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1 ge 6 to 11 years for children given neonatal BCG vaccination.
2 the human host response induced by neonatal BCG vaccination.
3 able to that provided by Mycobacterium bovis BCG vaccination.
4 t were strongest after BCG/rAd85A and rAd85A/BCG vaccination.
5 following M. tuberculosis infection or after BCG vaccination.
6 t in acquired immunity conferred by M. bovis BCG vaccination.
7 gens were significantly enhanced by M. bovis BCG vaccination.
8 ewer tubercles than did intradermal M. bovis BCG vaccination.
9 immune responses to mycobacteria induced by BCG vaccination.
10 ater than in vaccinees administered a single BCG vaccination.
11 ith degree of exposure to the index case and BCG vaccination.
12 , which was comparable with that afforded by BCG vaccination.
13 the levels were significantly enhanced after BCG vaccination.
14 phages infected with live mycobacteria after BCG vaccination.
15 fore, as well as 2 weeks and 3 months after, BCG vaccination.
16 ation of IFN-gamma mRNA expression following BCG vaccination.
17 xposed to various stimuli was enhanced after BCG vaccination.
18 uishes between M. tuberculosis infection and BCG vaccination.
19 s adjuvants to increase the effectiveness of BCG vaccination.
20 sting of 15 mm or greater 1 to 3 years after BCG vaccination.
21 investigate human T cell subsets induced by BCG vaccination.
22 rtially restored by concurrent or subsequent BCG vaccination.
23 ion status influenced the effect of neonatal BCG vaccination.
24 losis infection was strongly associated with BCG vaccination.
25 predominance of the Beijing genotype, after BCG vaccination.
26 y also contributes to the anti-TB effects of BCG vaccination.
27 ad presented with BCG osteitis after newborn BCG vaccination.
28 rs2275913 was associated with osteitis after BCG vaccination.
29 IP may provide a novel adjuvant strategy for BCG vaccination.
30 ection status, bacterial drug resistance, or BCG vaccination.
31 azimine selectively expands Tcm cells during BCG vaccination.
32 ) vaccination after infancy or with repeated BCG vaccinations.
33 deoxyglucose ((18)F-FDG) before versus after BCG vaccinations.
34 eous or intradermal bacille Calmette-Guerin (BCG) vaccination.
35 (TB) infection and bacillus Calmette Guerin (BCG) vaccination.
36 were 10 mm or greater than did percutaneous BCG vaccination (12 of 46 participants compared with 1 o
37 mune responses following Mycobacterium bovis BCG vaccination, 15-mer synthetic peptides were synthesi
38 (+) T cells, in immunity induced by M. bovis BCG vaccination, 4-week-old specific-pathogen-free pigs
43 s with a history of Bacille Calmette-Guerin (BCG) vaccination after infancy or with repeated BCG vacc
44 ext of experimental bacille Calmette-Guerin (BCG) vaccination, Ag-specific T cell responses to mycoba
46 ssess the heterologous protective effects of BCG vaccination against respiratory infection (RI) and s
47 s: this showed that the protective effect of BCG vaccination against the development of asthma identi
48 ariable efficacy of Bacille Calmette Guerin (BCG) vaccination against tuberculosis has prompted effor
49 ogy in four/eight parameters assessed, while BCG vaccination alone did so in only one parameter studi
50 Depletion of NK1.1(+) cells at the time of BCG vaccination also increased the bacillary burden and
51 s with active tuberculosis (P<.05), and oral BCG vaccination also induced significant increases in LA
52 ght be affected by various factors including BCG vaccination and age, our results suggest that the pr
55 he null hypothesis of no association between BCG vaccination and COVID-19 mortality, and suggest that
56 Our findings support a causal link between BCG vaccination and improved ability to control growth o
57 fected controls, while in kinetic studies of BCG vaccination and INH treatment we compared pre-experi
58 n both cattle models of protective immunity (BCG vaccination and INH treatment) was transient over ti
61 ted here, and to establish causality between BCG vaccination and protection from severe COVID-19.
