How Gut Health Affects Immune Responses to the Oral Rotavirus Vaccine in Adults in Zambia
NCT07626606 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 43
Last updated 2026-06-04
Summary
The Rotavirus SpatioTrasncriptomics (Rota-Omics) study is a multidisciplinary research project aimed at understanding why oral rotavirus vaccines perform less effectively in some low- and middle-income countries, including Zambia. Rotavirus remains one of the leading causes of severe diarrheal disease in infants and young children worldwide, despite the widespread introduction of vaccines such as Rotarix® and Rotavac®. Although these vaccines have greatly reduced childhood deaths in many countries, vaccine effectiveness is often lower in settings where the burden of disease is highest. Understanding the reasons behind this reduced protection is critical for improving child health globally.
A major focus of the study is Environmental Enteropathy (EE), also known as Environmental Enteric Dysfunction (EED), a chronic inflammatory condition of the small intestine that is common in low-resource settings. EE is associated with damage to the intestinal lining, chronic immune activation, poor nutrient absorption, and impaired gut barrier function. These changes are thought to interfere with the body's ability to respond effectively to oral vaccines, which rely on strong intestinal immune responses.
The RotaOmics study uses a systems biology approach to investigate how the immune system, gut microbiome, nutrition, and intestinal inflammation interact to influence rotavirus vaccine responses. The term "omics" refers to advanced technologies that allow researchers to study genes, proteins, microbes, and other biological processes at a large scale. By combining these approaches, the study aims to identify biological markers and immune pathways associated with strong or weak vaccine responses.
The study involves the collection of samples such as blood, stool, saliva, and breast milk from mothers and infants at different time points before and after vaccination. These samples are analysed using laboratory methods including antibody testing, molecular pathogen detection, microbiome sequencing, and immune profiling. The study also evaluates markers of gut inflammation and intestinal health.
One important goal of the project is to identify correlates of protection, which are measurable biological indicators that predict whether a vaccine is likely to protect against disease. Identifying these markers could help guide the development of improved vaccines or supportive interventions to enhance vaccine performance in vulnerable populations.
The study also contributes to a broader understanding of mucosal immunity, which refers to immune responses occurring in the gastrointestinal tract. Since many enteric infections begin in the gut, understanding intestinal immune function is important not only for rotavirus vaccines but also for other oral vaccines and diarrheal diseases.
In addition to its scientific objectives, RotaOmics includes a strong capacity-building component. The project supports training for local scientists, clinicians, and laboratory personnel in areas such as molecular biology, immunology, genomics, bioinformatics, and data analysis. By strengthening local research expertise and infrastructure, the study aims to support long-term scientific development and improve regional capacity for infectious disease research and outbreak response.
Overall, the RotaOmics study seeks to generate new insights into why oral rotavirus vaccines underperform in some settings and to identify strategies that may improve vaccine effectiveness and child health outcomes in Zambia and similar regions worldwide.
Conditions
- Feasibility Study
- Vaccine Immune Response
- Rota Virus Gastroenteritis
- Transcriptomics
Interventions
- BIOLOGICAL
-
Rotarix®,
This is an infant vaccine, but this study participants in this study will receive a double oral Rotarix dose at baseline as per study design.
