Immune non-interference and safety study of Vi-DT typhoid conjugate vaccine with a measles, mumps and rubella containing vaccine in 9-15 months old Nepalese infants.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
22 09 2022
Historique:
received: 25 12 2021
revised: 06 07 2022
accepted: 15 08 2022
pubmed: 6 9 2022
medline: 14 9 2022
entrez: 5 9 2022
Statut: ppublish

Résumé

Typhoid fever is a common disease in developing countries especially in the Indian subcontinent and Africa. The available typhoid conjugate vaccines (TCV) have been found to be highly immunogenic in infants and children less than 2 years of age. Many countries are planning to adopt TCV in their routine EPI programs around 9 months of age when measles containing vaccines are given. Therefore, Vi-DT TCV was tested in 9-15 months aged healthy infants in Nepal to demonstrate non-interference with a measles containing vaccine. This was a randomized, open label, phase III study to assess the immune non-interference, safety, and reactogenicity of Vi-DT typhoid conjugate vaccine when given concomitantly with measles, mumps and rubella (MMR) vaccine. A total of 360 participants aged 9-15 months were enrolled and randomized equally into Vi-DT + MMR (180 participants) or MMR alone (180 participants) group and were evaluated for immunogenicity and safety 28 days post vaccination. Using the immunogenicity set, difference between proportions (95% CI) of the Vi-DT + MMR group vs MMR alone group were -2.73% (-8.85, 3.38), -3.19% (-11.25, 4.88) and 2.91% (-3.36, 9.18) for sero-positivity rate of anti-measles, anti-mumps and anti- rubella, respectively. Only the lower bound of the range in difference of the proportions for sero-positivity rate of anti-mumps did not satisfy the non-inferiority criteria as it was above the -10% limit, which may not be of clinical significance. These results were confirmed in the per protocol set. There were no safety concerns reported from the study and both Vi-DT + MMR and MMR alone groups were comparable in terms of solicited and unsolicited adverse events . Results indicated that there is non-interference of MMR vaccine with Vi-DT and Vi-DT conjugate vaccine could be considered as an addition to the EPI schedule among children at risk of contracting typhoid.

Sections du résumé

BACKGROUND
Typhoid fever is a common disease in developing countries especially in the Indian subcontinent and Africa. The available typhoid conjugate vaccines (TCV) have been found to be highly immunogenic in infants and children less than 2 years of age. Many countries are planning to adopt TCV in their routine EPI programs around 9 months of age when measles containing vaccines are given. Therefore, Vi-DT TCV was tested in 9-15 months aged healthy infants in Nepal to demonstrate non-interference with a measles containing vaccine.
METHODS
This was a randomized, open label, phase III study to assess the immune non-interference, safety, and reactogenicity of Vi-DT typhoid conjugate vaccine when given concomitantly with measles, mumps and rubella (MMR) vaccine. A total of 360 participants aged 9-15 months were enrolled and randomized equally into Vi-DT + MMR (180 participants) or MMR alone (180 participants) group and were evaluated for immunogenicity and safety 28 days post vaccination.
RESULTS
Using the immunogenicity set, difference between proportions (95% CI) of the Vi-DT + MMR group vs MMR alone group were -2.73% (-8.85, 3.38), -3.19% (-11.25, 4.88) and 2.91% (-3.36, 9.18) for sero-positivity rate of anti-measles, anti-mumps and anti- rubella, respectively. Only the lower bound of the range in difference of the proportions for sero-positivity rate of anti-mumps did not satisfy the non-inferiority criteria as it was above the -10% limit, which may not be of clinical significance. These results were confirmed in the per protocol set. There were no safety concerns reported from the study and both Vi-DT + MMR and MMR alone groups were comparable in terms of solicited and unsolicited adverse events .
CONCLUSIONS
Results indicated that there is non-interference of MMR vaccine with Vi-DT and Vi-DT conjugate vaccine could be considered as an addition to the EPI schedule among children at risk of contracting typhoid.

Identifiants

pubmed: 36064672
pii: S0264-410X(22)01009-X
doi: 10.1016/j.vaccine.2022.08.034
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Diphtheria-Tetanus Vaccine 0
Measles Vaccine 0
Measles-Mumps-Rubella Vaccine 0
Typhoid-Paratyphoid Vaccines 0
Vaccines, Conjugate 0

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5828-5834

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest JHR, HKP, JHS, YL, and HK are employees of SK bioscience. JHK is a scientific consultant to SK bioscience for COVID 19 vaccine research. All remaining authors declare no competing interests.

Auteurs

Tarun Saluja (T)

International Vaccine Institute, Seoul, Republic of Korea. Electronic address: Tarun.Saluja@ivi.int.

Ganesh Kumar Rai (GK)

Kanti Children's Hospital, Kathmandu, Nepal.

Shipra Chaudhary (S)

B P Koirala Institute of Health Sciences, Dharan, Nepal.

Piush Kanodia (P)

Nepalgunj Medical College, Nepalgunj, Nepal.

Bishnu Rath Giri (BR)

Kanti Children's Hospital, Kathmandu, Nepal.

Deok Ryun Kim (DR)

International Vaccine Institute, Seoul, Republic of Korea.

Jae Seung Yang (JS)

International Vaccine Institute, Seoul, Republic of Korea.

Il-Yeon Park (IY)

International Vaccine Institute, Seoul, Republic of Korea.

Seung-Eun Kyung (SE)

International Vaccine Institute, Seoul, Republic of Korea.

Sridhar Vemula (S)

International Vaccine Institute, Seoul, Republic of Korea.

Jagadeesh Reddy E (J)

International Vaccine Institute, Seoul, Republic of Korea.

Bomi Kim (B)

International Vaccine Institute, Seoul, Republic of Korea.

Birendra Prasad Gupta (BP)

International Vaccine Institute, Seoul, Republic of Korea.

Sue Kyoung Jo (SK)

International Vaccine Institute, Seoul, Republic of Korea.

Ji Hwa Ryu (JH)

SK bioscience, Seoul, Republic of Korea.

Ho Keun Park (HK)

SK bioscience, Seoul, Republic of Korea.

Jong Hoon Shin (JH)

SK bioscience, Seoul, Republic of Korea.

Yoonyeong Lee (Y)

SK bioscience, Seoul, Republic of Korea.

Hun Kim (H)

SK bioscience, Seoul, Republic of Korea.

Jerome H Kim (JH)

International Vaccine Institute, Seoul, Republic of Korea.

Zenaida Reynoso Mojares (ZR)

International Vaccine Institute, Seoul, Republic of Korea.

T Anh Wartel (TA)

International Vaccine Institute, Seoul, Republic of Korea.

Sushant Sahastrabuddhe (S)

International Vaccine Institute, Seoul, Republic of Korea.

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