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1 ctiveness of HD influenza vaccination (vs SD influenza vaccination).
2 influenza-positive HCWs with fever and prior influenza vaccination.
3 After 21 d, subjects received the seasonal influenza vaccination.
4 r (aged >/=65 years) adults before and after influenza vaccination.
5 influenza, had lower odds of having received influenza vaccination.
6 recipients before and 1 month after seasonal influenza vaccination.
7 sponses get boosted in humans after seasonal influenza vaccination.
8 ple roles in inducing protective immunity to influenza vaccination.
9 ng the importance of primary prevention with influenza vaccination.
10 ression on recall T- and B-cell responses to influenza vaccination.
11 in depth both at baseline and in response to influenza vaccination.
12 is several times greater than that following influenza vaccination.
13 ollowing vaccinations of any kind, including influenza vaccination.
14 ous estimates of the disorder after seasonal influenza vaccination.
15 gnificantly influences the human response to influenza vaccination.
16 ssociation of GBS after 2009 monovalent H1N1 influenza vaccination.
17 nses to prophylactic vaccinations, including influenza vaccination.
18 n and memory B cells isolated after seasonal influenza vaccination.
19 to live-attenuated or trivalent-inactivated influenza vaccination.
20 ung and elderly individuals before and after influenza vaccination.
21 arly vaccinations with trivalent-inactivated influenza vaccination.
22 peptides and expansion of one of these after influenza vaccination.
23 ose subjects aged >/= 65 years, 78% received influenza vaccination.
24 ction during pregnancy and the importance of influenza vaccination.
25 After 21 d, all subjects received an influenza vaccination.
26 titers of hemagglutination inhibition after influenza vaccination.
27 are was associated with an increased rate of influenza vaccination.
28 ing is a novel, scalable approach to promote influenza vaccination.
29 mptoms and improved their immune response to influenza vaccination.
30 itamin D (25[OH]D), and humoral responses to influenza vaccination.
31 at baseline and at 2, 6, and 12 weeks after influenza vaccination.
32 elicited a de novo immune response following influenza vaccination.
33 d from 60 SLE patients at baseline and after influenza vaccination.
34 pronounced among patients with prior season influenza vaccination.
35 mount protective immunological responses to influenza vaccination.
36 lar immune reactivity in subjects undergoing influenza vaccination.
37 n coincident temporal association with novel influenza vaccination.
38 % protein) in an established murine model of influenza vaccination.
39 r in inducing protective immune responses to influenza vaccination.
40 e of stillbirth following seasonal trivalent influenza vaccination.
41 dy design, in assessing the effectiveness of influenza vaccination.
42 on therapy can mount effective responses to influenza vaccination.
43 hanisms underlying differential responses to influenza vaccination.
44 nd T-cell responses before and 4 weeks after influenza vaccination.
45 ation could also enhance immune responses to influenza vaccination.
46 ffect of L. casei 431 on immune responses to influenza vaccination.
47 All children had a history of prior influenza vaccinations.
48 za-infected HCWs, 20 had previously received influenza vaccination, 18 had declined the vaccine, and
51 ed hazard ratio, 1.04; 95% CI, 0.68-1.58) or influenza vaccination (adjusted hazard ratio, 1.10; 95%
56 nationwide sample of Medicare beneficiaries, influenza vaccination among adults aged 18-64 years was
58 n interferon transcriptional signature after influenza vaccination and by an inflammation signature a
60 t circulating TFR frequencies increase after influenza vaccination and correlate with anti-flu Ab res
61 conclude that bias is inherent in studies of influenza vaccination and death among elderly patients.
62 o guide and prioritize interventions such as influenza vaccination and HIV prevention in low- and mid
63 lecular events that take place in vivo after influenza vaccination and in the development of better p
64 ral strains could reduce the need for yearly influenza vaccination and increase our preparedness for
66 sought to determine the association between influenza vaccination and major adverse vascular events
67 There were no cases of recurrent GBS after influenza vaccination and none within 6 weeks after any
70 n the analyses revealed associations between influenza vaccination and outcome during noninfluenza se
71 dies have evaluated the relationship between influenza vaccination and pneumonia, a serious complicat
72 sights regarding the serological response to influenza vaccination and raise questions about the adde
73 reafter, L. casei 431) on immune response to influenza vaccination and respiratory symptoms in health
74 on days 0 to 1, adjusted for age group, past influenza vaccination and simultaneous receipt of select
76 ntigen, and there was no association between influenza vaccination and the outcome (adjusted OR, 0.96
78 anging from 10% lower for those who received influenza vaccinations and >or=2 A1c tests, to 43% lower
80 eceiving chemotherapy are able to respond to influenza vaccination, and because this intervention is
81 nd 9 lung transplant recipients who received influenza vaccination, and from 20 healthy unvaccinated
83 sease, were more likely to have received the influenza vaccination, and were less likely to report fe
84 ce; cardiovascular, lung, and renal disease; influenza vaccination; and antiviral administration.
