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1 co-stimulated with the TLR4-agonist adjuvant monophosphoryl lipid A.
2 OVA) 323-339 plus the inflammatory adjuvant, monophosphoryl lipid A.
3 by using the combined adjuvant of alum plus monophosphoryl lipid A.
4 AS04 comprising alum (Al) and 3-deactylated monophosphoryl lipid A (3-dMPL) afforded HSV-seronegativ
8 accine candidate, in conjunction with either monophosphoryl lipid A, a TLR4 agonist, or CpG, a TLR9 a
10 bined with aluminum and magnesium hydroxide, monophosphoryl lipid A + AddaVax, or Sigma adjuvant syst
11 ied in a dimethyldioctadecylammonium bromide-monophosphoryl lipid A adjuvant and tested for the abili
12 combinant HSV-2 glycoprotein D (gD2) in alum-monophosphoryl lipid A adjuvant only in HSV women serone
13 han the wild-type allergens and a registered monophosphoryl lipid A-adjuvanted vaccine based on natur
14 e in both flight and ground cohorts received monophosphoryl lipid A alone without additional OVA stim
15 ice with PppA protein and either a synthetic monophosphoryl lipid A analog, RC529AF, or a cholera tox
16 5/50 and 50/50 formulations) adjuvanted with monophosphoryl lipid A and Al(OH)3 We present safety and
17 led to incorporate the amphipathic adjuvants monophosphoryl lipid A and cholesterol-modified CpG olig
18 ose promoted by the well-studied TLR agonist monophosphoryl lipid A and comparable to a much larger d
19 10)-adjuvanted HIV-1 DNA prime followed by a monophosphoryl lipid A and QS-21 (MPLA+QS-21)-adjuvanted
20 somal Formulation (ALFQ) adjuvant containing monophosphoryl lipid A and QS-21 (SpFN/ALFQ) has shown p
21 ized with HCV-LP, HCV-LP and adjuvant AS01B (monophosphoryl lipid A and QS21), or HCV-LP and the comb
22 -in-water emulsion plus the immunostimulants monophosphoryl lipid A and the saponin derivative QS21 (
25 nd B5R proteins in an adjuvant consisting of monophosphoryl lipid A and trehalose dicorynomycolate or
26 stimulator of interferon genes pathway, and monophosphoryl lipid A, and a Toll-like receptor 4 agoni
27 free vaccine composed of aluminum hydroxide, monophosphoryl lipid A, and fungal mannan that improved
29 ke particle (VLP) vaccine (with chitosan and monophosphoryl lipid A as adjuvants) to prevent acute vi
32 in D from HSV-2 with alum and 3-O-deacylated monophosphoryl lipid A as an adjuvant; control subjects
33 ) product with MicroCrystalline Tyrosine and monophosphoryl lipid-A as an adjuvant system (Grass MATA
34 A1 was combined with commercially available monophosphoryl lipid A-based adjuvant, and after immuniz
35 determined that Pg OMVs are enriched for C4' monophosphoryl lipid A (C4'-MPLA), an established agonis
36 In this way, the immunostimulant activity of monophosphoryl lipid A can significantly improve the imm
37 protein formulated with either Alhydrogel or monophosphoryl lipid A-containing adjuvants resulted in
40 yrin-phospholipid (dose, 0.4 ug), along with monophosphoryl lipid A (dose, 0.16 ug) and QS-21 (dose,
41 as LPS on aHSCs, indicating specificity, and monophosphoryl lipid A down-regulated fibrogenic markers
42 albumin (OVA) and TLR agonists imiquimod and monophosphoryl Lipid A encapsulated in poly(d,l-lactide-
43 zation with rPhpA-79 protein adjuvanted with monophosphoryl lipid A (for subcutaneous immunization) o
44 dministration of ADX40-Id with 3-O-deacyl-4'-monophosphoryl lipid A further significantly enhanced va
45 ection induced by Leish-111f formulated with monophosphoryl lipid A in a stable emulsion (Leish-111f+
46 subunit vaccine with alum and 3-O-deacylated-monophosphoryl lipid A in subjects whose regular sexual
47 with Om-S-MERS-RBD and adjuvants (Alum plus monophosphoryl lipid A) induced broadly neutralizing ant
48 -MPL (aluminum hydroxide plus 3-O-desacyl-4'-monophosphoryl lipid A) induced robust L2 antibodies (EL
49 combination with lipopolysaccharide (LPS) or monophosphoryl lipid A led to strongly synergistic produ
51 l fatty acid chain length in the 3-O-desacyl monophosphoryl lipid A (MLA) series is shown to be a cri
52 e used to achieve early preconditioning, and Monophosphoryl lipid A (MLA) was used to induce late pre
54 s based on the structure of lipid A, such as monophosphoryl lipid A (MLA), have proven to be safe and
56 ss pollen allergoids containing the adjuvant monophosphoryl lipid A (MPL((R)) ); 51 control patients
57 th either a low or high dose of 3-deacylated monophosphoryl lipid A (MPL) and administered with alum
59 in CHO cells and given intramuscularly with monophosphoryl lipid A (MPL) and alum, or gC2 and gD2 we
61 the liposome-based AS01 with its components, monophosphoryl lipid A (MPL) and QS-21, and TLR ligands.
