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9 n December 2013 and January 2016, 36 bacille Calmette-Guerin-vaccinated, healthy UK adults were rando
10 e show in this article that although bacille Calmette-Guerin controlled M. tuberculosis growth for 7
11 odeficiency virus (HIV)-infected and bacille Calmette-Guerin (BCG)-immunized adults with CD4 cell cou
12 medical illness, isoniazid use, and bacille Calmette-Guerin strain did not substantially affect vacc
13 y to nontuberculous mycobacteria and bacille Calmette-Guerin vaccination may account for a proportion
14 n rates and responses to tetanus and Bacille Calmette-Guerin vaccines among HEU and HUU vaccinees.
15 rain of Mycobacterium bovis known as bacille Calmette-Guerin (BCG) has been widely used as a vaccine
19 erium tuberculosis vaccines to boost bacille Calmette-Guerin or for those who cannot be immunized wit
20 osis Ag 85A (M.85A), strongly boosts bacille Calmette-Guerin (BCG)-induced Ag 85A specific CD4(+) and
21 strict growth of Mycobacterium bovis bacille Calmette Guerin and Mycobacterium tuberculosis was impai
22 ollow the migration of live M. bovis Bacille Calmette-Guerin (BCG) and to observe interactions with e
23 Vaccination with Mycobacterium bovis bacille Calmette-Guerin (BCG) has variable efficacy in preventin
24 ells specific to Mycobacterium bovis bacille Calmette-Guerin (BCG) in the lungs, and the IFN-gamma CD
26 expansion during Mycobacterium bovis Bacille Calmette-Guerin (BCG) infection and a clear memory-type
27 ls responding to Mycobacterium bovis bacille Calmette-Guerin (BCG) infection and disrupt granuloma fo
30 sing intradermal Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination as a surrogate for M.
31 conferred by the Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccine are multifaceted and poorl
33 um smegmatis and Mycobacterium bovis bacille Calmette-Guerin (BCG), which respectively induce high an
37 that exposure of Mycobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thiacetazone
38 Infection with Mycobacterium bovis bacille Calmette-Guerin resulted in approximately 10-fold-higher
39 tuberculosis and Mycobacterium bovis bacille Calmette-Guerin similarly home to established granulomas
41 tuberculosis and Mycobacterium bovis bacille Calmette-Guerin, release MVs when growing in both liquid
43 detect antibody responses induced by bacille Calmette-Guerin (BCG) vaccination and active tuberculosi
45 days) than mice infected with either bacille Calmette-Guerin (BCG) vaccine or virulent M. tuberculosi
46 l Ags in the context of experimental bacille Calmette-Guerin (BCG) vaccination, Ag-specific T cell re
48 ries was 2.3 weeks (IQR 1.4-4.6) for bacille Calmette-Guerin (BCG); 2.4 weeks (1.2-3.3) for diphtheri
51 the standard-of-care immunotherapy, bacille Calmette-Guerin (BCG), constitute a challenging patient
52 une correlates of TB disease risk in Bacille Calmette-Guerin (BCG) immunized infants from the MVA85A
54 bovis bloodstream infection (BSI) in bacille Calmette-Guerin (BCG)-vaccinated children with human imm
55 ibit mycobacterial growth, including Bacille Calmette-Guerin (BCG) and Mycobacterium tuberculosis (MT
60 hown that systemic administration of Bacille Calmette-Guerin (BCG) or beta-glucan reprograms HSCs in
61 RAs in individuals with a history of Bacille Calmette-Guerin (BCG) vaccination after infancy or with
62 Approximately 100 million doses of bacille Calmette-Guerin (BCG) vaccine are given each year to pro
63 nd pyrazinamide restricted growth of bacille Calmette-Guerin but not wild-type Mycobacterium bovis, w
64 e, M72/AS01, in a phase IIa trial of bacille Calmette-Guerin-vaccinated, HIV-uninfected, and Mycobact
65 th environmental mycobacteria and/or bacille Calmette-Guerin (BCG) vaccination compromise the estimat
66 e-promastigote vaccine cocktail plus bacille Calmette-Guerin (BCG) adjuvant significantly reduced the
68 tion involves the use of recombinant bacille Calmette-Guerin (rBCG) overexpressing protective TB anti
70 ection in Mycobacterium bovis strain bacille Calmette-Guerin (BCG)-induced granulomas using an immuno
