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Journal ArticleDOI

T-cell quality in memory and protection: implications for vaccine design

TLDR
The importance of using multiparameter flow cytometry to better understand the functional capacity of effector and memory T-cell responses, thereby enabling the development of preventative and therapeutic vaccine strategies for infections is highlighted.
Abstract
T cells mediate effector functions through a variety of mechanisms. Recently, multiparameter flow cytometry has allowed a simultaneous assessment of the phenotype and multiple effector functions of single T cells; the delineation of T cells into distinct functional populations defines the quality of the response. New evidence suggests that the quality of T-cell responses is crucial for determining the disease outcome to various infections. This Review highlights the importance of using multiparameter flow cytometry to better understand the functional capacity of effector and memory T-cell responses, thereby enabling the development of preventative and therapeutic vaccine strategies for infections.

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Citations
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Journal ArticleDOI

Expanding roles for CD4 + T cells in immunity to viruses

TL;DR: The full range of antiviral functions of CD4+ T cells are reviewed, discussing the activities of these cells in helping other lymphocytes and in inducing innate immune responses, as well as their direct antiviral roles.
Journal ArticleDOI

Phenotype and function of human T lymphocyte subsets: Consensus and issues

TL;DR: An account of points of consensus and discord, including the relative heterogeneity of T cell subpopulations during infections with distinct pathogens, the relationship between phenotypic and functional T cell attributes, and the pathway(s) of Tcell differentiation are provided.
Journal ArticleDOI

Human memory T cells: generation, compartmentalization and homeostasis

TL;DR: Studies focused on human memory T cells that reveal key properties of these cells, including subset heterogeneity and diverse tissue residence in multiple mucosal and lymphoid tissue sites are discussed.
Journal ArticleDOI

The who's who of T-cell differentiation: human memory T-cell subsets.

TL;DR: Recent developments in the characterization of the heterogeneity of the memory T‐cell compartment are reviewed, and a unified classification of both human and nonhuman primate T cells on the basis of phenotypic traits and in vivo properties is proposed.
Journal ArticleDOI

Dendritic-cell-based therapeutic cancer vaccines.

TL;DR: The immunological basis for therapeutic cancer vaccines and how the current understanding of dendritic cell and T cell biology might enable the development of next-generation curative therapies for individuals with cancer are discussed.
References
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Journal Article

Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.

TL;DR: A panel of antigen-specific mouse helper T cell clones was characterized according to patterns of lymphokine activity production, and two types of T cell were distinguished.
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Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

TL;DR: It is shown that expression of CCR7, a chemokine receptor that controls homing to secondary lymphoid organs, divides human memory T cells into two functionally distinct subsets, which are named central memory (TCM) and effector memory (TEM).
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Identification of RANTES, MIP-1α, and MIP-1β as the Major HIV-Suppressive Factors Produced by CD8+ T Cells

TL;DR: Recombinant human RANTES, Mip-1α, and MIP-1β induced a dose-dependent inhibition of different strains of HIV-1, HIV-2, and simian immunodeficiency virus (SIV) and may have relevance for the prevention and therapy of AIDS.
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An essential role for interferon gamma in resistance to Mycobacterium tuberculosis infection.

TL;DR: Gko mice have been developed which fail to produce IFN-gamma (gko), because of a targeted disruption of the gene for IFNs, and succumb to a rapid and fatal course of tuberculosis that could be delayed, but not prevented, by treatment with exogenous recombinant IFN.
Journal ArticleDOI

Subsets of human dendritic cell precursors express different toll-like receptors and respond to different microbial antigens.

TL;DR: The expression of distinct sets of TLRs and the corresponding difference in reactivity to microbial molecules among subsets of pre-DCs and imDCs support the concept that they have developed through distinct evolutionary pathways to recognize different microbial antigens.
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