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1 ses antitumor T-cell responses by binding to cytotoxic T-lymphocyte antigen 4.
2 T, insulin like growth factor 1 receptor and cytotoxic T-lymphocyte antigen 4.
3 ssibly by a mechanism involving IL-10 and/or cytotoxic T-lymphocyte antigen 4.
4 as blocking PD-L1 or PD-1, but not PD-L2 and cytotoxic T-lymphocyte antigen 4, abrogated long-term su
6 Interestingly, the co-inhibitory molecules cytotoxic T lymphocyte antigen-4 and B and T lymphocyte
7 b is a human monoclonal antibody that blocks cytotoxic T-lymphocyte antigen 4 and has shown promising
8 more phenotypically exhausted with increased cytotoxic T-lymphocyte antigen 4 and reduced CD28 and CD
10 CD28 costimulation but required CD8+ cells, cytotoxic T lymphocyte antigen-4, and an intact signal t
11 tic melanoma using a fully human antibody to cytotoxic T-lymphocyte antigen-4 (anti-CTLA-4) in conjun
12 anide ISA 51 and received a fully human anti-cytotoxic T-lymphocyte antigen-4 (anti-CTLA-4) monoclona
13 T-cell responses, blocking antibodies (anti-cytotoxic T-lymphocyte antigen 4, anti-programmed death
14 e been developed include ipilimumab, an anti-cytotoxic T lymphocyte antigen 4 antibody that enhances
15 via monoclonal antibodies, such as the anti-cytotoxic T-lymphocyte antigen-4 antibody (ipilimumab),
16 checkpoints (eg, programmed cell death 1 and cytotoxic T-lymphocyte antigen 4), are under investigati
17 ock inhibitory molecules on T cells, such as cytotoxic T lymphocyte antigen-4, are currently under st
18 -induced tumor necrosis factor receptor, and cytotoxic T lymphocyte antigen 4) associated with the T
19 rget antigens, has led to the development of cytotoxic T lymphocyte antigen-4-blocking antibodies as
20 bitor), alone or combined with ipilimumab (a cytotoxic T-lymphocyte antigen-4 checkpoint inhibitor),
21 e for eight polymorphic markers spanning the cytotoxic T lymphocyte antigen-4 ( CTLA-4 ) region of ch
23 fects of blockade of the interaction between cytotoxic T lymphocyte antigen 4 (CTLA-4) and its ligand
25 ntibodies to block negative immune regulator cytotoxic T lymphocyte antigen 4 (CTLA-4) and programmed
26 It remains clear, however, that CD28 and cytotoxic T lymphocyte antigen 4 (CTLA-4) are the critic
30 advances in our understanding of the role of cytotoxic T lymphocyte antigen 4 (CTLA-4) in regulating
32 Ipilimumab, a monoclonal antibody against cytotoxic T lymphocyte antigen 4 (CTLA-4), has been show
33 ctivated T cells that is distinct from CD28, cytotoxic T lymphocyte antigen 4 (CTLA-4), inducible cos
36 s that constitutively express high levels of cytotoxic T lymphocyte antigen-4 (CTLA-4) and suppress T
39 ers of regulatory T cells (Tregs), increased cytotoxic T lymphocyte antigen-4 (CTLA-4) expression, an
46 ties in the phenotypes of mice deficient for cytotoxic T lymphocyte antigen-4 (CTLA-4) or transformin
51 he contribution of the coinhibitory receptor cytotoxic T lymphocyte antigen-4 (CTLA-4) to CD8 T cell
53 oimmunity by increasing surface retention of cytotoxic T lymphocyte antigen-4 (CTLA-4) via interactio
54 also induced by MAb blockade (inhibition) of cytotoxic T lymphocyte antigen-4 (CTLA-4) which downregu
55 ression of CD3 and the TCR, up-regulation of cytotoxic T lymphocyte antigen-4 (CTLA-4), and calcium m
58 co-stimulation blockade-based regimen using cytotoxic T lymphocyte antigen-4 (CTLA-4)-Ig, a CD80- an
60 nt of immune checkpoint inhibitors targeting cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed
61 dels have proven the concept for use of anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4) antibodies in
62 on T-cell activation, whereas engagement of cytotoxic T-lymphocyte antigen 4 (CTLA-4) by these molec
63 forkhead box P3 (FOXP3), and the inhibitory cytotoxic T-lymphocyte antigen 4 (CTLA-4) coreceptor.