62 patients with active tuberculosis even after BCG vaccination and suggest that combinatorial use of an
63 y ages are functionally enhanced by M. bovis BCG vaccination and suggests an important role for this
65 esponses induced by bacille Calmette-Guerin (BCG) vaccination and active tuberculosis infection were
66 ssociation between bacillus Calmette-Guerin (BCG) vaccination and childhood asthma in a birth cohort
67 g IFN-gamma during bacillus Calmette-Guerin (BCG) vaccination and subsequent M. tuberculosis challeng
68 mmune responses to bacillus Calmette-Guerin (BCG)-vaccination and susceptibility to pediatric tubercu
69 justing for other TB risk factors (age, sex, BCG-vaccination and stays >=3 months in Africa/Asia).
70 ce/ethnicity, poverty, education, history of BCG vaccination, and history of household exposure to tu
72 tatus of kidney transplantation, old age, no BCG vaccination, and positive donor-specific antibody ar
73 to investigate the immunogenicity of aerosol BCG vaccination, and the phenotypic profile of periphera
74 lation differences in immune responses after BCG vaccination are observed among infants, as well as a
75 ound to mount Th1-like responses to M. bovis BCG vaccination as determined by immunoproliferation and
77 ous for COVID-19 who did and did not receive BCG vaccination as part of routine childhood immunizatio
78 in skin test (TST) negative and eligible for BCG vaccination as part of the last round of Norway's ma
79 Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination as a surrogate for M. tuberculosis infe
80 nistration increased tuberculosis deaths-eg, BCG vaccination at 6 weeks, the recommended age of DTP1,
81 ed infants were randomly assigned to receive BCG vaccination at birth (the early vaccination arm) or
85 sitization biases T cell immunity induced by BCG vaccination away from type 1 IFN-gamma responses ass
87 ell and monocyte activation that occur after BCG vaccination but do not support the hypothesis that B
88 cells at an early time point after M. bovis BCG vaccination, but CD4(+) T cells were found to be mor
89 for age and sex, we found that a history of BCG vaccination, but not meningococcal, pneumococcal, or
91 reventing tuberculosis is uncertain and that BCG vaccination can interfere with the detection and tre
94 ts for age at vaccination, tribe, subsequent BCG vaccination, chronic medical illness, isoniazid use,
96 mycobacteria and/or bacille Calmette-Guerin (BCG) vaccination compromise the estimates derived from p
97 cytokine responses (trained immunity) after BCG vaccination.CONCLUSIONThe capacity of BCG to enhance
106 o-distribution of high TB prevalence and low BCG vaccination coverage were created by overlying spati
108 ex, an estimation of the degree of universal BCG vaccination deployment in a country, and COVID-19 mo
110 however, the addition of IL-12 or CpG ODN to BCG vaccination did not alter granuloma formation or res
113 vaccinated and unvaccinated groups, and that BCG vaccination did not perturb normal development.
114 atic review and meta-analysis suggested that BCG vaccination did not protect against allergic sensiti
116 ability to detect LTBI, was less affected by BCG vaccination, discriminated responses due to nontuber
117 w that treatment with these two drugs during BCG vaccination dramatically improves vaccine efficacy.
