Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
We performed genetic analysis of HLA and immune escape genes in samples from 44 patients sequenced by whole exome sequencing (34 tumor samples, 32 normal samples) and whole genome sequencing (10 tumor samples, 12 normal samples). We also performed HLA targeted sequencing in 26/44 patients (26 tumor samples, 26 normal samples).
- 139 samples
- DAC: EGAC00001002066
- Technologies: Illumina HiSeq 2000, unspecified
DAC for Study EGAS00001005054
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Authorized Institutional Representative Name: Title: Affiliation: Institutional email address: Signature: Date: Principal Investigator Name: Title: Affiliation: Institutional email address: Signature: Date: Agreed for COLUMBIA UNIVERSITY Signature: Name: Title: Date: APPENDIX I – DATASET DETAILS APPENDIX II ––PROJECT DETAILS APPENDIX III –– PUBLICATION POLICY APPENDIX I – DATASET DETAILS Dataset reference EGAS00001005054: Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma Name of project that created the dataset Genetic mechanisms of HLA-I loss and immune escape in Diffuse Large B Cell Lymphoma Research project that created the dataset Fifty percent of diffuse large B-cell lymphoma (DLBCL) cases lack cell-surface expression of the class-I major histocompatibility complex (MHC-I), thereby escaping immune recognition by cytotoxic T cells. In order to comprehensively identify the mechanisms involved in MHC-I loss, we first performed immunophenotypic analysis of both MHC class-I and -II in 657 cases across the spectrum of B-NHL, revealing that loss of MHC-I, but not MHC-II, is preferentially restricted to DLBCL. We then used whole exome and targeted deep-sequencing to examine genes involved in MHC-I expression in 74 DLBCL samples representative of MHC-I positive and negative cases. We show here that somatic biallelic or monoallelic inactivation of B2M and/or HLA-I is present in 80.9% (34/42) of MHC-I negative tumors. Furthermore, 68.8% (22/32) of MHC-I positive DLBCLs also harbored monoallelic HLA-I genetic alterations (MHC-I positivemono) that lead to allelic imbalance, suggesting allele-specific inactivation. Both MHC-I negative and MHC-I positivemono cases showed a significantly higher mutational burden as well as a higher number of inferred neo-antigens, suggesting co-selection of HLA-I loss and sustained neo-antigen production. Interestingly, the analysis of > 500.000 individuals in two databases revealed homozygosity of germline HLA-I genes in 26-38% of DLBCL patients, a frequency significantly higher than that observed in any other cancer type. In mice, germinal-center B cells lacking HLA-I expression did not progress to lymphoma and were counter-selected in the context of oncogene-driven lymphomagenesis, suggesting that additional events are needed to license immune evasion. These results suggest a multi-step process of HLA-I loss including both germ-line and somatic events in DLBCL development, and have direct implications for the pathogenesis and immunotherapeutic targeting of this disease. This study includes 3 datasets: 1) Whole exome sequencing (WES) of 34 DLBCL tumor samples and 32 paired normal samples 2) Whole genome sequencing (WGS) of 10 DLBCL tumor samples and 12 paired normal samples 3) Targeted HLA-I deep sequencing of 26 DLBCL tumor samples and 26 paired normal samples Specific limitations on areas of research Use of the dataset is limited to scientific genetic research related to cancer. The data will only be used for research purposes. Investigators must state in the DAR their intention to publish or otherwise broadly share any findings from their study with the scientific community. This consent group requires IRB approval. Minimum protection measures required File access: Data can be held in unencrypted files on an institutional compute system, with Unix user group read/write access for one or more appropriate groups but not Unix world read/write access behind a secure firewall. Laptops holding these data should have password protected logins and screenlocks (set to lock after 5 min of inactivity). If held on USB keys or other portable hard drives, the data must be encrypted. APPENDIX II – PROJECT DETAILS (to be completed by the Requestor) Genotype Data Requested (i.e., EGA Study and Dataset Accession Number) Title of Project In 30 words or less. Brief abstract of the Project in which the Data will be used (500 words max) Research Question Please provide a clear description of the project and its specific aims in no more than 750 words. This should include specific details of what you plan to do with the data and include key references. Feasibility Please describe your experience and expertise, and that of your collaborators, and how this will be applied to the proposed study. A publication list MUST be provided for the applicant, co-applicants and PhD supervisors where PhD students have applied. The committee needs assurance of competence in handling datasets of this size and nature. All Individuals who the User Institution wishes to be named as registered users Name of Registered User Email Job Title Supervisor All Individuals that should have an account created at the EGA Name of Registered User Email Job Title APPENDIX III – PUBLICATION POLICY Dr. Pasqualucci and Dr. Dalla-Favera intend to publish the results of their analysis of this dataset and do not consider its deposition into public databases to be the equivalent of such publications. Dr. Pasqualucci and Dr. Dalla-Favera anticipate that the dataset could be useful to other qualified researchers for a variety of purposes. However, some areas of work are subject to a publication moratorium. The publication moratorium covers any publications (including oral communications) that describe the use of the dataset. For research papers, submission for publication should not occur until 6 months after these data were first made available on the relevant hosting database, unless Dr. Pasqualucci and Dr. Dalla-Favera has provided written consent to earlier submission. We request that any publications based on these data acknowledge their use by citing their original publication: Fangazio et al., Genetic mechanisms of HLA-I loss and immune escape in Diffuse Large B-Cell Lymphoma, in revision. and describing how the data can be accessed, including the name of the hosting database (The European Genome-phenome Archive at the European Bioinformatics Institute) and its accession number (EGAS00001005054).
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
Study ID | Study Title | Study Type |
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EGAS00001005054 | Other |
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