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11 e show in this article that although bacille Calmette-Guerin controlled M. tuberculosis growth for 7
12 odeficiency virus (HIV)-infected and bacille Calmette-Guerin (BCG)-immunized adults with CD4 cell cou
13 medical illness, isoniazid use, and bacille Calmette-Guerin strain did not substantially affect vacc
14 y to nontuberculous mycobacteria and bacille Calmette-Guerin vaccination may account for a proportion
15 rain of Mycobacterium bovis known as bacille Calmette-Guerin (BCG) has been widely used as a vaccine
17 erium tuberculosis vaccines to boost bacille Calmette-Guerin or for those who cannot be immunized wit
18 osis Ag 85A (M.85A), strongly boosts bacille Calmette-Guerin (BCG)-induced Ag 85A specific CD4(+) and
19 strict growth of Mycobacterium bovis bacille Calmette Guerin and Mycobacterium tuberculosis was impai
20 AT)-6, that are absent from M. bovis bacille Calmette-Guerin (BCG) and most environmental mycobacteri
21 Vaccination with Mycobacterium bovis bacille Calmette-Guerin (BCG) has variable efficacy in preventin
22 ells specific to Mycobacterium bovis bacille Calmette-Guerin (BCG) in the lungs, and the IFN-gamma CD
24 um smegmatis and Mycobacterium bovis bacille Calmette-Guerin (BCG) in which a very high proportion of
25 expansion during Mycobacterium bovis Bacille Calmette-Guerin (BCG) infection and a clear memory-type
26 ls responding to Mycobacterium bovis bacille Calmette-Guerin (BCG) infection and disrupt granuloma fo
28 sing intradermal Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination as a surrogate for M.
29 conferred by the Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccine are multifaceted and poorl
31 ssed in M. tuberculosis and M. bovis Bacille Calmette-Guerin (BCG), using reverse transcription-polym
32 um smegmatis and Mycobacterium bovis bacille Calmette-Guerin (BCG), which respectively induce high an
38 that exposure of Mycobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thiacetazone
39 Infection with Mycobacterium bovis bacille Calmette-Guerin resulted in approximately 10-fold-higher
40 tuberculosis and Mycobacterium bovis bacille Calmette-Guerin similarly home to established granulomas
42 tuberculosis and Mycobacterium bovis bacille Calmette-Guerin, release MVs when growing in both liquid
44 detect antibody responses induced by bacille Calmette-Guerin (BCG) vaccination and active tuberculosi
46 days) than mice infected with either bacille Calmette-Guerin (BCG) vaccine or virulent M. tuberculosi
47 l Ags in the context of experimental bacille Calmette-Guerin (BCG) vaccination, Ag-specific T cell re
49 ries was 2.3 weeks (IQR 1.4-4.6) for bacille Calmette-Guerin (BCG); 2.4 weeks (1.2-3.3) for diphtheri
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
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
64 olled trials of the effectiveness of bacille Calmette-Guerin vaccine in preventing active tuberculosi
65 e, M72/AS01, in a phase IIa trial of bacille Calmette-Guerin-vaccinated, HIV-uninfected, and Mycobact
66 th environmental mycobacteria and/or bacille Calmette-Guerin (BCG) vaccination compromise the estimat
67 d with Mycobacterium tuberculosis or bacille Calmette-Guerin have been shown to facilitate presentati
68 by infection with M. tuberculosis or bacille Calmette-Guerin, or treatment with LPS or TNF-alpha.
69 e-promastigote vaccine cocktail plus bacille Calmette-Guerin (BCG) adjuvant significantly reduced the
71 tion involves the use of recombinant bacille Calmette-Guerin (rBCG) overexpressing protective TB anti
73 ection in Mycobacterium bovis strain bacille Calmette-Guerin (BCG)-induced granulomas using an immuno
75 n sharp contrast, the vaccine strain bacille Calmette-Guerin as well as RD-1 and ESAT-6 mutants of H3
77 We have previously established that bacille Calmette-Guerin (BCG), an attenuated form of Mycobacteri
78 erculosis every year even though the bacille Calmette Guerin (BCG) vaccine has been available for mor
79 Policies regarding the use of the Bacille Calmette-Guerin (BCG) vaccine for tuberculosis vary grea
80 stence of therapeutic agents and the bacille Calmette-Guerin (BCG) vaccine have not significantly aff
81 r specificity in those receiving the bacille Calmette-Guerin vaccine and poor sensitivity in individu
85 ected macaques previously exposed to bacille Calmette-Guerin (BCG) were reinfected with BCG, were tre
87 and existing ones improved to treat bacille Calmette-Guerin-refractory superficial bladder cancer.
