4.8 Article

High-dimensional intravital microscopy reveals major changes in splenic immune system during postnatal development

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.1002919

Keywords

spleen; malaria; development; immunology; in vivo imaging

Categories

Funding

  1. FAPEMIG (Brazil)
  2. CAPES (Brazil)
  3. CNPq (Brazil)
  4. INCT Vacinas
  5. Chang Zuckerberg Initiative (Bioimaging Brasil)

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This study used novel imaging techniques to describe the dynamic changes in immune development within the spleen for the first time. Adult and infant spleens had similar numbers and arrangement of lymphoid cells, while the immune environment in newborns was significantly different. In addition, the study showed how infections can alter the immune profile in the spleen, which may help in understanding the severity of infections.
Spleen is a key organ for immunologic surveillance, acting as a firewall for antigens and parasites that spread through the blood. However, how spleen leukocytes evolve across the developmental phase, and how they spatially organize and interact in vivo is still poorly understood. Using a novel combination of selected antibodies and fluorophores to image in vivo the spleen immune environment, we described for the first time the dynamics of immune development across postnatal period. We found that spleens from adults and infants had similar numbers and arrangement of lymphoid cells. In contrast, splenic immune environment in newborns is sharply different from adults in almost all parameters analysed. Using this in vivo approach, B cells were the most frequent subtype throughout the development. Also, we revealed how infections - using a model of malaria - can change the spleen immune profile in adults and infants, which could become the key to understanding different severity grades of infection. Our new imaging solutions can be extremely useful for different groups in all areas of biological investigation, paving a way for new intravital approaches and advances.

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