ライフサイエンスコーパス: cervical lymph node

1 onventional T cells in their exodus from the cervical lymph nodes).

2 try for prion protein was also positive in a cervical lymph node.

3 cursor CTL frequency in NALT compared with a cervical lymph node.

4 une cells entering the CNS from the draining cervical lymph node.

5 a bottleneck as the infection spread to the cervical lymph node.

6 l lymph node and increased interleukin-10 in cervical lymph node.

7 proliferation of both Treg and Th17 cells in cervical lymph nodes.

8 to invade the brain and metastasized to the cervical lymph nodes.

9 their ability to detect SCCHN metastases to cervical lymph nodes.

10 ich also captures drainage of Gd-DOTA to the cervical lymph nodes.

11 vivo exposure, latex beads could be found in cervical lymph nodes.

12 ated by this cell are rapidly transferred to cervical lymph nodes.

13 children in whom there were no metastases to cervical lymph nodes.

14 and IL-2 production were noted in spleen and cervical lymph nodes.

15 levels of ovalbumin-specific CTL in draining cervical lymph nodes.

16 ific CD8+ T cells were first detected in the cervical lymph nodes.

17 ency of activated CD44(+) lymphocytes in the cervical lymph nodes.

18 ced accumulation of primed CD8(+) T cells in cervical lymph nodes.

19 serovar Typhi-infected cells in spleens and cervical lymph nodes.

20 ased mRNA levels for IFN-gamma in cornea and cervical lymph nodes.

21 herent S. aureus and subsequently migrate to cervical lymph nodes.

22 ith more APCs present in the MLN than in the cervical lymph nodes.

23 lowed by spleen, mesenteric lymph nodes, and cervical lymph nodes.

24 the mesenteric lymph nodes and lowest in the cervical lymph nodes.

25 to its surrounding meninges and its draining cervical lymph nodes.

26 SF outflow through lymphatics to superficial cervical lymph nodes.

27 lexus is a major hub for CSF outflow to deep cervical lymph nodes.

28 inges drain interstitial fluid into the deep-cervical lymph nodes.

29 d spinal cord while wild type DC migrated to cervical lymph nodes.

30 a and hard palate and reduced CSF outflow to cervical lymph nodes.

31 anial nerves and vascular structures and the cervical lymph nodes.

32 d traditional secondary lymphoid organs, the cervical lymph nodes.

33 at the brain-draining skull bone marrow and cervical lymph nodes.

34 le coverage that transported CSF to the deep cervical lymph nodes.

35 tative site of human CNS lymphatic drainage, cervical lymph nodes.

36 F outflow to the neck drained to superficial cervical lymph nodes.

37 ption-quantitative PCR and flow cytometry in cervical lymph nodes.

38 sed CSF-derived protein in the draining deep cervical lymph nodes.

39 alivary glands and in particular parotid and cervical lymph nodes.

40 al nervous system (CNS) to the draining deep cervical lymph nodes.

41 specifically accumulated in the CNS-draining cervical lymph nodes.

42 ospinal fluid, and are connected to the deep cervical lymph nodes.

43 rdized uptake value of the primary tumor and cervical lymph nodes.

44 red to mediate their effects in the draining cervical lymph nodes.

45 in the corneal epithelium, conjunctiva, and cervical lymph nodes.

46 well as drainage to the deep and superficial cervical lymph nodes.

47 een known to drain through the lymphatics to cervical lymph nodes(1-17), but the connections and regu

48 e demonstrate that DCs migrate from brain to cervical lymph nodes, a process that can be blocked by f

49 al migratory stream to the olfactory bulb (a cervical lymph node access point) to dampen anti-CNS imm

50 Planar images missed residual cancer in high cervical lymph nodes adjacent to salivary gland activity

51 nage of interstitial fluid from the brain to cervical lymph nodes along periarterial spaces; similar

52 and pseudomonas Ag-associated LC in draining cervical lymph nodes also were increased significantly p

53 ack of cell-mediated antigen drainage to the cervical lymph nodes although soluble drainage to these

54 er receptor A) cells were found in blood and cervical lymph node and increased interleukin-10 in cerv

55 showed impaired activation of T cells in the cervical lymph node and relatively intact blood-brain ba

56 roliferative responses were also detected in cervical lymph node and spleen cell populations after in

57 detectable peptide-specific CTL in both the cervical lymph node and spleen.

58 ic IFN-gamma-secreting cells in the draining cervical lymph node and the lung.

59 epleted most B cells in peripheral blood and cervical lymph nodes and 50-80% of splenic B cells.