85 larly, the serological responses to seasonal influenza vaccination are also determined largely by non
86 dies in which the fetal benefits of maternal influenza vaccination are evaluated by estimating detect
87 ts suggest that allergic reactions following influenza vaccination are not necessarily related to egg
88 aluate the benefits to the fetus of maternal influenza vaccination because the causal benefit of vacc
91 significant benefit according to adherence, influenza vaccination, body mass index, or baseline vita
92 re, Thailand and Vietnam) had guidelines for influenza vaccination but only two were consistent with
93 on the components of the immune response to influenza vaccination but reduced the duration of upper
94 e the immune response of elderly subjects to influenza vaccination, but its effectiveness has not yet
95 recommendations and should encourage annual influenza vaccination by offering influenza vaccination
96 ark from pregnancies overlapping the A(H1N1) influenza vaccination campaign in Denmark, from November
104 r physicians and the percentage who received influenza vaccination, cholesterol screening, colorectal
105 ad impaired production of antibody following influenza vaccination compared to WT mice (mean antibody
106 ureus exhibited a reduced immune response to influenza vaccination compared with noncolonized partici
107 re to circulating human influenza viruses or influenza vaccination confers immunity to H7N9 strains.
109 examined the association between county-wide influenza vaccination coverage among 520 229 younger adu
113 potential for self-administration can expand influenza vaccination coverage in developing countries.
116 quently underperform in response to seasonal influenza vaccination, despite virologic control of HIV.
122 cination during pregnancy is safe, uptake of influenza vaccination during pregnancy remains low.
124 niors (65+ years) after high-risk groups for influenza vaccination during times of limited vaccine su
125 niors (65+ years) after high-risk groups for influenza vaccination during times of limited vaccine su
127 penic hematological conditions and uptake of influenza vaccination encouraged to further reduce the n
128 n suggests that evaluating immunogenicity of influenza vaccination exclusively by hemagglutination in
129 n Academy of Pediatrics now recommend annual influenza vaccination for all children 6 months through
131 systematic review and meta-analysis assesses influenza vaccination for immunocompromised patients in
134 splantation for annual trivalent inactivated influenza vaccination greater than 3 to 6 months post-ki
135 ategies, but little information exists about influenza vaccination guidelines and vaccine sales.
138 d a history of GBS within 6 weeks of a prior influenza vaccination if they are not at high risk of se
139 not (n = 29) immediately before inactivated influenza vaccination (IIV), 7 d after vaccination, and
142 n a randomized, controlled trial of seasonal influenza vaccination in 773 children aged 6-17 years, w
143 e for circulating Tfh cells (cTfh) following influenza vaccination in adults, but cTfh have not been
146 al decades on how to approach the subject of influenza vaccination in children with egg allergy.
148 teady-state and during the acute response to influenza vaccination in healthy donors, we identify the
149 ted with decreased antibody production after influenza vaccination in healthy human volunteers (P=0.0
152 thors analyzed rates of 2009 pandemic A/H1N1 influenza vaccination in Montreal, Quebec, Canada, using
155 ential strategies to improve the efficacy of influenza vaccination in patients with cancer, such as t
156 re is uncertainty about the effectiveness of influenza vaccination in persons with asthma and its imp
159 tional study in Laos to assess the effect of influenza vaccination in pregnant women on birth outcome
160 We estimated the effectiveness of documented influenza vaccination in preventing laboratory-confirmed
162 aphic factors that influence the response to influenza vaccination in SLE patients with a broad range
164 cumulative proportions of persons reporting influenza vaccination in the 2004-2005 through 2010-2011
165 icate that the inferior antibody response to influenza vaccination in the elderly is primarily due to
166 been implicated in poor Ab responsiveness to influenza vaccination in the elderly, most of whom are C
169 isk among children whose mothers received an influenza vaccination in their first trimester, but the
170 and meta-analyses to assess the evidence for influenza vaccination in this group, and we report our r
171 Safety and immunogenicity data of seasonal influenza vaccination in transplanted patients (Tps) are
172 public health agency initiated school-based influenza vaccination in two Wisconsin elementary school
173 .77, p = 0.001), and 66% compared to 59% had influenza vaccinations in the past year (odds ratio 1.35
178 CD4 T cell formation following cold-adapted influenza vaccination is boosted when Ag is administered
181 infection history in targeting and promoting influenza vaccination is predicted to be a highly effect
