Host Transcriptomic Response Following Administration of Rotavirus Vaccine in Infants' Mimics Wild Type Infection.

Front Immunol

Genetics, Vaccines and Pediatric Infectious Diseases Research Group (GENVIP), Instituto de Investigación Sanitaria de Santiago (IDIS) and Universidad de Santiago de Compostela (USC), Santiago de Compostela, Spain.

Published: June 2021

AI Article Synopsis

  • Rotavirus (RV) is a major cause of severe illness and death in children worldwide, but the immune response from RV vaccination is not fully understood.* -
  • A study compared gene expression in children with natural RV infections and those who received the RotaTeq vaccine, finding that vaccination produces similar gene changes as natural infection, affecting aspects like the immune response and gastrointestinal symptoms.* -
  • Key findings include the identification of a nine-transcript signature that can differentiate vaccinated children from those who are naturally infected, as well as the discovery of a specific microRNA that may help protect against viral infections, paving the way for better antiviral strategies and vaccines.*

Article Abstract

Background: Rotavirus (RV) is an enteric pathogen that has devastating impact on childhood morbidity and mortality worldwide. The immunologic mechanism underlying the protection achieved after RV vaccination is not yet fully understood.

Methods: We compared the transcriptome of children affected by community-acquired RV infection and children immunized with a live attenuated RV vaccine (RotaTeq).

Results: RV vaccination mimics the wild type infection causing similar changes in children's transcriptome, including transcripts associated with cell cycle, diarrhea, nausea, vomiting, intussusception, and abnormal morphology of midgut. A machine learning approach allowed to detect a combination of nine-transcripts that differentiates vaccinated from convalescent-naturally infected children (AUC: 90%; 95%CI: 70-100) and distinguishes between acute-infected and healthy control children (in both cases, AUC: 100%; 95%CI: 100-100). We identified a miRNA hsa-mir-149 that seems to play a role in the host defense against viral pathogens and may have an antiviral role.

Discussion: Our findings might shed further light in the understanding of RV infection, its functional link to intussusception causes, as well as guide development of antiviral treatments and safer and more effective vaccines. The nine-transcript signature may constitute a marker of vaccine protection and helps to differentiate vaccinated from naturally infected or susceptible children.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859632PMC
http://dx.doi.org/10.3389/fimmu.2020.580219DOI Listing

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