Mechanics of cytotoxic function revealed by HLH-associated gene mutations. Mechanics of cytotoxic function revealed by HLH-associated gene mutations. HLH-associated.

Slides:



Advertisements
Similar presentations
Lymphoma dissemination: the other face of lymphocyte homing by Steven T. Pals, David J. J. de Gorter, and Marcel Spaargaren Blood Volume 110(9):
Advertisements

Telomere dysfunction and fusion during the progression of chronic lymphocytic leukemia: evidence for a telomere crisis by Thet Thet Lin, Boitelo T. Letsolo,
Computational biology of cancer cell pathways Modelling of cancer cell function and response to therapy.
Validation of a flow cytometric scoring system as a prognostic indicator for posttransplantation outcome in patients with myelodysplastic syndrome by Bart.
The β2 integrin–kindlin-3 interaction is essential for T-cell homing but dispensable for T-cell activation in vivo by Vicky Louise Morrison, Matthew MacPherson,
Generating AML-Specific Peripheral Blood Autologous Cytotoxic T-Lymphocytes (CTLs)‏ by Rohtesh S. Mehta, Xiaohua Chen, Antony Jeyaraj, and Paul Szabolcs.
Pathogenesis beyond the cancer clone(s) in multiple myeloma by Giada Bianchi, and Nikhil C. Munshi Blood Volume 125(20): May 14, 2015 ©2015 by.
Human Genetic Mutations
Meeting with Hiren.
Characterization of VHL promoter variants in patients suspected of Von Hippel Lindau Saleh Albanyan, Rachel Giles, Raymond H Kim, MD/PhD Division of.
Noonan’s Syndrome Kimberly T. Edwards.
Uncontrolled Wnt signaling causes leukemia
Do HSCs divide asymmetrically?
by Robert F. Todd, Scott D. Gitlin, Linda J. Burns, and
MBL: mostly benign lymphocytes, but…
B-cell chronic lymphocytic leukemia cells express a surface membrane phenotype of activated, antigen-experienced B lymphocytes by Rajendra N. Damle, Fabio.
A Clinical Evaluation of the International Lymphoma Study Group Classification of Non-Hodgkin's Lymphoma Blood Volume 89(11): June 1, 1997 ©1997.
CD146 (Mel-CAM), an adhesion marker of endothelial cells, is a novel marker of lymphocyte subset activation in normal peripheral blood by Mohamed F. Elshal,
Lytic Replication of Epstein-Barr Virus in the Peripheral Blood: Analysis of Viral Gene Expression in B Lymphocytes During Infectious Mononucleosis and.
Nat. Rev. Clin. Oncol. doi: /nrclinonc
ERVmap reveals additional breast cancer-associated ERVs that correlate with cytolytic activity. ERVmap reveals additional breast cancer-associated ERVs.
Chediak-Higashi syndrome: Lysosomal trafficking regulator domains regulate exocytosis of lytic granules but not cytokine secretion by natural killer cells 
Rebuttal to Ajioka and Kushner
V617F “JAKs” up myeloproliferative signal
A novel immunoregulatory role for NK-cell cytotoxicity in protection from HLH-like immunopathology in mice by Fernando E. Sepulveda, Sophia Maschalidi,
Fusion genes in cord blood
An Unusual Cause of Abdominal Pain in Sickle Cell Disease
Genetic sequence analysis of inherited bleeding diseases
Mutation Analysis of the Rearranged Immunoglobulin Heavy Chain Genes of Marginal Zone Cell Lymphomas Indicates an Origin From Different Marginal Zone B.
Hemophagocytic Lympho Histiocytosis
Pedigrees of the families of patients 1 and 2 show that the clinical phenotype co-segregates with compound heterozygous CLDN10 variants. Pedigrees of the.
by Loïc Dupré, Grazia Andolfi, Stuart G
VWF sequence variants: innocent until proven guilty
Stephen M Prescott, Raymond L White  Cell 
Has MRD monitoring superseded other prognostic factors in adult ALL?
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences.
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia by Phil J. Ancliff, Michael P. Blundell, Giles.
Genetics of HLH (Hemophagocytic Lymphohistiocytosis)
Significant genes at the 1% nominal level either in Europe, Asia or both, present in the significant pathways obtained from the nSL (linkage disequilibrium)
