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1 rily presented in its membrane-bound form by follicular dendritic cells.
2 ght zone that compete for binding antigen on follicular dendritic cells.
3 ll follicles containing germinal centers and follicular dendritic cells.
4 e OZ are in contact with T cells and CD23(-) follicular dendritic cells.
5 and passive acquisition of FcgammaRIIB from follicular dendritic cells.
6 , with lymphoid aggregates, plasma cells and follicular dendritic cells.
7 receptor (CD21/35) expressed by B cells and follicular dendritic cells.
8 eta2, FLS did not acquire characteristics of follicular dendritic cells.
9 ells (mDC), IFN-gamma-treated monocytes, and follicular dendritic cells.
10 cells with subsequent transfer of the Ag to follicular dendritic cells.
11 igh expression of the LLT1 ligand, CD161, on follicular dendritic cells.
12 ed follicles and lacked germinal centers and follicular dendritic cells.
13 spective of the presence or absence of CD23+ follicular dendritic cells.
14 position of the IC-trapped Ag onto activated follicular dendritic cells.
15 inal centers and impaired retention of Ag by follicular dendritic cells.
16 affinity maturation, and less Ag trapping on follicular dendritic cells.
17 ctive, with variable reactivity observed for follicular dendritic cells.
18 , although these structures appeared to lack follicular dendritic cells.
19 anut agglutinin-positive regions, but lacked follicular dendritic cells.
20 l lymph nodes, splenic germinal centers, and follicular dendritic cells.
21 rimarily on the surface of B lymphocytes and follicular dendritic cells.
22 cells in lymphoid tissues and epidermis, and follicular dendritic cells.
23 ceptors expressed on either B lymphocytes or follicular dendritic cells.
24 to the white pulp allowed virus transfer to follicular dendritic cells.
25 receptor and expressed by mature B cells and follicular dendritic cells.
26 gA(+) B cells, antigen presenting cells, and follicular dendritic cells.
27 regates or germinal centers (GCs) containing follicular dendritic cells.
28 , including fibroblastic reticular cells and follicular dendritic cells.
29 gen-presenting properties of macrophages and follicular dendritic cells.
30 ery of small antigens to cognate B cells and follicular dendritic cells.
31 maturation, despite the lack of identifiable follicular dendritic cells.
32 GC reactions at least in part via effects on follicular dendritic cells.
33 eficiency of CD21/35 proteins on B cells and follicular dendritic cells.
34 endritic cells were unable to migrate toward follicular dendritic cells.
35 he follicle and transported the complexes to follicular dendritic cells.
36 for systemic antigen capture and delivery to follicular dendritic cells.
37 lear how immune complexes are transported to follicular dendritic cells.
38 he presence of germinal center centroblasts, follicular dendritic cells, activation-induced cytidine
39 ly stable pool of virions on the surfaces of follicular dendritic cells and a smaller pool of product
40 and B cell zone disruption, loss of CD35(+) follicular dendritic cells and abnormal recruitment of C
41 gh enhanced Ag retention and presentation by follicular dendritic cells and B cells, respectively.
43 Peyer's patches, splenic marginal zones, and follicular dendritic cells and failed to develop contact
45 ic lymphoid follicles, including networks of follicular dendritic cells and high endothelial venules.
46 sociated with trapping of cell-free virus on follicular dendritic cells and higher numbers of germina
47 ell as from macrophages and accessory cells (follicular dendritic cells and interdigitating cells) an
49 er demonstrated significant L1 expression on follicular dendritic cells and on endothelial cells asso
50 rt that cochlin is specifically expressed by follicular dendritic cells and selectively localized in
51 -cell-rich compartment: follicles containing follicular dendritic cells, and areas lacking such cells
52 ound B cells, CD4(+) cells, dendritic cells, follicular dendritic cells, and fibroblastic reticular c
55 ystem, intranodal prion replication by B and follicular dendritic cells, and potential prion strain s
56 lper cell precursors, and Ag-Ig complexes on follicular dendritic cells are not essential for the per
58 in situ hybridization revealed no detectable follicular dendritic cell-associated HIV RNA in either g
59 lar signature of AITL are contributed by the follicular dendritic cells, B-cell, and other stromal co
60 /-) mice, the NALT in Cxcl13(-/-) mice lacks follicular dendritic cells, BP3(+) stromal cells, and ER
61 NALT of plt/plt mice is nearly normal, with follicular dendritic cells, BP3(+) stromal cells, ERTR7(
62 is transcriptionally active in murine B and follicular dendritic cells, but not in murine T cells.
