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1 V-1 is a major challenge for both active and passive immunization.
2 to a more potent reagent for gene therapy or passive immunization.
3 the use of anti-E2 antibodies as a means of passive immunization.
4 protected mice from a lethal VV challenge by passive immunization.
5 domain Abs have reinvigorated the concept of passive immunization.
6 T-helper cell subset 1 response and enables passive immunization.
7 offers an attractive alternative option for passive immunization.
8 antibodies for virus following active versus passive immunization.
9 transplantation can be reduced by aggressive passive immunization.
10 of infants were protected through active or passive immunization.
11 medical interventions, including active and passive immunization.
12 ced by allergen-specific immunotherapy or by passive immunization.
13 more effective immunogens and antibodies for passive immunization.
14 ization, HSV-1 shedding, and latency through passive immunization.
15 mmunomodulatory effects as well as providing passive immunization.
16 cued spatial reference memory deficits after passive immunization.
17 IgG-FcgammaR interactions during active and passive immunization.
18 otected against systemic GAS challenge after passive immunization.
19 apsule is a potential therapeutic target via passive immunization.
20 prevention of viral acquisition by active or passive immunization.
21 uction before initiating a 12 week course of passive immunization.
22 rgy following prophylactic, therapeutic, and passive immunizations.
23 human immunodeficiency virus (HIV) has made passive immunization a potential strategy for the preven
26 ugh infections within 3 months occur despite passive immunization, affecting 11% in this series; howe
28 rides, an iron scavenging protein, isdB, and passive immunization against clumping factor A and lipot
32 utralizing antibodies that could be used for passive immunization against H5N1 virus or as guides for
34 antibodies (bnAbs) are crucial for effective passive immunization against infectious diseases as prot
35 n-sensitive P23 epitopes may have utility in passive immunization against murine C. parvum infection.
36 activates primary mouse neutrophils ex vivo Passive immunization against NeSt1 decreases pro-interle
37 monoclonal neutralizing antibody (MPV.A4) by passive immunization against papillomavirus infections a
38 D, we investigated the potency of active and passive immunization against the conserved microbial sur
41 tralizing antibodies (nAbs), applied through passive immunization, also provide broad and complete pr
43 Ab has an important potential in therapeutic passive immunization and could help HIV-1 infected patie
44 he importance of the antibody format in oral passive immunization and encourage future expression of
46 such infection that may be prevented by oral passive immunization and might avert recurrent economic
47 imely, given recent progress with active and passive immunization and novel approaches to HIV-1 cure.
48 app = 200 nM) was tested in a mouse model of passive immunization and subsequent mole-equivalent chal
49 man IsdB-specific antibodies also blunt IsdB passive immunization, and additional SA vaccines are sus
50 uorescence assays, growth inhibition assays, passive immunizations, and active immunizations indicate
52 fic antibodies, acquired by either active or passive immunization, are sufficient to protect against
53 We demonstrate that HCV can be blocked by passive immunization, as well as showing that a recombin
55 d; adjunctive therapies (e.g. phage therapy, passive immunization, augmentation of cell mediated bact
56 thermore, when MIP-2 was depleted in vivo by passive immunization, bleomycin-induced pulmonary fibros
58 Here we show that elements of active and passive immunization can be combined to create an effect
60 -CelTOS responses elicited by vaccination or passive immunization can inhibit sporozoite and ookinete
62 ed by active immunization or administered by passive immunization confer protection against S. aureus
63 us and vaccine-heterologous strains, whereas passive immunization confers only vaccine-homologous pro
69 mited the study's ability to address whether passive immunization diminishes perinatal transmission.
72 serum is sufficient to confer protection, a passive immunization experiment using pooled nHgbA antis
74 virus (ZEBOV) have been successfully used in passive immunization experiments in rodent models, but h
76 al passive immunity in fish and fish-to-fish passive immunization experiments supports the concept of
78 isms underlying host resistance, a series of passive immunization experiments were carried out using
81 ersies and summarize active-immunization and passive-immunization experiments in nonhuman primates th
82 om a lethal intranasal challenge with WU2 in passive-immunization experiments in which 10 mug of the
83 only a subset of G(C) MAbs protected mice in passive-immunization experiments, while some nonneutrali
85 eenth century, but the full potential to use passive immunization for infectious diseases has yet to
87 d subcutaneously alone and in combination as passive immunization for young women in South Africa.
90 soluble Abeta and tau levels after active or passive immunization in advanced aged 3xTg-AD mice that
91 omer-specific monoclonal antibody (TOMA) for passive immunization in mice expressing mutant human tau
95 l likely shape efforts to develop active and passive immunization interventions in response to the re
99 ocked TIGR4 adhesion in vitro and, following passive immunization, it protected mice against challeng
100 c antibodies in both the sera and lungs, and passive immunization led to the reduction of B. bronchis
101 a longer period of active immunotherapy, or passive immunization, may be required to provide suffici
102 enal disease is prevented in both active and passive immunization models by antigen-specific IgG1; ot
108 o the control normal mouse immunoglobulin G, passive immunization of BALB/c mice with MAb MoPn-23 res
112 culture systems or studies of protection by passive immunization of human liver chimeric mice offer
114 n of rheumatoid arthritis (RA) by active and passive immunization of mice results in the development
117 t, when performed during progression of HUS, passive immunization of mice with anti-Stx2 antibody pre
127 ight be paired with antibiotic treatment for passive immunization of patients suffering from P. aerug
132 This report examines the effects of chronic, passive immunization on VAbeta and microhemorrhage in PD
134 ns of ETA, may have therapeutic potential in passive immunization or topical treatment of burn patien
135 from nasopharyngeal infection; however, only passive immunization, or vaccination with inactive SpeA,
137 red to controls (5.64; P = 0.0480), and both passive immunizations (PLY = 31.34% loss of retinal func
138 This compensating effect was blocked by passive immunization pretreatment with the monoclonal Ig
139 HIV from infecting target cells and, through passive immunization, protect animals and humans from in
141 thers have demonstrated that both active and passive immunizations reduce Tau pathology and prevent c
145 s to examine pathological outcomes following passive immunization, sequential cross-infection, or vac
146 epithelial neutrophil activating protein by passive immunization significantly attenuated neutrophil
150 with a CD4+ T-cell count of <200 cells/muL, passive immunization strategies need to be explored to p
152 efore increase the potency and durability of passive immunization strategies to prevent HIV-1 infecti
153 s to date have focused on the development of passive immunization strategies to prevent or treat diss
158 e of antibody preparations as a prophylactic passive immunization strategy in large populations.
