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1 ILI) reports to create a weekly forecast for seasonal influenza.
2 r significantly when comparing pandemic with seasonal influenza.
3 ck/sepsis, and organ failure than those with seasonal influenza.
4 H1N1pdm09 than persons of the same ages with seasonal influenza.
5 ansmission patterns previously described for seasonal influenza.
6 ss hospitalizations that are attributable to seasonal influenza.
7 increase was not greater than observed with seasonal influenza.
8 in lessening the impact of both pandemic and seasonal influenza.
9 casting and vaccination strategies to combat seasonal influenza.
10 g of the much more predictable occurrence of seasonal influenza.
11 e important settings for the transmission of seasonal influenza.
12 erica: respiratory syncytial virus (RSV) and seasonal influenza.
13 ted to institutional outbreak management for seasonal influenza.
14 les in postmortem samples from patients with seasonal influenza.
15 ncidence and rates of antigenic evolution of seasonal influenza?
16 serial passage in MDCK cells inoculated with seasonal influenza A (H1N1) viruses at a low multiplicit
17 The strategy was validated on thousands of seasonal influenza A and B virus-positive specimens usin
18 [HA], neuraminidase [NA], and matrix [M]) of seasonal influenza A and B viruses for next-generation s
19 o the high morbidity and mortality caused by seasonal influenza A virus (IAV) infections in older ind
21 valent influenza vaccine (sTIV) containing a seasonal influenza A virus subtype H1N1 (A[H1N1]) compon
23 ting influenza virus pathogenesis.IMPORTANCE Seasonal influenza A viruses (IAVs) are among the most c
27 iod, with 20 discrete introductions of human seasonal influenza A viruses showing sustained onward tr
29 aused by individual influenza strains (i.e., seasonal influenza A(H1N1), pandemic A(H1N1), A(H3N2), a
30 ic cross-reactivity among humans primed with seasonal influenza A(H3N2) (sH3N2), using postinfection
33 mismatch on IAV reassortment using the human seasonal influenza A/Panama/2007/99 (H3N2) and pandemic
34 estimate was similar in magnitude to that of seasonal influenza, a marked shift toward mortality amon
36 rs for Disease Control and Prevention (CDC), seasonal influenza affects 5% to 20% of the U.S. populat
38 reat due to unpredictable antigenic drift in seasonal influenza and antigenic shifts caused by the em
39 tive as a broadly protective vaccine against seasonal influenza and emerging pandemic threats.IMPORTA
40 ntial for the treatment of both pandemic and seasonal influenza and has a distinct advantage over the
41 o assess human B cell responses to trivalent seasonal influenza and monovalent pandemic H1N1 vaccinat
42 level to quantify the relationships between seasonal influenza and monthly minimum temperature (MIT)
44 ntification of known risk factors for severe seasonal influenza and the more protracted clinical cour
45 Globally, these phenomena are observed with seasonal influenza and with the current coronavirus dise
46 associations between weather variability and seasonal influenza, and growth rates of seasonal influen
47 <5 years of age, the mean annual numbers of seasonal influenza- and RSV-associated all-respiratory d
50 childbearing age, the majority of estimated seasonal influenza-associated deaths occurred in HIV-inf
51 gnant women experienced an increased risk of seasonal influenza-associated mortality compared with no
52 nonpregnant women, the estimated mean annual seasonal influenza-associated mortality rate was 41.2 (8
53 During 1999-2009, the estimated mean annual seasonal influenza-associated mortality rates were 12.6
54 ng pregnant women, the estimated mean annual seasonal influenza-associated mortality rates were 74.9
58 ss analysis, we used a transmission model of seasonal influenza calibrated to 14 seasons of weekly co
59 suggest that previous exposure of humans to seasonal influenza can poise them to respond to avian H7
61 ain outcome is the percentage of prospective seasonal influenza cases identified by the ALERT algorit
69 in hospitalized children aged <18 years with seasonal influenza (during 2003-2009) and 2009 pandemic
71 and seasonal influenza, and growth rates of seasonal influenza epidemics among different age groups
72 of reduced air traffic and the asynchrony of seasonal influenza epidemics among West African countrie
74 vention and treatment for management of both seasonal influenza epidemics and pandemics are desirable
77 query data, this study investigated whether seasonal influenza epidemics in China, the US and the UK
78 evelopment of systems capable of forecasting seasonal influenza epidemics in temperate regions in rea
81 et represents a powerful tool for monitoring seasonal influenza epidemics thanks to aid of self-selec
