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1 Guerin et al. (2014) report the first direct experimenta
2 vation of the M. bovis bacillus Calmette and Guerin (BCG) vaccine strain selected for an M. bovis PK+
3 augmentation of KCs after Bacille-Calemette-Guerin vaccination largely increased hepatic CETP expres
4 The variable efficacy of Bacille Calmette Guerin (BCG) vaccination against tuberculosis has prompt
5 every year even though the bacille Calmette Guerin (BCG) vaccine has been available for more than 75
6 owth of Mycobacterium bovis bacille Calmette Guerin and Mycobacterium tuberculosis was impaired 7.3-
9 binant Mycobacterium bovis bacillus Calmette Guerin (BCG) expressing the vector only (BCG-vector) res
10 d with Mycobacterium bovis bacillus Calmette Guerin (BCG) represents a potential strategy for prevent
11 mutant Mycobacterium bovis bacillus Calmette Guerin (BCG) strains to identify genes that decrease maj
13 cine against tuberculosis, bacillus Calmette Guerin (BCG), has traditionally been viewed not to induc
15 ical agent in patients with bacille Calmette-Guerin (BCG) -refractory transitional cell carcinoma of
16 igote vaccine cocktail plus bacille Calmette-Guerin (BCG) adjuvant significantly reduced the incidenc
18 rial challenge model, using bacille Calmette-Guerin (BCG) as a surrogate for a Mycobacterium tubercul
21 ycobacterium bovis known as bacille Calmette-Guerin (BCG) has been widely used as a vaccine for preve
22 on with Mycobacterium bovis bacille Calmette-Guerin (BCG) has variable efficacy in preventing tubercu
23 lates of TB disease risk in Bacille Calmette-Guerin (BCG) immunized infants from the MVA85A efficacy
24 ific to Mycobacterium bovis bacille Calmette-Guerin (BCG) in the lungs, and the IFN-gamma CD8 T cell
25 n PMCs were stimulated with bacille Calmette-Guerin (BCG) in vitro, they expressed ICAM-1 in a time-d
27 tis and Mycobacterium bovis bacille Calmette-Guerin (BCG) in which a very high proportion of infected
28 during Mycobacterium bovis Bacille Calmette-Guerin (BCG) infection and a clear memory-type response
29 ding to Mycobacterium bovis bacille Calmette-Guerin (BCG) infection and disrupt granuloma formation,
31 e tuberculosis (TB) vaccine bacille Calmette-Guerin (BCG) is a live attenuated organism, but the muta
33 dividuals with a history of Bacille Calmette-Guerin (BCG) vaccination after infancy or with repeated
34 tibody responses induced by bacille Calmette-Guerin (BCG) vaccination and active tuberculosis infecti
35 adermal Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination as a surrogate for M. tuberculo
36 nmental mycobacteria and/or bacille Calmette-Guerin (BCG) vaccination compromise the estimates derive
41 the context of experimental bacille Calmette-Guerin (BCG) vaccination, Ag-specific T cell responses t
43 mately 100 million doses of bacille Calmette-Guerin (BCG) vaccine are given each year to protect agai
44 by the Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccine are multifaceted and poorly underst
45 Because Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccine can confer protection against fatal
46 es regarding the use of the Bacille Calmette-Guerin (BCG) vaccine for tuberculosis vary greatly throu
47 therapeutic agents and the bacille Calmette-Guerin (BCG) vaccine have not significantly affected the
48 n mice infected with either bacille Calmette-Guerin (BCG) vaccine or virulent M. tuberculosis (77 and
51 aques previously exposed to bacille Calmette-Guerin (BCG) were reinfected with BCG, were treated eith
52 previously established that bacille Calmette-Guerin (BCG), an attenuated form of Mycobacterium bovis,
54 he cells were infected with bacille Calmette-Guerin (BCG), and intracellular mycobacterial traffickin
55 . tuberculosis and M. bovis Bacille Calmette-Guerin (BCG), using reverse transcription-polymerase cha
56 tis and Mycobacterium bovis bacille Calmette-Guerin (BCG), which respectively induce high and low aut
58 cy virus (HIV)-infected and bacille Calmette-Guerin (BCG)-immunized adults with CD4 cell counts of >o
59 5A (M.85A), strongly boosts bacille Calmette-Guerin (BCG)-induced Ag 85A specific CD4(+) and CD8(+) T
60 Mycobacterium bovis strain bacille Calmette-Guerin (BCG)-induced granulomas using an immunocompetent
63 odstream infection (BSI) in bacille Calmette-Guerin (BCG)-vaccinated children with human immunodefici
70 2.3 weeks (IQR 1.4-4.6) for bacille Calmette-Guerin (BCG); 2.4 weeks (1.2-3.3) for diphtheria, tetanu
72 lves the use of recombinant bacille Calmette-Guerin (rBCG) overexpressing protective TB antigens.