72 n sharp contrast, the vaccine strain bacille Calmette-Guerin as well as RD-1 and ESAT-6 mutants of H3
74 We have previously established that bacille Calmette-Guerin (BCG), an attenuated form of Mycobacteri
75 erculosis every year even though the bacille Calmette Guerin (BCG) vaccine has been available for mor
76 Policies regarding the use of the Bacille Calmette-Guerin (BCG) vaccine for tuberculosis vary grea
77 stence of therapeutic agents and the bacille Calmette-Guerin (BCG) vaccine have not significantly aff
78 r specificity in those receiving the bacille Calmette-Guerin vaccine and poor sensitivity in individu
82 ected macaques previously exposed to bacille Calmette-Guerin (BCG) were reinfected with BCG, were tre
84 and existing ones improved to treat bacille Calmette-Guerin-refractory superficial bladder cancer.
86 mycobacterial challenge model, using bacille Calmette-Guerin (BCG) as a surrogate for a Mycobacterium
90 intravesical agent in patients with bacille Calmette-Guerin (BCG) -refractory transitional cell carc
91 ho receive intravesical therapy with bacille Calmette-Guerin should be considered for ongoing mainten
96 exposure to M. tuberculosis from the Bacille-Calmette-Guerin vaccine strain, they currently lack the
112 ements, other dietary approaches, a Bacillus Calmette-Guerin trial in 1976, molecular-targeted agents
113 dder cancer (NMIBC) recurrent after bacillus Calmette-Guerin therapy is complex and further complicat
114 Multivariate analyses examined age, bacillus Calmette-Guerin (BCG) vaccination status, and sex as pre
118 y of interventions, such as IPT and bacillus Calmette-Guerin (BCG) vaccination for preventing TB dise
119 ium tuberculosis (strain H37Rv) and bacillus Calmette-Guerin (BCG) vaccine inhibit phagosome maturati
120 ate tuberculosis susceptibility and bacillus Calmette-Guerin (BCG)-induced immunity are mostly unknow
121 that Mycobacterium tuberculosis and bacillus Calmette-Guerin infections of macaques induced expressio
122 status of index cases, the age and bacillus Calmette-Guerin vaccination status of contacts, and stud
125 ted TLR ligands or bacteria such as bacillus Calmette-Guerin increases antitumor immune responses and
126 was also observed during S. aureus, bacillus Calmette-Guerin (BCG), or E. coli infection, as well as
128 on after stimulation with live BCG (Bacillus Calmette-Guerin), and a second locus on chromosome regio
129 The only available vaccine, BCG (Bacillus Calmette-Guerin), is given intradermally and has variabl
130 e estimated the association between bacillus Calmette-Guerin (BCG) vaccination and childhood asthma i
131 culosis (TB) vaccine trial to boost bacillus Calmette-Guerin-mediated anti-TB immunity despite the in
132 for the derivation of the M. bovis bacillus Calmette and Guerin (BCG) vaccine strain selected for an
133 n combined with Mycobacterium bovis bacillus Calmette Guerin (BCG) represents a potential strategy fo
134 ed 3,290 mutant Mycobacterium bovis bacillus Calmette Guerin (BCG) strains to identify genes that dec
136 nes, based upon Mycobacterium bovis bacillus Calmette-Guerin (BCG) all interfere with the action of t
137 accination with Mycobacterium bovis bacillus Calmette-Guerin (BCG) alone or as a BCG prime/Mtb72F-boo
138 vaccinated with Mycobacterium bovis bacillus Calmette-Guerin (BCG) and were then challenged with viru
139 en expressed in Mycobacterium bovis bacillus Calmette-Guerin (BCG) but not when all seven phosphoryla
140 wall lipids of Mycobacterium bovis bacillus Calmette-Guerin (BCG) by coating the lipids onto 90-micr
141 ministration of Mycobacterium bovis bacillus Calmette-Guerin (BCG) continues to be a successful immun
143 In contrast, the vaccine M. bovis bacillus Calmette-Guerin (BCG) does not stimulate MMP-1 secretion
144 cobacteria since avirulent M. bovis bacillus Calmette-Guerin (BCG) fails to trigger significant expre
147 uberculosis and Mycobacterium bovis bacillus Calmette-Guerin (BCG) induce potent expansions of human
149 vaccinated with Mycobacterium bovis bacillus Calmette-Guerin (BCG) nor tuberculin skin test (TST) pos
150 ses to M. tuberculosis and M. bovis bacillus Calmette-Guerin (BCG) Pasteur in vivo and in vitro.