183 R, a booster strategy 5 weeks after standard influenza vaccination is safe and effective and induces
188 sequencing to dynamically track responses to influenza vaccination, Jackson et al. find evidence of c
191 observational studies suggest that previous influenza vaccination may influence the immunogenicity a
192 from some recent studies have suggested that influenza vaccination might also prevent adverse pregnan
194 0 years ago, it was observed that sequential influenza vaccination might lead to reduced vaccine effe
198 suggests that the large fetal benefits from influenza vaccination observed in epidemiologic studies
199 BS cases' occurring during the 6 weeks after influenza vaccination of 45 million persons, an 8.8-fold
203 Many national guidelines recommend annual influenza vaccination of immunocompromised patients, alt
204 dy evaluated the effectiveness of postpartum influenza vaccination of mothers and household members i
205 formed to determine the efficacy of antennal influenza vaccination of mothers plus pneumococcal conju
213 network to further investigate the effect of influenza vaccination on influenza severity in adults ag
214 ough June 2012 to evaluate the effect of HCP influenza vaccination on mortality, hospitalization, and
215 pothesis, we examined the effect of seasonal influenza vaccination on NK cell function and phenotype
216 ecent reports of a negative impact of serial influenza vaccination on vaccine effectiveness (VE) rais
217 red memory T cell and Ab responses following influenza vaccination or infection, we investigated the
219 be concluded from these recent studies that influenza vaccination overall is of public health benefi
220 ere not correlated with humoral responses to influenza vaccination (P = 0.863), and BLyS levels incre
221 reinforce current recommendations for annual influenza vaccination, particularly those at greatest ri
222 mework to evaluate the cost-effectiveness of influenza vaccination policies in developing countries a
225 , and for therapeutic applications including influenza vaccination, polio vaccination, and diabetes a
227 italizations during 3 influenza seasons, and influenza vaccination prevented 61.2% of such hospitaliz
236 t activation of the RIG-I pathway along with influenza vaccination programs the innate immunity to in
240 ghlights the need to assess whether seasonal influenza vaccination provides cross-protection against
241 emonstrate that the early B-cell response to influenza vaccination, quantified by the frequency of in
242 Antibody titers decrease with time following influenza vaccination, raising concerns that vaccine eff
244 gh recommended by many and mandated by some, influenza vaccination rates among health care workers, e
246 nal and infant mortality/morbidity; however, influenza vaccination rates of pregnant women remain und
247 ons to vaccinate surgical inpatients against influenza, vaccination rates remain low in this populati
254 vel, physician office visits, and history of influenza vaccination (RR(9-17 years) = 1.20, RR(18-26 y
255 D are colonized with S aureus, intramuscular influenza vaccination should be given preference in thes
257 ithout laboratory-confirmed influenza and by influenza vaccination status among subjects with influen
260 had adequate respiratory samples, had known influenza vaccination status, and were community-dwellin
265 duction of memory T- and B-cell responses to influenza vaccination supports the recommendation to vac
266 in inducing protective antibody responses to influenza vaccination than CD4 T cell-deficient mice.
268 to innate cytokines were also enhanced after influenza vaccination; this was associated with prolifer
269 took advantage of the pandemic 2009 A(H1N1) influenza vaccination to conduct a longitudinal integrat
270 accination, as well as pre-pandemic seasonal influenza vaccination to elucidate the effect of the adj
271 these findings reinforce the need for yearly influenza vaccination to prevent infection, and raise ne
273 introduce dissolving microneedle patches for influenza vaccination using a simple patch-based system
277 We assessed the relative effectiveness of HD influenza vaccination (vs SD influenza vaccination).
283 010-2011 and 2011-2012 US influenza seasons, influenza vaccination was associated with a three-quarte
284 l IgG or anti-Gal IgG, respectively, whereas influenza vaccination was associated with higher anti-no
289 Of patients for whom data was available, influenza vaccination was reported in 3289 (28.7%) of 11
290 tic regression analyses showed that maternal influenza vaccination was significantly associated with
291 trimester-specific analyses, first-trimester influenza vaccination was the only period associated wit
293 : Use of dissolvable microneedle patches for influenza vaccination was well tolerated and generated r
294 wing BCG vaccination, nonspecific effects of influenza vaccination were also observed, with modulatio
296 ancy modifies the humoral immune response to influenza vaccination will aid in maximizing vaccine eff
297 ctiveness of the Scottish pandemic H1N1 2009 influenza vaccination with a retrospective cohort design
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