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.

Scientific Reports
|June 2, 2023
PubMed

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.