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Protection by vaccination of children against typhoid fever with a Vi-tetanus toxoid conjugate vaccine in urban Bangladesh: a cluster-randomised trial.
Qadri, Firdausi; Khanam, Farhana; Liu, Xinxue; Theiss-Nyland, Katherine; Biswas, Prasanta Kumar; Bhuiyan, Amirul Islam; Ahmmed, Faisal; Colin-Jones, Rachel; Smith, Nicola; Tonks, Susan; Voysey, Merryn; Mujadidi, Yama F; Mazur, Olga; Rajib, Nazmul Hasan; Hossen, Md Ismail; Ahmed, Shams Uddin; Khan, Arifuzzaman; Rahman, Nazia; Babu, Golap; Greenland, Melanie; Kelly, Sarah; Ireen, Mahzabeen; Islam, Kamrul; O'Reilly, Peter; Scherrer, Karin Sofia; Pitzer, Virginia E; Neuzil, Kathleen M; Zaman, K; Pollard, Andrew J; Clemens, John D.
Afiliación
  • Qadri F; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh. Electronic address: fqadri@icddrb.org.
  • Khanam F; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Liu X; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Theiss-Nyland K; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Biswas PK; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Bhuiyan AI; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Ahmmed F; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Colin-Jones R; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Smith N; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Tonks S; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Voysey M; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Mujadidi YF; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Mazur O; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Rajib NH; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Hossen MI; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Ahmed SU; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Khan A; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Rahman N; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Babu G; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Greenland M; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Kelly S; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Ireen M; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Islam K; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • O'Reilly P; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Scherrer KS; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Pitzer VE; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, Yale University, New Haven, CT USA.
  • Neuzil KM; University of Maryland School of Medicine, Baltimore MD, USA.
  • Zaman K; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Pollard AJ; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Clemens JD; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; University of California Los Angeles, Fielding School of Public Health, Los Angeles, CA, USA.
Lancet ; 398(10301): 675-684, 2021 08 21.
Article en En | MEDLINE | ID: mdl-34384540
ABSTRACT

BACKGROUND:

Typhoid fever remains a major cause of morbidity and mortality in low-income and middle-income countries. Vi-tetanus toxoid conjugate vaccine (Vi-TT) is recommended by WHO for implementation in high-burden countries, but there is little evidence about its ability to protect against clinical typhoid in such settings.

METHODS:

We did a participant-masked and observer-masked cluster-randomised trial preceded by a safety pilot phase in an urban endemic setting in Dhaka, Bangladesh. 150 clusters, each with approximately 1350 residents, were randomly assigned (11) to either Vi-TT or SA 14-14-2 Japanese encephalitis (JE) vaccine. Children aged 9 months to less than 16 years were invited via parent or guardian to receive a single, parenteral dose of vaccine according to their cluster of residence. The study population was followed for an average of 17·1 months. Total and overall protection by Vi-TT against blood culture-confirmed typhoid were the primary endpoints assessed in the intention-to-treat population of vaccinees or all residents in the clusters. A subset of approximately 4800 participants was assessed with active surveillance for adverse events. The trial is registered at www.isrctn.com, ISRCTN11643110.

FINDINGS:

41 344 children were vaccinated in April-May, 2018, with another 20 412 children vaccinated at catch-up vaccination campaigns between September and December, 2018, and April and May, 2019. The incidence of typhoid fever (cases per 100 000 person-years) was 635 in JE vaccinees and 96 in Vi-TT vaccinees (total Vi-TT protection 85%; 97·5% CI 76 to 91, p<0·0001). Total vaccine protection was consistent in different age groups, including children vaccinated at ages under 2 years (81%; 95% CI 39 to 94, p=0·0052). The incidence was 213 among all residents in the JE clusters and 93 in the Vi-TT clusters (overall Vi-TT protection 57%; 97·5% CI 43 to 68, p<0·0001). We did not observe significant indirect vaccine protection by Vi-TT (19%; 95% CI -12 to 41, p=0·20). The vaccines were well tolerated, and no serious adverse events judged to be vaccine-related were observed.

INTERPRETATION:

Vi-TT provided protection against typhoid fever to children vaccinated between 9 months and less than 16 years. Longer-term follow-up will be needed to assess the duration of protection and the need for booster doses.

FUNDING:

The study was funded by the Bill & Melinda Gates Foundation.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polisacáridos Bacterianos / Fiebre Tifoidea / Toxoide Tetánico / Vacunas Tifoides-Paratifoides / Vacunación / Vacunas Conjugadas Tipo de estudio: Clinical_trials País/Región como asunto: Asia Idioma: En Revista: Lancet Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polisacáridos Bacterianos / Fiebre Tifoidea / Toxoide Tetánico / Vacunas Tifoides-Paratifoides / Vacunación / Vacunas Conjugadas Tipo de estudio: Clinical_trials País/Región como asunto: Asia Idioma: En Revista: Lancet Año: 2021 Tipo del documento: Article