74 ontrast, the vaccine strain bacille Calmette-Guerin as well as RD-1 and ESAT-6 mutants of H37Rv faile
76 this article that although bacille Calmette-Guerin controlled M. tuberculosis growth for 7 wk of inf
77 o macrophages infected with bacille Calmette-Guerin expressing the green fluorescent protein, molecul
80 e addition of interferon to bacille Calmette-Guerin has proven to be an effective combination therapy
81 cobacterium tuberculosis or bacille Calmette-Guerin have been shown to facilitate presentation of ova
83 erculosis vaccines to boost bacille Calmette-Guerin or for those who cannot be immunized with bacille
84 sure of Mycobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thiacetazone, a secon
86 on with Mycobacterium bovis bacille Calmette-Guerin resulted in approximately 10-fold-higher bacteria
87 e intravesical therapy with bacille Calmette-Guerin should be considered for ongoing maintenance ther
88 sis and Mycobacterium bovis bacille Calmette-Guerin similarly home to established granulomas in mice.
89 illness, isoniazid use, and bacille Calmette-Guerin strain did not substantially affect vaccine effic
90 uberculous mycobacteria and bacille Calmette-Guerin vaccination may account for a proportion of test
93 city in those receiving the bacille Calmette-Guerin vaccine and poor sensitivity in individuals with
95 als of the effectiveness of bacille Calmette-Guerin vaccine in preventing active tuberculosis yielded
101 sis and Mycobacterium bovis bacille Calmette-Guerin, release MVs when growing in both liquid culture
104 01, in a phase IIa trial of bacille Calmette-Guerin-vaccinated, HIV-uninfected, and Mycobacterium tub
110 to M. tuberculosis from the Bacille-Calmette-Guerin vaccine strain, they currently lack the specifici
113 d upon Mycobacterium bovis bacillus Calmette-Guerin (BCG) all interfere with the action of the tuberc
114 n with Mycobacterium bovis bacillus Calmette-Guerin (BCG) alone or as a BCG prime/Mtb72F-boost regime
115 y by endotoxin but also by bacillus Calmette-Guerin (BCG) and CD40 ligand and was associated with (an
117 l injection of heat-killed bacillus Calmette-Guerin (BCG) and subsequent activation using an intrader
118 onkeys were immunized with bacillus Calmette-Guerin (BCG) and then boosted with Mtb72F in AS02A, prot
119 this study, we found that bacillus Calmette-Guerin (BCG) and viable M. tuberculosis as well as M. tu
120 d with Mycobacterium bovis bacillus Calmette-Guerin (BCG) and were then challenged with virulent M. b
121 s a carrier and given with Bacillus Calmette-Guerin (BCG) as an adjuvant, elicited HMW-MAA-specific a
122 sed in Mycobacterium bovis bacillus Calmette-Guerin (BCG) but not when all seven phosphorylation site
123 ids of Mycobacterium bovis bacillus Calmette-Guerin (BCG) by coating the lipids onto 90-microm diamet
124 ion of Mycobacterium bovis bacillus Calmette-Guerin (BCG) continues to be a successful immunotherapy
125 rast, the vaccine M. bovis bacillus Calmette-Guerin (BCG) does not stimulate MMP-1 secretion from hum
126 unization with recombinant bacillus Calmette-Guerin (BCG) expressing RSV nucleoprotein prevented beha
127 a since avirulent M. bovis bacillus Calmette-Guerin (BCG) fails to trigger significant expression of
129 ents who fail intravesical bacillus Calmette-Guerin (BCG) for nonmuscle invasive bladder cancer (NMIB
130 though Mycobacterium bovis bacillus Calmette-Guerin (BCG) has been accepted as the most effective age
134 ation of patients for whom bacillus Calmette-Guerin (BCG) has failed, the type of failure (BCG unresp
135 routinely vaccinated with bacillus Calmette-Guerin (BCG) in areas of the world where worm infections
136 before revaccination with bacillus Calmette-Guerin (BCG) in healthy, tuberculin skin test-positive (
139 is and Mycobacterium bovis bacillus Calmette-Guerin (BCG) induce potent expansions of human memory Vg
141 Mycobacterium bovis strain bacillus Calmette-Guerin (BCG) infection we studied the extent of T cell h
146 d with Mycobacterium bovis bacillus Calmette-Guerin (BCG) nor tuberculin skin test (TST) positive (gr
148 e dose (1 x 10(5) CFUs) of bacillus Calmette-Guerin (BCG) or Mycobacterium vaccae via nasal or perito
151 um bovis Ravenel, M. bovis bacillus Calmette-Guerin (BCG) Pasteur, and M. bovis BCG Montreal were com
153 therapy with intravesical bacillus Calmette-Guerin (BCG) plus IFN-alpha for superficial bladder canc
154 h live Mycobacterium bovis Bacillus Calmette-Guerin (BCG) produced large amounts of CXCL1 and CXCL2,
