The Effects of Antibiotic Exposure in Early Infancy on Vaccine Responses

Antibiotic Treatment Clinical Trial

Official title: The Effects of Antibiotic Exposure in Early Infancy on Vaccine Responses

Status Active, not recruiting

Clinical Trial Summary

This prospective cohort study will include 200 term children born in Landspitali University Hospital in Iceland. The cohort will be divided into four groups according to antibiotic exposure of which one is the control group. Children's immune responses to live oral rotavirus vaccine as well as conventional vaccinations given at three, five and 12 months old will be determined by measuring salivary and serologic responses. Responses will be compared between the four groups. Stool samples will also be collected from participants and the composition of the microbiome compared between the four groups.

Clinical Trial Description

This prospective cohort study will evaluate the development of the immune system by means of evaluating the immune responses to oral rotavirus vaccine and the scheduled childhood vaccinations in Iceland, at the age of three, five and 12 months, in four different groups of term children born in Iceland. The cohort will be divided into the following groups: - Group A: Term children born with elective caesarean section (their mothers received intra-operative antibiotics). - Group B: Term vaginally born children and their mothers received intra-partum antibiotics. - Group C: Term vaginally born children that received systemic antibiotics during the first week of life for at least 48 hours. - Group D: Term vaginally born children that had not received systemic antibiotics at the time of recruitment. Parents of children born with elective caesarean section in Landspitali or born vaginally and their mothers received intra-partum antibiotics as well as parents of children in the Neonatal Intensive Care Unit receiving systemic antibiotics during the first week of life will be offered to take part in the study (Groups A, B and C). Parents of children coming to a five day old check up at the Children's Hospital in Landspitali will also be offered to take part in the study (Group D). Sample size calculations show that to detect a 30% difference in immune responses to vaccines with 80% power, 40 infants are needed for analysis in each group. To account for late exclusions due to antibiotic use or drop-out due to other reasons, 50 infants will be recruited to each group. Participants will receive vaccination with the oral live attenuated rotavirus vaccine, Rotarix, at six weeks old and again at three months old. Participants will receive vaccinations with Pentavac against diphtheria, tetanus, pertussis, haemophilus influenza type B and polio and Synflorix against pneumococci at their Health Care Centre according to scheduled childhood vaccinations in Iceland at three, five and 12 months old. Salivary and blood samples will be taken from participants just before the first vaccination with Rotarix at six weeks old and again at six months (four weeks after the second dose of Pentavac and Synflorix) and at 13 months old (four weeks after the third dose of Pentavac and Synflorix). Specific antibody levels against rotavirus, pertussis, diphtheria, tetanus, haemophilus influenzae type B, polio virus and pneumococci will be measured. Parents of participants will be given two stool sample kits and asked to take one from their child at six weeks old (before the first dose of rotavirus vaccine) and then another at three months old. In case of detection of differences in antibody response, these samples will be sent for microbiome analysis. ;

Related Conditions & MeSH terms

• Antibiotic Treatment
• Immune Responses

• NCT number: NCT06079606
• Study type: Observational
• Source: Landspitali University Hospital
• Status: Active, not recruiting
• Start date: September 10, 2022
• Completion date: December 31, 2027