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1 is a plausible correlate of attenuation for live viral vaccines.
2 vaccines and most other strategies involving live virus vaccines.
3 ing immunization of a 78-year-old woman with live zoster vaccine.
4 ping a safe and potentially more efficacious live attenuated vaccine.
5 l tropism of a virus is a new approach for a live attenuated vaccine.
6 th -19% (95% CI, -113 to 33; P=0.55) for the live attenuated vaccine.
7 culated for the inactivated vaccines and the live attenuated vaccine.
8 n vivo and supports targeting the SH gene in live attenuated vaccines.
9 ations are good candidates for the design of live attenuated vaccines.
10 ored ILTV vaccines are less efficacious than live attenuated vaccines.
11 onally attenuate hMPV for the development of live attenuated vaccines.
12 man paramyxoviruses for rationally designing live attenuated vaccines.
13 gy, which combines the advantages of DNA and live attenuated vaccines.
14 s that can be mutated to generate successful live attenuated vaccines.
15 o understand virus biology and develop novel live attenuated vaccines.
16 option as safe, immunogenic, and protective live-attenuated vaccines.
17 cell culture has hindered the development of live-attenuated vaccines.
18 ty and activity is a strategy for generating live-attenuated vaccines.
19 ize may be more informative on the safety of live-attenuated vaccines.
20 ortant determinants of the immunogenicity of live-virus oral vaccines.
21 l adjuvants and licensed vaccines, including live attenuated BCG vaccine.
22 should improve the safety and efficacy of a live attenuated RSV vaccine.
23 athology is a key correlate of the safety of live mycobacterial vaccines.
24 because of the potential to generate better live attenuated NDV vaccines.
25 value of including such a mutation in future live attenuated RSV vaccines.
26 eviously exposed to DENV4 infections or to a live attenuated DENV4 vaccine.
27 mune responses following nasal delivery of a live attenuated viral vaccine.
28 d may translate into improved manufacture of live-attenuated hRSV vaccines.
29 lenge model to better evaluate the candidate live attenuated dengue vaccines.
30 une responses elicited by vaccination with a live attenuated type II vaccine.
31 rovirus-like particle vaccines but also as a live-attenuated vectored vaccine.
32 H2N2), the backbone of the licensed seasonal live attenuated influenza vaccine.
33 ich is the backbone of the licensed seasonal live attenuated influenza vaccine.
34 have emerged about the effectiveness of the live attenuated influenza vaccine.
35 oing testing, including genetically modified live-attenuated parasite vaccines.
36 safe and effective platform for creation of live attenuated RNA viral vaccines.
37 he rational development of other efficacious live attenuated flavivirus vaccines.
38 development of safe, stable, and protective live-attenuated arenavirus vaccines.
39 ased approach as a novel strategy to develop live-attenuated arenavirus vaccines.
40 vaccine as well as further reduce costs for live-attenuated oral polio vaccines.
41 ccine, but not to adjuvanted vaccines or the live-attenuated yellow fever vaccine.
42 cell-inducing vaccines, including vectored, live attenuated, and subunit vaccines.
43 enic influenza virus and immunization with a live attenuated influenza virus vaccine.
44 hallenge the level of protection provided by live attenuated oral rotavirus vaccines.
45 ter randomized controlled trial [cRCT]) used live attenuated influenza vaccine, 11 (7 cRCTs) used ina
47 d and the polymerase could be used to design live attenuated vaccines against serious pathogens withi
49 ications for development of both subunit and live-attenuated vaccines against ETEC and other enteric
50 A similar approach may guide the design of live-attenuated vaccines against Lassa and other arenavi
52 88(-/-) and Card9(-/-) mice immunized with a live, attenuated vaccine also fail to acquire protective
54 4 T cell responses elicited by a tetravalent live attenuated dengue vaccine and show that they resemb
55 confirmed in 210 (18%) of 1173 recipients of live attenuated influenza vaccine and 105 (18%) of place
56 dren were randomly assigned, 1174 to receive live attenuated influenza vaccine and 587 to receive pla
57 or the observed reduced effectiveness of the live attenuated influenza vaccine and highlight the unde
58 ht is critical for future rational design of live virus vaccines and their safety evaluation; attenua
59 d, these macaques were boosted i.m. with the live-attenuated trachoma vaccine and their peripheral T
60 r quality control of new lots of the current live-attenuated vaccine and provide insight for the rati
61 applied to current commercial PRRSV modified live-virus (MLV) vaccines and other candidate vaccines.