155 n with Mycobacterium bovis bacillus Calmette-Guerin (BCG) remains the only prophylactic vaccine again
158 refractory to intravesical bacillus Calmette-Guerin (BCG) therapy and refusing a cystectomy were cons
159 using Mycobacterium bovis bacillus Calmette-Guerin (BCG) to prime and modified vaccinia virus Ankara
160 ure of Mycobacterium bovis bacillus Calmette-Guerin (BCG) to protect against disease, new vaccines ag
161 n apoptotic regulation and bacillus Calmette-Guerin (BCG) treatment in murine peritoneal exudate macr
162 ) are either refractory to bacillus Calmette-Guerin (BCG) treatment or may experience disease relapse
163 according to intravesical Bacillus Calmette-Guerin (BCG) treatment status: no BCG, induction BCG (iB
165 IGRAs was associated with bacillus Calmette-Guerin (BCG) vaccination (odds ratio: 25.1 [95% confiden
166 ed the association between bacillus Calmette-Guerin (BCG) vaccination and childhood asthma in a birth
167 producing IFN-gamma during bacillus Calmette-Guerin (BCG) vaccination and subsequent M. tuberculosis
168 rventions, such as IPT and bacillus Calmette-Guerin (BCG) vaccination for preventing TB disease among
170 tudies have suggested that Bacillus Calmette-Guerin (BCG) vaccination may reduce the risk of allergic
171 ate analyses examined age, bacillus Calmette-Guerin (BCG) vaccination status, and sex as predictor va
172 ced by Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccination to protect against mycobacteria
173 after primary or secondary bacillus Calmette-Guerin (BCG) vaccination were assessed for Ab responses
174 culosis (strain H37Rv) and bacillus Calmette-Guerin (BCG) vaccine inhibit phagosome maturation in mac
177 h an autologous tumor cell-bacillus Calmette-Guerin (BCG) vaccine was conducted to determine whether
178 inations studied comprised Bacillus Calmette-Guerin (BCG) vaccine, Triple vaccine, Hepatitis B vaccin
179 proved Mycobacterium bovis bacillus Calmette-Guerin (BCG) vaccine-induced protection was lost in the
183 ad previously received the bacillus Calmette-Guerin (BCG) vaccine; among this vaccinated group, the r
185 ion, recombinant clones of bacillus Calmette-Guerin (BCG) were engineered to express the natural anta
186 ), and Mycobacterium bovis bacillus Calmette-Guerin (BCG) were studied for their ability to be activa
187 strain Mycobacterium bovis bacillus Calmette-Guerin (BCG), and it is hypothesized that these proteins
188 ates, based on recombinant bacillus Calmette-Guerin (BCG), attenuated Mycobacterium tuberculosis, or
189 model of vaccination with bacillus Calmette-Guerin (BCG), followed by challenge with virulent M. tub
190 he only vaccine available, Bacillus Calmette-Guerin (BCG), has been used since its inception in 1921.
191 ccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is contraindicated for immunocompromised i
193 ccine, Mycobacterium bovis bacillus Calmette-Guerin (BCG), is largely ineffective, and ways to enhanc
194 ages infected with M bovis Bacillus Calmette-Guerin (BCG), M phlei, M avium 2151-rough, and M tubercu
198 log in Mycobacterium bovis Bacillus Calmette-Guerin (BCG), we show for the first time that acetylatio
199 ity is Mycobacterium bovis bacillus Calmette-Guerin (BCG), which has been used in newborns for many d
200 ed descendant of M. bovis, bacillus Calmette-Guerin (BCG), widely used as a vaccine against human tub
201 vel breast cancer vaccine, Bacillus Calmette-Guerin (BCG)-hIL2MUC1, that consists of BCG and expresse
203 e that Mycobacterium bovis bacillus Calmette-Guerin (BCG)-mediated TLR2 signaling-induced iNOS/NO exp
205 blood mononuclear cells of bacillus Calmette-Guerin (BCG)-vaccinated individuals with live Mycobacter
214 ts the use of intravesical Bacillus Calmette-Guerin (including a maintenance regimen) for those at hi
215 rt the use of intravesical bacillus Calmette-Guerin (including a maintenance regimen) for those at hi
216 ty of Danish patients were bacillus Calmette-Guerin (Mycobacterium bovis BCG) vaccinated (CD, 77.5%;
217 th the attenuated M. bovis bacillus Calmette-Guerin [BCG]), and Mycobacterium microti; increasingly r
218 cell responses induced by bacillus Calmette-Guerin and a recombinant subunit protein vaccine to hepa
219 Immunomodulators such as Bacillus Calmette-Guerin and interferon are clinically active in transitio
220 eport, Mycobacterium bovis bacillus Calmette-Guerin and M. tuberculosis H37Ra were used as models of
