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1 cine rollouts and extensively drug-resistant typhoid.
2 patients developed complications related to typhoid.
3 n of TCVs in countries with a high burden of typhoid.
4 ation of a coalition to act as a steward for typhoid.
5 ffort to reduce morbidity and mortality from typhoid.
6 easured a high but heterogenous incidence of typhoid.
9 eated in 2010 with the mission of preventing typhoid among vulnerable populations through research, e
12 First, we assess how varying perceptions of typhoid and conflicts of interest led to a nonlinear evo
13 on was particularly successful in preventing typhoid and greatly reduced the number of casualties fro
14 elationships of rainfall or temperature with typhoid and iNTS incidence might infer differences in ep
15 tegies, including a combined introduction of typhoid and iNTS vaccines, aimed at reducing transmissio
17 ion can significantly decrease the burden of typhoid and may also impact antimicrobial resistance, wa
18 ght major differences in the pathogenesis of typhoid and non-typhoidal Salmonella infections and demo
22 During the 11th International Conference on Typhoid and Other Invasive Salmonelloses held in Hanoi,
23 onvened the 11th International Conference on Typhoid and Other Invasive Salmonelloses in Hanoi, Vietn
24 onvened the 10th International Conference on Typhoid and Other Invasive Salmonelloses in Kampala, Uga
26 f children (<12 years old) hospitalized with typhoid and paratyphoid (32% and 21%, respectively) decr
27 ecific introduction, but questions regarding typhoid and paratyphoid epidemiology persist, especially
30 Hospital (YGH) to estimate the incidence of typhoid and paratyphoid fevers among person >=12 years o
32 te the cost of illness due to enteric fever (typhoid and paratyphoid) at selected sites in Nepal.
33 mate the cost of illness from enteric fever (typhoid and paratyphoid) at selected sites in Pakistan.
35 imination, effective interventions exist for typhoid, and humans are the organism's only known reserv
37 innovative solutions, the Coalition Against Typhoid, based at the Sabin Vaccine Institute, convened
38 es at the local level, the Coalition against Typhoid, based at the Sabin Vaccine Institute, convened
39 he recent rise of extensively drug-resistant typhoid bears the biosocial footprint of more than half
46 ability weights to estimate the reduction in typhoid burden, identify the strategy that maximised ave
47 country, there is still a significant annual typhoid burden, which particularly affects children.
48 s were introduced to deal with the spread of typhoid but these varied between the 3 countries, depend
52 ious serology signature to distinguish acute typhoid cases from controls and then validated our findi
55 he majority (>90%) of blood culture-positive typhoid cases remain unobserved in surveillance studies.
58 Vaccine Acceleration Consortium to "Take on Typhoid," combining advocacy and communications efforts
61 arch 2018 calling for integration of a novel typhoid conjugate vaccine (TCV) into routine immunizatio
64 is study aims to determine the efficacy of a typhoid conjugate vaccine (TCV) that was recently prequa
65 World Health Organization (WHO)-prequalified typhoid conjugate vaccine (TCV), Gavi funding for eligib
66 ease elimination through the introduction of typhoid conjugate vaccine (TCV), we again need to recons
67 accine Alliance (Gavi), for the use of a new typhoid conjugate vaccine (TCV), we should turn our mind
69 ends studies to evaluate co-administering Vi-typhoid conjugate vaccine (Vi-TCV) with routine childhoo
72 eir deliberations on strategies to introduce typhoid conjugate vaccine as a preventive tool against e
74 evaluating the efficacy of a newly developed typhoid conjugate vaccine in an urban setting in Nepal.