89 mycobacterial challenge model, using bacille Calmette-Guerin (BCG) as a surrogate for a Mycobacterium
92 intravesical agent in patients with bacille Calmette-Guerin (BCG) -refractory transitional cell carc
95 cally into macrophages infected with bacille Calmette-Guerin expressing the green fluorescent protein
96 ho receive intravesical therapy with bacille Calmette-Guerin should be considered for ongoing mainten
101 exposure to M. tuberculosis from the Bacille-Calmette-Guerin vaccine strain, they currently lack the
111 ements, other dietary approaches, a Bacillus Calmette-Guerin trial in 1976, molecular-targeted agents
112 dder cancer (NMIBC) recurrent after bacillus Calmette-Guerin therapy is complex and further complicat
113 Multivariate analyses examined age, bacillus Calmette-Guerin (BCG) vaccination status, and sex as pre
117 ip between apoptotic regulation and bacillus Calmette-Guerin (BCG) treatment in murine peritoneal exu
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
128 on after stimulation with live BCG (Bacillus Calmette-Guerin), and a second locus on chromosome regio
129 e estimated the association between bacillus Calmette-Guerin (BCG) vaccination and childhood asthma i
130 for the derivation of the M. bovis bacillus Calmette and Guerin (BCG) vaccine strain selected for an
131 ith recombinant Mycobacterium bovis bacillus Calmette Guerin (BCG) expressing the vector only (BCG-ve
132 n combined with Mycobacterium bovis bacillus Calmette Guerin (BCG) represents a potential strategy fo
133 ed 3,290 mutant Mycobacterium bovis bacillus Calmette Guerin (BCG) strains to identify genes that dec
134 ound M. avium, Mycobacterium bovis (bacillus Calmette-Guerin), and Mycobacterium tuberculosis (strain
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
139 vaccinated with Mycobacterium bovis bacillus Calmette-Guerin (BCG) and were then challenged with viru
140 en expressed in Mycobacterium bovis bacillus Calmette-Guerin (BCG) but not when all seven phosphoryla
141 wall lipids of Mycobacterium bovis bacillus Calmette-Guerin (BCG) by coating the lipids onto 90-micr
142 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
148 uberculosis and Mycobacterium bovis bacillus Calmette-Guerin (BCG) induce potent expansions of human
152 vaccinated with Mycobacterium bovis bacillus Calmette-Guerin (BCG) nor tuberculin skin test (TST) pos
154 ses to M. tuberculosis and M. bovis bacillus Calmette-Guerin (BCG) Pasteur in vivo and in vitro.
155 cobacterium bovis Ravenel, M. bovis bacillus Calmette-Guerin (BCG) Pasteur, and M. bovis BCG Montreal
156 the control of Mycobacterium bovis bacillus Calmette-Guerin (BCG) pleural infection in a murine mode
157 ected with live Mycobacterium bovis Bacillus Calmette-Guerin (BCG) produced large amounts of CXCL1 an
158 accination with Mycobacterium bovis bacillus Calmette-Guerin (BCG) remains the only prophylactic vacc
159 protocols using Mycobacterium bovis bacillus Calmette-Guerin (BCG) to prime and modified vaccinia vir
160 the failure of Mycobacterium bovis bacillus Calmette-Guerin (BCG) to protect against disease, new va
163 dies induced by Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccination to protect against myc
164 eover, improved Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccine-induced protection was los
165 osis (Mtb), and Mycobacterium bovis bacillus Calmette-Guerin (BCG) were studied for their ability to
166 vaccine strain Mycobacterium bovis bacillus Calmette-Guerin (BCG), and it is hypothesized that these
167 ulosis vaccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is contraindicated for immunocomp
168 e only vaccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is largely ineffective, and ways
169 r macrophages infected with M bovis Bacillus Calmette-Guerin (BCG), M phlei, M avium 2151-rough, and
170 infection with Mycobacterium bovis bacillus Calmette-Guerin (BCG), peaking by days 14-21 posttreatme
171 Tmt ortholog in Mycobacterium bovis Bacillus Calmette-Guerin (BCG), we show for the first time that a
172 Th1 immunity is Mycobacterium bovis bacillus Calmette-Guerin (BCG), which has been used in newborns f
173 emonstrate that Mycobacterium bovis bacillus Calmette-Guerin (BCG)-mediated TLR2 signaling-induced iN
180 ven heat-killed Mycobacterium bovis bacillus Calmette-Guerin (HK-BCG) i.p. did not release PGE(2).
