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1 get IL-5R and attenuate eosinophilia through antibody-dependent cellular cytotoxicity.
2 th IgG Fc-mediated complement activation and antibody-dependent cellular cytotoxicity.
3 ors via complement-dependent cytotoxicity or antibody-dependent cellular cytotoxicity.
4 ody for easy-to-neutralize SIV isolates, and antibody-dependent cellular cytotoxicity.
5 r natural killer cells, nor does it diminish antibody-dependent cellular cytotoxicity.
6 ivation of PP2A also decreases human NK-cell antibody-dependent cellular cytotoxicity.
7 diates complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity.
8 esponse, presumably because of their role in antibody-dependent cellular cytotoxicity.
9 zing antibody titers and better induction of antibody-dependent cellular cytotoxicity.
10 suggesting that it is mediated by a form of antibody-dependent cellular cytotoxicity.
11 -mediated phagocytosis, oxidative burst, and antibody-dependent cellular cytotoxicity.
12 ents C1q, C3, C5, and properdin and blocking antibody-dependent cellular cytotoxicity.
13 for immune responses such as phagocytosis or antibody-dependent cellular cytotoxicity.
14 ces from diverse HIV-1 isolates and mediated antibody-dependent cellular cytotoxicity.
15 ces from diverse HIV-1 isolates and mediated antibody-dependent cellular cytotoxicity.
16 -induced (CD4i) antibodies capable of potent antibody-dependent cellular cytotoxicity.
17 elevated natural cytotoxicity, and increased antibody-dependent cellular cytotoxicity.
18 enhancing NK cell-mediated cytotoxicity and antibody-dependent cellular cytotoxicity.
19 ediated by donor-specific antibodies through antibody-dependent cellular cytotoxicity.
20 us virion capture, virus neutralization, and antibody-dependent cellular cytotoxicity.
22 g to FcgammaRIIIA and thereby decreasing the antibody-dependent cellular cytotoxicity activities.
23 te fucose-deficient antibodies with enhanced antibody-dependent cellular cytotoxicity activities.
24 No alteration in gamma-receptor binding and antibody-dependent cellular cytotoxicity activity was ob
25 dy incapable of Fcgamma receptor binding and antibody-dependent cellular cytotoxicity activity, aboli
26 ed with higher serum binding titer, stronger antibody-dependent cellular cytotoxicity activity, and p
27 by generation of reactive oxygen species or antibody-dependent cellular cytotoxicity activity, but l
30 antibodies (Abs), those capable of mediating antibody-dependent cellular cytotoxicity (ADCC) activity
31 oclonal antibodies and subsequently modulate antibody-dependent cellular cytotoxicity (ADCC) activity
32 (Abs) to the V1V2 region of gp120 with high antibody-dependent cellular cytotoxicity (ADCC) activity
33 and that this protection may correlate with antibody-dependent cellular cytotoxicity (ADCC) activity
34 lobulin G1 antibody variant with compromised antibody-dependent cellular cytotoxicity (ADCC) activity
35 ust cross-clade binding and neutralizing and antibody-dependent cellular cytotoxicity (ADCC) activity
36 ngly, the presence of antibodies with potent antibody-dependent cellular cytotoxicity (ADCC) activity
38 ility to opsonize viral particles, to direct antibody-dependent cellular cytotoxicity (ADCC) against
39 b) directs natural killer (NK) cell-mediated antibody-dependent cellular cytotoxicity (ADCC) against
43 cantly greater antibody activities mediating antibody-dependent cellular cytotoxicity (ADCC) and anti
44 iminating latent HIV infection, specifically antibody-dependent cellular cytotoxicity (ADCC) and anti
47 2 immune functions, cytomegalovirus-specific antibody-dependent cellular cytotoxicity (ADCC) and natu
48 These Treg suppressed cetuximab-mediated antibody-dependent cellular cytotoxicity (ADCC) and thei
49 munodeficiency virus type 1 (HIV-1)-specific antibody-dependent cellular cytotoxicity (ADCC) antibody
52 y-dependent cellular phagocytosis (ADCP) and antibody-dependent cellular cytotoxicity (ADCC) assays w
54 phagocytosis, NK cell activation assays, and antibody-dependent cellular cytotoxicity (ADCC) assays.