63 from norovirus GI.1 genotype adjuvanted with monophosphoryl lipid A (MPL) and the mucoadherent chitos
64 ype lectin receptor (CLR) agonist pairing of monophosphoryl lipid A (MPL) and trehalose-6,6'-dicoryno
66 ory molecule SA-4-1BBL with the TLR4 agonist monophosphoryl lipid A (MPL) as a novel vaccine adjuvant
67 uble truncated gD protein (gD2t) in alum and monophosphoryl lipid A (MPL) elicited high neutralizing
69 djuvants microcrystalline tyrosine (MCT) and monophosphoryl lipid A (MPL) in a murine model of HDM al
73 nsisting of glycoprotein D (gD2) in alum and monophosphoryl lipid A (MPL) reduced genital herpes dise
74 capsulation of RTS,S in liposomes containing monophosphoryl lipid A (MPL) resulted in a dose-dependen
75 essed whether prophylactic administration of monophosphoryl lipid A (MPL), a nontoxic derivative of l
76 tranasal (i.n.) immunization of rHagB and if monophosphoryl lipid A (MPL), a nontoxic derivative of t
77 e investigated whether nHgbAI dispensed with monophosphoryl lipid A (MPL), an adjuvant approved for u
78 ) vaccine candidate adjuvanted with alum and monophosphoryl lipid A (MPL), blockade Ab titers peaked
79 the nonspecific biological response modifier monophosphoryl lipid A (MPL), given in vivo or incubated
81 -gp160, formulated with liposomes containing monophosphoryl lipid A (MPL), MPL-AF, proteosomes, emuls
84 (dmLT), when combined with the TLR4 agonist monophosphoryl lipid A (MPL-A), impacted innate and adap
85 we evaluated the effects of adjuvant AS01B (monophosphoryl lipid A [MPL] and QS21), CpG 10105, and t
86 ing IP-10) followed by gp140 formulated with monophosphoryl lipid A (MPLA) +QS-21 adjuvant predominan
87 uvant, with microcrystalline tyrosine (MCT), monophosphoryl lipid A (MPLA) and calcium phosphate (CaP
88 ynthetic particulate carriers co-loaded with monophosphoryl lipid A (MPLA) and CpG as pathogen-like p
89 s can be polarized to kill cancer cells with monophosphoryl lipid A (MPLA) and interferon (IFN) y.
90 The strategy, established with a synthetic monophosphoryl lipid A (MPLA) and known MPLA and diphosp
94 nal adjuvant alum or the molecular adjuvants monophosphoryl lipid A (MPLA) or alpha-galactosylceramid
95 th ovalbumin (OVA) and a molecular adjuvant, monophosphoryl lipid A (MPLA) promoted BMDC maturation a
96 ounds 1 and 33 when used as coadjuvants with monophosphoryl lipid A (MPLA) showed significant enhance
97 inked to keyhole limpet hemocyanin (KLH) and monophosphoryl lipid A (MPLA) to form novel therapeutic
98 (Rha) attached to the 1- and 6'-positions of monophosphoryl lipid A (MPLA) was designed, synthesized,
99 ncapsulated the toll-like receptor 4 agonist monophosphoryl lipid A (MPLA) within hyperbranched polyg
108 cts of VTX-294 and R-848 in combination with monophosphoryl lipid A (MPLA; TLR4) were also assessed.
109 nt synthesizing an adjuvant form of lipid A (monophosphoryl lipid A, MPLA) displayed increased biogen
110 erule-derived proline-rich antigen (rPRA) in monophosphoryl lipid A-oil emulsion adjuvant or a DNA va
111 stable emulsion (SE) with the TLR4 agonists monophosphoryl lipid A or glucopyranosyl lipid A (GLA) h
112 functions were enhanced after treatment with monophosphoryl lipid A or phosphorylated hexa-acyl disac
113 significantly decreased in mice treated with monophosphoryl lipid A or phosphorylated hexa-acyl disac
114 d with lactated Ringer's (vehicle) solution, monophosphoryl lipid A, or phosphorylated hexa-acyl disa
117 CD14 that functionally affects LPS, but not monophosphoryl lipid A, pro-inflammatory cytokine produc
118 d with alum and the detoxified LPS adjuvant, monophosphoryl lipid A, provided some protection to the
119 terol-rich liposomes containing the adjuvant monophosphoryl lipid A results in the production of anti
120 The endogenous production of calcitriol by monophosphoryl lipid A-stimulated DCs appeared to be Tol
121 reas the TLR4 ligands lipopolysaccharide and monophosphoryl lipid A substantially augmented the magni
122 onstrated a lipid-based adjuvant composed of monophosphoryl lipid A, synthetic cord factor, and squal
124 nosinic-polycytidylic acid [poly-IC]), TLR4 (monophosphoryl lipid A), TLR7/8 (3M-012), TLR9 (CpG), or
127 adjuvant, Freund's incomplete adjuvant, and monophosphoryl-lipid A/trehalose dicorynomycolate adjuva