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Updated: Jul 28, 2025

Assays for the Specific Growth Rate and Cell-binding Ability of Rotavirus
Published on: January 28, 2019
Acute rotavirus infection is associated with the induction of circulating memory CD4
Chikondi Malamba-Banda1,2,3,4, Chimwemwe Mhango2, Prisca Benedicto-Matambo2,3,4
1Biological Sciences Departments, Malawi University of Science and Technology, Thyolo, Malawi.
Insights
Rotavirus infection in Malawian children showed limited induction of antiviral CD4+ T cells. While T helper 2 cells increased during infection, key cytokine-producing T cells were rarely detected, impacting immune protection understanding.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- CD4+ T cell-mediated immunity is crucial for protection against rotavirus in animal models, but human relevance is not well understood.
- Understanding T cell responses in children is vital for assessing vaccine efficacy and disease pathogenesis.
Purpose of the Study:
- To characterize acute and convalescent CD4+ T cell responses in Malawian children hospitalized with rotavirus infection.
- To investigate the induction of cytokine-producing rotavirus-specific CD4+ T cells.
Main Methods:
- Analysis of CD4+ T cell subsets (effector, central memory, T helper 2) in acute and convalescent blood samples.
- Detection of rotavirus-specific VP6-specific CD4+ T cells producing IFN-γ and/or TNF-α.
- Whole blood mitogenic stimulation to assess CD4+ T cell cytokine production.
Main Results:
- Children with rotavirus infection showed increased effector and central memory T helper 2 cells during acute illness compared to convalescence.
- Circulating rotavirus-specific CD4+ T cells producing IFN-γ and/or TNF-α were rarely detected.
- Most CD4+ T cells responding to mitogenic stimulation were non-cytokine producers of IFN-γ and/or TNF-α.
Conclusions:
- Limited induction of antiviral IFN-γ and/or TNF-α-producing CD4+ T cells was observed in Malawian children with confirmed rotavirus infection.
- These findings suggest restricted cellular immune responses despite T helper 2 cell changes, impacting protective immunity understanding.
Abstract:
Strong CD4+ T cell-mediated immune protection following rotavirus infection has been observed in animal models, but its relevance in humans remains unclear. Here, we characterized acute and convalescent CD4+ T cell responses in children who were hospitalized with rotavirus-positive and rotavirus-negative diarrhoea in Blantyre, Malawi. Children presenting with laboratory-confirmed rotavirus infection had higher proportions of effector and central memory T helper 2 cells during acute infection i.e., at disease presentation compared to convalescence, 28 days post-infection defined by a follow-up 28 days after acute infection. However, circulating cytokine-producing (IFN-γ and/or TNF-α) rotavirus-specific VP6-specific CD4+ T cells were rarely detectable in children with rotavirus infection at both acute and convalescent stages. Moreover, following whole blood mitogenic stimulation, the responding CD4+ T cells were predominantly non-cytokine producers of IFN-γ and/or TNF-α. Our findings demonstrate limited induction of anti-viral IFN-γ and/or TNF-α-producing CD4+ T cells in rotavirus-vaccinated Malawian children following the development of laboratory-confirmed rotavirus infection.
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