181 (along with the attenuated M. bovis bacillus Calmette-Guerin [BCG]), and Mycobacterium microti; incre
182 In this report, Mycobacterium bovis bacillus Calmette-Guerin and M. tuberculosis H37Ra were used as m
184 accination with Mycobacterium bovis bacillus Calmette-Guerin compared with control mice after infecti
185 nduced cross processing of M. bovis bacillus Calmette-Guerin expressing OVA could be circumvented by
186 hanced cross processing of M. bovis bacillus Calmette-Guerin expressing OVA, bypassing the inhibition
187 le infection by Mycobacterium bovis bacillus Calmette-Guerin failed to induce IRF-1 expression and ha
188 tuberculosis or Mycobacterium bovis bacillus Calmette-Guerin failed to induce TLR-dependent activatio
191 the attenuated Mycobacterium bovis bacillus Calmette-Guerin induces less PPARgamma and preferentiall
193 t that M. tuberculosis and M. bovis bacillus Calmette-Guerin infection down-regulated the expression
195 d nonpathogenic Mycobacterium bovis bacillus Calmette-Guerin intracellular survival, downregulated an
197 enuated vaccine Mycobacterium bovis bacillus Calmette-Guerin or the adoptive transfer of mycobacteria
199 ith recombinant Mycobacterium bovis bacillus Calmette-Guerin overexpressing the 30-kDa antigen, C3HeB
200 ported that M. marinum and M. bovis bacillus Calmette-Guerin produce a type of spore known as an endo
201 izing mice with Mycobacterium bovis bacillus Calmette-Guerin to augment host immunity before infectio
204 rculosis H37Ra, Mycobacterium bovis bacillus Calmette-Guerin, and M. kansasii) induced significantly
205 lular bacterium Mycobacterium bovis bacillus Calmette-Guerin, macrophages recovered from the peritone
206 by bcg_1279c in Mycobacterium bovis bacillus Calmette-Guerin, plays an important role in mycobacteria
208 ition of M. tuberculosis var. bovis Bacillus Calmette-Guerin-induced p38 MAPK activity caused a marke
210 isolated from the serum of M. bovis bacillus Calmette-Guerin-infected mice could also stimulate macro
217 attenuated descendant of M. bovis, bacillus Calmette-Guerin (BCG), widely used as a vaccine against
218 nuated vaccine, Mycobacterium bovis-bacillus Calmette-Guerin as well as in mice infected i.v. with M.
219 d not only by endotoxin but also by bacillus Calmette-Guerin (BCG) and CD40 ligand and was associated
220 nd CD8+ T cell responses induced by bacillus Calmette-Guerin and a recombinant subunit protein vaccin
223 (ASI) with an autologous tumor cell-bacillus Calmette-Guerin (BCG) vaccine was conducted to determine
224 Vaccinations studied comprised Bacillus Calmette-Guerin (BCG) vaccine, Triple vaccine, Hepatitis
225 bject 1 presented with disseminated Bacillus Calmette-Guerin infection and oligoclonal T cells with n
227 or cells producing IFN-gamma during bacillus Calmette-Guerin (BCG) vaccination and subsequent M. tube
229 fforts toward developing agents for bacillus Calmette-Guerin-refractory superficial bladder cancer co
230 es in the development of agents for bacillus Calmette-Guerin-refractory superficial bladder cancer.
231 he underwent cystoprostatectomy for bacillus Calmette-Guerin-refractory, high-grade noninvasive UC.
