CD8 T-cell memory: The other half of the story

David Masopust; Leo Lefrançois

doi:10.1016/S1286-4579(03)00014-5

CD8 T-cell memory: The other half of the story

David Masopust, Leo Lefrançois

Microbiology

Research output: Contribution to journal › Review article › peer-review

29 Scopus citations

Abstract

Historically, most immune response studies have been limited to analyses of lymphoid tissue. However, peripheral sites of infection are likely to represent important sites of cell-mediated immune surveillance and effector function. Recent debates have centered on the persistence, trafficking patterns, effector activity, and protective role of non-lymphoid memory T cells.

Original language	English (US)
Pages (from-to)	221-226
Number of pages	6
Journal	Microbes and Infection
Volume	5
Issue number	3
DOIs	https://doi.org/10.1016/S1286-4579(03)00014-5
State	Published - Mar 1 2003

Bibliographical note

Funding Information:
This work was supported by USPHS grants DK45260 and AI41576. DM was supported by USPHS Training Grant T32-AI07080.

Keywords

Infection
Memory
Migration
Non-lymphoid
T cell

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/S1286-4579(03)00014-5

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abstract = "Historically, most immune response studies have been limited to analyses of lymphoid tissue. However, peripheral sites of infection are likely to represent important sites of cell-mediated immune surveillance and effector function. Recent debates have centered on the persistence, trafficking patterns, effector activity, and protective role of non-lymphoid memory T cells.",

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author = "David Masopust and Leo Lefran{\c c}ois",

note = "Funding Information: This work was supported by USPHS grants DK45260 and AI41576. DM was supported by USPHS Training Grant T32-AI07080.",

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T1 - CD8 T-cell memory

T2 - The other half of the story

AU - Masopust, David

AU - Lefrançois, Leo

N1 - Funding Information: This work was supported by USPHS grants DK45260 and AI41576. DM was supported by USPHS Training Grant T32-AI07080.

PY - 2003/3/1

Y1 - 2003/3/1

N2 - Historically, most immune response studies have been limited to analyses of lymphoid tissue. However, peripheral sites of infection are likely to represent important sites of cell-mediated immune surveillance and effector function. Recent debates have centered on the persistence, trafficking patterns, effector activity, and protective role of non-lymphoid memory T cells.

AB - Historically, most immune response studies have been limited to analyses of lymphoid tissue. However, peripheral sites of infection are likely to represent important sites of cell-mediated immune surveillance and effector function. Recent debates have centered on the persistence, trafficking patterns, effector activity, and protective role of non-lymphoid memory T cells.

KW - Infection

KW - Memory

KW - Migration

KW - Non-lymphoid

KW - T cell

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JF - Microbes and Infection

IS - 3

ER -

CD8 T-cell memory: The other half of the story

Abstract

Bibliographical note

Keywords

UN SDGs

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