Perforin expression by CD8 T cells is sufficient to cause fatal brain edema during experimental cerebral malaria

Matthew A. Huggins, Holly L. Johnson, Fang Jin, Aurelie N'Songo, Lisa M. Hanson, Stephanie J. LaFrance, Noah S. Butler, John T. Harty, Aaron J. Johnson

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Human cerebral malaria (HCM) is a serious complication of Plasmodium falciparum infection. The most severe outcomes for patients include coma, permanent neurological deficits, and death. Recently, a large-scale magnetic resonance imaging (MRI) study in humans identified brain swelling as the most prominent predictor of fatal HCM. Therefore, in this study, we sought to define the mechanism controlling brain edema through the use of the murine experimental cerebral malaria (ECM) model. Specifically, we investigated the ability of CD8 T cells to initiate brain edema during ECM. We determined that areas of blood-brain barrier (BBB) permeability colocalized with a reduction of the cerebral endothelial cell tight-junction proteins claudin-5 and occludin. Furthermore, through small-animal MRI, we analyzed edema and vascular leakage. Using gadolinium-enhanced T1-weighted MRI, we determined that vascular permeability is not homogeneous but rather confined to specific regions of the brain. Our findings show that BBB permeability was localized within the brainstem, olfactory bulb, and lateral ventricle. Concurrently with the initiation of vascular permeability, T2-weighted MRI revealed edema and brain swelling. Importantly, ablation of the cytolytic effector molecule perforin fully protected against vascular permeability and edema. Furthermore, perforin production specifically by CD8 T cells was required to cause fatal edema during ECM. We propose that CD8 T cells initiate BBB breakdown through perforin-mediated disruption of tight junctions. In turn, leakage from the vasculature into the parenchyma causes brain swelling and edema. This results in a breakdown of homeostatic maintenance that likely contributes to ECM pathology.

Original languageEnglish (US)
Article numbere00985-16
JournalInfection and Immunity
Volume85
Issue number5
DOIs
StatePublished - May 1 2017

Fingerprint

Cerebral Malaria
Perforin
Brain Edema
T-Lymphocytes
Edema
Capillary Permeability
Blood-Brain Barrier
Magnetic Resonance Imaging
Permeability
Claudin-5
Occludin
Tight Junction Proteins
Intercellular Junctions
Tight Junctions
Lateral Ventricles
Olfactory Bulb
Gadolinium
Plasmodium falciparum
Coma
Malaria

Keywords

  • Blood-brain barrier
  • CD8 T cell
  • Experimental cerebral malaria
  • Perforin

ASJC Scopus subject areas

  • Parasitology
  • Microbiology
  • Immunology
  • Infectious Diseases

Cite this

Perforin expression by CD8 T cells is sufficient to cause fatal brain edema during experimental cerebral malaria. / Huggins, Matthew A.; Johnson, Holly L.; Jin, Fang; N'Songo, Aurelie; Hanson, Lisa M.; LaFrance, Stephanie J.; Butler, Noah S.; Harty, John T.; Johnson, Aaron J.

In: Infection and Immunity, Vol. 85, No. 5, e00985-16, 01.05.2017.

Research output: Contribution to journalArticle

Huggins, MA, Johnson, HL, Jin, F, N'Songo, A, Hanson, LM, LaFrance, SJ, Butler, NS, Harty, JT & Johnson, AJ 2017, 'Perforin expression by CD8 T cells is sufficient to cause fatal brain edema during experimental cerebral malaria', Infection and Immunity, vol. 85, no. 5, e00985-16. https://doi.org/10.1128/IAI.00985-16
Huggins, Matthew A. ; Johnson, Holly L. ; Jin, Fang ; N'Songo, Aurelie ; Hanson, Lisa M. ; LaFrance, Stephanie J. ; Butler, Noah S. ; Harty, John T. ; Johnson, Aaron J. / Perforin expression by CD8 T cells is sufficient to cause fatal brain edema during experimental cerebral malaria. In: Infection and Immunity. 2017 ; Vol. 85, No. 5.
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