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1 beta epitope (in a prior nomenclature for e-antigen specificity).
2 aid in the design of antibodies with altered antigen specificity.
3 described, based on their TCR repertoire and antigen specificity.
4 n induce tumor-specific T cells with defined antigen specificity.
5 s to redirect T cell and natural killer cell antigen specificity.
6 ild-type IgG1 (IgG1/wt) or IgG2 of identical antigen specificity.
7 ditioned secondary recipients, demonstrating antigen specificity.
8 ved with IgG1/wt, IgG2, or IgG4 of identical antigen specificity.
9 fetal antigen, demonstrating their inherent antigen specificity.
10 for ERCC1-XPF were not rigorously tested for antigen specificity.
11 model antigens were preserved demonstrating antigen specificity.
12 tly regulated event and is governed by islet antigen specificity.
13 + regulatory T cells (T(reg)) independent of antigen specificity.
14 reased on memory CD8(+) T cells according to antigen specificity.
15 T cell antigen receptors (TCRs) that confer antigen specificity.
16 terminant of preferential infection based on antigen specificity.
17 ls without impairing phenotype, function, or antigen specificity.
18 emory CD4(+) T-cell subsets, irrespective of antigen specificity.
19 s and effector Th2 cells displaying the same antigen specificity.
20 lation likely requires in vivo generation of antigen specificity.
21 previously derived from IAC, without losing antigen specificity.
22 munoglobulin (Ig) gene usage, clonality, and antigen specificity.
23 entify and isolate NK T cells based on their antigen specificity.
24 gy to produce therapeutic T cells of defined antigen specificity.
25 in, and entered the CNS independent of their antigen specificity.
26 x T cell populations that differ in size and antigen specificity.
27 he heavy and the light chains contributed to antigen specificity.
28 f B cells and for determining their eventual antigen specificity.
29 y time to LAT condensation and alters T cell antigen specificity.
30 ed antitumor CD8(+) T-cell responses require antigen specificity.
31 ing regions (CDR1-CDR3), which contribute to antigen specificity.
32 toire consolidation directly correlated with antigen specificity.
33 tibody properties, such as immunogenicity or antigen specificity.
34 ceptor (TCR) sequence features provide about antigen specificity.
35 fort to tackle the problem of predicting TCR-antigen specificity.
36 ltimodal over unimodal approaches to capture antigen specificity.
37 long-term memory with a broad repertoire of antigen specificity.
38 rally unrelated hapten-BSA adducts confirmed antigen specificity.
39 therapeutics for autoimmunity is the lack of antigen specificity.
40 tumor progression regardless of CD8(+) TILs' antigen specificity.
41 beta chain libraries pre-enriched for target antigen specificity.
42 ss II molecules is as or more important than antigen specificity.
43 sely adjacent Treg cells regardless of their antigen specificity.
44 -specific antibodies is separable from their antigen specificity.
45 B cell helper quality differed depending on antigen specificity.
46 therapeutic functions while still retaining antigen specificity.
47 nd beta-chains contribute to determining TCR antigen specificity.
48 the infused T-cell population had restricted antigen specificity.
49 at allows proliferative responses, enforcing antigen specificity.
50 , thus providing greater scope for differing antigen specificities.
51 n enormous array of receptors with different antigen specificities.
52 madelta T cells rather than constrains their antigen specificities.
53 ment has little role in generating different antigen specificities.
54 e an almost infinitely diverse repertoire of antigen specificities.
55 autoimmune hepatitis, and they have diverse antigen specificities.
56 from different individuals, pathologies, and antigen specificities.
57 (V(H)3-30), despite an apparent diversity of antigen specificities.
58 he generation of pMHC-I molecules of desired antigen specificities.
59 d light-chain BCR sequences to their cognate antigen specificities.
60 fic TILs without previous knowledge of their antigen specificities.
61 ssion, rapid effector responses and 'public' antigen specificities.
62 of the VDJdb in the task of exploring T-cell antigen specificities.
63 te repertoires with extensive collections of antigen specificities.
64 fection of CD4 T cells of different pathogen/antigen specificities.
