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1 anti-CD14, anti-HLA-DR, anti-CD54, and anti-interleukin 2 receptor.
2 body directed against the alpha chain of the interleukin 2 receptor.
3 activated cells expressing the high-affinity interleukin 2 receptor.
4 is directed against the alpha subunit of the interleukin 2 receptor.
5 -activated T cells express the high-affinity interleukin-2 receptor.
6 FR, VEGFR, PDGFR, NGFR and IGF1R, as well as interleukin-2 receptor.
7 ed the internalization of the complex spCD25-interleukin-2 receptor.
8 sor-cytotoxic, and natural killer cells) and interleukin 2 receptors.
9 , and serum samples were assayed for soluble interleukin-2 receptors.
10 or and also interacts with the CD4, CD8, and interleukin-2 receptors.
11 , or a combination (29/37), elevated soluble interleukin 2 receptor (20/21), and elevated VEGF (16/20
12 in the expression of CD25, the low-affinity interleukin 2 receptor (34% +/- 15% versus 40% +/- 16%).
13 r burden and the presence of soluble (serum) interleukin-2 receptor, a marker associated with a subse
14 ent clinical evidence for the Treg-selective interleukin-2 receptor agonist rezpegaldesleukin (REZPEG
16 nistered intravenously (i.v.) to bind to the interleukin 2 receptor alpha (IL-2R alpha; CD25)-express
17 the type 1 diabetes (T1D) association in the interleukin 2 receptor alpha (IL2RA) gene region to two
20 te (gamma interferon [IFN-gamma] and soluble interleukin 2 receptor alpha [sIL-2Ralpha]) and adaptive
21 co-expressing a chimeric receptor containing interleukin 2 receptor alpha and GP Ibalpha cytoplasmic
22 T-MMP), nor a chimeric MT-MMP containing the interleukin 2 receptor alpha chain (IL-2R) TM and cytopl
24 reased expression of the CD25 marker and the interleukin 2 receptor alpha chain and perturbation of C
25 le-negative CD4-8- thymocytes expressing the interleukin 2 receptor alpha chain, CD25, was also obser
26 stocompatibility complex class I (MHCI), and interleukin 2 receptor alpha subunit (Tac) was compared
27 that transmembrane secretory cargos, such as interleukin 2 receptor alpha subunit or Tac, transferrin
29 h humanized anti-Tac (HAT) directed to CD25 (interleukin 2 receptor alpha) or with MEDI-507 directed
30 le tumor necrosis factor receptor 2, soluble interleukin 2 receptor alpha, soluble gp130, soluble CD2
31 in the absence of CD4(+) T cells express the interleukin 2 receptor alpha-chain (CD25) at lower level
32 hen transferred to the lumenal domain of the interleukin 2 receptor alpha-chain (Tac protein), the cy
33 s of T-cell activation, such as induction of interleukin 2 receptor alpha-chain expression and cytoki
36 zed anti-Tac (HAT) directed toward CD25, the interleukin-2 receptor alpha (IL-2Ralpha) using a human
38 tosis reporter system using a chimera of the interleukin-2 receptor alpha (previously referred to as
40 ecrosis factor receptor 2 (sTNF-R2), soluble interleukin-2 receptor alpha (sIL-2Ralpha), sCD27, B-cel
42 iggered proliferation and of upregulation of interleukin-2 receptor alpha chain (CD25) molecules, but
43 alphabeta T cells expressing high levels of interleukin-2 receptor alpha chain (IL-2R alpha) and maj
45 ipheral immune activation, including soluble interleukin-2 receptor alpha chain (sCD25) levels, as we
46 measured for soluble KIT (sKIT) and soluble interleukin-2 receptor alpha chain (sCD25), which are kn
47 tracellular and transmembrane domains of the interleukin-2 receptor alpha chain (Tac) and the cytopla
48 ) showed a decrease in the expression of the interleukin-2 receptor alpha chain following PMA stimula
49 manized monoclonal antibody specific for the interleukin-2 receptor alpha chain, was safe and efficac
52 I interferon signaling and the interleukin-2/interleukin-2 receptor alpha pathway for the induction o
54 ochemical routes by expression of a chimeric interleukin-2 receptor alpha subunit (Tac)-FcepsilonRI g
55 sterase release, gamma interferon secretion, interleukin-2 receptor alpha upregulation) were neverthe