82 stems that are able to predict irregular non-seasonal influenza epidemics, using either the ensemble
87 e Control and Prevention (CDC) has organized seasonal influenza forecasting challenges since the 2013
89 Asn 177, but not Asn 71 and Asn 104) from a seasonal influenza H1N1 virus, A/Solomon Islands/2006 (S
90 ledge, this is the first time predictions of seasonal influenza have been made in real time and with
91 es was sequence divergence between avian and seasonal influenza hemagglutinin proteins, thus limiting
96 ng oseltamivir with placebo for treatment of seasonal influenza in adults regarding symptom alleviati
99 r burden than the 2009 influenza pandemic or seasonal influenza in terms of hospitalization and morta
102 when there was essentially no circulation of seasonal influenza in the United States, and 2007/2008,
103 fected-recovered type transmission model for seasonal influenza, incorporating the four main strains
104 to currently circulating strains.IMPORTANCE Seasonal influenza infection remains a major cause of di
106 ly with ADCC-Abs to H7N9 NP, suggesting that seasonal influenza infections and vaccinations may induc
117 showed that the antigenic evolution of H3N2 seasonal influenza is generally S-shaped while the genet
118 unger (median age, 47 years) than those with seasonal influenza (median age, 68 years; P < .01), and
119 opical and temperate zones, but estimates of seasonal influenza mortality in developing countries in
120 diagnosis codes in adults hospitalized with seasonal influenza (n = 5270) or 2009 pandemic influenza
123 perience of gradual or regional closures for seasonal influenza outbreaks demonstrates that logistic
124 ing, peak incidence, and total incidence for seasonal influenza outbreaks in 48 states and 95 cities
126 such as a pandemic strain versus a previous seasonal influenza, plays a crucial role in the monitori
127 nts reported assessing need for and stocking seasonal influenza; pneumococcal; tetanus and diphtheria
133 lts aged 65 years and older account for most seasonal influenza-related hospital admissions and death
135 ipants in 15 European countries during three seasonal influenza seasons, allocated 1629 to usual care
139 ccine containing 15 mug of each of the three seasonal influenza strains for that year, as a single do
140 ults indicate prior infection with different seasonal influenza strains leads to radically different
142 ren in Senegal against circulating, pre-2010 seasonal influenza strains, but not against A/H1N1pdm09,
143 model was applied to citywide primary school seasonal influenza surveillance and household surveys fr
144 al-time risk assessments hinging on reliable seasonal influenza surveillance and precise estimates of
146 ate data involving 269 ferrets infected with seasonal influenza, swine influenza, and highly pathogen
147 lutinin (HA)-specific CD4 T-cell memory with seasonal influenza to facilitate antibody production to
148 n this study, we quantified the potential of seasonal influenza to provide memory CD4 T cells that ca
149 ariability appears to be more influential on seasonal influenza transmission in younger (0-14) age gr
152 Similarly, the serological responses to seasonal influenza vaccination are also determined large
159 t this hypothesis, we examined the effect of seasonal influenza vaccination on NK cell function and p
160 e optimal target age groups when extending a seasonal influenza vaccination programme of at-risk indi
161 3N2)v] highlights the need to assess whether seasonal influenza vaccination provides cross-protection
162 ic H1N1 vaccination, as well as pre-pandemic seasonal influenza vaccination to elucidate the effect o
166 ages frequently underperform in response to seasonal influenza vaccination, despite virologic contro
175 el vaccine platforms have been developed for seasonal influenza vaccination: a recombinant HA vaccine
177 antibody response to a trivalent inactivated seasonal influenza vaccine (TIV) and a large number of i
179 l investigation of 274 children who received seasonal influenza vaccine (trivalent inactivated vaccin
180 y, and diabetic subjects vaccinated with the seasonal influenza vaccine across five consecutive seaso
181 determine the effectiveness of the 2010-2011 seasonal influenza vaccine against laboratory-confirmed
183 hildren previously vaccinated with 2009-2010 seasonal influenza vaccine also showed greater expansion
184 e effectiveness (VE) estimates for 2015-2016 seasonal influenza vaccine are reported from Canada's Se
185 nd adaptive response to vaccination with the seasonal influenza vaccine during early childhood, and i
189 a substantial burden worldwide, and current seasonal influenza vaccine has suboptimal effectiveness.
