Zilberberg Jenny, Feinman Rena, Korngold Robert
Research Department and John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
Research Department and John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
Biol Blood Marrow Transplant. 2015 Jun;21(6):1000-7. doi: 10.1016/j.bbmt.2014.11.001. Epub 2014 Nov 20.
Allogeneic blood and marrow transplantation (allo-BMT) is an effective immunotherapeutic treatment that can provide partial or complete remission for patients with hematological malignancies. Mature donor T cells in the donor inoculum play a central role in mediating graft-versus-tumor (GVT) responses by destroying residual tumor cells that persist after conditioning regimens. Alloreactivity towards minor histocompatibility antigens (miHA), which are varied tissue-related self-peptides presented in the context of major histocompatibility complex (MHC) molecules on recipient cells, some of which may be shared on tumor cells, is a dominant factor for the development of GVT. Potentially, GVT can also be directed to tumor-associated antigens or tumor-specific antigens that are more specific to the tumor cells themselves. The full exploitation of allo-BMT, however, is greatly limited by the development of graft-versus-host disease (GVHD), which is mediated by the donor T cell response against the miHA expressed in the recipient's cells of the intestine, skin, and liver. Because of the significance of GVT and GVHD responses in determining the clinical outcome of patients, miHA and tumor antigens have been intensively studied, and one active immunotherapeutic approach to separate these two responses has been cancer vaccination after allo-BMT. The combination of these two strategies has an advantage over vaccination of the patient without allo-BMT because his or her immune system has already been exposed and rendered unresponsive to the tumor antigens. The conditioning for allo-BMT eliminates the patient's existing immune system, including regulatory elements, and provides a more permissive environment for the newly developing donor immune compartment to selectively target the malignant cells. Utilizing recent technological advances, the identities of many human miHA and tumor antigenic peptides have been defined and are currently being evaluated in clinical and basic immunological studies for their ability to produce effective T cell responses. The first step towards this goal is the identification of targetable tumor antigens. In this review, we will highlight some of the technologies currently used to identify tumor antigens and anti-tumor T cell clones in hematological malignancies.
异基因血液和骨髓移植(allo-BMT)是一种有效的免疫治疗方法,可为血液系统恶性肿瘤患者提供部分或完全缓解。供体接种物中的成熟供体T细胞通过破坏预处理方案后残留的肿瘤细胞,在介导移植物抗肿瘤(GVT)反应中起核心作用。对次要组织相容性抗原(miHA)的同种异体反应性是GVT发展的主要因素,miHA是受体细胞上主要组织相容性复合体(MHC)分子背景下呈现的各种组织相关自身肽,其中一些可能在肿瘤细胞上共享。潜在地,GVT也可以针对肿瘤相关抗原或肿瘤特异性抗原,这些抗原对肿瘤细胞本身更具特异性。然而,allo-BMT的充分利用受到移植物抗宿主病(GVHD)发展的极大限制,GVHD由供体T细胞对受体肠道、皮肤和肝脏细胞中表达的miHA的反应介导。由于GVT和GVHD反应在决定患者临床结局方面的重要性,miHA和肿瘤抗原已得到深入研究,一种分离这两种反应的主动免疫治疗方法是allo-BMT后的癌症疫苗接种。这两种策略的结合比未进行allo-BMT的患者接种疫苗具有优势,因为其免疫系统已经接触过肿瘤抗原并对其无反应。allo-BMT的预处理消除了患者现有的免疫系统,包括调节元件,并为新发展的供体免疫区室选择性靶向恶性细胞提供了更宽松的环境。利用最近的技术进步,许多人类miHA和肿瘤抗原肽的身份已被确定,目前正在临床和基础免疫学研究中评估它们产生有效T细胞反应的能力。实现这一目标的第一步是鉴定可靶向的肿瘤抗原。在本综述中,我们将重点介绍目前用于鉴定血液系统恶性肿瘤中肿瘤抗原和抗肿瘤T细胞克隆的一些技术。