65 on of DSA (including two new human leukocyte antigen specificities) 2 months after initial bortezomib
66 currently under investigation to (1) confer antigen specificity, (2) enhance T cell effector functio
67 to chronic stimulation, regardless of their antigen specificities, a phenotype reversed by the expre
68 gA and FcgammaR-binding antibodies and among antigen specificities accurately predicted infection sta
72 T cells that regulate CD4(+) and CD8(+) self-antigen specificities and autoimmune diabetes in NOD mic
74 These two subsets differ in their principal antigen specificities and in the T-cell receptor signal
76 unresolved, especially with regard to their antigen specificities and the cellular and molecular pat
78 f CAR T cell products for therapy, including antigen specificity and affinity, metabolic fitness, phe
79 gic memory that has 2 basic characteristics, antigen specificity and an amplified response upon subse
80 two-step staining approach is used to detect antigen specificity and antibody expression: in order to
81 innate immune system, are considered to lack antigen specificity and be devoid of immunological memor
82 ion and purification, the Mbs retained their antigen specificity and bound primary CD8(+) T cells fro
83 combinant IgG-DAF chimeric proteins retained antigen specificity and bound to dansylated Chinese hams
87 ovel TCR transgenic mice with a defined self-antigen specificity and conventional mouse models, we de
89 MHC) tetramer staining to directly correlate antigen specificity and cytolytic ability on a single-ce
90 ts priming of naive CD8+ T cells that retain antigen specificity and cytotoxic function for more than
91 ine staining was used to determine the viral antigen specificity and expression levels of various cyt
94 f human malignancies and, given their target antigen specificity and generally minimal toxicity, are
95 infiltrate into the CNS regardless of their antigen specificity and have the potential to be re-stim
96 erein, we discuss different forms of NK cell antigen specificity and how these responses may be tuned
97 re, we screened related LS-specific TCRs for antigen specificity and identified a peptide derived fro
99 tional techniques being developed to predict antigen specificity and mechanistic basis of TCR targeti
100 and characterization of B-CLL mAbs to study antigen specificity and of B-CLL DNA to investigate mole
102 ed probes and flow cytometry to evaluate the antigen specificity and phenotype of RSV F-specific B ce
108 ition of the signal on the array defined the antigen specificity and the antibody class was defined b
109 iew, the mechanism of action of Tregs, their antigen specificity and their frequency and function in
111 c anaphylaxis in vivo and to investigate the antigen specificity and underlying mechanisms of rapid d
113 Expression of LIR-1 was dependent on CTL-antigen specificity and was associated with a differenti
116 between antibody features (IgG subclass and antigen specificity) and effector function activities (a
117 surface immunoglobulin (sIg), which provides antigen specificity, and a noncovalently associated sign
118 repertoires, classifying CDR3 repertoires by antigen specificity, and distinguishing general patholog
120 tility owing to their biocompatibility, high antigen specificity, and targeted immune stimulation.
121 Despite unorthodox binding, TCR signaling, antigen specificity, and the ability to use CD8 are main
122 of the T cell receptor (TCR), which confers antigen specificity, and the CD8 coreceptor, which stabi
123 populations, which have not taken account of antigen specificity, and understanding their properties
124 e diseases, self-reactive T cells with known antigen specificity appear to be particularly promising
126 is system, clonal naive T cells with defined antigen specificity are generated by retrovirus-mediated
128 d version of E16 was generated that retained antigen specificity, avidity and neutralizing activity.
131 n does little to constrain gammadelta T cell antigen specificities, but instead determines their effe
132 lood-brain barrier (BBB) regardless of their antigen specificity, but studies have focused on CD4 T c
134 Fv and IgG mutant forms were then tested for antigen specificity by ELISA, for tissue specificity by
136 ocytes were quantified by flow cytometry and antigen specificity by in vitro cytokine production.
140 dicate that BCR signal strength, rather than antigen specificity, determines mature B cell fate.
141 crosomal type 1 (LKM-1) showing a remarkable antigen-specificity directed against cytochrome P4502D6.
