» Articles » PMID: 17682068

An Antigen-specific Pathway for CD8 T Cells Across the Blood-brain Barrier

Overview
Journal J Exp Med
Date 2007 Aug 8
PMID 17682068
Citations 124
Authors
Affiliations
Soon will be listed here.
Abstract

CD8 T cells are nature's foremost defense in encephalitis and brain tumors. Antigen-specific CD8 T cells need to enter the brain to exert their beneficial effects. On the other hand, traffic of CD8 T cells specific for neural antigen may trigger autoimmune diseases like multiple sclerosis. T cell traffic into the central nervous system is thought to occur when activated T cells cross the blood-brain barrier (BBB) regardless of their antigen specificity, but studies have focused on CD4 T cells. Here, we show that selective traffic of antigen-specific CD8 T cells into the brain occurs in vivo and is dependent on luminal expression of major histocompatibility complex (MHC) class I by cerebral endothelium. After intracerebral antigen injection, using a minimally invasive technique, transgenic CD8 T cells only infiltrated the brain when and where their cognate antigen was present. This was independent of antigen presentation by perivascular macrophages. Marked reduction of antigen-specific CD8 T cell infiltration was observed after intravenous injection of blocking anti-MHC class I antibody. These results expose a hitherto unappreciated route by which CD8 T cells home onto their cognate antigen behind the BBB: luminal MHC class I antigen presentation by cerebral endothelium to circulating CD8 T cells. This has implications for a variety of diseases in which antigen-specific CD8 T cell traffic into the brain is a beneficial or deleterious feature.

Citing Articles

Pooled screening for CAR function identifies novel IL-13Rα2-targeted CARs for treatment of glioblastoma.

Gordon K, Perez C, Garmilla A, Lam M, Aw J, Datta A J Immunother Cancer. 2025; 13(2).

PMID: 39933837 PMC: 11815465. DOI: 10.1136/jitc-2024-009574.


CD8 T cells exacerbate AD-like symptoms in mouse model of amyloidosis.

Wang X, Campbell B, Bodogai M, McDevitt R, Patrikeev A, Gusev F Brain Behav Immun. 2024; 122:444-455.

PMID: 39191349 PMC: 11409913. DOI: 10.1016/j.bbi.2024.08.045.


The choroid plexus maintains adult brain ventricles and subventricular zone neuroblast pool, which facilitates poststroke neurogenesis.

Taranov A, Bedolla A, Iwasawa E, Brown F, Baumgartner S, Fugate E Proc Natl Acad Sci U S A. 2024; 121(28):e2400213121.

PMID: 38954546 PMC: 11252789. DOI: 10.1073/pnas.2400213121.


Immunotherapy With Radiotherapy for Brain Metastases in Patients With NSCLC: NEJ060.

Tozuka T, Minegishi Y, Yamaguchi O, Watanabe K, Toi Y, Saito R JTO Clin Res Rep. 2024; 5(4):100655.

PMID: 38706978 PMC: 11069015. DOI: 10.1016/j.jtocrr.2024.100655.


Reprogramming T cells as an emerging treatment to slow human age-related decline in health.

Peplow P Front Med Technol. 2024; 6:1384648.

PMID: 38666066 PMC: 11043517. DOI: 10.3389/fmedt.2024.1384648.


References
1.
Krakowski M, Owens T . Naive T lymphocytes traffic to inflamed central nervous system, but require antigen recognition for activation. Eur J Immunol. 2000; 30(4):1002-9. DOI: 10.1002/(SICI)1521-4141(200004)30:4<1002::AID-IMMU1002>3.0.CO;2-2. View

2.
Yeager M, DeLeo J, Hoopes P, Hartov A, Hildebrandt L, Hickey W . Trauma and inflammation modulate lymphocyte localization in vivo: quantitation of tissue entry and retention using indium-111-labeled lymphocytes. Crit Care Med. 2000; 28(5):1477-82. DOI: 10.1097/00003246-200005000-00037. View

3.
Carrithers M, Visintin I, Kang S, Janeway Jr C . Differential adhesion molecule requirements for immune surveillance and inflammatory recruitment. Brain. 2000; 123 ( Pt 6):1092-101. DOI: 10.1093/brain/123.6.1092. View

4.
Bitsch A, Schuchardt J, Bunkowski S, Kuhlmann T, Bruck W . Acute axonal injury in multiple sclerosis. Correlation with demyelination and inflammation. Brain. 2000; 123 ( Pt 6):1174-83. DOI: 10.1093/brain/123.6.1174. View

5.
Babbe H, Roers A, Waisman A, Lassmann H, Goebels N, Hohlfeld R . Clonal expansions of CD8(+) T cells dominate the T cell infiltrate in active multiple sclerosis lesions as shown by micromanipulation and single cell polymerase chain reaction. J Exp Med. 2000; 192(3):393-404. PMC: 2193223. DOI: 10.1084/jem.192.3.393. View