64 eatments which prevent prions from infecting follicular dendritic cells can block their spread to the
65 les comprising clusters of B lymphocytes and follicular dendritic cells (DC), associated with high en
69 n in SMs; and (4) LT viral burden, including follicular dendritic cell deposition of virus, is increa
70 otoxin alpha1beta2, a cytokine that promotes follicular dendritic cell development and BLC expression
71 idly attenuated and accompanied by perturbed follicular dendritic cell development and immune complex
73 ociated with MAdCAM-1 or alone, whereas NALT follicular dendritic cells expressed both MAdCAM-1 and V
75 ormal B cell-T cell compartmentalization, of follicular dendritic cell (FDC) clusters, and of ability
76 oss of discrete T and B lymphocyte zones, of follicular dendritic cell (FDC) clusters, and of germina
80 rs tend to acquire the most antigen from the follicular dendritic cell (FDC) network and present the
81 cific colocalization of osteopontin with the follicular dendritic cell (FDC) network in lymphatic tis
82 ronment, treatment resulted in a collapse of follicular dendritic cell (FDC) networks and in the disa
83 deficient (TNF-alpha(-/-)) mice lack GCs and follicular dendritic cell (FDC) networks in lymphoid tis
84 cell follicles and are unable to form proper follicular dendritic cell (FDC) networks upon antigenic
85 GC B cells and reduced proliferation in the follicular dendritic cell (FDC) zone of GC, and causes f
87 We have cloned a TNFR family member from a follicular dendritic cell (FDC)-like cell line, FDC-1.
88 es suggested that lymph node macrophages and follicular dendritic cells (FDC) accumulate PrP(Sc).
89 nd adaptive immunity by targeting antigen to follicular dendritic cells (FDC) and B cells via specifi
90 ent studies point to the involvement of both follicular dendritic cells (FDC) and CD11c(+) lymphoid d
91 tor receptor (TNFR-I), organized clusters of follicular dendritic cells (FDC) and germinal centers (G
92 C) B cells undergo complex interactions with follicular dendritic cells (FDC) and T cells in the cour
95 -regulated on GC B cells and up-regulated on follicular dendritic cells (FDC) at all times during the
96 ly, the conduits not only deliver antigen to follicular dendritic cells (FDC) but also provide a rich
97 (Dll1) and Jagged 1 (Jg1), are expressed by follicular dendritic cells (FDC) but not by B cells in t
99 persistence of antigen-antibody complexes on follicular dendritic cells (FDC) have been implicated in
100 r, coreceptor expression was not detected on follicular dendritic cells (FDC) in lymph nodes, suggest
101 pheral exposure, prions replicate first upon follicular dendritic cells (FDC) in the draining lymphoi
103 tain prion strains upon stromal cell-derived follicular dendritic cells (FDC) in the Peyer's patches
104 he formation of germinal centers (GC) around follicular dendritic cells (FDC) is a critical step in t
111 arly replication of some prion isolates upon follicular dendritic cells (FDC) within gut-associated l
112 pulp in neonates, expand in association with follicular dendritic cells (FDC), and localize more cent
113 y enhanced (10-1000-fold) by the addition of follicular dendritic cells (FDC), suggesting that FDC ma
119 ed by proliferating Ki67(+) B cells close to follicular dendritic cells (FDCs) and lacked polarizatio
120 The initial interaction between B cells and follicular dendritic cells (FDCs) appears to be essentia
122 lar within the germinal centers (GCs), where follicular dendritic cells (FDCs) are adjacent to CD4(+)
125 the amount of HIV-1 RNA in virus trapped on follicular dendritic cells (FDCs) decreased almost as qu
127 germinal center (GC) origin, is dependent on follicular dendritic cells (FDCs) for survival and proli
128 he prominent display of opsonized antigen by follicular dendritic cells (FDCs) has long favored the v
129 rminal center (GC) B cells and Ag-presenting follicular dendritic cells (FDCs) have been suggested to
130 dramatically increased deposition of ICs on follicular dendritic cells (FDCs) in germinal centers (G
131 al exposure, many TSE agents accumulate upon follicular dendritic cells (FDCs) in lymphoid tissues be
133 To investigate the role of HIV-1 retained on follicular dendritic cells (FDCs) in this process, we ha
136 ndary lymphoid organs, intimate contact with follicular dendritic cells (FDCs) is required for B cell
137 In the host response to foreign antigens, follicular dendritic cells (FDCs) maintain GCs through t
140 inking also occurs in germinal centers where follicular dendritic cells (FDCs) present multimerized a
141 We reasoned that immune complex (IC)-bearing follicular dendritic cells (FDCs) promote somatic hyperm
146 elieved that Ag in immune complexes (ICs) on follicular dendritic cells (FDCs) selects high affinity
147 ndirect role by promoting the development of follicular dendritic cells (FDCs) that accumulate abnorm
148 ced disease, the network of the processes of follicular dendritic cells (FDCs) that serve as antigen
149 rtmentalization and granular C4d deposits on follicular dendritic cells (FDCs) that typify tertiary l
150 uman immunodeficiency virus (HIV) infection, follicular dendritic cells (FDCs) trap and retain large
152 c interdigitating dendritic cells (IDCs) and follicular dendritic cells (FDCs) using a clinically rel
155 Early PrPSc accumulation takes place on follicular dendritic cells (FDCs) within germinal center
157 s of HIV are found trapped on the surface of follicular dendritic cells (FDCs), and virus persists on
158 mouse scrapie models have shown that mature follicular dendritic cells (FDCs), expressing the host p
159 the presence of highly infectious virions on follicular dendritic cells (FDCs), low frequencies of vi
