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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 301b(+) dendritic cell subset located in the cervical lymph nodes but not the spleen.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 Cervical lymph nodes contained the highest relative conc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 Cervical lymph node metastases are recognized as a progn

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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