62 rts superseded by a final report, studies of live-attenuated vaccine, and studies of prepandemic seas
63 mmune responses similar to those elicited by live-attenuated vaccines, and its flexibility permits th
72 ger studies of intradermal administration of live, attenuated zoster vaccine are needed to provide co
74 ults suggest that EHV-1 KyA may be used as a live attenuated EHV-1 vaccine as well as a prophylactic
75 ion may serve as a novel approach to develop live attenuated vaccines as well as antiviral drugs for
76 tivity can lead to the development of novel, live attenuated vaccines, as well as antiviral drugs for
77 ong children whose last vaccine received was live compared with inactivated vaccine, as well as concu
78 l vaccines are typically not as efficient as live attenuated or inactivated vaccines at inducing prot
80 al, we assessed the efficacy and safety of a live attenuated influenza vaccine based on Russian-deriv
81 consideration should be taken when designing live attenuated vaccines based on deletions of nonstruct
82 new avenue for the development of arenavirus live attenuated vaccines based on rearrangement of their
83 se findings provide a pathway for developing live attenuated virus vaccines based on engineering the
84 n children who received minimally attenuated live RSV vaccines but not in children who received highl
85 y exposed to DENV and was immunized with the live attenuated tetravalent vaccine Butantan-DV, develop
86 /1/1981 (eq/GA/81) was selected to produce a live attenuated candidate vaccine by reverse genetics wi
88 excellent safety profile and high stability, live-attenuated CDV vaccines can retain residual virulen
94 DeltamsbB double mutant could provide a new live-attenuated background vaccine candidate strain, and
95 letion (DeltaNS2) to produce the recombinant live-attenuated RSV vaccine candidate DeltaNS2/Delta1313
99 rational development of safe and protective live attenuated vaccine candidates based on genome reorg
101 can be assembled and have been developed as live attenuated vaccine candidates for several flaviviru
102 h potential for further development as novel live attenuated vaccine candidates that may rapidly cont
103 to safely attenuate FMDV and further develop live attenuated vaccine candidates to control such a fea
108 bility of a CD-based approach for developing live-attenuated vaccine candidates against human-pathoge
111 or the rational design of second-generation, live-attenuated, recombinant JEV vaccine candidates.
115 ved at least 1 dose of either inactivated or live attenuated influenza vaccine compared with 0.8%-4.3
116 91, respectively) and for those who received live and inactivated vaccines concurrently compared with
117 have improved the safety of a mouse-adapted live attenuated influenza vaccine containing the same at
118 to receive three injections of recombinant, live, attenuated, tetravalent dengue vaccine (CYD-TDV) o
119 o receive three injections of a recombinant, live, attenuated, tetravalent dengue vaccine (CYD-TDV),
120 as developed a chimeric yellow fever-dengue, live-attenuated, tetravalent dengue vaccine (CYD-TDV) th
121 ve previously shown that a plasmid-deficient live-attenuated trachoma vaccine delivered ocularly to m
122 demonstrated the efficacy of a recombinant, live-attenuated dengue vaccine (Dengvaxia) over the firs
123 People exposed to serotype 4 infections or a live attenuated serotype 4 vaccine developed neutralizin
126 ach to the development of safe and effective live attenuated vaccines directed against VEEV and other
127 ach to the development of safe and effective live attenuated vaccines directed against VEEV and perha
128 ants receiving the monovalent or tetravalent live attenuated DENV vaccine (DLAV), developed by the U.
130 id a combination of a commercially available live fowl poxvirus vaccine expressing the H5 influenza v
132 rtance of the production capabilities of the live attenuated influenza vaccine for pandemic preparedn
133 ade an interim recommendation not to use the live attenuated influenza vaccine for the 2016-2017 infl
136 serve as a novel target to rationally design live attenuated vaccines for aMPV and perhaps other para
137 rstanding may also enable the development of live attenuated vaccines for both RSV and other members
138 for the development of safe and efficacious live attenuated vaccines for hMPV and other human paramy
139 serve as a novel target to rationally design live attenuated vaccines for hMPV and perhaps other para
140 aches would add an HPV component to existing live attenuated vaccines for measles and typhoid fever.