160 nts in this pathological process is lysis of follicular dendritic cells (FDCs), we investigated the c
161 a mouse scrapie model have shown that mature follicular dendritic cells (FDCs), which express the hos
162 early-life immunity is delayed maturation of follicular dendritic cells (FDCs), which play a central
163 he form of an immune complex (IC) trapped on follicular dendritic cells (FDCs), with germinal center
173 in the form of immune complexes retained on follicular dendritic cells, has been implicated in the d
175 are located in follicles, and contain mature follicular dendritic cells, immune complex deposits, and
176 nd memory cells; B-cell follicles containing follicular dendritic cells in activated germinal centers
182 the virus is trapped within the processes of follicular dendritic cells in the germinal centers of ly
183 not readily infected by HIV, are similar to follicular dendritic cells in their capacity to serve as
184 y CD23+ CD21+ cellular networks representing follicular dendritic cells involved in germinal center r
185 studies indicate that localization of Ag on follicular dendritic cells is not necessary for developm
186 ed that CD21 expression on either B cells or follicular dendritic cells is sufficient to acquire dise
187 of viral antigens by stromal cells, such as follicular dendritic cells, is critical for optimal main
188 suggest that CD21/CD35 on stroma, including follicular dendritic cells, is critical to the maintenan
189 the susceptibility of a human tonsil-derived follicular dendritic cell-like cell line (HK) to prion i
190 ival of GC B cells is supported by a defined follicular dendritic cell-like cell line, we investigate
192 d that MAdCAM-1 and VCAM-1 expressed by NALT follicular dendritic cells may play an important role in
193 B cells, and these include dendritic cells, follicular dendritic cells, monocytes, macrophages, mast
194 lls and NK cells, CD137 is also expressed by follicular dendritic cells, monocytes, mast cells, granu
197 porting the formation and maintenance of the follicular dendritic cell network and of primary B cell
198 ured by the slower decay or increases in the follicular dendritic cell network pool of virions and wi
199 ement within this domain, whereas a distinct follicular dendritic cell network similarly served as th
200 llular phase followed by localization in the follicular dendritic cell network with relatively few in
201 y to the follicle-associated epithelium, the follicular dendritic cell network, the B cell/T cell bou
202 n anti-TNF (etanercept) display a paucity of follicular dendritic cell networks and germinal center (
204 tent with an absence of B cell follicles and follicular dendritic cell networks in secondary lymphoid
206 on, had fewer follicular Th cells, decreased follicular dendritic cell networks, and altered chemokin
207 emistry for T cell/B cell segregation, CD21+ follicular dendritic cell networks, and peripheral lymph
208 , the formation of high endothelial venules, follicular dendritic cell networks, functional B cell ac
209 and have profound defects in development of follicular dendritic cell networks, germinal center form
213 r long term retention of immune complexes on follicular dendritic cells, nor for B cells as antigen-p
214 mocytes, dermal dendritic cells in the skin, follicular dendritic cells of lymph nodes, and in the B
216 xpression on the metastatic cells and within follicular dendritic cells of the metastasis-infiltrated
217 s virions in vivo, such as those surrounding follicular dendritic cells, participate in immune suppre
218 aggregates were screened for the presence of follicular dendritic cells, proliferating B cells and pl
219 ctor secreted by activated T and B cells and follicular dendritic cells promotes B cell growth, survi
220 phocyte compartmentalization, attenuation of follicular dendritic cell reticula, excessive collagen d
223 iver the tonic lymphotoxin signal supporting follicular dendritic cell structure are B cells; thus, B
224 ymphocyte zones with interdigitating CD21(+) follicular dendritic cells, suggesting an in situ immune
226 Our results suggest a possible role for follicular dendritic cells that pick up immune complexes
227 e have identified key molecules expressed on follicular dendritic cells that support the differentiat
228 ent receptor 1 (CR1[CD35]) and CR2 (CD21) on follicular dendritic cells, these mice have a profound d
229 to facilitate their initial delivery toward follicular dendritic cells to establish host infection.
231 t is one of the survival signals provided by follicular dendritic cells to prevent apoptosis in germi
232 ver, adjuvants cannot improve the ability of follicular dendritic cells to retain Ags in the form of
233 ence of high viral replication and extensive follicular dendritic cell virus trapping in one of them.
234 ese mice the early accumulation of prions on follicular dendritic cells was impaired and oral prion d
236 odes and subsequent encounter by B cells and follicular dendritic cells, we used the approach of mult
237 ion of T and B cell zones and development of follicular dendritic cells were affected by the lack of
238 r, immunodeficient mice, which have impaired follicular dendritic cells, were susceptible to scrapie
239 r sinus macrophages and are transferred onto follicular dendritic cells, where they persist for weeks
240 may express HIV-1 for prolonged periods; and follicular dendritic cells, which may hold infectious HI
242 tor 2 (CR2)--which is present on B cells and follicular dendritic cells--with its antigen-bound ligan
243 gut to the brain, they first replicate upon follicular dendritic cells within intestinal Peyer's pat
244 mice exhibited decreased uptake of III-PS by follicular dendritic cells within the germinal centers a
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