159 c principles and scientific premises for the passive immunization strategy, including existing and em
160 over, vaccine-induced IgGs were purified for passive immunization studies and for in vitro experiment
168 binations can be validated in vivo in future passive immunization studies using the SHIV challenge mo
172 ccine design, our data have implications for passive-immunization studies in countries where clade C
175 uggest the potential of combining active and passive immunization targeting different immunologic mec
177 clinical studies demonstrate that active and passive immunizations targeting alpha-syn partially amel
178 ct against S. aureus infection of active and passive immunization that targeted 3 proteins involved i
181 ely developed is immunotherapy-specifically, passive immunization through administration of exogenous
182 nfants at high risk of severe RSV disease is passive immunization through monoclonal antibodies.
185 in the presence of maternal immunity or upon passive immunization to rabies virus with the pSG5rab.gp
186 mune evasion tactics of the VoC, we utilized passive immunization to study the effect of early-pandem
187 sceptible populations are often compromised, passive immunization treatments using broadly neutralizi
188 e use this model to test our hypothesis that passive immunization using a single neutralizing monoclo
190 n the absence of an effective HIV-1 vaccine, passive immunization using broadly neutralizing Abs or A
191 of FcRn-transported IgG was demonstrated by passive immunization using herpes simplex virus-2 (HSV-2
195 tly, for the first time, we demonstrate that passive immunization using the antibody NT4X is therapeu
196 -influenza treatments are acutely needed and passive immunizations using broadly neutralizing anti-in
198 r, virus isolated from 1 mouse 3 weeks after passive immunization with 13.2 mg/kg antibody proved res
200 e protected against lethality by intravenous passive immunization with a CPB antibody prior to intrag
206 to Abp2D(RBD) vaccination, demonstrate that passive immunization with Abp2D(RBD)-immune serum transf
209 vent or treat AD, we compared the effects of passive immunization with an anti-Abeta42 mAb, an anti-A
210 laboratory has previously demonstrated that passive immunization with an anti-tau antibody, HJ8.5, d
213 e protected against lethality by intravenous passive immunization with an epsilon toxin antibody prio
214 ion with the amyloid beta (Abeta) protein or passive immunization with anti-Abeta antibodies has bene
215 protein transgenic mice have suggested that passive immunization with anti-Abeta antibodies may clea
220 ction and therefore may benefit greatly from passive immunization with anti-spike monoclonal antibodi
228 he disease are currently available, although passive immunization with C. parvum-specific antibodies
229 ly, studies in these same mice indicate that passive immunization with certain anti-Abeta antibodies
233 studies were designed to compare active and passive immunization with DeltagD-2 versus an adjuvanted
239 on and survival) was completely abrogated by passive immunization with high-titer human anti-MV antib
242 We and others have previously shown that passive immunization with human nMAbs protected adult or
243 AIDS, the potential of pre- and postexposure passive immunization with hyperimmune serum to prevent o
244 llenging with the immunizing antigen, and by passive immunization with IgG or IgE anti-2,4,6-trinitro
247 roups of animals were given one prechallenge passive immunization with immune rabbit serum (IRS), M13
248 uire Ag in sensitized Ig-deficient mice, and passive immunization with immune serum or Ag-specific Ig
249 ministration of additional vaccine doses and passive immunization with long-acting monoclonal antibod
257 (FnBPA) and fibronectin-binding protein B or passive immunization with monoclonal antibodies against
258 e to bind to the surface of M. tuberculosis, passive immunization with monoclonal antibodies directed
261 tion with recombinant PR (rPR) molecules and passive immunization with monoclonal antibodies reactive
266 pithelial neutrophil activating protein; (2) passive immunization with neutralizing antibodies to TNF
267 immunization with nontoxigenic Hla(H35L) or passive immunization with neutralizing monoclonal antibo
269 udy have implications for the improvement of passive immunization with polyclonal or monoclonal antib
271 al challenge with P. yoelii sporozoites than passive immunization with purified IgG from rabbits immu
273 Active immunization with recombinant SasX or passive immunization with rabbit polyclonal anti-SasX Ig
274 ne mice challenged by transplantation and by passive immunization with sera from mice infected with e
275 amyloid peptide (Alphabeta) with vaccines or passive immunization with systemic monoclonal anti-Abeta
276 he aim of this study is to determine whether passive immunization with the 23-valent pneumococcal pol
278 This study reports the effect of active or passive immunization with the conjugates or their antise
283 e we show that the combination of active and passive immunization with vesatolimod may lead to higher