151 the control of Mycobacterium bovis bacillus Calmette-Guerin (BCG) pleural infection in a murine mode
152 ected with live Mycobacterium bovis Bacillus Calmette-Guerin (BCG) produced large amounts of CXCL1 an
153 accination with Mycobacterium bovis bacillus Calmette-Guerin (BCG) remains the only prophylactic vacc
154 protocols using Mycobacterium bovis bacillus Calmette-Guerin (BCG) to prime and modified vaccinia vir
155 the failure of Mycobacterium bovis bacillus Calmette-Guerin (BCG) to protect against disease, new va
158 dies induced by Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccination to protect against myc
160 eover, improved Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccine-induced protection was los
161 osis (Mtb), and Mycobacterium bovis bacillus Calmette-Guerin (BCG) were studied for their ability to
162 vaccine strain Mycobacterium bovis bacillus Calmette-Guerin (BCG), and it is hypothesized that these
163 ulosis vaccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is contraindicated for immunocomp
164 e only vaccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is largely ineffective, and ways
165 r macrophages infected with M bovis Bacillus Calmette-Guerin (BCG), M phlei, M avium 2151-rough, and
166 infection with Mycobacterium bovis bacillus Calmette-Guerin (BCG), peaking by days 14-21 posttreatme
168 Tmt ortholog in Mycobacterium bovis Bacillus Calmette-Guerin (BCG), we show for the first time that a
169 Th1 immunity is Mycobacterium bovis bacillus Calmette-Guerin (BCG), which has been used in newborns f
170 emonstrate that Mycobacterium bovis bacillus Calmette-Guerin (BCG)-mediated TLR2 signaling-induced iN
177 ven heat-killed Mycobacterium bovis bacillus Calmette-Guerin (HK-BCG) i.p. did not release PGE(2).