142 infiltrate dynamics and the requirement for antigen specificity during progression of autoimmune dia
143 olecular phenotypes, architectural contexts, antigen specificities, effector mechanisms and regulator
144 urprisingly, T cell populations differing in antigen specificity expand, contract, and enter the T ce
145 tailored generation of T cells of unlimited antigen specificity for improving the effectiveness of a
146 of the TCR-repertoire underpins the distinct antigen specificity for iNKT cells in peripheral tissues
147 eering of novel T-cell receptors that impart antigen specificity for virally infected or malignant ce
148 very different clinical features relative to antigen specificity; for example, most patients with Weg
151 e of immunosuppressive medications that lack antigen specificity, have many adverse side effects, and
152 and antibody expression: in order to detect antigen specificity, hybridoma cells are incubated with
153 onstraint of fitting a diverse repertoire of antigen specificities in a limited total population of l
155 cells (LT-HSCs) alters the representation of antigen specificities in the peripheral B-cell repertoir
156 The consistency of CD2, CD3, CD11a, and CD45 antigen specificities in thymoglobulin was determined us
157 t parasites and venoms and are the source of antigen specificity in allergic patients, yet the develo
161 these cells lack polyreactivity yet manifest antigen specificity in the context of lipids, shaping MP
162 gether, our data highlight the importance of antigen specificity in the functional dynamics of the T-
163 -related TCR, and therefore sharing the same antigen specificity, invariably shared the same NKG2A co
168 logous peripheral CD8(+) T lymphocytes whose antigen specificity is redirected by transduction with l
169 munity, Lennon et al. demonstrate that islet-antigen specificity is required for accumulation in the
170 The match of T-cell effector function with antigen specificity is thus determined by the type of ba
176 ation and cytokine production independent of antigen specificity, its therapeutic effect is abrogated
179 the post-translational acquisition of novel antigen specificities might play an important role in th
180 ale proteome array to systematically profile antigen specificities of antibody responses to C. tracho
181 current knowledge on the cellular states and antigen specificities of antitumour T cells and examine
183 emory T cells, the developmental origins and antigen specificities of CD8-MP cells remain incompletel
185 the CDR3 regions were found to determine the antigen specificities of T10- and T22-reactive gammadelt
186 roteome and used them to determine the major antigen specificities of the human humoral immune respon
188 ic response after adoptive transfer, but the antigen specificities of the T cells transferred have no
189 cell responses against tumors; however, the antigen specificities of tumor-infiltrating lymphocytes
190 Bispecific antibodies (bsAbs) combine the antigen specificities of two distinct Abs and demonstrat
194 ation is needed to identify the mechanism of antigen specificity of adverse reactions to foods in FPI
196 cells), these entities combine the exquisite antigen specificity of antibodies with the polyfunctiona
198 polyclonal and virus-specific processes, the antigen specificity of B cells in lymphoid tissues of mo
199 emic associated with the origin, target, and antigen specificity of both endogenous and induced regul
201 ase inhibitor (SLPI), and to investigate the antigen specificity of both NE and PR3 ANCA in patients
204 olipin binding, raising the possibility that antigen specificity of certain antibodies may exclusivel
206 ted that costimulatory molecule B7 modulates antigen specificity of CTLs, and provides a missing link
207 regulatory T cells alone can account for the antigen specificity of dominant transplantation toleranc
209 esults challenge current paradigms about the antigen specificity of GvHD effector mechanisms and conf
213 ime (MST), and alloimmune responses, and the antigen specificity of induced tolerance were studied.
214 Furthermore, these studies revealed that the antigen specificity of influenza virus-reactive CD4 and
216 ant role for negative selection in mediating antigen specificity of mature T cells and a molecular me
217 tometry profiling of CD8+ T-cell subsets and antigen specificity of reconstituting CD4+ and CD8+ T ce
220 om KRASMUT have been described, but the fine antigen specificity of T cell responses directed against
221 However, data on lymphocyte dynamics and the antigen specificity of T cells in Ebola survivors are sc
222 ively link intratumoural phenotypes with the antigen specificity of T cells provided by T cell recept
224 ity complex (MHC) multimers which mirror the antigen specificity of T-cell receptor recognition.
