes and in skin itself.

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

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

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

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

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

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

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

104 performed to determine specific intragraft, draining lymph nodes and spleen T-cell population, and s

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

106 al cellular cytokine response in splenic and draining lymph nodes and the antibody response in serum

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

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

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

110 ivation of tumor antigen-specific T cells in draining lymph nodes, and a reduction in regulatory T ce

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

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

113 mice showed increased levels of MCP-1 in the draining lymph nodes, and in vivo administration of MCP-

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

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

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

117 uency increased significantly in the spleen, draining lymph nodes, and transplanted islets and remain

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

119 Recurrent tumors and draining lymph nodes are infiltrated with M2 (CD11b(+)F4

120 nstrated that migratory DCs from the stomach-draining lymph nodes are the only DC subset capable of c

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

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

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

124 After immunization, draining lymph nodes became replenished with terminally

125 ars not to alter dendritic cell migration to draining lymph nodes but is associated with enhanced flu

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

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

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

129 al inflammatory response develops in the paw-draining lymph nodes by an IL-17-dependent mechanism.

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

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

132 decreased in the in vitro restimulated skin-draining lymph node cells from the EGF-treated mice.

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

134 sociated with little or no reduction in lung-draining lymph node cells or their cytokine production a

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

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

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

138 However, the cecum draining lymph node (cLN), the gut tissue, and the splee

139 ll trafficking, diverting migration from the draining lymph nodes/CNS route to the mesenteric lymph n

140 tially at the injection site and the nearest draining lymph nodes compared with the attenuated varian

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

142 us that targets dendritic cells (DCs) in the draining lymph node (DLN) and produces intracellular vir

143 mice, followed by the analysis of lungs and draining lymph node (DLN) cell infiltrates, immunoglobul

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

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

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

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

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

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

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

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

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

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

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

155 with decreased lymphocyte migration into the draining lymph nodes (dLNs) of infected Cd22(-/-) mice.

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

157 lammation, LAPCs accumulate in the lungs and draining lymph nodes (DLNs), concomitant with the onset

158 interferon response systemically and in the draining lymph node during WNV infection.

159 cells beyond their initial activation in the draining lymph nodes during influenza infection.

160 a population of monocyte-derived DCs in the draining lymph node, early release of IL-12p70 and IFN-g

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

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

163 tivation and migration from the intestine to draining lymph nodes, events necessary for Th2 priming.

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

165 red into Rag1(-/-) mice proliferated in skin-draining lymph nodes, expressed a restricted T-cell rece

166 of Ag-loaded dendritic cells (DCs) into the draining lymph nodes following allergen challenge.

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

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

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

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

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

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

173 nt, activation, and apoptosis of DCs in lung-draining lymph nodes; granulocyte and macrophage infiltr

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

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

176 i) the suppression Th1/Th17 pathways in lung-draining lymph nodes, (iii) the recruitment of effector

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

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

179 nt, these two DC populations appeared in the draining lymph nodes in comparable numbers and with simi

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

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

182 regs), which are induced locally in the skin-draining lymph nodes in response to UVB exposure, connec

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

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

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

186 n induces naive T cell proliferation in skin-draining lymph nodes, in an Ag-dependent fashion.

187 aerobic bacteria from the neonatal gut into draining lymph nodes, including the opportunistic pathog

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

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

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

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

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

193 pathogen transport from the lung to a local draining lymph node (LN).

194 DC in the lung, but exclusively by DC in the draining lymph node (LN).

195 demonstrate in this study that Tregs in the draining lymph nodes (LN) of allograft acceptors, but no

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

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

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

199 In response to lymph-borne antigens, draining lymph nodes (LNs) expand several folds in size,

200 econd population migrated from the skin into draining lymph nodes (LNs) in a CCR7-dependent manner.

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

202 The invasion status of tumour-draining lymph nodes (LNs) is a critical indicator of ca

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

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

205 c T cell responses are initiated in the lung draining lymph nodes (LNs), and lymphocytes subsequently

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

207 45(+) leukocytes present in tumor tissue and draining lymph nodes (LNs).

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

209 igens and constitutively migrate to the skin-draining lymph nodes (LNs).

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

211 accumulation of slanDCs in metastatic tumour-draining lymph nodes (M-TDLN) from carcinoma patients.

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

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

214 ice with PIN lesions exhibited metastases to draining lymph nodes, marked by relatively differentiate

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

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

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

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

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

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

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

222 In lung-draining lymph nodes of C3aR(-/-) mice the total number

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

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

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

226 ved instead from influenza virus in the lung-draining lymph nodes of infected mice, they proliferated

227 migratory dermal dendritic cells in the skin-draining lymph nodes of L. donovani-infected malnourishe

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

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

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

231 ized by major populations of T cells in skin-draining lymph nodes of mice.

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

233 T cells from skin-draining lymph nodes of normal mice were shown, in vitro

234 ntly, CD31-conditioned DCs purified from the draining lymph nodes of ovalbumin-immunized mice favored

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

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

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

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

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

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

241 D8(+) and/or CD103(+) dendritic cells in the draining lymph node played a critical role in the primin

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

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

244 transiently at the muscle injection site and draining lymph node postinjection, consistent with the r

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

246 heral tissues via afferent lymphatics to the draining lymph node remains poorly understood.

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

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

249 4+ T cell hyporesponsiveness within the skin-draining lymph nodes (sdLN), manifested as reduced CD4+

250 R-signaled DCs required their homing in skin-draining lymph nodes (sDLNs) where they induced inflamma

251 After TAC, enlarged heart mediastinal draining lymph nodes showed a high density of both CD4(+

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

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

254 creased the numbers and percentage of Tregs (draining lymph node, spleen), which resulted in reduced

255 for 105 days by size measurements, and skin, draining lymph node, spleen, and sera were investigated

256 maturation and plasma cell responses in the draining lymph nodes, spleen, and bone marrow and confer

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

258 egulatory T (T(reg)) cells within the tumor, draining lymph nodes, spleen, and lung metastases.

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

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

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

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

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

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

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

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

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

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

269 pression of CD86 and rapidly migrated to the draining lymph node to become the most abundant skin-der

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

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

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

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

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

275 T cells from skin-draining lymph nodes, transferred into Rag1(-/-) mice pr

276 Accordingly, draining lymph nodes turned out to be dispensable for th

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

278 sition in peripheral tissues, DCs migrate to draining lymph nodes via the lymphatics to present antig

279 rrested on vessel walls within inflamed skin-draining lymph nodes was also reduced.

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

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

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

283 atory agents, the hypertrophy induced in the draining lymph nodes was minimal and significantly less

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

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

286 tive and cytokine-producing potential in the draining lymph nodes, when the animals were challenged 2

287 n of activated lung dendritic cells into the draining lymph node where they primed naive T cells to d

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

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

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

291 airment is limited to the lungs and the lung-draining lymph nodes, where viral Ags are unusually pers

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

293 rly proinflammatory cytokine response in the draining lymph node, which impacts immunity and control

294 ping the early innate immune response in the draining lymph node, which impacts the spread of virus i

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

296 ciency results in increased T cell egress to draining lymph nodes, which is associated with impaired

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

298 7BL/6 mice enhanced resident DC migration to draining lymph nodes, which was verified by imaging lymp

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