75 tion and control interventions including the typhoid conjugate vaccine in the poor communities that h
76 sistance was common, highlighting a role for typhoid conjugate vaccine into routine infant vaccine sc
77 th Organization prequalification should make typhoid conjugate vaccine more accessible and affordable
79 ts are implemented in high-burden countries, typhoid conjugate vaccine presents a promising disease-p
80 be brought to bear on the current context of typhoid conjugate vaccine rollouts and extensively drug-
82 oach to accelerate the introduction of a new typhoid conjugate vaccine to reduce the burden of typhoi
83 tion and control, including consideration of typhoid conjugate vaccine use as well as nonvaccine cont
87 safety, tolerability, and immunogenicity of typhoid conjugate vaccine, and early efficacy results ar
91 orld Health Organization now recommends that typhoid conjugate vaccines (TCV) be used in settings wit
92 etween Gavi's investment decision to support typhoid conjugate vaccines (TCVs) in 2008 and Gavi suppo
94 stance, and licensure of a new generation of typhoid conjugate vaccines (TCVs) were instrumental in p
95 , the results of ground-breaking research on typhoid conjugate vaccines (TCVs), the World Health Orga
96 s have centered on supporting development of typhoid conjugate vaccines and expanding disease surveil
98 The World Health Organization recommends typhoid conjugate vaccines for country-specific introduc
99 ation recommendation for the introduction of typhoid conjugate vaccines for infants and children aged
101 (TyVAC) aims to support the introduction of typhoid conjugate vaccines into Gavi-eligible countries
106 address the impact of polysaccharide length, typhoid conjugates made with short- and long-chain fract
107 ts to analyze how historical and new data on typhoid control can be brought to bear on the current co
108 ssume neither unanticipated breakthroughs in typhoid control nor any chaotic shocks, history suggests
109 s to introduce TCVs as part of an integrated typhoid control program, particularly in light of the in
110 lloses in Africa and will help inform future typhoid control strategies, namely, introduction of typh
111 ood safety are critical for robust long-term typhoid control, and the recent Strategic Advisory Group
113 se developments are encouraging, all current typhoid diagnostics are inadequate, having either poor p
114 CV), we again need to reconsider the role of typhoid diagnostics in how they can aid in facilitating
116 typhoid fever, three to 25 patients without typhoid disease are treated with antimicrobials unnecess
119 Salmonella typhoid toxin contributes to typhoid disease progression and chronic infection, but l
123 s for infants and children aged >6 months in typhoid-endemic countries is likely to require further i
125 Empiric prescribing of antimicrobials in typhoid-endemic settings has increased selective pressur
126 tion of these parameter values in real-world typhoid-endemic settings will improve model predictions
127 e to the paucity of diagnostic facilities in typhoid-endemic settings, including microbiology, histop
128 timate excess perforations attributed to the typhoid epidemic, using temporal trends in S. Typhi bloo
131 radication classified the political will for typhoid eradication as "none." Here we revisit the Task
132 ropean armies that were regularly ravaged by typhoid, especially garrisons stationed in the colonies.
133 emonstrated an overall adjusted incidence of typhoid fever 2-3 times higher than previous estimates i
135 var Typhi (Salmonella Typhi) is the cause of typhoid fever and a human host-restricted organism.
137 l and non-typhoidal Salmonelleae (NTS) cause typhoid fever and gastroenteritis, respectively, in huma
138 anding of age and geographic distribution of typhoid fever and other invasive salmonelloses in Africa
139 ng by studies that reported the incidence of typhoid fever and those that estimated incidence by usin
147 nd acceleration of the global agenda towards typhoid fever control with a strong World Health Organiz
148 development of a diagnostic assay for acute typhoid fever focused on detecting IgA responses against