232 differentiation of Th17 cells from bacillus Calmette-Guerin-challenged (BCG-challenged) lung CD4+ T
233 e observed in livers and lungs from bacillus Calmette-Guerin-infected humanized mice but not in nonhu
234 4 expression by CD4(+) T cells from bacillus Calmette-Guerin-vaccinated mice and show that high-quali
236 is Ags Ag85A, Ag85B, and TB10.4, in bacillus Calmette-Guerin (BCG)-primed or unprimed rhesus macaques
237 th factor Vegf-c is up-regulated in Bacillus Calmette-Guerin- and Mycobacterium tuberculosis-induced
238 target, also lowered intracellular Bacillus Calmette-Guerin levels in mammary epithelial cancer MCF-
239 for patients who fail intravesical bacillus Calmette-Guerin (BCG) for nonmuscle invasive bladder can
240 mbination therapy with intravesical bacillus Calmette-Guerin (BCG) plus IFN-alpha for superficial bla
241 r cancer refractory to intravesical bacillus Calmette-Guerin (BCG) therapy and refusing a cystectomy
242 patients according to intravesical Bacillus Calmette-Guerin (BCG) treatment status: no BCG, inductio
243 ta supports the use of intravesical Bacillus Calmette-Guerin (including a maintenance regimen) for th
244 ata support the use of intravesical bacillus Calmette-Guerin (including a maintenance regimen) for th
245 rastriatal injection of heat-killed bacillus Calmette-Guerin (BCG) and subsequent activation using an
247 n response to stimulation with live bacillus Calmette-Guerin (BCG; LOD score, 3.81; P = 1.40 x 10(-5)
249 e considered the childhood measles, bacillus Calmette-Guerin, diphtheria-pertussis-tetanus, polio, an
252 r a single dose (1 x 10(5) CFUs) of bacillus Calmette-Guerin (BCG) or Mycobacterium vaccae via nasal
253 al infection, recombinant clones of bacillus Calmette-Guerin (BCG) were engineered to express the nat
254 ripheral blood mononuclear cells of bacillus Calmette-Guerin (BCG)-vaccinated individuals with live M
255 of PBMCs with the Moreau strain of bacillus Calmette-Guerin but not after infection with other strai
256 he primary attenuating mechanism of bacillus Calmette-Guerin is the loss of cytolytic activity mediat
257 H65 gave protection at the level of bacillus Calmette-Guerin, and the fusion protein exhibited high p
258 ciated carcinoma in situ, nonuse of bacillus Calmette-Guerin, tumor size > 3 cm, and older age; HRs f
261 us pneumoniae, Helicobacter pylori, bacillus Calmette-Guerin, and Mycobacterium tuberculosis) in a mu
262 tion, immunization with recombinant bacillus Calmette-Guerin (BCG) expressing RSV nucleoprotein preve
263 CV candidates, based on recombinant bacillus Calmette-Guerin (BCG), attenuated Mycobacterium tubercul
264 fore and after primary or secondary bacillus Calmette-Guerin (BCG) vaccination were assessed for Ab r
266 model of Mycobacterium bovis strain bacillus Calmette-Guerin (BCG) infection we studied the extent of
275 atients had previously received the bacillus Calmette-Guerin (BCG) vaccine; among this vaccinated gro
276 Mycobacterium tuberculosis and the bacillus Calmette-Guerin can be tracked directly in the lungs of
277 among persons who had received the Bacillus Calmette-Guerin vaccine in households with and without a
279 er (NMIBC) are either refractory to bacillus Calmette-Guerin (BCG) treatment or may experience diseas
282 ated as alternatives to traditional Bacillus Calmette-Guerin needles and syringes for the administrat
283 lable vaccine against tuberculosis, bacillus Calmette Guerin (BCG), has traditionally been viewed not
284 ccines revealed that currently used bacillus Calmette-Guerin strains vary in their ability to affect
286 cted a novel breast cancer vaccine, Bacillus Calmette-Guerin (BCG)-hIL2MUC1, that consists of BCG and
287 he majority of Danish patients were bacillus Calmette-Guerin (Mycobacterium bovis BCG) vaccinated (CD
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 ldren are routinely vaccinated with bacillus Calmette-Guerin (BCG) in areas of the world where worm i
294 apy (IPT) before revaccination with bacillus Calmette-Guerin (BCG) in healthy, tuberculin skin test-p
295 negative IGRAs was associated with bacillus Calmette-Guerin (BCG) vaccination (odds ratio: 25.1 [95%
296 n a mouse model of vaccination with bacillus Calmette-Guerin (BCG), followed by challenge with virule
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