226 o, but the extent of this activation and the antigen specificity of the CD8(+) T cells remain uncerta
227 a, implying a common mechanism, the issue of antigen specificity of the cells involved has not yet be
228 enzymes may enable pathogens to subvert the antigen specificity of the humoral immune response to fa
229 for extracellular bacteria, we assessed the antigen specificity of the induction and recall of this
231 s more compelling if concordance between the antigen specificity of the leukocyte antibodies in the d
232 which does not depend upon knowledge of the antigen specificity of the original T cell clone trigger
233 with other dietary proteins, which suggests antigen specificity of the secretion of dietary protein
237 udy, we used two approaches to determine the antigen specificity of the T-cell response to C. neoform
240 lesions (CIMDL), but the pathogenic role and antigen specificity of these antibodies are unknown.
242 comprehensive understanding of the roles and antigen specificity of these endogenous T cells at the i
243 ten contain B cells and plasma cells but the antigen specificity of these intratumoral B cells is not
244 rotection following CNS injury; however, the antigen specificity of these T cells and how they mediat
249 e unresolved issue of antigen-dependency and antigen-specificity of autoimmune disease suppression by
254 the isotype and IgG subclasses, but not the antigen specificity, of the local antibody response.
258 and warn that care must be taken when using antigen-specificity or surface IgG as an indicator of B
260 ave a large antibody repertoire with diverse antigen specificities, poised to react to invading patho
262 Tregs), their anergic phenotype, and diverse antigen specificity present major challenges to harnessi
263 responses of CTL populations that differ in antigen specificity range in magnitude from large, domin
264 let membrane preparations, others have known antigen specificities, reacting with defined islet cell
267 ng the ontogeny of the divergent IgG and IgA antigen specificity repertoires and their effects on ant
269 mber injection of antigen, as shown by their antigen specificity, surface expression of CD8, and capa
270 ces of adaptive immunity, which is built for antigen specificity, tend to produce organ-specific auto
271 ur data indicated that despite their similar antigen specificity, the functional NKT cell subsets wer
272 , and despite the lack of information on TCR antigen specificity, the sharing of top abundant clones
273 uencing approach (linking B cell receptor to antigen specificity through sequencing (LIBRA-seq)) enab
274 resent LIBRA-seq (linking B cell receptor to antigen specificity through sequencing), a technology fo
275 diversity of immune functions by coupling of antigen specificity through the Fab domain to signal tra
276 ith ARLA living in Europe, we aimed to infer antigen specificity through unbiased analysis of TCR rep
277 e we define the minimal requirements for TCR antigen specificity, through an analysis of TCR sequence
278 formation is currently available about their antigen specificity, tissue distribution, and biological
281 ed that CD4(+) T cell clones in mice exhibit antigen specificity towards self-peptides of myelin and
282 y their functional heterogeneity, breadth in antigen specificity, transient appearance in circulation
287 rent regions of the TCR play in affinity and antigen specificity, we have studied the TCR from T cell
288 r bulk CXCR5(+) CD4(+) T cells nor other HIV antigen specificities were associated with gp120-specifi
289 tibodies, 20-1 and NZA6, with very different antigen specificities were found to be highly homologous
291 reg and their immunosuppressive function and antigen specificity were assessed using flow cytometry,
292 hat cytotoxic CD8+ T cells with relevant EBV antigen specificity were detectable in the blood of the
293 O1, O4, A2B5, and HNK-1), each with distinct antigen specificities, were evaluated and found to promo
294 cells from CHB patients, regardless of their antigen specificity, were impaired in their ability to p
295 contain antibodies with numerous and diverse antigen specificities, whereas sera from conidium-expose
296 press either VLRAs or VLRCs of yet undefined antigen specificity, whereas the VLRB antibodies secrete
298 ional plasticity enabling the integration of antigen specificity with environmentally responsive immu
299 s, including surface markers, cytokines, and antigen specificity with modified peptide-MHC tetramers.