4.8 Article

Developmental Origin Governs CD8(+) T Cell Fate Decisions during Infection

Journal

CELL
Volume 174, Issue 1, Pages 117-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.05.029

Keywords

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Funding

  1. NIH from the National Institute of Allergy and Infectious Disease [R01AI105265, R01AI110613, U01AI131348]
  2. NIH from the National Institute of Child Health and Human Development [P50HD076210]
  3. NHMRC (Australia) [1080001]
  4. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [P50HD076210] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI110613, U01AI131348, R01AI105265] Funding Source: NIH RePORTER

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Heterogeneity is a hallmark feature of the adaptive immune system in vertebrates. Following infection, naive T cells differentiate into various subsets of effector and memory T cells, which help to eliminate pathogens and maintain long-term immunity. The current model suggests there is a single lineage of naive T cells that give rise to different populations of effector and memory T cells depending on the type and amounts of stimulation they encounter during infection. Here, we have discovered that multiple sub-populations of cells exist in the naive CD8(+) T cell pool that are distinguished by their developmental origin, unique transcriptional profiles, distinct chromatin landscapes, and different kinetics and phenotypes after microbial challenge. These data demonstrate that the naive CD8(+) T cell pool is not as homogeneous as previously thought and offers a new framework for explaining the remarkable heterogeneity in the effector and memory T cell subsets that arise after infection.

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