Andreescu Mihaela, Berbec Nicoleta, Tanase Alina Daniela
Department of Clinical Sciences, Hematology, Faculty of Medicine, Titu Maiorescu University of Bucharest, 040051 Bucharest, Romania.
Department of Hematology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
J Clin Med. 2023 Apr 6;12(7):2731. doi: 10.3390/jcm12072731.
Tumor growth and metastasis are reliant on intricate interactions between the host immune system and various counter-regulatory immune escape mechanisms employed by the tumor. Tumors can resist immune surveillance by modifying the expression of human leukocyte antigen (HLA) molecules, which results in the impaired presentation of tumor-associated antigens, subsequently evading detection and destruction by the immune system. The management of chronic lymphocytic leukemia (CLL) is based on symptom severity and includes various types of targeted therapies, including rituximab, obinutuzumab, ibrutinib, acalabrutinib, zanubrutinib, idelalisib, and venetoclax. These therapies rely on the recognition of specific peptides presented by HLAs on the surface of tumor cells by T cells, leading to an immune response. HLA class I molecules are found in most human cell types and interact with T-cell receptors (TCRs) to activate T cells, which play a vital role in inducing adaptive immune responses. However, tumor cells may evade T-cell attack by downregulating HLA expression, limiting the efficacy of HLA-dependent immunotherapy. The prognosis of CLL largely depends on the presence or absence of genetic abnormalities, such as del(17p), TP53 point mutations, and IGHV somatic hypermutation status. These oral targeted therapies alone or in combination with anti-CD20 antibodies have replaced chemoimmunotherapy as the primary treatment for CLL. In this review, we summarize the current clinical evidence on the impact of HLA- and cytokine-type responses on outcomes after targeted therapies currently used to treat CLL.
肿瘤的生长和转移依赖于宿主免疫系统与肿瘤所采用的各种反调节免疫逃逸机制之间的复杂相互作用。肿瘤可通过改变人类白细胞抗原(HLA)分子的表达来抵抗免疫监视,这会导致肿瘤相关抗原的呈递受损,进而逃避免疫系统的检测和破坏。慢性淋巴细胞白血病(CLL)的治疗基于症状严重程度,包括多种类型的靶向治疗,如利妥昔单抗、奥妥珠单抗、伊布替尼、阿卡拉布替尼、泽布替尼、idelalisib和维奈克拉。这些治疗依赖于T细胞识别肿瘤细胞表面HLA呈递的特定肽段,从而引发免疫反应。I类HLA分子存在于大多数人类细胞类型中,并与T细胞受体(TCR)相互作用以激活T细胞,T细胞在诱导适应性免疫反应中起关键作用。然而,肿瘤细胞可能通过下调HLA表达来逃避T细胞攻击,从而限制了依赖HLA的免疫治疗的疗效。CLL的预后很大程度上取决于是否存在基因异常,如del(17p)、TP53点突变和IGHV体细胞超突变状态。这些口服靶向治疗单独使用或与抗CD20抗体联合使用已取代化疗免疫疗法成为CLL的主要治疗方法。在本综述中,我们总结了目前关于HLA和细胞因子类型反应对目前用于治疗CLL的靶向治疗后结局影响的临床证据。