The role of regulatory T cells and TH17 cells in multiple myeloma.

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The role of regulatory T cells and TH17 cells in multiple myeloma. / Braga, Walter M T; Atanackovic, Djordje; Colleoni, Gisele W B.

In: Clin Dev Immunol, Vol. 2012, 2012, p. 293479.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Braga, WMT, Atanackovic, D & Colleoni, GWB 2012, 'The role of regulatory T cells and TH17 cells in multiple myeloma.', Clin Dev Immunol, vol. 2012, pp. 293479. https://doi.org/10.1155/2012/293479

APA

Braga, W. M. T., Atanackovic, D., & Colleoni, G. W. B. (2012). The role of regulatory T cells and TH17 cells in multiple myeloma. Clin Dev Immunol, 2012, 293479. https://doi.org/10.1155/2012/293479

Vancouver

Braga WMT, Atanackovic D, Colleoni GWB. The role of regulatory T cells and TH17 cells in multiple myeloma. Clin Dev Immunol. 2012;2012:293479. https://doi.org/10.1155/2012/293479

Bibtex

@article{7f018ed880404beaa1d691a89308c75b,
title = "The role of regulatory T cells and TH17 cells in multiple myeloma.",
abstract = "The development of multiple myeloma (MM) involves a series of genetic alterations and changes in the bone marrow microenvironment, favoring the growth of the tumor and failure of local immune control. Quantitative and functional alterations in CD4(+) and CD8(+) T cells have been described in MM. The balance between T regulatory cells (Treg) and T helper (Th) 17 cells represents one essential prerequisite for maintaining anti-tumor immunity in MM. Tregs play an important role in the preservation of self-tolerance and modulation of overall immune responses against infections and tumor cells. In MM patients, Tregs seem to contribute to myeloma-related immune dysfunction and targeting them could, therefore, help to restore and enhance vital immune responses. Th17 cells protect against fungal and parasitic infections and participate in inflammatory reactions and autoimmunity. The interplay of TGF-? and IL-6, expressed at high levels in the bone marrow of myeloma patients, may affect generation of Th17 cells both directly or via other pro-inflammatory cytokines and thereby modulate antitumor immune responses. A detailed analysis of the balance between Tregs and Th17 cells seems necessary in order to design more effective and less toxic modes of immunotherapy myeloma which still is an uncurable malignancy.",
keywords = "Humans, CD8-Positive T-Lymphocytes/immunology/pathology, Forkhead Transcription Factors/biosynthesis/immunology, Immune Tolerance, Interleukin-6/biosynthesis/immunology, Multiple Myeloma/*immunology/pathology, T-Lymphocytes, Regulatory/*immunology/pathology, Th17 Cells/*immunology/pathology, Transforming Growth Factor beta/biosynthesis/immunology, Tumor Markers, Biological/biosynthesis/immunology, Humans, CD8-Positive T-Lymphocytes/immunology/pathology, Forkhead Transcription Factors/biosynthesis/immunology, Immune Tolerance, Interleukin-6/biosynthesis/immunology, Multiple Myeloma/*immunology/pathology, T-Lymphocytes, Regulatory/*immunology/pathology, Th17 Cells/*immunology/pathology, Transforming Growth Factor beta/biosynthesis/immunology, Tumor Markers, Biological/biosynthesis/immunology",
author = "Braga, {Walter M T} and Djordje Atanackovic and Colleoni, {Gisele W B}",
year = "2012",
doi = "10.1155/2012/293479",
language = "English",
volume = "2012",
pages = "293479",

}

RIS

TY - JOUR

T1 - The role of regulatory T cells and TH17 cells in multiple myeloma.

AU - Braga, Walter M T

AU - Atanackovic, Djordje

AU - Colleoni, Gisele W B

PY - 2012

Y1 - 2012

N2 - The development of multiple myeloma (MM) involves a series of genetic alterations and changes in the bone marrow microenvironment, favoring the growth of the tumor and failure of local immune control. Quantitative and functional alterations in CD4(+) and CD8(+) T cells have been described in MM. The balance between T regulatory cells (Treg) and T helper (Th) 17 cells represents one essential prerequisite for maintaining anti-tumor immunity in MM. Tregs play an important role in the preservation of self-tolerance and modulation of overall immune responses against infections and tumor cells. In MM patients, Tregs seem to contribute to myeloma-related immune dysfunction and targeting them could, therefore, help to restore and enhance vital immune responses. Th17 cells protect against fungal and parasitic infections and participate in inflammatory reactions and autoimmunity. The interplay of TGF-? and IL-6, expressed at high levels in the bone marrow of myeloma patients, may affect generation of Th17 cells both directly or via other pro-inflammatory cytokines and thereby modulate antitumor immune responses. A detailed analysis of the balance between Tregs and Th17 cells seems necessary in order to design more effective and less toxic modes of immunotherapy myeloma which still is an uncurable malignancy.

AB - The development of multiple myeloma (MM) involves a series of genetic alterations and changes in the bone marrow microenvironment, favoring the growth of the tumor and failure of local immune control. Quantitative and functional alterations in CD4(+) and CD8(+) T cells have been described in MM. The balance between T regulatory cells (Treg) and T helper (Th) 17 cells represents one essential prerequisite for maintaining anti-tumor immunity in MM. Tregs play an important role in the preservation of self-tolerance and modulation of overall immune responses against infections and tumor cells. In MM patients, Tregs seem to contribute to myeloma-related immune dysfunction and targeting them could, therefore, help to restore and enhance vital immune responses. Th17 cells protect against fungal and parasitic infections and participate in inflammatory reactions and autoimmunity. The interplay of TGF-? and IL-6, expressed at high levels in the bone marrow of myeloma patients, may affect generation of Th17 cells both directly or via other pro-inflammatory cytokines and thereby modulate antitumor immune responses. A detailed analysis of the balance between Tregs and Th17 cells seems necessary in order to design more effective and less toxic modes of immunotherapy myeloma which still is an uncurable malignancy.

KW - Humans

KW - CD8-Positive T-Lymphocytes/immunology/pathology

KW - Forkhead Transcription Factors/biosynthesis/immunology

KW - Immune Tolerance

KW - Interleukin-6/biosynthesis/immunology

KW - Multiple Myeloma/immunology/pathology

KW - T-Lymphocytes, Regulatory/immunology/pathology

KW - Th17 Cells/immunology/pathology

KW - Transforming Growth Factor beta/biosynthesis/immunology

KW - Tumor Markers, Biological/biosynthesis/immunology

KW - Humans

KW - CD8-Positive T-Lymphocytes/immunology/pathology

KW - Forkhead Transcription Factors/biosynthesis/immunology

KW - Immune Tolerance

KW - Interleukin-6/biosynthesis/immunology

KW - Multiple Myeloma/immunology/pathology

KW - T-Lymphocytes, Regulatory/immunology/pathology

KW - Th17 Cells/immunology/pathology

KW - Transforming Growth Factor beta/biosynthesis/immunology

KW - Tumor Markers, Biological/biosynthesis/immunology

U2 - 10.1155/2012/293479

DO - 10.1155/2012/293479

M3 - SCORING: Journal article

VL - 2012

SP - 293479

ER -