56 t of a CD8-Nef chimera or in a fusion of the interleukin-2 receptor alpha with an 11-amino-acid regio
57 ts chromatin remodelling to the IL-2Ralpha ('interleukin-2 receptor alpha') gene, which is ectopicall
58 express FasL and Fas, but not CD69 or CD25 (interleukin-2 receptor alpha) and eventually die via apo
59 n, soluble interleukin-1 receptor I, soluble interleukin-2 receptor alpha, and tumor necrosis factor
60 any genes expressed in the thymus, including interleukin-2 receptor alpha, c-myc, and those encoded b
64 orting signal to the cytoplasmic tail of the interleukin-2 receptor alpha-chain caused significant ba
65 2Mit80, an interval that includes Il2ra (for interleukin 2 receptor, alpha chain), a gene that is kno
67 s in interleukin-7 receptor-alpha (IL7RA*C), interleukin-2 receptor-alpha (IL2RA*T), MGAT1 (IV(A)V(T-
68 1beta, and interleukin-7) as well as soluble interleukin-2 receptor-alpha were significantly elevated
69 ry group, whereas interleukin-1beta, soluble interleukin-2 receptor-alpha, interleukin-4, interleukin
70 d a composite biomarker panel of 4 proteins (interleukin-2-receptor-alpha, tumor-necrosis-factor-rece
71 rease induced monocyte expression of surface interleukin 2 receptors and increased expression of HLA-
72 binds specifically to the alpha chain of the interleukin-2 receptor and may thus reduce the risk of r
73 ody that binds to CD25 (alpha subunit of the interleukin-2 receptor) and modulates interleukin-2 sign
74 nd endothelin-1), T cell activation (soluble interleukin-2 receptors), and collagen synthesis (carbox
75 ion through the T cell antigen receptor, the interleukin-2 receptor, and by stimulation of protein ki
76 tients correlate with interleukin-6, soluble interleukin-2 receptor, and interleukin-10 concentration
77 rsely correlated with interleukin-6, soluble interleukin-2 receptor, and interleukin-10 concentration
78 ell depletion induction, 1635 (32%) received interleukin 2 receptor antagonist (IL2-RA), and 2596 (50
79 recipients in 1999-2016 who received ATG or interleukin-2 receptor antagonist (IL2RA) for induction.
80 recipients in 1999-2016 who received ATG or interleukin-2 receptor antagonist (IL2RA) for induction.
83 e clearance was also similar between groups (interleukin-2 receptor antagonist group 56 +/- 20 mL/min
84 e low and similar between groups (10% in the interleukin-2 receptor antagonist group vs 6% in the RAT
85 /plasmapheresis preconditioning regimen with interleukin-2 receptor antagonist induction along with t
86 an 60 min, absence of recipient splenectomy, interleukin-2 receptor antagonist induction, and era.
87 nsplant recipients receive induction with an interleukin-2 receptor antagonist, and basiliximab is th
89 364), antithymocyte globulin (ATG; n=4,930), interleukin-2 receptor antagonists (IL-2RA; n=4,378), or
91 antithymocyte globulin (RATG) compared with interleukin-2 receptor antagonists in a racially diverse
93 tandard induction immunosuppression was with interleukin-2 receptor antagonists, and antithymocyte gl
95 match, rabbit antithymocyte globulin (RATG), interleukin-2 receptor antagonists, tacrolimus (FK), cyc
96 n cells activated in vitro with MTg and anti-interleukin-2 receptor (anti-IL-2R), anti-IL-2, or anti-
97 is more effective than Thymoglobulin or anti-interleukin 2 receptor antibodies cannot be answered at
98 .1%) when compared with those receiving anti-interleukin-2 receptor antibodies (2%) and non-induction
99 splantation outcomes between alemtuzumab and interleukin-2 receptor antibodies (IL-2RA) in living don
100 isk of BPAR compared with induction with the interleukin-2 receptor antibodies (IL-2RAs): basiliximab
102 lso distinguished patients who received anti-interleukin-2 receptor antibodies from those who receive
105 polyclonal antibody or OKT3 (n = 62, 33.5%), interleukin-2 receptor antibody (n = 61, 33%), and no in
106 unosuppressive protocol consisted of an anti-interleukin-2 receptor antibody for induction, and mycop
107 phenolate mofetil, corticosteroids, and anti-interleukin-2 receptor antibody induction, results in im
