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The Safety and Immunogenicity of Rotavirus Vaccination in Infants With Intestinal Failure
Patrick J Javid1, Sabrina E Sanchez2, Susan Jacob3
1Division of Pediatric General and Thoracic Surgery, Seattle Children's Hospital and University of Washington School of Medicine, and patrick.javid@seattlechildrens.org.
Insights
Rotavirus vaccination is safe and effective in infants with intestinal failure, demonstrating immunogenicity without increased viral shedding. This supports further studies on rotavirus vaccine efficacy in this vulnerable pediatric population.
Area of Science:
- Pediatric Gastroenterology
- Vaccinology
- Immunology
Background:
- Infants with intestinal failure face risks from rotavirus gastroenteritis.
- Safety and immunogenicity of rotavirus vaccines in this group are unknown.
- This study investigated rotavirus vaccination in infants with intestinal failure and prior abdominal surgery.
Purpose of the Study:
- To assess the safety and immunogenicity of rotavirus vaccination in infants with intestinal failure.
- To evaluate potential risks such as viral shedding and adverse events.
- To determine if vaccination confers immunity in this high-risk cohort.
Main Methods:
- Enrolled infants with early intestinal failure requiring surgery and parenteral nutrition.
- Administered rotavirus vaccine series and monitored for adverse events.
- Assessed viral stool shedding and measured serum rotavirus immunoglobulin A for seroconversion.
Main Results:
- Mild, transient side effects like diarrhea and emesis were observed.
- No serious adverse events including intussusception or dehydration occurred.
- All unvaccinated infants achieved seroconversion, indicating vaccine immunogenicity.
Conclusions:
- Rotavirus vaccination is safe and immunogenic in infants with intestinal failure.
- No evidence of altered viral shedding was found.
- Multicenter trials are recommended to confirm rotavirus vaccine efficacy in this population.
Background:
Young children with intestinal failure are at risk for complications from rotavirus gastroenteritis. To date, the safety and immunogenicity of rotavirus vaccines in these children are not known. We hypothesized that rotavirus vaccination would be safe and confer immunity to infants with intestinal failure and a history of abdominal surgery.
Methods:
The study population consisted of infants with early intestinal failure who required abdominal surgery and parenteral nutrition for necrotizing enterocolitis, gastroschisis, jejunoileal atresia, or meconium peritonitis. Subjects received a rotavirus vaccine series at the appropriate age. Safety assessments were performed for the first 5 days after each vaccine dose. Viral stool shedding and serum rotavirus antigen were measured at multiple time points after each dose of the vaccine. A 3-fold increase in rotavirus immunoglobulin A titer at study completion defined seroconversion.
Results:
Fifteen infants were enrolled and 14 infants completed the study protocol. Mild diarrhea, emesis, and fever were noted after vaccination in 33%, 40%, and 7% of subjects, respectively. No subject experienced postvaccine intussusception, viremia, dehydration, or required alterations in nutritional care. Viral stool shedding was noted in 47%, but only 1 child shed virus beyond 2 weeks postvaccination. All subjects who were not considered immune at baseline developed seroconversion to rotavirus after vaccination.
Conclusions:
In infants with intestinal failure, rotavirus vaccination appears to be safe and immunogenic. We found no evidence for altered viral shedding in this population. Given the profound consequences associated with rotavirus infection and potential benefits of rotavirus vaccine in this cohort, multicenter studies focusing on vaccine efficacy are warranted.
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