60 currences within the thyroid bed or anterior cervical lymph nodes and as a guidance system for direct

61 in CD103(+) cDC1 and cDC2 number in the deep cervical lymph nodes and caused an impairment in cDC1 an

62 the pathological findings of oral ulcers and cervical lymph nodes and chemotherapy was prescribed.

63 were progressively enriched in the draining cervical lymph nodes and CNS as compared with spleen.

64 e in IFN-gamma mRNA levels in the cornea and cervical lymph nodes and decreased TNF-alpha protein lev

65 restricted to the cribriform plate and deep cervical lymph nodes and is regulated by VEGF-C/VEGFR-3

66 h2 cytokine were observed in ocular surface, cervical lymph nodes and isolated CD4(+) T cells of BALB

67 dy-secreting cells in corresponding draining cervical lymph nodes and lacrimal glands than did ocular

68 ers of IgG and IgA antibody forming cells in cervical lymph nodes and lung tissues of mice intranasal

69 he primary Ab-forming cell (AFC) response in cervical lymph nodes and mediastinal lymph nodes of mice

70 nd Th2-type cytokine responses were noted in cervical lymph nodes and spleen of 1-year-old mice.

71 CTL from both cervical lymph nodes and spleens failed to recognize Sal

72 s and cytokine assays using lymphocytes from cervical lymph nodes and spleens from mice immunized wit

73 Mast cell numbers in the cervical lymph nodes and the lungs progressively increas

74 the mediastinal lymph nodes and then in the cervical lymph nodes and the spleen.

75 ed the lymphomatous tissue from the parotid, cervical lymph node, and spleen using molecular genetic

76 atures including strawberry tongue, enlarged cervical lymph node, and subacute periungual desquamatio

77 draining mediastinal lymph nodes (MLNs), in cervical lymph nodes, and also in the spleen.

78 cell counts in nasal mucosa, fecal samples, cervical lymph nodes, and blood.

79 geal lymphangiogenesis, drainage to the deep cervical lymph nodes, and brain-CSF perfusion.

80 drains cerebrospinal fluid (CSF) to the deep cervical lymph nodes, and consider the implications of a

81 sults were confirmed in the Waldeyer's ring, cervical lymph nodes, and small bowel with either nondes

82 ted in the nasal tract compared to the lung, cervical lymph nodes, and spleen 1, 2, 4, 7, 14, and 21

83 haryngeal-associated lymphoreticular tissue, cervical lymph nodes, and spleen of aged mice, which wer

84 m both the nasal associated lymphoid tissue, cervical lymph nodes, and spleen.

85 duced IFN-gamma and IL-4 production in NALT, cervical lymph nodes, and spleen.

86 , most commonly the preauricular nodes, deep cervical lymph nodes, and the salivary gland.

87 ent or exudate; tender and enlarged anterior cervical lymph nodes; and the absence of cough.

88 Metastases are often to preauricular and cervical lymph nodes as well as to the salivary gland.

89 ) T cell activation required intact draining cervical lymph nodes, as cervical lymphadenectomy also i

90 PrP(d) was first identified in cervical lymph nodes at 8 weeks, in the mesenteric lymph

91 ulate activation markers in the CNS-draining cervical lymph nodes at a time when there is no T cell a

92 was detected in either facial lymph nodes or cervical lymph nodes at any time point.

93 We also identify age-related cervical lymph node atrophy and thickening of lymphatics

94 There were enlarged cervical lymph nodes bilaterally in 10 cases (100%).

95 otollin was observed in the nasal cavity and cervical lymph node but not in the brain.

96 rew from 68% of lungs and 36% of spleens and cervical lymph nodes but fewer than 20% of axillary lymp

97 o was also found at early time points in the cervical lymph nodes but not in the mediastinal lymph no

98 301b(+) dendritic cell subset located in the cervical lymph nodes but not the spleen.

99 in all brains and spinal cords and rarely in cervical lymph nodes, but leukemic DNA was not detected

100 CD4(+) T cells isolated from the cervical lymph nodes, but not spleens, of diseased 5B6 t

101 sigma1 could be adoptively transferred using cervical lymph node CD4(+) T cells, which failed to unde

102 ma+ T4p2553-specific cells is observed among cervical lymph node cells and intrathyroidal lymphocytes

103 e profile was observed in ex vivo culture of cervical lymph node cells and splenocytes, indicating th

104 Spleen, mediastinal, and cervical lymph node cells from infected mice produced hi

105 a cells constitute a significant fraction of cervical lymph node cells from older mice deficient in b

106 In contrast i.v. injection of cervical lymph node cells harvested 8 days after OVA inj

107 nd a broad spectrum of cytokine responses by cervical lymph node cells in vitro.

