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Immunogenicity, safety and reactogenicity of a Phase II trial of Vi-DT typhoid conjugate vaccine in healthy Filipino infants and toddlers: A preliminary report.

Authors :
Capeding, Maria Rosario
Alberto, Edison
Sil, Arijit
Saluja, Tarun
Teshome, Samuel
Kim, Deok Ryun
Park, Ju Yeon
Yang, Jae Seung
Chinaworapong, Suchada
Park, Jiwook
Jo, Sue-Kyoung
Chon, Yun
Yang, Seon-Young
Ham, Dong Soo
Ryu, Ji Hwa
Lynch, Julia
Kim, Jerome H.
Kim, Hun
Excler, Jean-Louis
Wartel, T. Anh
Source :
Vaccine. Jun2020, Vol. 38 Issue 28, p4476-4483. 8p.
Publication Year :
2020

Abstract

• Vi-DT is safe and well tolerated in infants and toddlers aged 6–23 months. • Vi-DT showed >1000-fold higher Geometric Mean Titer (GMT) compared to Placebo. • 100% seroconversion reported in Vi-DT group in all age strata. Typhoid fever remains an important public health problem in developing countries and is endemic in many parts of Asia and Africa where the incidence of disease typically peaks in school-aged children. Age restrictions and other limitations of existing oral live-attenuated typhoid and parenteral Vi polysaccharide vaccines have triggered the development of Vi conjugate vaccines with improved immunological properties, use in younger age range, and longer durability of protection. We present the safety, reactogenicity, and immunogenicity data from a Phase II study after a single dose of Vi polysaccharide conjugated to diphtheria toxoid (Vi-DT) conducted in 6–23-month old Filipino children. This is a randomized, observer-blinded Phase II study to assess the immunogenicity, safety and reactogenicity of Vi-DT compared to placebo, conducted in Muntinlupa City, The Philippines. Participants aged 6–23 months were enrolled and randomized to Vi-DT (25 µg) or placebo (0.9% sodium chloride) and evaluated for immunogenicity and overall safety 28 days post vaccination. A total of 285 participants were enrolled and age-stratified: 6 to < 9 months, 9–12 months, and 13–23 months. Seventy-six (76) participants received Vi-DT and 19 received placebo per each strata. All participants seroconverted after a single dose of Vi-DT versus 7% of placebo recipients. Anti-Vi IgG GMT was 444.38 [95% CI (400.28; 493.34)] after a single dose of Vi-DT; there was no change in GMT after placebo administration, 0.41 [95% CI (0.33; 0.51), p < 0.0001]. A similar pattern of immunogenicity was reported across all age strata. The vaccine reported to be safe and well tolerated. Vi-DT vaccine was immunogenic, safe, and well tolerated in children aged 6–23 months. ClinicalTrials.gov registration number: NCT03527355. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0264410X
Volume :
38
Issue :
28
Database :
Academic Search Index
Journal :
Vaccine
Publication Type :
Academic Journal
Accession number :
143458525
Full Text :
https://doi.org/10.1016/j.vaccine.2019.09.074