153 Our understanding of the global burden of typhoid fever has improved in recent decades, with both
154 Available commercial serologic assays for typhoid fever have limited sensitivity and specificity.
156 ance in Africa Program (TSAP) and the Severe Typhoid Fever in Africa (SETA) program have refined our
157 -restricted pathogen that is responsible for typhoid fever in approximately 10.9 million people annua
158 the diagnosis, treatment, and prevention of typhoid fever in different locations with endemic diseas
163 he rate reduction of blood culture-confirmed typhoid fever in the vaccination arm as compared to the
165 nd geographic representation of high-quality typhoid fever incidence studies, and greater sophisticat
176 el estimates that culture-confirmed cases of typhoid fever lead to an excess of 0.046 perforations pe
183 d for infection and the development of early typhoid fever symptoms within the context of a human cha
185 terica serovar Typhi, the causative agent of typhoid fever, and is thought to be responsible for the
186 tion by examining its estimated incidence of typhoid fever, its history of introducing new vaccines,
188 g causative agents of dysentery, plague, and typhoid fever, rely on a type III secretion system - a m
190 a, including the causative agents of plague, typhoid fever, whooping cough, sexually transmitted infe
199 h 1 antibody isotype (IgA) could distinguish typhoid from other invasive bacterial infections (area u
204 id conjugate vaccine to reduce the burden of typhoid in countries eligible for support from Gavi, the
207 in studying the epidemiology and control of typhoid in these settings can provide insights to guide
208 lowing the discovery of the bacillus causing typhoid, in 1880, understanding of the disease formerly
209 t the probability of hospital admission (and typhoid incidence and mortality) had the greatest influe
214 vaccines (TCV) be used in settings with high typhoid incidence; consequently, governments face a chal
217 ved no significant difference in the rate of typhoid infection (fever >=38 degrees C for >=12 h and/o
219 phical areas by water-based risk factors for typhoid infection or broader measures of health and deve
221 trial designs that use serologically defined typhoid infections (seroefficacy trials) rather than blo
223 the total number of antimicrobial-resistant typhoid infections but not affect the proportion of case
224 io with 80% vaccination coverage, 35% of all typhoid infections were antimicrobial resistant, and 44%
228 e infection with S. Typhimurium is used as a typhoid model, but its relevance to human typhoid is lim
229 cause they bear a substantial burden of both typhoid morbidity and mortality in this population.
231 ere have been no population-based studies of typhoid outside of this community in the past 3 decades.
235 ere are huge opportunities for mainstreaming typhoid prevention and control strategies within the SDG
236 any knowledge we have of its engagement with typhoid prevention, including intention to apply for Gav
237 and town"), as well as competing theories of typhoid proliferation stalled sanitary reform until the
238 e databases, covering 2000-2017, to identify typhoid-related cost-of-illness (COI) studies, cost-of-d
239 a literature review and critical overview of typhoid-related economic issues to inform vaccine introd
242 ultidrug resistance, new antibiotic classes, typhoid's cultural status as a supposedly ancient diseas
245 no validated road map for the elimination of typhoid, the lessons learned in studying the epidemiolog
247 some of the approaches that may help elevate typhoid to a higher level of awareness in public health
248 nifestations ranging from systemic infection typhoid to invasive nontyphoidal Salmonella disease in h
254 cilitate secretion, whereas the secretion of Typhoid toxin in Salmonella enterica serovar Typhi relie
255 ical data are required to assess the role of typhoid toxin in severe disease or the establishment of
260 ter its synthesis by intracellular bacteria, typhoid toxin is secreted into the lumen of the Salmonel
261 e glycan binding specificity of a variant of typhoid toxin produced by a non-typhoidal Salmonellae se
262 human cells, S. Typhi produces two forms of typhoid toxin that have distinct delivery components but
263 e results indicate that the evolution of two typhoid toxin variants has conferred functional versatil
264 tes the host DNA damage response through the typhoid toxin, facilitating typhoid symptoms and chronic
265 cribe the generation and characterization of typhoid toxin-neutralizing human monoclonal antibodies b
273 sing antimicrobial resistance, and therefore typhoid vaccination is recommended as a preventive measu
274 yses might underestimate crucial benefits of typhoid vaccination programmes, because the potential ef
275 We propose that large-scale, more aggressive typhoid vaccination programmes-including catch-up campai
279 n endemic setting in sub-Saharan Africa, the Typhoid Vaccine Acceleration Consortium is conducting a
283 e introduction of a single-dose, efficacious typhoid vaccine into countries with high burden of disea
285 rce's assessment in light of developments in typhoid vaccines and increasing antimicrobial resistance
290 monstrating the efficacy of new Vi-conjugate typhoid vaccines is challenging, due to the cost of fiel
291 programmes, because the potential effect of typhoid vaccines on the treatment of patients with non-s
294 017, WHO recommended the programmatic use of typhoid Vi-conjugate vaccine (TCV) in endemic settings,
295 ine British and American attempts to control typhoid via sanitary interventions from the 1840s to 194
296 s, we estimated that the annual incidence of typhoid was 391 per 100 000 persons and paratyphoid was
297 he relative-risk function of temperature for typhoid was bimodal, with higher risk at both lower (wit
298 fter the onset of the rains, whereas that of typhoid was long-lasting but with a two months delayed s
299 eal perforation with a clinical diagnosis of typhoid were enrolled from 4 tertiary care hospitals in