108 ble on dendritic cells obtained ex vivo from cervical lymph node cells of NaI-fed or control mice, su

109 Single-cell suspensions of spleen and cervical lymph node cells prepared from normal C57BL/6 a

110 Supernatants from superficial cervical lymph node cells were examined by ELISA for IFN

111 ma) are produced by spleen, mediastinal, and cervical lymph node cells.

112 vely activated macrophages, in the draining (cervical) lymph node cells.

113 led visualization of regions coinciding with cervical lymph node chains as important for outcome pred

114 Here we show that a brain-to-cervical lymph node (CLN) pathway is involved.

115 T-cells from draining cervical lymph nodes (CLN) and distant inguinal lymph no

116 Cells were then isolated from the cervical lymph nodes (CLN) and the nasal mucosa-associat

117 nasal-associated lymphoid tissue (NALT) and cervical lymph nodes (CLN) are involved in the generatio

118 tribution of peripheral activation events in cervical lymph nodes (CLN) to driving humoral immune res

119 ting cells and antigen-responsive T cells in cervical lymph nodes (CLN) were compared with those foun

120 nasal-associated lymphoid tissue (NALT), and cervical lymph nodes (CLN) were determined after primary

121 d IgA anti-PspA Ab-forming cells in spleens, cervical lymph nodes (CLN), and lung tissue when compare

122 RA59 replicated to appreciable levels in the cervical lymph nodes (CLN), the site of T-cell priming d

123 cell (AFC) reaction in mediastinal (MLN) and cervical lymph nodes (CLN), which drain the lungs and up

124 reverse transcription (RT)-PCR in lungs and cervical lymph nodes (CLN).

125 s in the intestinal lamina propria (LPL) and cervical lymph nodes (CLN).

126 The frequencies of Th17 and Treg cells in cervical lymph nodes (CLNs) and spleen were determined b

127 Vs) act as a drainage path directly into the cervical lymph nodes (CLNs) for macromolecules contained

128 To elucidate the role of draining cervical lymph nodes (CLNs) in corneal alloimmunity.

129 itial ovalbumin to both superficial and deep cervical lymph nodes (cLNs) ipsilateral to sonication, w

130 Cross-talk between the brain and cervical lymph nodes (CLNs) is crucial in brain patholog

131 rain neurodegeneration biomarkers drain into cervical lymph nodes (CLNs), and this drainage function

132 acromolecules and immune cells from CSF into cervical lymph nodes (CLNs).

133 yngeal-associated lymphoid tissue (NALT) and cervical lymph nodes (CLNs).

134 -secreting cells in the draining superficial cervical lymph nodes compared to LT-IIa and CT.

135 ng a 2- to 3-fold increase in the spleen and cervical lymph nodes compared with AM14 Tg Act1(+/+) mic

136 Cervical lymph nodes contained the highest relative conc

137 To investigate this directly, deep cervical lymph node (dCLN) aspirates (n = 36) and blood

138 al fluid (CSF) into the deep and superficial cervical lymph nodes (dcLN and scLN) and tested how the

139 -mVEGF-C) increased CSF drainage to the deep cervical lymph nodes (dCLNs) by enhancing lymphatic grow

140 a the lymphatic pathway, traveling from deep cervical lymph nodes (dCLNs) to the meninges and subsequ

141 ced lymphocyte proliferation in the draining cervical lymph nodes, decreased leukocyte infiltration i

142 ndergone total thyroidectomy with or without cervical lymph node dissection and had received (124)I P

143 Total thyroidectomy with 'therapeutic' cervical lymph node dissection for involved lymph nodes

144 idectomy; some advocate prophylactic central cervical lymph node dissection, whereas others only rare

145 ability to measure glymphatic transport and cervical lymph node drainage in the same animal longitud

146 ls showed that ASCs produced in the draining cervical lymph nodes during the early germinal center re

147 brospinal fluid, and their delivery into the cervical lymph nodes, especially during neuroinflammator

148 rebrospinal fluid from the brain to the deep cervical lymph nodes, fenestrated blood vessels that all

149 Among 352 samples and one cervical lymph node fine needle aspirate, one sample was

150 innate immune response both in the brain and cervical lymph node, followed by an influx of lymphocyte

151 c CD4(+) T cells were first activated in the cervical lymph nodes following i.n. inoculation and then

152 ted for the primary tumor and (18)F-FLT-avid cervical lymph nodes for all scans.