141 s but also facilitate the development of new live attenuated vaccines for VSV, and perhaps other NNS
142 amed BPZE1, is being developed as a possible live nasal vaccine for the prevention of whooping cough.
143 ation highlights the potential need to defer live virus vaccines for at least 6 months in exposed neo
144 r (HZ) vaccines may be an alternative to the live-attenuated HZ vaccine for immunocompromised individ
146 ovided an opportunity to design a successful live-attenuated vaccine for SARS-CoV and opens avenues f
147 novel approach to produce safe and effective live-attenuated vaccines for DENV and other insect-borne
155 ompared with inactivated alone or concurrent live and inactivated vaccines (HR, 0.50; 95% confidence
158 Taken together, our data indicate that a live attenuated HSV-2 vaccine impaired for infection of
159 n could improve the safety and efficacy of a live attenuated RSV vaccine.IMPORTANCE RSV binds to the
161 f protection conferred by a highly effective live attenuated SIV vaccine in the rhesus macaque animal
164 assess the dynamics of genetic reversion of live poliovirus vaccine in humans, we studied molecular
165 nitiated a pilot introduction of the Rotarix live, oral rotavirus vaccine in all public health facili
167 Because concerns exist about the use of live-attenuated vaccines in immunocompromised individual
169 1 envelope (Env) antigens (Ag) for more long-lived, efficacious HIV-1 vaccine-induced B-cell response
170 V biology, including human host-pathogen and live, attenuated vaccine interactions; host and cell typ
175 vaccines.IMPORTANCE The genetic stability of live viral vaccines is important for safety and efficacy
177 tant to prevent the spread of disease, and a live-attenuated MP-12 vaccine is currently the only vacc
179 Rs.IMPORTANCE A chimeric yellow fever-dengue live-attenuated tetravalent vaccine is now being markete
180 rse genetics techniques, we have developed a live-attenuated CIV vaccine (LACIV) for the prevention o
181 za virus infection in humans, we developed a live attenuated H7N9 influenza vaccine (LAIV) with two a
182 e safety and immunogenicity of an avian H5N2 live attenuated influenza vaccine (LAIV H5N2) in healthy
184 the 2 currently licensed influenza vaccines, live attenuated influenza vaccine (LAIV) and inactivated
186 al efficacy and safety of a Russian-backbone live attenuated influenza vaccine (LAIV) at two field si
188 omized, placebo-controlled clinical trial of live attenuated influenza vaccine (LAIV) in children age
190 Whether vaccinating children with intranasal live attenuated influenza vaccine (LAIV) is more effecti
193 on Practices recommended preferential use of live attenuated influenza vaccine (LAIV) over inactivate
194 onses in tonsils and saliva after intranasal live attenuated influenza vaccine (LAIV) vaccination in
195 s of inactivated influenza vaccine (IIV) and live attenuated influenza vaccine (LAIV) were tested by
197 tivated influenza vaccine (TIV) or trivalent live-attenuated influenza vaccine (LAIV) in Thailand.
198 ent 2009 pandemic influenza A(H1N1) virus or live-attenuated influenza vaccine (LAIV) or who had labo
199 l of inactivated influenza vaccine (IIV) and live-attenuated influenza vaccine (LAIV) performed durin
200 mbinant, temperature-sensitive H3N8 CIV as a live-attenuated influenza vaccine (LAIV), which was atte
201 limited immune responses and, in the case of live-attenuated influenza virus vaccines (LAIV), there a
202 months and the effectiveness of quadrivalent live attenuated influenza vaccine (LAIV4) among children
208 pproach to generate safer and more efficient live-attenuated influenza virus vaccines (LAIVs) based o
209 completion, and the chances that one or more live attenuated tetravalent vaccines (LATVs) will be int
210 /LASV reassortant (ML29) is a LASV candidate live-attenuated vaccine (LAV) that has shown promising r
211 ain Edmonston-Zagreb has long been used as a live-attenuated vaccine (LAV) to protect against measles
217 These results suggest that the success of live dengue vaccines may depend on their ability to stim
219 lls play an important but unexpected role in live-attenuated trachoma vaccine-mediated protective imm
221 of illness, and reactogenicity of candidate live dengue virus vaccines of uncertain attenuation.
