Acyl CoA binding protein (ACBP): an autophagy checkpoint that can be targeted for improving cancer immunosurveillance.

IF 6.5 2区 医学 Q1 IMMUNOLOGY Oncoimmunology Pub Date : 2024-10-07 eCollection Date: 2024-01-01 DOI:10.1080/2162402X.2024.2413200
Léa Montégut, Isabelle Martins, Guido Kroemer
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引用次数: 0

Abstract

Acyl CoA binding protein (ACBP) encoded by DBI is a tissue hormone that limits autophagy in multiple cell types, hence acting as an extracellular autophagy checkpoint. We recently reported in Molecular Cancer that monoclonal antibodies neutralizing ACBP improve immunosurveillance of breast and lung carcinomas. Moreover, ACBP neutralization improves the outcome of neoadjuvant chemoimmunotherapy with PD-1 blockade in preclinical models.

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酰基辅酶A结合蛋白(ACBP):自噬检查点,可作为改善癌症免疫监视的靶点。
由DBI编码的酰基辅酶A结合蛋白(ACBP)是一种组织激素,可限制多种类型细胞的自噬,从而起到细胞外自噬检查点的作用。我们最近在《分子癌症》(Molecular Cancer)杂志上报道,中和 ACBP 的单克隆抗体能改善乳腺癌和肺癌的免疫监视。此外,在临床前模型中,中和 ACBP 可改善 PD-1 阻断新辅助化疗免疫疗法的疗效。
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来源期刊
Oncoimmunology
Oncoimmunology ONCOLOGYIMMUNOLOGY-IMMUNOLOGY
CiteScore
12.50
自引率
2.80%
发文量
276
审稿时长
24 weeks
期刊介绍: OncoImmunology is a dynamic, high-profile, open access journal that comprehensively covers tumor immunology and immunotherapy. As cancer immunotherapy advances, OncoImmunology is committed to publishing top-tier research encompassing all facets of basic and applied tumor immunology. The journal covers a wide range of topics, including: -Basic and translational studies in immunology of both solid and hematological malignancies -Inflammation, innate and acquired immune responses against cancer -Mechanisms of cancer immunoediting and immune evasion -Modern immunotherapies, including immunomodulators, immune checkpoint inhibitors, T-cell, NK-cell, and macrophage engagers, and CAR T cells -Immunological effects of conventional anticancer therapies.
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