64 and/or Mgat5 prevents T cell hyperactivity, cytotoxic T-lymphocyte antigen 4 (CTLA-4) endocytosis, s
65 ssion of programmed death 1 (PD-1) and lower cytotoxic T-lymphocyte antigen 4 (CTLA-4) expression tha
68 or ovalbumin in vivo or in vitro, and CD28, cytotoxic T-lymphocyte antigen 4 (CTLA-4), CD69, and pho
71 ed in a murine tumor xenograft model of anti-cytotoxic T-lymphocyte antigen-4 (CTLA-4) immunotherapy
73 ssion of the negative costimulatory molecule cytotoxic T-lymphocyte antigen-4 (CTLA-4) on T cells mod
74 f the negative T-cell costimulatory receptor cytotoxic T-lymphocyte antigen-4 (CTLA-4) promotes rejec
75 tment with recombinant Wnt-3a and found that cytotoxic T-lymphocyte antigen-4 (CTLA-4) was the most h
76 dies (ipilimumab and tremelimumab) targeting cytotoxic T-lymphocyte antigen-4 (CTLA-4), an inhibitory
77 cytokine secretion without binding to CD28, cytotoxic T-lymphocyte antigen-4 (CTLA-4), and inducible
78 nd SNP descriptor) were studied in subjects: cytotoxic T-lymphocyte antigen-4 (CTLA-4, 49 A>G), human
79 rected against the immune checkpoint protein cytotoxic T-lymphocyte antigen-4 (CTLA-4; CD152)-ipilimu
80 kers for differentiation (CD127) and anergy (cytotoxic T lymphocyte antigen 4 [CTLA-4] and programmed
81 pression (programmed cell death 1 [PD-1] and cytotoxic T-lymphocyte antigen 4 [CTLA-4]) was similar t
84 ulating T cell immune responses via CD28 and cytotoxic T lymphocyte antigen 4 (CTLA4) on T cells.
85 death ligand-1 (PD-1/PD-L1), but not through cytotoxic T lymphocyte antigen 4 (CTLA4), was shown to b
88 New immune checkpoint inhibitors blocking cytotoxic T lymphocyte antigen-4 (CTLA4) or programmed d
94 ween HLA class II genotypes and rs3087243 at cytotoxic T-lymphocyte antigen 4 (CTLA4)/2q33.2 was obta
96 lyses were done to assess the association of cytotoxic T-lymphocyte-antigen 4 (CTLA4) and protein tyr
97 defensin, beta 4A [DEFB4A]) or dermal (IL22, cytotoxic T-lymphocyte antigen 4 [CTLA4], and CCR7) and
98 ion of soluble recombinant fusion protein of cytotoxic T lymphocyte antigen 4 (CTLA4Ig) induces block
99 The dNP2-conjugated cytoplasmic domain of cytotoxic T-lymphocyte antigen 4 (dNP2-ctCTLA-4) negativ
100 latory blockade by in vivo administration of Cytotoxic T-Lymphocyte Antigen 4 fusion protein (CTLA4-I
104 a human monoclonal antibody targeted against cytotoxic T-lymphocyte antigen 4, has shown promise in t
105 of metastatic urothelial carcinoma, tubulin, cytotoxic T-lymphocyte antigen 4, Hsp27, and p53 are nov
106 ectin antagonist; and (ii) a fusion protein, cytotoxic T lymphocyte antigen 4-Ig, which blocks B7-med
107 s combined with suboptimal concentrations of cytotoxic T-lymphocyte antigen 4-Ig or cyclosporine.
108 r does FE depend on Fas, TNF-alpha receptor, cytotoxic T-lymphocyte antigen-4, IL-2, or IFN-gamma.
110 ach of monoclonal antibody against CD154 and cytotoxic T-lymphocyte antigen 4 immunoglobulin, resulte
111 ver, when combined with a suboptimal dose of cytotoxic T-lymphocyte antigen-4 immunoglobulin (200 mic
112 when administered with a suboptimal dose of cytotoxic T-lymphocyte antigen-4 immunoglobulin or cyclo
113 provement in response to abatacept, a CTLA4 (cytotoxic T lymphocyte antigen-4)-immunoglobulin fusion
114 liferation triggered by DCs was abrogated by cytotoxic T lymphocyte antigen 4-immunoglobulin (CTLA-4-
117 cell costimulatory signal from B7-->CD28 by cytotoxic T lymphocyte antigen 4-immunoglobulin fusion p
118 dies reactive against CD80 or by recombinant cytotoxic T-lymphocyte antigen 4-immunoglobulin fusion p
119 from FL-treated B10 (H2b) donors were given cytotoxic T-lymphocyte antigen 4: immunoglobulin (CTLA4I
120 -induced tumor necrosis factor receptor, and cytotoxic T lymphocyte antigen 4 increased significantly
121 rejection, whereas ipilimumab (anti-CTLA-4 [cytotoxic T-lymphocyte antigen-4] mAb) treatment acceler
122 lines how the coinhibitory receptors CTLA-4 (cytotoxic T-lymphocyte antigen-4), PD-1 (programed death
124 and overexpression of regulatory molecules (cytotoxic T-lymphocyte antigen 4, programmed cell death
126 engraftment remains absolutely dependent on cytotoxic T lymphocyte antigen 4 signaling, even after g
127 fts contained high levels of mRNA for foxp3, cytotoxic T lymphocyte antigen-4, TGF-beta, IL-10, and I
128 nd 1 expression, BRAF status, and best prior cytotoxic T-lymphocyte antigen-4 therapy response, then
129 a fully human monoclonal antibody that binds cytotoxic T-lymphocyte antigen 4 to enhance antitumour i
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