223 forts include high vaccination coverage with live oral polio vaccine (OPV), surveillance for acute fl
225 er polio eradication is achieved, the use of live-attenuated oral poliovirus vaccine (OPV) must be di
226 cations containing mouse protection data for live attenuated Brucella vaccines or vaccine candidates.
228 ess and safety concerns regarding the use of live attenuated vaccines or potent adjuvants in this pop
229 ated a candidate A/Anhui/2013(H7N9) pandemic live attenuated influenza vaccine (pLAIV) in healthy adu
230 We investigated the HA stability of pandemic live attenuated influenza vaccine (pLAIV) viruses and ob
231 valuation of pairs of wild-type and pandemic live attenuated influenza virus vaccines (pLAIV) represe
233 We generated seven reassortant pandemic live attenuated influenza vaccines (pLAIVs) with the hem
235 us, opening the possibility for its use as a live-attenuated vaccine platform for ZIKV and other clin
238 ls spanning the past 28 years, opposition to live-attenuated HSV vaccines predicated on unfounded saf
240 ere Shan et al. show that a single dose of a live-attenuated Zika vaccine prevents infection, testis
241 In 2013 England and Wales began to fund a live attenuated influenza vaccine programme for individu
242 ummary, our data indicate that attenuated or live viral vaccines promote cytokine-induced memory-like
243 bo-controlled trial of inactivated (IIV) and live-attenuated (LAIV) influenza vaccines provided blood
246 CD8(+) T cell responses elicited by a dengue live attenuated virus (DLAV) vaccine resemble those obse
248 While RABV vaccines are inactivated, the live-attenuated CDV vaccines retain residual virulence f
254 This has implications for the design of live attenuated HPIV3 vaccines; specifically, the antibo
257 d-generation Candid#1 vaccine.IMPORTANCE The live-attenuated Candid#1 vaccine strain of Junin virus i
258 generated a reverse genetics system for the live-attenuated MV vaccine strain Edmonston-Zagreb (EZ),
259 th protection against plague, we developed a live-attenuated vaccine strain by deleting the Braun lip
260 tibility of the glycoprotein of the Candid#1 live-attenuated vaccine strain of JUNV in MACV replicati
262 , we developed nonreverting, nonreplicating, live attenuated uracil auxotroph vaccine strains in the
269 viral infection or as an adverse reaction to live-virus vaccines such as measles, mumps and rubella (
271 Ten subjects previously vaccinated with a live attenuated tetravalent dengue vaccine (TDV) and 4 D
273 sults of vaccinating mice with a new type of live attenuated HSV-2 vaccine that is impaired for infec
274 that might be deleted for the development of live attenuated vaccines that would be safer to use in s
275 enetic engineering now enables the design of live viral vaccines that are potentially transmissible.
276 ica serovar Enteritidis DeltaguaBA DeltaclpX live oral vaccines to protect mice against a highly leth
277 etermine the ability of a single dose of the live attenuated tetravalent dengue vaccine TV003 to indu
278 monstrate the safety and immunogenicity of a live attenuated tetravalent dengue vaccine (TV003), comp
281 o preserve the transcriptional competence of live recombinant viral vaccine vectors in the absence of
284 The A(H1N1)pdm09 virus strain used in the live attenuated influenza vaccine was changed for the 20
287 fective (95% CI, 47 to 70; P<0.001), and the live attenuated vaccine was not observed to be effective
288 t the stalk and catalytic domains of NA as a live attenuated vaccine was shown to confer a strong IAV
289 he 2016-2017 A(H1N1)pdm09 strain used in the live attenuated vaccine was unchanged from 2015-2016, th
291 a VLP, whole inactivated influenza virus, or live attenuated influenza virus vaccines were not protec
292 ruses and human infections, new candidate H5 live attenuated vaccines were developed by using two dif
294 rinary RVF vaccine in the United States is a live-attenuated MP-12 vaccine, which is conditionally li
295 ical disease similar to that provided by the live attenuated commercial vaccines, with no decrease in
296 means to increase the antibody response to a live attenuated HPIV3 vaccine without affecting viral re
298 cohort of 80 individuals immunized with the live attenuated yellow fever vaccine (YFV-17D) by sampli
300 on against herpes zoster (HZ) induced by the live attenuated zoster vaccine Zostavax (ZVL) wanes with
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