108 phenolate mofetil, corticosteroids, and anti-interleukin-2 receptor antibody induction, was associate
112 trates the common gamma chain, impairing the interleukin-2 receptor assembly and downstream signallin
113 on the cell surface such as Fas and CD69 and interleukin 2 receptor, at comparable levels as those T
115 n of a chimeric cytokine receptor (the mouse interleukin 2 receptor beta chain [IL-2Rbeta] extracellu
116 n a lymphopenic host upregulate CD44, CD122 (interleukin 2 receptor beta) and Ly6C expression, acquir
118 be relevant in vivo, since p12(I) binds the interleukin-2 receptor beta and gammac chains, raising t
120 sion of the antiapoptotic molecule Bcl-2 and interleukin-2 receptor beta chain and diminished IL-15-d
121 s are indistinguishable, except for enhanced interleukin 2 receptor-beta (IL-2Rbeta) and suppressed i
124 e-1 diabetes, baseline femoral neck T-score, interleukin-2 receptor blockade, and proteinuria (HR 2.0
125 tandard immunosuppression with Thymoglobulin/interleukin 2 receptor blocker and mycophenolate mofetil
126 Daclizumab, a highly humanized, specific interleukin-2 receptor blocker, may be efficacious to th
127 tion treatments (alemtuzumab, thymoglobulin, interleukin-2 receptor blockers, and no induction) given
128 nt reports have demonstrated the efficacy of interleukin-2-receptor blockers in lowering the incidenc
129 lung transplant subjects also expressed the interleukin-2 receptor, but only during the early post-t
130 body directed against the alpha-chain of the interleukin 2 receptor (CD25), has been extensively eval
131 dy directed against the alpha chain of human interleukin-2 receptor (CD25), reduces the incidence of
132 disorders expressing Tac (alpha chain of the interleukin 2 receptor; CD25), physiologic shedding of t
133 organ-based disease, serum levels of soluble interleukin-2 receptor, collagen propeptides (N propepti
135 ed, SIN lentiviral vector encoding the human interleukin 2 receptor common gamma chain (IL2RG) gene a
137 a humanized monoclonal antibody recognizing interleukin-2 receptor (daclizumab), which has proven to
138 onal antibodies that block the high-affinity interleukin-2 receptor expressed on alloantigen-reactive
139 e CD4:CD8 inversion, and marked reduction in interleukin-2 receptor expression by CD4(+) T cells.
141 composed of Tac antigen, the alpha-chain of interleukin 2-receptor, fused to the first five amino ac
142 odeficiency (SCID-X1) caused by mutations in interleukin 2 receptor gamma (IL2RG) gene threatens the
143 nterferon, CCL5, CXCL1, CXCL2, CXCL7, CXCL9, interleukin 2 receptor gamma (IL2Rgamma), IL21R, CCR2, a
144 letely abolished in interleukin 33 (IL-33)-, interleukin 2 receptor gamma chain (IL2ry)-, and interle
146 ), Recombination Activating Gene (Rag)-2 and Interleukin-2 Receptor Gamma (Il2rg) genes were inactiva
147 is due to mutations in the gene encoding the Interleukin-2 receptor gamma chain (IL-2Rgamma), leading
148 of iCD8alpha cells depends on expression of interleukin-2 receptor gamma chain (IL-2Rgammac), IL-15,
149 se of more highly immunocompromised NOD/SCID interleukin-2 receptor gamma chain null (Il2rg(-/-)) mic
150 nicity studies in immunocompromised NOD/SCID interleukin-2 receptor gamma chain null (NSG), immunocom
151 rus-based gamma-retrovirus vector expressing interleukin-2 receptor gamma-chain (gammac) complementar
152 se diabetic/severe combined immunodeficiency/interleukin-2 receptor-gamma-null (NOD-SCID IL2Rgamma(nu
153 se diabetic/severe combined immunodeficiency/interleukin-2 receptor-gamma-null (NSgamma) mice with li
154 brane domain of the Tac subunit of the human interleukin 2 receptor (gp55) fused to the cytoplasmic d
155 body directed against the alpha chain of the interleukin 2 receptor, has been shown to reduce the inc
156 genitors by augmenting responsiveness of the interleukin 2 receptor (IL-2R) and transcription factor
157 or (TfR) expression follows the induction of interleukin 2 receptor (IL-2R) expression in a sequence