118 ta activity augments the initial response to BCG vaccination, early bacterial clearance may adversely
119 ng novel vaccines, since Mycobacterium bovis BCG vaccination effectively prolongs survival after low-
120 used to assess trained immunity.RESULTSWhile BCG vaccination enhanced cytokine responses to restimula
122 icate that inclusion of CT in the intranasal BCG vaccination enhances COX-2-mediated PGE(2) release b
123 ow that inhibition of IL-10 signaling during BCG vaccination enhances host-generated Ag-specific IFN-
124 ermore, mice that received clofazimine after BCG vaccination exhibited significantly enhanced resista
125 ovis infected animals, including those where BCG vaccination failed to prevent bovine TB pathology fo
126 s, such as IPT and bacillus Calmette-Guerin (BCG) vaccination for preventing TB disease among exposed
129 Although widely used, Mycobacterium bovis BCG vaccination given at birth does not protect against
135 immunity may suggest increased inflammation, BCG vaccination has been epidemiologically associated wi
141 ormation following bacillus Calmette-Guerin (BCG) vaccination has been associated with lower all-caus
144 y against mycobacteria are upregulated after BCG vaccination; however, a significantly weaker respons
145 ing system, we were able to demonstrate that BCG vaccination imparted significant protection by reduc
146 BCG (BCG lux), to study immune responses to BCG vaccination in 50 neonates in a setting in Cape Town
147 Organization recommends Mycobacterium bovis BCG vaccination in areas of high tuberculosis prevalence
152 BCG-reactive memory NK cells were induced by BCG vaccination in infants, whereas in vitro IFN-gamma e
153 ere, we perform a dose-ranging study of i.v. BCG vaccination in macaques to generate a range of immun
154 studies on mucosal and intravenous routes of BCG vaccination in non-human primate models have renewed
155 erable debate regarding the effectiveness of BCG vaccination in preventing tuberculosis and death, pa
156 ults differ from those of studies of delayed BCG vaccination in South Africa and the Gambia, suggesti
157 demonstration of known vaccine effects (eg, BCG vaccination in specific populations), and by compari
158 cellular and molecular responses induced by BCG vaccination in the guinea pig model of pulmonary tub
161 Here we show that bacille Calmette-Guerin (BCG) vaccination in healthy volunteers led not only to a
162 study suggests a temporal window soon after BCG vaccination, in which STAT1-dependent activation of
164 Depletion of NK1.1(+) cells at the time of BCG vaccination increased the number of immunosuppressiv
166 ig IFN-gamma (gpIFN-gamma) and reported that BCG vaccination induced a significant increase in the IF
168 with nonsensitized controls, indicating that BCG vaccination induced gamma delta T cell activation as
169 lts in a low tuberculosis incidence setting, BCG vaccination induced heterologous innate cytokine pro
173 Our findings demonstrated that intranasal BCG vaccination induces the expansion of CD3-NK1.1+CD69+
180 ogether with the unexpected observation that BCG vaccination influenced M. avium subsp. paratuberculo
181 als randomizing low-weight neonates to early BCG vaccination (intervention) versus no BCG vaccination
183 ation but do not support the hypothesis that BCG vaccination is a risk factor for postnatal HIV trans
184 e generation of host Th1 responses following BCG vaccination is accepted as the major mechanism of pr
187 ycobacterium bovis bacillus Calmette-Guerin (BCG) vaccination is efficacious for newborns or adults w
190 in 1975, where discontinuation of newborns' BCG vaccination led to a dramatic decrease in BCG covera
191 in vaccinated and nonvaccinated populations, BCG vaccination led to TB case declines of 15.4% and 21.
194 idly from antigen-presenting cells following BCG vaccination, maintenance of OX40-expressing vaccine-
195 date of birth was negatively associated with BCG vaccination (marginal RD = -1.5; 95% CI -2.2, -0.9),
198 have suggested that bacille Calmette-Guerin (BCG) vaccination may lessen the severity of Coronavirus
199 ave suggested that Bacillus Calmette-Guerin (BCG) vaccination may reduce the risk of allergic disease
200 justment for prior bacillus Calmette-Guerin [BCG] vaccination).Measurements and Main Results: For all
202 roinflammatory leukocyte responses following BCG vaccination, nonspecific effects of influenza vaccin
203 as associated with bacillus Calmette-Guerin (BCG) vaccination (odds ratio: 25.1 [95% confidence inter
205 the effectiveness of treatment programs, and BCG vaccination of HIV-negative homeless individuals hav
207 o have beneficial nonspecific effects; early BCG vaccination of low-birth-weight (LBW) newborns reduc
208 vestigated the effects of M.tb infection and BCG vaccination on B cell responses to heterologous path
209 earer evidence that any protective effect of BCG vaccination on childhood asthma is likely to be tran
210 r understanding of the effect of respiratory BCG vaccination on gammadelta T cell responses in the lu
216 the effectiveness of preventive therapy and BCG vaccination on the risk of developing tuberculosis.
217 as performed to examine the effects of early BCG vaccination on the risk, cause, and severity of infa
218 t to assess whether the protective effect of BCG vaccination on wheeze observed in the MANCAS cohort
220 adily trafficked to the airway or lung after BCG vaccination or M. tuberculosis infection, and some o
222 ically significant waning of the efficacy of BCG vaccination over time, greater among men than women.