55 ed cells at all doses and a 52% reduction in antibody-dependent cellular cytotoxicity (ADCC) at doses
56 riggered lysis of multiple myeloma cells via antibody-dependent cellular cytotoxicity (ADCC) but did
57 Natural killer (NK) immune cells mediate antibody-dependent cellular cytotoxicity (ADCC) by aggre
58 ycan fucosylation have been shown to improve antibody-dependent cellular cytotoxicity (ADCC) by allow
59 eptor expressed on NK cells that facilitates antibody-dependent cellular cytotoxicity (ADCC) by bindi
60 ee medium, but had not been shown to inhibit antibody-dependent cellular cytotoxicity (ADCC) by CD16+
63 g antibodies with effector functions such as antibody-dependent cellular cytotoxicity (ADCC) contribu
65 ible (CDi) neutralizing epitopes targeted by antibody-dependent cellular cytotoxicity (ADCC) effector
66 ll-sorting (FACS) analysis, and had enhanced antibody-dependent cellular cytotoxicity (ADCC) effector
67 oss-reactive antibodies capable of mediating antibody-dependent cellular cytotoxicity (ADCC) effector
68 onses at an early time point correlated with antibody-dependent cellular cytotoxicity (ADCC) function
69 virus type 1 (HIV-1) Env and able to mediate antibody-dependent cellular cytotoxicity (ADCC) have bee
70 ng evidence supports a role for HIV-specific antibody-dependent cellular cytotoxicity (ADCC) in contr
71 Although anti-CD52 functions primarily by antibody-dependent cellular cytotoxicity (ADCC) in vivo,
72 -HIV-1 Env IgA antibodies and high levels of antibody-dependent cellular cytotoxicity (ADCC) inversel
74 16-mediated NK cell IFN-gamma production and antibody-dependent cellular cytotoxicity (ADCC) is uncle
77 Nonneutralizing antibodies (Abs) involved in antibody-dependent cellular cytotoxicity (ADCC) may prov
78 and neutrophils for killing of L3 through an antibody-dependent cellular cytotoxicity (ADCC) mechanis
79 able to induce complement-mediated lysis and antibody-dependent cellular cytotoxicity (ADCC) of trans
80 uce CD16 modulation, CD54 up-regulation, and antibody-dependent cellular cytotoxicity (ADCC) on NK ce
82 levels of HIV-1-neutralizing antibodies and antibody-dependent cellular cytotoxicity (ADCC) response
83 itopes) as targets of potentially protective antibody-dependent cellular cytotoxicity (ADCC) response
84 ding IgG and IgA as well as neutralizing and antibody-dependent cellular cytotoxicity (ADCC) response
86 complement-dependent cytotoxicity (CDC) and antibody-dependent cellular cytotoxicity (ADCC) through
87 ith prechallenge serum antienvelope avidity, antibody-dependent cellular cytotoxicity (ADCC) titers,
89 e HIV-1 reservoir.IMPORTANCE Mobilization of antibody-dependent cellular cytotoxicity (ADCC) to elimi
90 protein expressed by infected cells mobilize antibody-dependent cellular cytotoxicity (ADCC) to elimi
92 tes biological effector functions, including antibody-dependent cellular cytotoxicity (ADCC) which is
93 ating the factors that modulate HIV-specific antibody-dependent cellular cytotoxicity (ADCC) will hel
94 t PBMC also kill antibody-opsonized cells by antibody-dependent cellular cytotoxicity (ADCC), a react
96 e breadth of HIV-1 gp120 and V1V2 responses, antibody-dependent cellular cytotoxicity (ADCC), and low
98 Very high IgG binding titers, substantial antibody-dependent cellular cytotoxicity (ADCC), and mod
99 b triggers natural killer (NK)-cell-mediated antibody-dependent cellular cytotoxicity (ADCC), but lit
100 rituximab-mediated antitumor effects include antibody-dependent cellular cytotoxicity (ADCC), complem
101 s may mediate protective effects by means of antibody-dependent cellular cytotoxicity (ADCC), in whic
102 functions, including tier 1 neutralization, antibody-dependent cellular cytotoxicity (ADCC), infecte
103 ide, an immunomodulatory agent that enhances antibody-dependent cellular cytotoxicity (ADCC), is curr
104 hermore, HCD122 is also a potent mediator of antibody-dependent cellular cytotoxicity (ADCC), lysing
105 we demonstrate that XmAb5574 mediates potent antibody-dependent cellular cytotoxicity (ADCC), modest
106 ed up to 3 mg of mAb that possesses enhanced antibody-dependent cellular cytotoxicity (ADCC), nonanti