160 ells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 prod
161 of alpha, beta, and gamma(c) subunits of the interleukin 2 receptors (IL-2R) in plasma membranes of K
162 f the erythropoietin receptor (EPO-R) or the interleukin-2 receptor (IL-2-R) by their respective liga
165 was associated with a specific deficiency of interleukin-2 receptor (IL-2R) alpha-chain up-regulation
166 expressed activation markers, as measured by interleukin-2 receptor (IL-2R) and transcription factor
167 immunostaining with DEC-205, B7-1, CD4, and interleukin-2 receptor (IL-2R) antibodies and histopatho
169 12(I) binds to the cytoplasmic domain of the interleukin-2 receptor (IL-2R) beta chain that is involv
173 STAT5 transcription factor downstream of the Interleukin-2 receptor (IL-2R) induces expression of Fox
175 (SRL) in combination with chimeric (c-) anti-interleukin-2 receptor (IL-2R) monoclonal antibodies (mA
177 lerance and anti-inflammatory responses, and interleukin-2 receptor (IL-2R) signaling is critical for
180 IgG1 directed against the alpha chain of the interleukin-2 receptor (IL-2R), is a competitive inhibit
181 cts with the beta and gamma(c) chains of the interleukin-2 receptor (IL-2R), the heavy chain of the m
186 ntibody that binds to the alpha chain of the interleukin-2 receptor (IL-2Ralpha), administered for a
187 pansion of alloreactive donor T cells, their interleukin-2-receptor (IL-2R) alpha-chain expression an
190 mmon cytokine receptor gamma chain (NOD/SCID/interleukin 2 receptor [IL2r] gamma(null)) efficiently s
191 dy directed against the alpha subunit of the interleukin 2 receptor, in reducing acute rejection afte
192 IL2RG, which encodes the gamma-chain of the interleukin-2 receptor, in a mouse model of the disease
193 rothrombin activity, urea, white blood cell, interleukin-2 receptor, indirect bilirubin, myoglobin, a
198 ited by the fact that CD25, the low-affinity interleukin-2 receptor, is up-regulated on conventional
199 was distinguished by less T-cell activation (interleukin-2 receptor+), less proliferation (proliferat
200 cells, absolute number of CD8 cells, soluble interleukin-2 receptor level) were sufficient to define
203 d Nf1-deficient T cells, T-cell receptor and interleukin-2 receptor-mediated proliferation of thymocy
204 mes to the more commonly used combination of interleukin-2 receptor monoclonal antibody induction wit
205 inhibitor, cyclosporine A, the chimeric anti-interleukin-2 receptor monoclonal antibody, basiliximab,
206 ocyte polyclonal antibody or basiliximab, an interleukin-2 receptor monoclonal antibody, is most comm
208 assess whether basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, reduced the
211 the absence of downstream events related to interleukin 2 receptor occupancy and/or cell division.
212 and day 4-was selected to block detection of interleukin-2 receptor on 97% of peripheral blood lympho
214 b (Roche Laboratories, Nutley, NJ) block the interleukin-2 receptor on the surface of activated T cel
215 tively, act by binding to the alpha chain of interleukin-2 receptors on activated T lymphocytes.
217 es composed of R73-positive T cells and rare interleukin-2 receptor-positive cells, which was not obs
218 3-positive cells and 88% for the presence of interleukin-2 receptor-positive or HLA-DR-positive cells
219 tion of IgG anti-HLA class II antibodies and interleukin-2 receptor--positive T-cell outgrowth from b
221 a humanized monoclonal antibody against the interleukin-2 receptor, reduced the risk of rejection wi
227 r-like effector nucleases (TALENs) to target interleukin-2 receptor subunit gamma (IL2RG) in pronucle
228 pathogenic germline mutation in the X-linked interleukin-2 receptor subunit gamma gene (IL2RG), which
231 s enzyme provides a crucial link between the interleukin-2 receptor, the protooncogene PKB, and p70 S
233 ride, interleukin-6, interleukin-10, soluble interleukin-2 receptor, tumor necrosis factor-alpha, and
234 tive cells expressing the alpha chain of the interleukin 2 receptor) were removed by immunomagnetic s