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Immune responses to typhoid conjugate vaccine in a two dose schedule among Nepalese children <2 years of age.
Bijukchhe, Sanjeev M; Gurung, Meeru; Pokhrel, Bhishma; Shakya, Mila; Pant, Dikshya; Maskey, Pratistha; Maskey, Himang; Dhakal, Babita; Rajkarkinar, Shristy; Bista, Sabitri; Voysey, Merryn; Mujadidi, Yama F; Kim, Young Chan; Atherton, Rachel; Jones, Elizabeth; Mclean, Florence; Shrestha, Sonu; Hill, Matilda; Nyland, Katherine Theiss; Kelly, Sarah; O'reilly, Peter; Sah, Ganesh Prasad; Basnyat, Buddha; Pollard, Andrew J; Shrestha, Shrijana.
Affiliation
  • Bijukchhe SM; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal; Department of Paediatrics, University of Oxford, Oxford, United Kingdom. Electronic address: sanjeev.bijukchhe@st-hildas.ox.ac.uk.
  • Gurung M; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Pokhrel B; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Shakya M; Oxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Pant D; Oxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Maskey P; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Maskey H; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Dhakal B; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Rajkarkinar S; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Bista S; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Voysey M; Department of Paediatrics, University of Oxford, Oxford, United Kingdom; NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.
  • Mujadidi YF; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Kim YC; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Atherton R; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Jones E; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Mclean F; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Shrestha S; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Hill M; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Nyland KT; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Kelly S; Department of Paediatrics, University of Oxford, Oxford, United Kingdom; NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.
  • O'reilly P; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
  • Sah GP; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Basnyat B; Oxford University Clinical Research Unit, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Pollard AJ; Department of Paediatrics, University of Oxford, Oxford, United Kingdom; NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.
  • Shrestha S; Deparment of Paediatrics, Patan Academy of Health Sciences, Kathmandu, Nepal.
Vaccine ; 42(8): 2018-2025, 2024 Mar 19.
Article in En | MEDLINE | ID: mdl-38395723
ABSTRACT

BACKGROUND:

Previously, the Vi-typhoid conjugate vaccine (Vi-TT) was found to be highly efficacious in Nepalese children under 16 years of age. We assessed the immunogenicity of Vi-TT at 9 and 12 months of age and response to a booster dose at 15 months of age.

METHODS:

Infants were recruited at Patan Hospital, Kathmandu and received an initial dose of Vi-TT at 9 or 12 months of age with a booster dose at 15 months of age. Blood was taken at four timepoints, and antibody titres were measured using a commercial ELISA kit. The primary study outcome was seroconversion (4-fold rise in antibody titre) of IgG one month after both the doses.

FINDINGS:

Fifty children were recruited to each study group.Some visits were disrupted by the COVID19 pandemic and occurred out of protocol windows.Both the study groups attained 100 % IgG seroconversion after the initial dose. IgG seroconversion in the 9-month group was significantly higher than in the 12-month group (68.42 % vs 25.8 %, p < 0.001). Among individuals who attended visits per protocol, IgG seroconversion after the first dose occurred in 100 % of individuals (n = 27/27 in 9-month and n = 32/32 in 12-month group). However, seroconversion rates after the second dose were 80 % in the 9-month and 0 % in the shorter dose-interval 12-month group (p < 0.001) (n = 16/20 and n = 0/8, respectively).

INTERPRETATION:

Vi-TT is highly immunogenic at both 9 and 12 months of age. Stronger response to a booster in the 9-month group is likely due to the longer interval between doses.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Typhoid Fever / Typhoid-Paratyphoid Vaccines Limits: Child / Humans / Infant Country/Region as subject: Asia Language: En Journal: Vaccine Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Typhoid Fever / Typhoid-Paratyphoid Vaccines Limits: Child / Humans / Infant Country/Region as subject: Asia Language: En Journal: Vaccine Year: 2024 Document type: Article
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