Role of the BCR in B Cell Chronic Lymphocytic Leukemia

BCR 在 B 细胞慢性淋巴细胞白血病中的作用

• 批准号: 8025981
• 负责人: Diane F Jelinek
• 金额: $ 30.41万
• 依托单位: MAYO CLINIC ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-05-01 至 2014-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8025981
• 关键词: Address; Affinity; Aliquot; Alleles; Antibodies; Antigens; Apoptosis; B-Cell Activation; B-Lymphocytes; Behavior; Biochemical; Biological; Biology; Biopsy; Bone Marrow; Categories; Cell Survival; Cell physiology; Cells; Cellular biology; Characteristics; Chromosome abnormality; Chronic Lymphocytic Leukemia; Clinic; Clinical; Clinical Data; Clinical Research; Clonal Evolution; Clonal Expansion; Coculture Techniques; Collecting Cell; Commit; Complementarity Determining Region III; Country; Cryopreserved Cell; Cytogenetics; DNA Sequence Rearrangement; Data; Databases; Development; Disease; Disease Outcome; Elderly; Enzymes; Epitopes; Etiology; Evaluation; Event; Exclusion; Exhibits; Flow Cytometry; Frequencies; Genes; Genetic; Genomic Instability; Growth; Health; Heavy-Chain Immunoglobulins; Heterogeneity; Human; IGH@ gene cluster; Immunoglobulin Somatic Hypermutation; Immunoglobulin Variable Region; In Vitro; Indolent; Institutional Review Boards; Leukemic Cell; Link; Longitudinal Studies; Malignant - descriptor; Marrow; Measures; Mediating; Memory; Mining; Molecular; Molecular Abnormality; Morbidity - disease rate; Mutate; Mutation; Outcome; Patients; Peptide Phage Display Library; Peptides; Physiological; Play; Population; Positioning Attribute; Prognostic Factor; Prognostic Marker; Property; Protein Microchips; Proteins; Publishing; Quality of life; RNA Interference; Reading Frames; Receptor Signaling; Receptors, Antigen, B-Cell; Risk; Role; Sampling; Sampling Studies; Screening procedure; Signal Transduction; Signaling Molecule; Staging; Stereotyping; Stratification; Stromal Cells; Testing; Time; Vial device; base; cell bank; cell growth; cohort; complementarity-determining region 3; density; design; experience; follow-up; in vivo; inhibitor/antagonist; insight; interest; leukemia; lymph nodes; molecular phenotype; mortality; novel; novel therapeutic intervention; prognostic; receptor; receptor expression; receptor-mediated signaling; response; variable region gene

DESCRIPTION (provided by applicant): B cell chronic lymphocytic leukemia (B-CLL) is the most common form of leukemia among older adults in Western countries and is a significant cause of morbidity and mortality in the older adult population. We believe the B cell receptor (BCR) plays a crucial role in dictating the behavior of the malignant clone in B-CLL and in turn dictates clinical behavior of B-CLL. Our data and that obtained by others provide compelling evidence that the use of specific immunoglobulin heavy chain variable region (IGHV) genes in CLL is non-random and the IGH complementarity determining region 3 (CDR3) is remarkably homologous in certain CLL patients. In addition, the somatic hypermutation (SHM) status of the IGHV gene in the leukemic cell BCR is now a validated and powerful prognostic factor. Regardless of SHM status, all CLL B cells more closely resemble antigen experienced memory rather than naive B cells and some CLL B cells display a molecular phenotype which is similar to BCR-stimulated normal B cells. These observations collectively support the hypothesis that antigenic stimulation influences the development and/or course of B-CLL. Several broad questions concerning the biological role of the BCR in this disease remain unanswered. First, does the BCR continue to play an ongoing role in the biology of B-CLL, and if so, is this uniformly displayed by all patient leukemic B cells? Two, do CLL B cells expressing stereotyped BCRs recognize similar antigens, and if so, does this feature permit insight into the etiology of this disease and can this information be used to devise timely novel therapeutic interventions? Third, what is the relationship between molecular features of the BCR and clinical outcome? We are uniquely positioned to answer these questions because of our exceptional access to primary CLL B cells and an extensive cell bank of over 3000 cryopreserved vials of high quality cells collected as a result of our ongoing efforts to determine the IGHV molecular features of B-CLL patients, now numbering over 1000 patients. In addition, these data are integrated into a clinical data base which features invaluable long term clinical outcome data on each patient as well as expression levels of other biologically relevant molecules with prognostic significance and cytogenetic (FISH) data characterizing the most common CLL-associated genetic abnormalities. Thus, to answer these questions and test our unifying hypothesis that the BCR is functional and plays a critical role in the biology of malignant B cells in B-CLL and clinical outcome of this disease, we propose a comprehensive experimental strategy that will: i) systematically link BCR mediated signaling competencies with molecular BCR features that are critical for in vivo leukemic B cell survival, growth, and accumulation over time; ii) investigate BCR antigen recognition and identify shared epitopes recognized by CLL B cells expressing canonical receptors; and iii) probe the relevance of the BCR to the leukemic B cell process in CLL by correlating various IGHV molecular features with patient clinical outcome and other prognostic factors via our access to an invaluable clinical and research database. PUBLIC HEALTH RELEVANCE: B cell chronic lymphocytic leukemia is a very common leukemia in this country and is currently incurable. Because at least 70 percent of all patients will ultimately require treatment in order to have an enhanced quality of life, avoidance of complications of the disease, and increased survival, we are committed to better understanding the underlying mechanisms that contribute to leukemic cell growth and survival in the patients. This proposal will take a comprehensive approach to define the role of the leukemic B cell antigen receptor in determining the behavior of the malignant B cells and how this in turn dictates patient clinical outcome. Through these studies, we aim to add novel insight into the etiology of this disease and are optimistic that this information can be used to devise timely novel therapeutic interventions.

