The tumor-driven antibody-mediated immune response in cancer

被引：1

作者：

Paparoditis, Philipp ^{[1
]}

Shulman, Ziv ^{[1
]}

机构：

[1] Weizmann Inst Sci, Dept Syst Immunol, Rehovot, Israel

来源：

CURRENT OPINION IN IMMUNOLOGY | 2024年 / 88卷

基金：

瑞士国家科学基金会; 以色列科学基金会;

关键词：

TERTIARY LYMPHOID STRUCTURES; B-CELLS; SOMATIC HYPERMUTATION; AUTOANTIBODIES; IMMUNOTHERAPY; RECOGNITION; NEOANTIGENS; REDEMPTION; GENERATION; SURVIVAL;

D O I：

10.1016/j.coi.2024.102431

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

Immune cells in the tumor microenvironment play a crucial role in cancer prognosis and response to immunotherapy. Recent studies highlight the significance of tumor-infiltrating B cells and tertiary lymphoid structures as markers of favorable prognosis and patient-positive response to immune checkpoint blockers in some types of cancer. Although the presence of germinal center B cells and plasma cells in the tumor microenvironment has been established, determining their tumor reactivity remains challenging. The few known tumor targets range from viral proteins to self and altered self- proteins. The emergence of self-reactive antibodies in patients with cancer, involves the opposing forces of antigen-driven affinity increase and peripheral tolerance mechanisms. Here, B cell tumor antigen specificity and affinity maturation in tumor- directed immune responses in cancer are discussed.

引用

页数：7

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