B Cells and Tertiary Lymphoid Structures: Friends or Foes in Cancer Immunotherapy?

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Standard

B Cells and Tertiary Lymphoid Structures : Friends or Foes in Cancer Immunotherapy? / Lauss, Martin; Donia, Marco; Svane, Inge Marie; Jönsson, Göran.

I: Clinical Cancer Research, Bind 28, Nr. 9, 2022, s. 1751–1758.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lauss, M, Donia, M, Svane, IM & Jönsson, G 2022, 'B Cells and Tertiary Lymphoid Structures: Friends or Foes in Cancer Immunotherapy?', Clinical Cancer Research, bind 28, nr. 9, s. 1751–1758. https://doi.org/10.1158/1078-0432.CCR-21-1130

APA

Lauss, M., Donia, M., Svane, I. M., & Jönsson, G. (2022). B Cells and Tertiary Lymphoid Structures: Friends or Foes in Cancer Immunotherapy? Clinical Cancer Research, 28(9), 1751–1758. https://doi.org/10.1158/1078-0432.CCR-21-1130

Vancouver

Lauss M, Donia M, Svane IM, Jönsson G. B Cells and Tertiary Lymphoid Structures: Friends or Foes in Cancer Immunotherapy? Clinical Cancer Research. 2022;28(9):1751–1758. https://doi.org/10.1158/1078-0432.CCR-21-1130

Author

Lauss, Martin ; Donia, Marco ; Svane, Inge Marie ; Jönsson, Göran. / B Cells and Tertiary Lymphoid Structures : Friends or Foes in Cancer Immunotherapy?. I: Clinical Cancer Research. 2022 ; Bind 28, Nr. 9. s. 1751–1758.

Bibtex

@article{66dd342d897943e79135bf7e87e161ee,
title = "B Cells and Tertiary Lymphoid Structures: Friends or Foes in Cancer Immunotherapy?",
abstract = "Tumor cells pose a challenge to the adaptive immune system, and its key cell types, T and B cells, have frequently been associated with an improved prognosis. The success of immune checkpoint blockade has confirmed the relevance of T cells. However, the role of B cells is increasingly recognized, and highlighted in this review. Recent data suggest that tumors contain a diverse set of B cells reflecting different developmental states and exerting functions such as antigen presentation, antibody production, and regulatory effects. Further, B cells are frequently located in tertiary lymphoid structures (TLS), which are immune cell niches that sustain an immune response at sites of chronic inflammation. TLSs in tumors display substantial heterogeneity, ranging from cell aggregates to mature structures with an active germinal center. Recent studies have provided insights into initiation, cellular and spatial composition, and function of TLS in a variety of cancer types; however, several critical issues still need to be resolved. Currently, initial reports are discerning the role of TLSs in immunotherapy, with the majority of studies observing TLSs to confer favorable patient outcome. Finally, TLS induction in tumors is evaluated, with the therapeutic aim to reactivate the host immune response.",
author = "Martin Lauss and Marco Donia and Svane, {Inge Marie} and G{\"o}ran J{\"o}nsson",
year = "2022",
doi = "10.1158/1078-0432.CCR-21-1130",
language = "English",
volume = "28",
pages = "1751–1758",
journal = "Clinical Cancer Research",
issn = "1078-0432",
publisher = "American Association for Cancer Research (A A C R)",
number = "9",

}

RIS

TY - JOUR

T1 - B Cells and Tertiary Lymphoid Structures

T2 - Friends or Foes in Cancer Immunotherapy?

AU - Lauss, Martin

AU - Donia, Marco

AU - Svane, Inge Marie

AU - Jönsson, Göran

PY - 2022

Y1 - 2022

N2 - Tumor cells pose a challenge to the adaptive immune system, and its key cell types, T and B cells, have frequently been associated with an improved prognosis. The success of immune checkpoint blockade has confirmed the relevance of T cells. However, the role of B cells is increasingly recognized, and highlighted in this review. Recent data suggest that tumors contain a diverse set of B cells reflecting different developmental states and exerting functions such as antigen presentation, antibody production, and regulatory effects. Further, B cells are frequently located in tertiary lymphoid structures (TLS), which are immune cell niches that sustain an immune response at sites of chronic inflammation. TLSs in tumors display substantial heterogeneity, ranging from cell aggregates to mature structures with an active germinal center. Recent studies have provided insights into initiation, cellular and spatial composition, and function of TLS in a variety of cancer types; however, several critical issues still need to be resolved. Currently, initial reports are discerning the role of TLSs in immunotherapy, with the majority of studies observing TLSs to confer favorable patient outcome. Finally, TLS induction in tumors is evaluated, with the therapeutic aim to reactivate the host immune response.

AB - Tumor cells pose a challenge to the adaptive immune system, and its key cell types, T and B cells, have frequently been associated with an improved prognosis. The success of immune checkpoint blockade has confirmed the relevance of T cells. However, the role of B cells is increasingly recognized, and highlighted in this review. Recent data suggest that tumors contain a diverse set of B cells reflecting different developmental states and exerting functions such as antigen presentation, antibody production, and regulatory effects. Further, B cells are frequently located in tertiary lymphoid structures (TLS), which are immune cell niches that sustain an immune response at sites of chronic inflammation. TLSs in tumors display substantial heterogeneity, ranging from cell aggregates to mature structures with an active germinal center. Recent studies have provided insights into initiation, cellular and spatial composition, and function of TLS in a variety of cancer types; however, several critical issues still need to be resolved. Currently, initial reports are discerning the role of TLSs in immunotherapy, with the majority of studies observing TLSs to confer favorable patient outcome. Finally, TLS induction in tumors is evaluated, with the therapeutic aim to reactivate the host immune response.

U2 - 10.1158/1078-0432.CCR-21-1130

DO - 10.1158/1078-0432.CCR-21-1130

M3 - Journal article

C2 - 34965949

VL - 28

SP - 1751

EP - 1758

JO - Clinical Cancer Research

JF - Clinical Cancer Research

SN - 1078-0432

IS - 9

ER -

ID: 304065393