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1 significantly increased with reinfection and active immunization.
2 successful strategy to develop a vaccine for active immunization.
3 autoimmune encephalomyelitis independent of active immunization.
4 b titers define protection in the setting of active immunization.
5 ular effectors in the neutropenic host after active immunization.
6 opriate serologic testing and counseling for active immunization.
7 , significantly enhanced T cell responses to active immunization.
8 valuate potential vaccine candidates through active immunization.
9 tion was enhanced in SCI rats via passive or active immunization.
10 e quality of immune responses induced during active immunizations.
11 ng antibody responses, whether by passive or active immunization, a genotyping monitor will be necess
12 evaluated the basis for immunity induced by active immunization against a melanoma differentiation A
13 tive tumor immunity in models of passive and active immunization against a relevant tumor differentia
18 assive immunization with mAb against gp75 or active immunization against gp75 prevented the developme
19 ivable that an immunomodulatory strategy via active immunization against many of these antigens could
20 rpose of this study was to determine whether active immunization against pneumolysin (PLY), or polysa
26 e of the newly characterized oligomers as an active immunization agent targeting amyloid self- assemb
27 n wild-type mice an alternative approach for active immunization: an epitope vaccine that selectively
30 early effector T cells, in combination with active immunization and IL-2, resulted in the eradicatio
31 fficacy of recombinant PotD was evaluated by active immunization and intravenous challenge with capsu
34 We address these controversies and summarize active-immunization and passive-immunization experiments
35 mice are highly resistant to EAE induced by active immunization, and this resistance appears to be m
37 ing viral antigens may be useful for in vivo active immunization as well as ex vivo priming of cytoto
38 ollowing primary infection, reinfection, and active immunization, as well as immune protection in mic
39 e receptor (CCR)2, did not develop EAE after active immunization but generated effector cells that co
42 e in BMT patients is the first evidence that active immunization can reduce morbidity due to herpesvi
43 virus-neutralizing antibodies, together with active immunization, can prevent development of the dise
45 cells, or two injections 7 and 10 days after active immunization, completely blocked development of E
46 vity with anti-IgE autoantibodies induced by active immunization could potentially offer an efficient
47 ired antibody following primary infection or active immunization demonstrated no significant alterati
48 Anti-TECK Ab, elicited in the female mice by active immunization, depleted the ovarian CD8alpha alpha
50 f SasX as a vaccine component in passive and active immunization efforts using mouse infection models
51 In immunoblots, sera from rabbits following active immunization elicited cross-reactive antibodies t
54 ntrast, engagement of OX40 in the setting of active immunization has potent adjuvant properties, lead
58 ndritic cells (DC) as a cellular vaccine for active immunization in healthy volunteers and allogeneic
61 of inducing tumor-specific immunity through active immunization in the absence of defined tumor-asso
63 nhibition assays, passive immunizations, and active immunizations indicated that this outer membrane-
65 from mucosal SIV challenge in the setting of active immunization is more complex than previously reco
70 and complete Freund's adjuvant (CFA)-evoked active immunization models compared to the reference SSA
76 suggest that intervention strategies such as active immunization of human immunodeficiency virus (HIV
77 to improve DC-based immunotherapy; i.e., the active immunization of humans with autologous DCs that h
78 oxidized low-density lipoprotein (oxLDL) and active immunization of hypercholesterolemic mice with ox
83 potential role in host-pathogen interaction, active immunization of mice with recombinant enolase fai
88 to address the effects of anti-amyloid-beta active immunization on neurite trajectories and the path
90 optimal formulation of either a vaccine for active immunization or a polyclonal intravenous IgG or m
91 at S. aureus type 5 CP antibodies induced by active immunization or administered by passive immunizat
92 c T cells, either spontaneously or following active immunization or adoptive transfer, immune-mediate
93 potential of PNAG as a vaccine component for active immunization or as a target for passive antibody
94 ce with MP4 after induction of EAE either by active immunization or by adoptive transfer of activated
95 antibodies may be most efficacious following active immunization or passive administration.IMPORTANCE
96 f this Ab in mice, as a result of passive or active immunization, or by enforced expression of the SM
97 ivation can be elicited in viral infections, active immunization, or cancer immunotherapy, leading to
98 IL-6 deficiency in models of EAE induced by active immunization, passive transfer, T cell transfer,
99 ce of maternal antibody also interferes with active immunization, placing infants at risk for severe
102 ation of efficacy is important in support of active immunization protocols as therapy for, or potenti
109 Together, these data reveal passive and active immunization strategies for prevention or therapy
112 Here, we show the beneficial effects of an active immunization strategy using the SEDI antigenic pe
115 the inter-species cytokine as immunogen for active immunization (TISCAI) to induce anti-cytokine ant
117 the combination strategy using passive plus active immunization to provide protection of infants bor
118 PLP) 139-151 peptide EAE model, we show that active immunizations using CFA but not CpG 1826/IFA as a
119 One notable difference from GN induced by active immunization was a T cell infiltration in the ren
122 everity, or histopathology of EAE induced by active immunization with 100 micro g of myelin oligodend
123 monoclonal antibody GNC92H2 was elicited by active immunization with a cocaine immunoconjugate and b
126 e immunization with Hla-specific antisera or active immunization with a nontoxigenic form of Hla sign
128 cal, and immununological responses following active immunization with a purified Porphyromonas gingiv
130 immunotherapy for human Alzheimer's disease, active immunization with amyloid-beta 1-42 results in th
132 in combination with existing medications is active immunization with antiopioid vaccines, which stim
134 ntine leukocidin (PVL), we evaluated whether active immunization with attenuated forms of Hla (HlaH35
138 iated mortality were effectively reversed by active immunization with dendritic cells treated with HM
140 treptococcal pyrogenic exotoxin A (SpeA), or active immunization with either wild-type or a nonfuncti
141 of murine WN virus infection, and the use of active immunization with envelope protein and passive tr
149 perimental autoimmune uveoretinitis (EAU) by active immunization with interphotoreceptor retinal bind
150 s and the protective efficacy of passive and active immunization with J5 vaccine against experimental
153 y Neisseria meningitidis can be prevented by active immunization with meningococcal polysaccharide or
156 toimmune encephalomyelitis (EAE) produced by active immunization with myelin oligodendrocyte glycopro
161 rosinase-related protein-1 (Tyrp1; gp75) and active immunization with plasmid DNA encoding altered Ty
162 AICAR), in active and passive EAE induced by active immunization with PLP(139-151) or MOG(35-55) and
164 of ligature-induced periodontitis, and that active immunization with porphypain-2 appeared capable o
168 created an experimental mouse model through active immunization with recombinant murine nephrin.
171 In a genetically humanized mouse model, active immunization with sE2 efficiently protected again
175 e present study investigated the efficacy of active immunization with the C-terminal domain of alpha
177 neumococcal keratitis in the rabbit, whereas active immunization with the conserved protein virulence
180 experimental autoimmune uveoretinitis after active immunization with the interphotoreceptor retinoid
184 charide (CP)-specific antibodies elicited by active immunization with vaccines composed of Staphyloco
185 Four groups of infant macaques received active immunizations with subunit Env protein or modifie
186 ll mice were markedly resistant to EAE after active immunization, with drastically impaired recruitme