153 Clinical staging of cervical lymph nodes from patients with squamous cell ca

154 Tregs from cervical lymph nodes had reduced Foxp3 expression (> 25%

155 he presence of brain-derived constituents in cervical lymph nodes has been associated with the activa

156 l lymphatic drainage by ligation of the deep cervical lymph nodes impaired clearance of senescent ast

157 NR1-IgG secretion was observed neither from cervical lymph nodes in disease controls nor in patients

158 Cervical lymph nodes in E(-/-)P(-/-)Rag-1(-/-) mice were

159 Surgical excision of the cervical lymph nodes in healthy pre-EAE transgenic mice

160 mory T-helper 17 (Th17) cells in the retina, cervical lymph nodes, inguinal lymph nodes, and spleen.

161 mory T-helper 17 (Th17) cells in the retina, cervical lymph nodes, inguinal lymph nodes, and spleen.

162 e cerebrospinal fluid and are present in the cervical lymph nodes, into which cerebrospinal fluid dra

163 ality (beta [SE], 0.40 [0.23]; P = .045) and cervical lymph node involvement (N stage) (beta [SE], 0.

164 IIIB patients with pathologically confirmed cervical lymph node involvement did not show any uptake

165 stage IIIA patients with clinically negative cervical lymph node involvement were found to have uptak

166 response against Porphyromonas gingivalis in cervical lymph node is abrogated by diphtheria toxin-dri

167 oth IFN-gamma and IL-17, indicating that the cervical lymph node is the initial peripheral activation

168 an from the AC to the facial lymph nodes and cervical lymph nodes is markedly more efficient than tha

169 Primary tumor (PT) and metastatic cervical lymph node (LN) characteristics are highly asso

170 d uptake value (SUVmax) of primary OCSCC and cervical lymph nodes (LNs) at T0 and T1 and new LN uptak

171 h for cellular migration from the eye to the cervical lymph nodes (LNs) during CNV.

172 We examined 71 excised cervical lymph nodes (LNs) from persons with HIV and M.

173 he cerebrospinal fluid (CSF) drains into the cervical lymph nodes (LNs).

174 lls as well as CD11b(+) cells in the spleen, cervical lymph node, lung, and nasopharyngeal associated

175 pleens, nasally associated lymphoid tissues, cervical lymph nodes, lungs, and Peyer's patches using a

176 trated that LT-IIa(T34I) had no affinity for cervical lymph node lymphocytes.

177 ung (CL), abdominal-pelvic (AP), mediastinal/cervical lymph node (MC), and liver (L).

178 While cervical lymph node metastases (cLNM) are well-recognize

179 Four of 5 patients had cervical lymph node metastases and/or extrathyroid exten

180 Our results suggest that cervical lymph node metastases are associated with compr

181 Cervical lymph node metastases are recognized as a progn

182 e hypothesis that the presence and number of cervical lymph node metastases have an adverse impact on

183 r categorized by location (thyroid remnants, cervical lymph node metastases, or distant metastases).

184 s younger than age 45 years does not include cervical lymph node metastases.

185 hat BMI1(+) CSCs mediate invasive growth and cervical lymph node metastasis in a mouse model of HNSCC

186 high negative predictive value in detecting cervical lymph node metastasis in patients with newly di

187 Cervical lymph node metastasis is the leading cause of p

188 Use of FDG PET/CT detected cervical lymph node metastasis with 83.3% sensitivity (9

189 On follow-up, 1 patient developed cervical lymph node metastasis, thus giving a false-nega

190 MDAR epitope spreading, which along the deep cervical lymph nodes, might contribute to fine-tune the

191 unization of LT-beta(-/-) mice, which retain cervical lymph nodes, might generate such a response.

192 priming of CD8 T cells in the draining deep cervical lymph nodes, migration of CD8 T cells into the

193 general, both PsaA- and PspA-specific lung-, cervical lymph node-, nasal tract-, and spleen-derived C

194 rocyte glycoprotein) in palatine tonsils and cervical lymph nodes of 28 acute stroke patients and 17

195 CD4(+) T cells (>75% FoxP3(+)) purified from cervical lymph nodes of commensal bacteria reduced mice

196 in the corneal limbus, lacrimal glands, and cervical lymph nodes of healthy male and female mice.

197 significantly in the cornea and in draining cervical lymph nodes of mAb-treated mice.

198 OVA-specific CTL responses in the spleen and cervical lymph nodes of mice given nasal OVA plus Ad-FL

199 macytoid dendritic cells were upregulated in cervical lymph nodes of minocycline-treated SPF mice.