Sponsors & Collaborators
-
Bill and Melinda Gates Foundation
collaborator OTHER -
Centre for Infectious Disease Research in Zambia
lead OTHER
Principal Investigators
-
Michelo Simuyandi, Master's Degree (MSc) · Centre for Infectious Disease Research in Zambia
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-03-30
- Primary Completion
- 2026-09-30
- Completion
- 2026-12-31
- FDA Drug
- Yes
Countries
- Zambia
Study Locations
More Related Trials
-
Improving Rotavirus Vaccine Immune Response
NCT01825109 ·Status: COMPLETED ·Phase: PHASE3
-
Rotavirus Vaccine Produced by Butantan Institute
NCT00981669 ·Status: COMPLETED ·Phase: PHASE1
-
Effectiveness of Rotarix™ Against Rotavirus Severe Gastroenteritis (RV SGE) in Infants in Panama
NCT00653198 ·Status: COMPLETED
-
Development of a Live Attenuated Rotavirus Vaccine as a Human Infection Challenge Model
NCT04123119 ·Status: COMPLETED ·Phase: NA
-
Potential Mechanisms for Intussusception After Rotavirus Vaccine-Pilot Study
NCT02542462 ·Status: COMPLETED ·Phase: PHASE4
-
Reactogenicity, Safety and Immunological Efficacy of the Live, Pentavalent Rotavirus Vaccine in Childhood Immunization
NCT05032391 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Immunogenicity of Sequential Rotavirus Vaccine Schedules
NCT01266850 ·Status: COMPLETED ·Phase: PHASE4
-
To Determine the Safety and Efficacy of Liquid ROTAVAC 5C Vaccine Against Childhood Diarrhea Caused by Rotavirus
NCT04819412 ·Status: COMPLETED ·Phase: PHASE3
-
Observational Study on Rotavirus Gastroenteritis Epidemiology, Impact of Lyophilised vs. Liquid Formulation of Rotarix™
NCT01435967 ·Status: COMPLETED
-
Safety and Immunogenicity of MT-5625 in Healthy Adults, Toddlers and Infants
NCT03507738 ·Status: COMPLETED ·Phase: PHASE1
-
Impact of Rotavirus Vaccination on Hospitalisations for Rotavirus Gastroenteritis in Children Aged <5 Years in Australia
NCT01236066 ·Status: COMPLETED
-
Serologic Response to Porcine Circovirus Type 1 (PCV-1) in Infants Following Administration of Rotarix™
NCT02153333 ·Status: COMPLETED
-
Epidemiological, Observational and Post Marketing Study of Rotarix™ in Children With Severe Gastroenteritis in Belgium
NCT01339221 ·Status: COMPLETED
-
Study to Evaluate the Safety of Rotarix™ in Chinese Children
NCT01086436 ·Status: COMPLETED ·Phase: PHASE1
-
The Efficacy of Oral Rotavirus Vaccine 116E (ROTAVAC 5D) in Chilean Infants
NCT06200844 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Effectiveness Study of GSK Biologicals' Rotarix TM Vaccine in Hospitalized Children
NCT01177826 ·Status: COMPLETED
-
Evaluation of Universal Rotavirus Vaccination Program
NCT01273077 ·Status: COMPLETED
-
Safety and Immunogenicity Study of Recombinant Trivalent Rotavirus Subunit Vaccine in Healthy Infants and Toddlers
NCT05621655 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study of V260 in Healthy Chinese Adults, Children and Infants (V260-028)(COMPLETED)
NCT00953056 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluate Immunogenicity, Safety, and Reactogenicity of Rotavac in Healthy Infants in Vietnam
NCT04596696 ·Status: COMPLETED ·Phase: PHASE3
-
Introduction of an Oral Live Human Rotavirus (Rotarix) Vaccine in Matlab
NCT00737503 ·Status: COMPLETED ·Phase: PHASE4
-
Phase Three Clinical Trials of Trivalent Rotavirus Genetic Reassortment Vaccine
NCT01738074 ·Status: UNKNOWN ·Phase: PHASE3
-
Optimising Rotavirus Vaccine in Aboriginal Children
NCT02941107 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
A Trial to Assess the Safety, Immunogenicity and Efficacy of a Trivalent Rotavirus P2-VP8 Subunit Vaccine in Prevention of Severe Rotavirus Gastroenteritis in Healthy Infants in Africa and India
NCT04010448 ·Status: RECRUITING ·Phase: PHASE3
-
Safety,Tolerability and Immunogenicity of Vaccination With Rotateq in Healthy Infants in India (V260-021)
NCT00496054 ·Status: COMPLETED ·Phase: PHASE3