107 cts on virus infectivity, antibodies mediate antibody-dependent cellular cytotoxicity (ADCC), the kil
108 ese epitopes and sensitize infected cells to antibody-dependent cellular cytotoxicity (ADCC), we trea
109 e, core fucosylation significantly decreases antibody-dependent cellular cytotoxicity (ADCC), whereas
111 Polymorphonuclear leukocytes (PMNs) mediate antibody-dependent cellular cytotoxicity (ADCC), which i
112 Fc N-glycans leads to drastic enhancement of antibody-dependent cellular cytotoxicity (ADCC), while t
113 Cross-reactive influenza virus-specific antibody-dependent cellular cytotoxicity (ADCC)-activati
114 ed that human natural killer (NK) cells, via antibody-dependent cellular cytotoxicity (ADCC)-like mec
115 tion with either lineage induces HA-specific antibody-dependent cellular cytotoxicity (ADCC)-mediatin
135 t complement-dependent cytotoxicity (CDC) or antibody-dependent cellular-cytotoxicity (ADCC), so as t
136 infected cells by natural killer (NK) cells (antibody-dependent cellular cytotoxicity [ADCC]) or comp
138 tosis in the presence of a cross-linker, and antibody-dependent cellular cytotoxicity against B-cell
140 nt, enhances NK-cell direct cytotoxicity and antibody-dependent cellular cytotoxicity against hematop
141 cking core N-glycan residues mediated higher antibody-dependent cellular cytotoxicity against human t
142 An afucosylated Fc form (Pr20M) directed antibody-dependent cellular cytotoxicity against PRAME+H
143 atural killer cells with concurrent enhanced antibody-dependent cellular cytotoxicity against rituxim
144 fic CD16(pos) gammadelta T cells can perform antibody-dependent cellular cytotoxicity against stromal
146 ed in N. benthamiana are capable of inducing antibody-dependent cellular cytotoxicity, an activity no
147 e that immunostimulatory CpG ODN can enhance antibody dependent cellular cytotoxicity and warrant fur
148 ti-IL1RAP antibody capable of both achieving antibody-dependent cellular cytotoxicity and blocking of
149 pecific monoclonal antibodies display robust antibody-dependent cellular cytotoxicity and CD4-depende
150 y programmed immune responses were driven by antibody-dependent cellular cytotoxicity and complement-
151 nal epitopes and mediated both AQP4-directed antibody-dependent cellular cytotoxicity and complement-
152 osed for this therapeutic antibody including antibody-dependent cellular cytotoxicity and complement-
153 ) can induce lysis of neuroblastoma cells by antibody-dependent cellular cytotoxicity and complement-
155 tes killing of infected cells by Fc-mediated antibody-dependent cellular cytotoxicity and complement-
156 f a CD20-targeting antibody had no impact on antibody-dependent cellular cytotoxicity and did not cha
157 emistry, and a target for cetuximab-mediated antibody-dependent cellular cytotoxicity and in vivo eli
158 different cell surface antigens, but not to antibody-dependent cellular cytotoxicity and lymphokine-
159 ne phosphorylation during the development of antibody-dependent cellular cytotoxicity and natural kil
160 redicted susceptibility to cetuximab-induced antibody-dependent cellular cytotoxicity and occurred in
161 tes immunological effector functions such as antibody-dependent cellular cytotoxicity and phagocytosi
162 -negative tumor cells were resistant to both antibody-dependent cellular cytotoxicity and signaling-i
163 lear leukocytes and macrophages that mediate antibody-dependent cellular cytotoxicity and/or trigger
164 ion by activating innate immunity, enhancing antibody dependent cellular cytotoxicity, and serving as
165 both macrophage-dependent FcgammaR-mediated antibody-dependent cellular cytotoxicity, and by direct
166 ability of lumiliximab to mediate apoptosis, antibody-dependent cellular cytotoxicity, and complement
167 ng of infected targets through direct lysis, antibody-dependent cellular cytotoxicity, and production
168 ate effector pathways, such as phagocytosis, antibody-dependent cellular cytotoxicity, and the recrui
169 arcinoma cells were shown to be sensitive to antibody-dependent cellular cytotoxicity, and their in v