描述（由申请人提供）：B细胞慢性淋巴细胞白血病（B- cll）是西方国家老年人中最常见的白血病形式，是老年人发病率和死亡率的重要原因。我们认为B细胞受体（BCR）在决定B- cll恶性克隆的行为中起着至关重要的作用，进而决定B- cll的临床行为。我们的数据和其他人获得的数据提供了令人信服的证据，证明特异性免疫球蛋白重链可变区（IGHV）基因在CLL中的使用是非随机的，并且在某些CLL患者中，IGH互补决定区3 （CDR3）具有显著的同源性。此外，白血病细胞BCR中IGHV基因的体细胞超突变（SHM）状态现在是一个经过验证的强大预后因素。无论SHM状态如何，所有的CLL B细胞都更接近于抗原记忆，而不是幼稚的B细胞，一些CLL B细胞表现出与bcr刺激的正常B细胞相似的分子表型。这些观察结果共同支持抗原刺激影响B-CLL发展和/或病程的假设。关于BCR在该疾病中的生物学作用的几个广泛问题仍未得到解答。首先，BCR是否继续在B- cll的生物学中发挥持续的作用，如果是，这是否在所有患者的白血病B细胞中一致表现出来？第二，表达刻板bcr的CLL B细胞是否识别类似的抗原，如果是这样，这种特征是否允许深入了解这种疾病的病因，这些信息是否可以用于及时设计新的治疗干预措施？第三，BCR的分子特征与临床结果有何关系？我们有独特的优势来回答这些问题，因为我们拥有独特的CLL原代B细胞和广泛的细胞库，其中有3000多瓶低温保存的高质量细胞，这是我们持续努力确定B-CLL患者的IGHV分子特征的结果，现在有超过1000名患者。此外，这些数据被整合到临床数据库中，该数据库具有每位患者宝贵的长期临床结果数据，以及具有预后意义的其他生物学相关分子的表达水平，以及表征最常见的cll相关遗传异常的细胞遗传学（FISH）数据。因此，为了回答这些问题并验证我们的统一假设，即BCR是功能性的，在B- cll恶性B细胞的生物学和这种疾病的临床结果中起着关键作用，我们提出了一个全面的实验策略，它将：i)系统地将BCR介导的信号能力与分子BCR特征联系起来，这些特征对体内白血病B细胞的生存、生长和积累至关重要；ii)研究BCR抗原识别并确定表达典型受体的CLL B细胞识别的共享表位；iii)通过访问宝贵的临床和研究数据库，将各种IGHV分子特征与患者临床结果和其他预后因素联系起来，探讨BCR与CLL中白血病B细胞过程的相关性。公共卫生相关性：B细胞慢性淋巴细胞白血病是一种非常常见的白血病在这个国家，目前是无法治愈的。因为至少70%的患者最终需要治疗，以提高生活质量，避免疾病并发症，提高生存率，我们致力于更好地了解促进白血病细胞生长和患者生存的潜在机制。本提案将采取全面的方法来确定白血病B细胞抗原受体在决定恶性B细胞行为中的作用，以及这反过来如何决定患者的临床结果。通过这些研究，我们的目标是为这种疾病的病因增加新的见解，并乐观地认为这些信息可以用于及时设计新的治疗干预措施。