178 (along with the attenuated M. bovis bacillus Calmette-Guerin [BCG]), and Mycobacterium microti; incre
179 In this report, Mycobacterium bovis bacillus Calmette-Guerin and M. tuberculosis H37Ra were used as m
180 ed in increased Mycobacterium bovis bacillus Calmette-Guerin and Mycobacterium tuberculosis H(37)R(v)
182 accination with Mycobacterium bovis bacillus Calmette-Guerin compared with control mice after infecti
183 nduced cross processing of M. bovis bacillus Calmette-Guerin expressing OVA could be circumvented by
184 hanced cross processing of M. bovis bacillus Calmette-Guerin expressing OVA, bypassing the inhibition
185 le infection by Mycobacterium bovis bacillus Calmette-Guerin failed to induce IRF-1 expression and ha
187 the attenuated Mycobacterium bovis bacillus Calmette-Guerin induces less PPARgamma and preferentiall
189 t that M. tuberculosis and M. bovis bacillus Calmette-Guerin infection down-regulated the expression
191 d nonpathogenic Mycobacterium bovis bacillus Calmette-Guerin intracellular survival, downregulated an
192 enuated vaccine Mycobacterium bovis bacillus Calmette-Guerin or the adoptive transfer of mycobacteria
194 ith recombinant Mycobacterium bovis bacillus Calmette-Guerin overexpressing the 30-kDa antigen, C3HeB
195 ported that M. marinum and M. bovis bacillus Calmette-Guerin produce a type of spore known as an endo
196 izing mice with Mycobacterium bovis bacillus Calmette-Guerin to augment host immunity before infectio
198 obacter pylori, Mycobacterium bovis bacillus Calmette-Guerin, and Citrobacter rodentium and of tumor
199 by bcg_1279c in Mycobacterium bovis bacillus Calmette-Guerin, plays an important role in mycobacteria
201 ition of M. tuberculosis var. bovis Bacillus Calmette-Guerin-induced p38 MAPK activity caused a marke
202 isolated from the serum of M. bovis bacillus Calmette-Guerin-infected mice could also stimulate macro
209 sis; the vaccine strain of M. bovis Bacillus Calmette-Guerin; and M. kansasii to demonstrate detectio
210 nd CD8+ T cell responses induced by bacillus Calmette-Guerin and a recombinant subunit protein vaccin
211 Vaccinations studied comprised Bacillus Calmette-Guerin (BCG) vaccine, Triple vaccine, Hepatitis
213 bject 1 presented with disseminated Bacillus Calmette-Guerin infection and oligoclonal T cells with n
215 or cells producing IFN-gamma during bacillus Calmette-Guerin (BCG) vaccination and subsequent M. tube
217 fforts toward developing agents for bacillus Calmette-Guerin-refractory superficial bladder cancer co
218 es in the development of agents for bacillus Calmette-Guerin-refractory superficial bladder cancer.
219 he underwent cystoprostatectomy for bacillus Calmette-Guerin-refractory, high-grade noninvasive UC.
220 differentiation of Th17 cells from bacillus Calmette-Guerin-challenged (BCG-challenged) lung CD4+ T
221 e observed in livers and lungs from bacillus Calmette-Guerin-infected humanized mice but not in nonhu
222 4 expression by CD4(+) T cells from bacillus Calmette-Guerin-vaccinated mice and show that high-quali
224 is Ags Ag85A, Ag85B, and TB10.4, in bacillus Calmette-Guerin (BCG)-primed or unprimed rhesus macaques
225 tifs within AM and its functions in bacillus Calmette-Guerin vaccination and/or in controlled (latent
226 th factor Vegf-c is up-regulated in Bacillus Calmette-Guerin- and Mycobacterium tuberculosis-induced
229 target, also lowered intracellular Bacillus Calmette-Guerin levels in mammary epithelial cancer MCF-
230 for patients who fail intravesical bacillus Calmette-Guerin (BCG) for nonmuscle invasive bladder can
231 r cancer refractory to intravesical bacillus Calmette-Guerin (BCG) therapy and refusing a cystectomy
232 patients according to intravesical Bacillus Calmette-Guerin (BCG) treatment status: no BCG, inductio
233 ta supports the use of intravesical Bacillus Calmette-Guerin (including a maintenance regimen) for th
234 ata support the use of intravesical bacillus Calmette-Guerin (including a maintenance regimen) for th
235 rastriatal injection of heat-killed bacillus Calmette-Guerin (BCG) and subsequent activation using an
236 safety, and immunogenicity of live bacillus Calmette-Guerin (BCG) in a lung-oriented controlled huma
238 Mtb- specific antigens and live bacillus Calmette-Guerin (BCG) were used as stimuli, with direct
239 n response to stimulation with live bacillus Calmette-Guerin (BCG; LOD score, 3.81; P = 1.40 x 10(-5)
241 ts include intravesical maintenance Bacillus Calmette-Guerin (mBCG) and radical cystectomy (RC).