226 ting rates, there was no association between BCG vaccination policy and COVD-19 spread rate or percen
227 s lower for the majority of countries with a BCG vaccination policy for at least the preceding 15 yea
228 do not provide evidence to correlate overall BCG vaccination policy with the spread of CoV-2 and its
230 n between national bacillus Calmette-Guerin (BCG) vaccination policy and the prevalence and mortality
234 tive therapy and treatment, coupled with the BCG vaccination program, would lead to a 47% decline in
236 s including slum clearances, introduction of BCG vaccination programmes, and the ending of postwar fo
239 used to the Ag 85B epitope showed that prior BCG vaccination promoted high-affinity IgG1 responses th
241 Taken together, these data demonstrate that BCG vaccination protects against infection with diverse
243 ges of gammadelta T cells caused by M. bovis BCG vaccination rather than being due solely to help fro
248 e, Ab blockade of IL-10R specifically during BCG vaccination resulted in additional protection agains
252 cy, exposure to environmental tobacco smoke, BCG vaccination, season, and body habitus on susceptibil
256 , rMtb72F delivered by coadministration with BCG vaccination significantly improved the survival of t
258 erculin skin test or IFNgamma release assay, BCG vaccination significantly protected against tubercul
260 st, ELISPOT results were not correlated with BCG vaccination status (p=0.7), whereas TST results were
261 uestionnaires, which included information on BCG vaccination status and preexisting demographic and c
264 n Immunity and Health (1974-1994), including BCG vaccination status, perinatal and sociodemographic c
265 tal zone of residence, country of birth, and BCG vaccination status, while occupations were placed in
266 yses examined age, bacillus Calmette-Guerin (BCG) vaccination status, and sex as predictor variables
270 and the type of immune responses elicited by BCG vaccination to enable comparisons with potential new
273 ycobacterium bovis bacillus Calmette-Guerin (BCG) vaccination to protect against mycobacterial infect
274 y, an in vivo immunisation model showed that BCG vaccination under PD-L1 blockade could enhance antig
276 rly BCG vaccination (intervention) versus no BCG vaccination (usual practice in low-weight neonates,
278 FN-gamma production evaluated 10-14 mo after BCG vaccination was 26-fold higher for infants who were
279 ry immunity conferred by Mycobacterium bovis BCG vaccination was affected in mice with chronic enteri
280 2 IgG seroconversion.CONCLUSIONSA history of BCG vaccination was associated with a decrease in the se
283 Here, we determined whether a history of BCG vaccination was associated with decreased SARS-CoV-2
285 trend was observed with guinea pigs in which BCG vaccination was boosted by DNA vaccination, although
286 oluble, substrate of the circadian effect of BCG vaccination was demonstrated by the enhanced capacit
287 ve tuberculin skin test (OR, 2.21; P = .03); BCG vaccination was particularly protective, especially
288 In the four studies with mortality data, BCG vaccination was significantly protective against dea
289 e majority of gamma delta T cells induced by BCG vaccination were gamma 9+ delta 2+ T cells reactive
290 ut of ten macaques that received intravenous BCG vaccination were highly protected, with six macaques
291 Effects of primary and booster intradermal BCG vaccinations were assessed in 3 distinct assays of m
294 imary or secondary bacillus Calmette-Guerin (BCG) vaccination were assessed for Ab responses to AM vi
295 Finally, i.v. bacillus Calmette-Guerin (BCG) vaccination (which activates multiple TLRs, especia
296 of INH can be augmented following historical BCG vaccination, which support findings from previous ob
297 ating inflammatory proteins before and after BCG vaccination, while ex vivo Mycobacterium tuberculosi
298 sis that the coadministration or boosting of BCG vaccination with Mtb72F may limit the lung consolida
299 To determine whether Mycobacterium bovis BCG vaccination would alter gamma interferon (IFN-gamma)
300 hesized that Mtb PPD-induced IFN-gamma after BCG vaccination would be similar in infants from these 2