222 ccine, Mycobacterium bovis-bacillus Calmette-Guerin as well as in mice infected i.v. with M. tubercul
224 erium tuberculosis and the bacillus Calmette-Guerin can be tracked directly in the lungs of living mi
225 n with Mycobacterium bovis bacillus Calmette-Guerin compared with control mice after infection with M
226 oss processing of M. bovis bacillus Calmette-Guerin expressing OVA could be circumvented by pretreati
227 oss processing of M. bovis bacillus Calmette-Guerin expressing OVA, bypassing the inhibition of induc
228 ion by Mycobacterium bovis bacillus Calmette-Guerin failed to induce IRF-1 expression and had no effe
233 igands or bacteria such as bacillus Calmette-Guerin increases antitumor immune responses and delays t
234 nuated Mycobacterium bovis bacillus Calmette-Guerin induces less PPARgamma and preferentially uses th
235 lowing Mycobacterium bovis bacillus Calmette-Guerin infection and costimulation with IFN-gamma, we ob
236 resented with disseminated Bacillus Calmette-Guerin infection and oligoclonal T cells with no naive m
237 tuberculosis and M. bovis bacillus Calmette-Guerin infection down-regulated the expression of CIITA/
240 bacterium tuberculosis and bacillus Calmette-Guerin infections of macaques induced expression of vari
242 ogenic Mycobacterium bovis bacillus Calmette-Guerin intracellular survival, downregulated antimicrobi
243 y attenuating mechanism of bacillus Calmette-Guerin is the loss of cytolytic activity mediated by sec
244 Evidence suggests that bacillus Calmette-Guerin is the most effective intravesical therapy for th
246 also lowered intracellular Bacillus Calmette-Guerin levels in mammary epithelial cancer MCF-7 cells.
247 lternatives to traditional Bacillus Calmette-Guerin needles and syringes for the administration of fI
249 accine Mycobacterium bovis bacillus Calmette-Guerin or the adoptive transfer of mycobacteria-activate
251 binant Mycobacterium bovis bacillus Calmette-Guerin overexpressing the 30-kDa antigen, C3HeB/FeJ mice
252 at M. marinum and M. bovis bacillus Calmette-Guerin produce a type of spore known as an endospore, wh
253 vealed that currently used bacillus Calmette-Guerin strains vary in their ability to affect correlate
254 er (NMIBC) recurrent after bacillus Calmette-Guerin therapy is complex and further complicated by hig
255 e with Mycobacterium bovis bacillus Calmette-Guerin to augment host immunity before infection with vi
256 ther dietary approaches, a Bacillus Calmette-Guerin trial in 1976, molecular-targeted agents, and age
258 f index cases, the age and bacillus Calmette-Guerin vaccination status of contacts, and study design
262 rsons who had received the Bacillus Calmette-Guerin vaccine in households with and without a microbio
265 stimulation with live BCG (Bacillus Calmette-Guerin), and a second locus on chromosome region 3q affe
266 vium, Mycobacterium bovis (bacillus Calmette-Guerin), and Mycobacterium tuberculosis (strain H37Rv),
267 H37Ra, Mycobacterium bovis bacillus Calmette-Guerin, and M. kansasii) induced significantly more AMph
268 niae, Helicobacter pylori, bacillus Calmette-Guerin, and Mycobacterium tuberculosis) in a murine mode
269 protection at the level of bacillus Calmette-Guerin, and the fusion protein exhibited high predicted
270 red the childhood measles, bacillus Calmette-Guerin, diphtheria-pertussis-tetanus, polio, and materna
271 terium Mycobacterium bovis bacillus Calmette-Guerin, macrophages recovered from the peritoneal cavity
272 79c in Mycobacterium bovis bacillus Calmette-Guerin, plays an important role in mycobacterial surviva
274 rcinoma in situ, nonuse of bacillus Calmette-Guerin, tumor size > 3 cm, and older age; HRs for progre
276 Vegf-c is up-regulated in Bacillus Calmette-Guerin- and Mycobacterium tuberculosis-induced granuloma
277 tiation of Th17 cells from bacillus Calmette-Guerin-challenged (BCG-challenged) lung CD4+ T cells.
278 M. tuberculosis var. bovis Bacillus Calmette-Guerin-induced p38 MAPK activity caused a marked increas
281 d in livers and lungs from bacillus Calmette-Guerin-infected humanized mice but not in nonhumanized i
284 from the serum of M. bovis bacillus Calmette-Guerin-infected mice could also stimulate macrophage pro
287 ward developing agents for bacillus Calmette-Guerin-refractory superficial bladder cancer continue, h
291 ion by CD4(+) T cells from bacillus Calmette-Guerin-vaccinated mice and show that high-quality microa
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