170 including complement-dependent cytotoxicity, antibody-dependent cellular cytotoxicity, antibody-depen
171 le mechanisms including apoptosis induction, antibody-dependent cellular cytotoxicity, antibody-depen
174 odification in the Fc domain that eliminates antibody-dependent cellular cytotoxicity at clinically r
175 gest that enhancement of Fc gamma R-mediated antibody-dependent cellular cytotoxicity by inflammatory
176 ivation of the classical complement pathway, antibody-dependent cellular cytotoxicity by innate immun
177 proved complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity compared with r
179 uce Fc-mediated effector functions including antibody-dependent cellular cytotoxicity, complement-dep
180 pe glycans and reported to display increased antibody-dependent cellular cytotoxicity, demonstrates t
181 s, of which the major mechanism of action is antibody-dependent cellular cytotoxicity (eg, trastuzuma
182 he asymmetrically engineered Fc variants for antibody-dependent cellular cytotoxicity enhancement cou
183 an anti-CD38 monoclonal antibody in reverse antibody-dependent cellular cytotoxicity experiments, it
185 Specific killing of C15 cells in in vitro antibody-dependent cellular cytotoxicity has been observ
186 ation and degradation and mediates effective antibody-dependent cellular cytotoxicity in a variety of
187 ing of CD16 (Fc gamma RIIIA), which mediates antibody-dependent cellular cytotoxicity in LAKs, also l
190 3-specific and fusion-inhibition antibodies, antibody-dependent cellular cytotoxicity, lymphoprolifer
192 FL, mechanisms of tumor clearance other than antibody-dependent cellular cytotoxicity may be more imp
193 We consider two alternatives: the first, antibody-dependent cellular cytotoxicity mediated by FcR
194 2M activates natural killer cells to enhance antibody-dependent cellular cytotoxicity, mediates compl
195 ) arm that was derived from broadly binding, antibody-dependent cellular cytotoxicity-mediating antib
196 highest titers of binding, neutralizing, and antibody-dependent cellular cytotoxicity-mediating antib
197 ecific MAbs that showed Galcer blocking, the antibody-dependent cellular cytotoxicity-mediating CH38
198 Our study highlights the potential role that antibody-dependent cellular cytotoxicity might play in a
199 gocytosis of antibody-coated tachyzoites nor antibody-dependent cellular cytotoxicity nor antibody-an
200 diates complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity of CD20-positiv
201 dy inhibits cell growth and induces in vitro antibody-dependent cellular cytotoxicity of human neurob
202 ne neutralization of RANKL with induction of antibody-dependent cellular cytotoxicity of natural kill
204 mulation, by the use of antibodies to induce antibody-dependent cellular cytotoxicity or to block iKI
205 d functional activity (virus neutralization, antibody-dependent cellular cytotoxicity, phagocytosis,
206 nses can be induced through the induction of antibody-dependent cellular cytotoxicity, promotion of a
207 NSCC sensitivity in a manner associated with antibody-dependent cellular cytotoxicity rather than EGF
209 levels of IgA antibodies, and high levels of antibody-dependent cellular cytotoxicity responses and H
210 In each study, protection correlated with antibody-dependent cellular cytotoxicity specific for CD
211 1 Fc protein variant that exhibited enhanced antibody-dependent cellular cytotoxicity, the lack of fu
212 f natural killer cells, the key mediators of antibody-dependent cellular cytotoxicity, to human AMR i
213 ariety of rodent tumor models by stimulating antibody-dependent cellular cytotoxicity toward tumor ve
214 sis of Fc gamma R+ target cells in a reverse antibody-dependent cellular cytotoxicity-type assay and
215 a generalized defect in cytotoxicity because antibody-dependent cellular cytotoxicity was intact.
217 IFN-gamma treatment of monocytes enhanced antibody-dependent cellular cytotoxicity, whereas IFN-ga
218 biting complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity, which suggests
219 In addition, the antibodies did not manifest antibody-dependent cellular cytotoxicity with NOD/SCID s
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