190 s were stratified by documented receipt of a seasonal influenza vaccine in each Medicare beneficiary.
191 experimental studies of the effectiveness of seasonal influenza vaccine in older adults have found 40
195 ed, the medical community's understanding of seasonal influenza vaccine performance remains limited.
196 would be difficult to capture during routine seasonal influenza vaccine programmes, which have extens
201 study there was no evidence to suggest that seasonal influenza vaccine was associated with major mal
203 Influenza C is not included in the annual seasonal influenza vaccine, and has historically been re
204 tudy, 51 healthy adults were vaccinated with seasonal influenza vaccine, and PBMC were collected befo
205 ple, we analyse CD4+ T-cell responses to the seasonal influenza vaccine, establishing a frequency hie
212 riable epitopes in the HA head; (ii) current seasonal influenza vaccines are efficient in inducing B-
216 Finally, we confirm that currently licensed seasonal influenza vaccines can boost preexisting memory
217 from adults ages 48-64 who received multiple seasonal influenza vaccines from 2004 to 2009 for cross-
224 Both natural influenza infection and current seasonal influenza vaccines primarily induce neutralizin
226 barriers, the adjuvant MF59 has been used in seasonal influenza vaccines to increase antibody titers
227 hould be specifically dedicated to improving seasonal influenza vaccines while developing entirely ne
229 ly in the MF59 adjuvant, a component in some seasonal influenza vaccines, in stockpiled, emulsion-bas
233 slightly higher than that seen with previous seasonal influenza vaccines; however, additional results
234 nogenic influenza A epitopes as putative non-seasonal influenza vaccines; one specifically targets th
235 effectiveness against illness caused by the seasonal influenza virus (presumed to all be drifted A/H
241 nza A virus is less stable than other recent seasonal influenza virus HAs, but the molecular interact
242 nogenicity to provide better protection from seasonal influenza virus infection and improve pandemic
249 protective neutralizing Abs, as seen during seasonal influenza virus infections, can be expected to
253 or without CLDC, and challenged with a human seasonal influenza virus isolate, A/Memphis/7/2001(H1N1)
254 which exhibit unusual features compared with seasonal influenza virus NA proteins, are ill-defined.
256 tions about the makeup of the future A(H3N2) seasonal influenza virus population, and we compare pred
257 ragine or threonine in over 99% of all human seasonal influenza virus pre-2009 H1N1, H2N2, and H3N2 s
258 ich prior infection with specific strains of seasonal influenza virus protect from lethal H5N1 challe
259 Thus, in primate cells, MxA inhibits human seasonal influenza virus replication at a step prior to
261 satory effect of E214D is applicable in both seasonal influenza virus strain A/New Caledonia/20/1999
262 sed to determine when sequence variations in seasonal influenza virus strains have affected regions r
263 cross-reactivity between strains in pigs and seasonal influenza virus strains in humans is also impor
266 thesized that it is possible to make a human seasonal influenza virus that is specifically attenuated
268 orating NA, including PIV5-NA, could improve seasonal influenza virus vaccine efficacy and provide pr
271 ns of emergence and circulation of new human seasonal influenza virus variants is a key scientific an
277 nza and emerging pandemic threats.IMPORTANCE Seasonal influenza viruses cause considerable morbidity
286 in the proteolytic activation and spread of seasonal influenza viruses in humans.IMPORTANCE Influenz
289 rule out cross-reactive antibodies to other seasonal influenza viruses to determine whether addition
291 owever, the specific proteases that activate seasonal influenza viruses, especially H3N2 viruses, in
292 way epithelial cells was on par with that of seasonal influenza viruses, mild-to-moderate disease was
294 A(H3N2)v viruses transmit as efficiently as seasonal influenza viruses, raising concern over the pan
295 role of H5N1 PA in altering the virulence of seasonal influenza viruses, we generated a recombinant s
300 volution allows the continual circulation of seasonal influenza, while novel influenza viruses invade