Cytokine-Release Syndrome in Patients With B-Cell Chronic Lymphocytic Leukemia and High Lymphocyte Counts After Treatment With an Anti-CD20 Monoclonal.
Chediak-Higashi syndrome: pathognomonic feature
Exam Three, packet 4 Antigen Recognition
by Alex Aleshin, and Peter L. Greenberg
by Dana T. Lounder, Qiong Bin, Cristina de Min, and Michael B. Jordan
Microbiome contribution and metabolite intervention in post-dieting weight-regain MSc. Lenka Dohnalová, July 2017, Munich.
Significant differences in translational efficiencies of DNA damage repair pathway genes between patient clusters. Significant differences in translational.
Predicted number of joint bleeds according to factor activity level and age group for patients with hemophilia A or B based on a regression model. Predicted.
Roles and functions of α1-AT in lungs of a) individuals with normal levels of protein, b) patients with deficient or null mutations, and c) patients with.
Platelet ATP secretion in response to agonist stimulation.
Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin by Sarah L. Reeves, Hannah K. Jary, Jennifer.
LITERATURE REVIEW.
HoxA9 directly regulates cell cycle control genes.
Distribution of podocyte gene mutations in patients with genetic congenital nephrotic syndrome (CNS) and steroid–resistant nephrotic syndrome (SRNS). Distribution.
Erratum in Ledru et al. Alteration of tumor necrosis factor–α T-cell homeostasis following potent antiretroviral therapy: contribution to the development.
Characteristic ocular features in women with Alport syndrome.
Proposed model of molecular pathogenesis in the development and progression of major subtypes of MCL. Precursor B cells usually with but sometimes without.
How I treat thrombocytopenia in pregnancy
CD16 uses additional pathways for killing.
Survival based on V gene mutation status and CD38 expression among B-CLL patients who stratify to the Rai intermediate risk category. Survival based on.
Glomerular basement membrane (GBM) appearance and patterns of hearing loss in women with Alport syndrome. Glomerular basement membrane (GBM) appearance.
by Elisa Rumi, and Mario Cazzola
How I treat hemophagocytic lymphohistiocytosis
Biology and treatment of Richter syndrome
Myeloproliferative neoplasms and thrombosis
Reduced number and impaired effector functions of TILs in tumors with PTEN deletion or loss-of-function mutations in PTEN. Cutaneous melanoma patients.
Single nucleotide polymorphism array analysis can distinguish different genetic mechanisms that lead to loss of heterozygosity (LOH). Single nucleotide.
Schematic model of the role of complement activation, cell damage, and thrombosis in various severe diseases or conditions with major thrombotic problems.
The interplay of leukemia cells and the bone marrow microenvironment
Driver pathways and key genes in OSCC
Bioinformatic analyses suggest that PI3K/AKT signaling may be a key downstream pathway of tazarotene signaling. Bioinformatic analyses suggest that PI3K/AKT.
Presentation transcript:

Mechanics of cytotoxic function revealed by HLH-associated gene mutations. Mechanics of cytotoxic function revealed by HLH-associated gene mutations. HLH-associated genetic abnormalities (in the indicated genes) may affect granule-dependent lymphocyte cytotoxicity by impairing trafficking, docking, priming for exocytosis, or membrane fusion of cytolytic granules. The function of this pathway may also be severely impaired by loss of functional perforin, the key delivery molecule for proapoptotic granzymes. Diverse mutations in this pathway all give rise to similar clinical phenotypes (albeit of variable severity). Lyst (the gene affected in Chediak-Higashi syndrome) is not portrayed because its function is not entirely clear, although it appears to play an important role in the maintenance of normally sized (and functional) cytolytic granules. Michael B. Jordan et al. Blood 2011;118:4041-4052 ©2011 by American Society of Hematology