200 ting) CD4+ T cells was increased in the deep cervical lymph nodes of NTG-treated control mice but not

201 ndary lymphoid organs, B cells cultured from cervical lymph nodes of patients with NMDAR-antibody enc

202 Further, the cervical lymph nodes of RSA59 infected Ifit2(-/-) mice s

203 were significantly higher in the cornea and cervical lymph nodes of sham- versus bead-treated animal

204 frequent among isotypically switched AFC in cervical lymph nodes of the same mice; this pattern was

205 ode involvement were found to have uptake in cervical lymph nodes on PET/CT-1, and 2 of 3 IRSS stage

206 before the disease onset in thyroid-draining cervical lymph nodes only in mice placed on an iodide-ri

207 DD occurs directly in the CNS and not in the cervical lymph nodes or other peripheral lymphoid organs

208 s bearing this specificity were found in the cervical lymph nodes or spleens of TMEV-infected mice.

209 n patients with PTLD in the Waldeyer's ring, cervical lymph nodes, or small bowel with either nondest

210 alues were significantly higher after THW in cervical lymph node (P = 0.005) and distant (P = 0.001)

211 ecovery of 500-kDa dextran in the facial and cervical lymph nodes peaked at 1.8% of amount the inject

212 recovery of 40-kDa dextran in the facial and cervical lymph nodes peaked at 52.6% of the amount injec

213 id sinus, as well as a notable delay in deep cervical lymph node perfusion, compared to patients with

214 d-producing CD8alpha+ dendritic cells in the cervical lymph node postinfection.

215 involved lymph node sites, increased size of cervical lymph nodes, presence of 17p deletion or 11q de

216 tomy and the high rates of recurrence in the cervical lymph nodes reported in retrospective studies.

217 Furthermore, we develop a cervical lymph node sampling protocol that can be used t

218 luate 46 tissue cores of surgically resected cervical lymph nodes, some of which harboured oral squam

219 d detection of Mycobacterium tuberculosis in cervical lymph node specimens obtained from patients in

220 in LT beta retain mesenteric lymph nodes and cervical lymph nodes, suggesting that an LT beta-indepen

221 ikuchi-Fujimoto disease usually involves the cervical lymph nodes, there are also atypical presentati

222 e dissemination of HNSCC cancer cells to the cervical lymph nodes, thereby prolonging animal survival

223 ystems, with the latter draining to the deep cervical lymph nodes through lymphatic vasculature in th

224 d by drainage from the brain directly to the cervical lymph nodes through the brain's primitive lymph

225 generated within the CNS and migrate to deep cervical lymph nodes through the CSF after antigen captu

226 novel mechanisms of autoimmunization in deep cervical lymph nodes to explore hypotheses around post-H

227 Transcutaneous exposure of the cervical lymph nodes to violet light permitted punctual

228 of blood cells, which accumulate in the deep cervical lymph nodes via meningeal lymphatics.

229 rainage of Gd-DOTA to submandibular and deep cervical lymph nodes was demonstrated as 25-50% T1 reduc

230 ical or histologically proven enlargement of cervical lymph nodes was present in 7 of 14 patients.

231 cells in the MLN, while the response in the cervical lymph nodes was still greatly inhibited.

232 body synthesis in cultured inguinal and deep cervical lymph nodes were assessed with techniques inclu

233 ge, the corneal epithelium, conjunctiva, and cervical lymph nodes were harvested for total RNA extrac

234 urs later, the eyes, facial lymph nodes, and cervical lymph nodes were isolated, and the total conten

235 anced numbers of Foxp3(+)T(reg) cells in the cervical lymph nodes were observed after intestinal reco

236 oved PTLD of the Waldeyer (lymphoid) ring or cervical lymph nodes were retrospectively reviewed for a

237 art, liver, kidney, spleen, bone marrow, and cervical lymph nodes were subjected to histopathologic e

238 ntigen-loaded bone marrow DC migrate to deep cervical lymph nodes where they prime antigen-specific T

239 specific T and B cell populations within the cervical lymph nodes, where brain-derived antigens are p

240 opic tumors spontaneously metastasize to the cervical lymph nodes, where the presence of HNSCC cells

241 eals significantly less drainage to the deep cervical lymph nodes, which is indicative of impaired ly

242 tiviral immune response was initiated in the cervical lymph nodes with rapid extrafollicular producti

243 neutrophil counts and develop hypercellular cervical lymph nodes with substantial plasma cell infilt

244 and neck (SCCHN) metastasizes predictably to cervical lymph nodes, with low rates of distant metastas

245 after FIV infection was most dramatic in the cervical lymph nodes, with the greatest increase in inte