242 e considered the childhood measles, bacillus Calmette-Guerin, diphtheria-pertussis-tetanus, polio, an
243 gative association between national bacillus Calmette-Guerin (BCG) vaccination policy and the prevale
245 r a single dose (1 x 10(5) CFUs) of bacillus Calmette-Guerin (BCG) or Mycobacterium vaccae via nasal
246 ion showed that old age, absence of bacillus Calmette-Guerin (BCG) scar, presence of donor-specific a
248 of PBMCs with the Moreau strain of bacillus Calmette-Guerin but not after infection with other strai
249 he primary attenuating mechanism of bacillus Calmette-Guerin is the loss of cytolytic activity mediat
250 H65 gave protection at the level of bacillus Calmette-Guerin, and the fusion protein exhibited high p
251 ciated carcinoma in situ, nonuse of bacillus Calmette-Guerin, tumor size > 3 cm, and older age; HRs f
255 and TST (with adjustment for prior bacillus Calmette-Guerin [BCG] vaccination).Measurements and Main
256 us pneumoniae, Helicobacter pylori, bacillus Calmette-Guerin, and Mycobacterium tuberculosis) in a mu
258 tion, immunization with recombinant bacillus Calmette-Guerin (BCG) expressing RSV nucleoprotein preve
259 CV candidates, based on recombinant bacillus Calmette-Guerin (BCG), attenuated Mycobacterium tubercul
260 fore and after primary or secondary bacillus Calmette-Guerin (BCG) vaccination were assessed for Ab r
261 parison of the efficacy of standard bacillus Calmette-Guerin vaccination as well as novel TB vaccines
271 atients had previously received the bacillus Calmette-Guerin (BCG) vaccine; among this vaccinated gro
272 Mycobacterium tuberculosis and the bacillus Calmette-Guerin can be tracked directly in the lungs of
273 among persons who had received the Bacillus Calmette-Guerin vaccine in households with and without a
275 er (NMIBC) are either refractory to bacillus Calmette-Guerin (BCG) treatment or may experience diseas
278 ated as alternatives to traditional Bacillus Calmette-Guerin needles and syringes for the administrat
279 lable vaccine against tuberculosis, bacillus Calmette Guerin (BCG), has traditionally been viewed not
280 mans as a vaccine for tuberculosis, Bacillus Calmette-Guerin (BCG) has been suggested as a possible a
282 ccines revealed that currently used bacillus Calmette-Guerin strains vary in their ability to affect
283 ty, by the antituberculosis vaccine bacillus Calmette-Guerin (BCG) contributes to protection against
284 KGROUNDThe antituberculosis vaccine bacillus Calmette-Guerin (BCG) reduces overall infant mortality.
286 w the current tuberculosis vaccine, bacillus Calmette-Guerin (BCG), impacts early immunity is poorly
287 cted a novel breast cancer vaccine, Bacillus Calmette-Guerin (BCG)-hIL2MUC1, that consists of BCG and
289 the population of patients for whom bacillus Calmette-Guerin (BCG) has failed, the type of failure (B
290 When monkeys were immunized with bacillus Calmette-Guerin (BCG) and then boosted with Mtb72F in AS
291 n (KLH) as a carrier and given with Bacillus Calmette-Guerin (BCG) as an adjuvant, elicited HMW-MAA-s
293 apy (IPT) before revaccination with bacillus Calmette-Guerin (BCG) in healthy, tuberculin skin test-p
294 negative IGRAs was associated with bacillus Calmette-Guerin (BCG) vaccination (odds ratio: 25.1 [95%
295 n a mouse model of vaccination with bacillus Calmette-Guerin (BCG), followed by challenge with virule
296 and vaccination, in particular with Bacillus Calmette-Guerin (BCG), remain the main strategies to con