Lymph Node Cytology
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Immunodeficiency Patients Differentiation of Common Variable
Defined Blocks in Terminal Plasma Cell Differentiation of Common Variable Immunodeficiency Patients This information is current as Nadine Taubenheim, Marcus von Hornung, Anne Durandy, of September 24, 2021. Klaus Warnatz, Lynn Corcoran, Hans-Hartmut Peter and Hermann Eibel J Immunol 2005; 175:5498-5503; ; doi: 10.4049/jimmunol.175.8.5498 http://www.jimmunol.org/content/175/8/5498 Downloaded from References This article cites 35 articles, 13 of which you can access for free at: http://www.jimmunol.org/content/175/8/5498.full#ref-list-1 http://www.jimmunol.org/ Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication by guest on September 24, 2021 *average Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2005 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. The Journal of Immunology Defined Blocks in Terminal Plasma Cell Differentiation of Common Variable Immunodeficiency Patients1 Nadine Taubenheim,* Marcus von Hornung,* Anne Durandy,† Klaus Warnatz,‡ Lynn Corcoran,§ Hans-Hartmut Peter,‡ and Hermann Eibel2* Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by defective Ab production and recurrent bacterial infections. -
Evaluation of the Effects of Activation Dependent Regulation of Cd40l on Germinal Center Response Using Cd40lδ5 Mouse Model
EVALUATION OF THE EFFECTS OF ACTIVATION DEPENDENT REGULATION OF CD40L ON GERMINAL CENTER RESPONSE USING CD40LΔ5 MOUSE MODEL By BITHA NARAYANAN A dissertation submitted to the School of Graduate Studies Rutgers, The State University of New Jersey In partial fulfillment of the requirements For the degree of Doctor of Philosophy Graduate Program in Microbiology and Molecular Genetics written under the direction of Lori R. Covey and approved by _____________________________________ _____________________________________ _____________________________________ _____________________________________ New Brunswick, New Jersey January 2020 ©[2020] Bitha Narayanan ALL RIGHTS RESERVED ABSTRACT OF THE DISSERTATION ACTIVATION-DEPENDENT POSTTRANSCRIPTIONAL REGULATION OF CD40L IS REQUIRED FOR AN OPTIMAL GERMINAL CENTER (GC) RESPONSE. by BITHA NARAYANAN Dissertation Director Dr. Lori R. Covey The interaction between cognate T and B cells decides the progression of an immune response to a pathogen or self-antigen. Of the multiple signals that synchronize to fine-tune this union, the binding of CD40 on the surface of B cells to CD40L expressed on CD4 T cells is of paramount importance. Ligation of CD40 on antigen- experienced B cells is associated with the initiation and development of germinal centers (GCs) resulting in the subsequent generation of high affinity antibodies and B cell memory. Post-transcriptional regulation of CD40L has been implicated in regulating the activation dependent expression of this protein. Our lab has previously shown a polypyrimidine tract binding protein complex binds to the 3’ UTR of the CD40L mRNA ii and that the deletion of a PTBP1 binding stability element in the same results in a significant decrease in the half-life of the CD40L transcript and subsequently the surface expression at later stages of activation in vitro. -
Modelling the Affinity Maturation of B Lymphocytes in the Germinal Centre
Modelling the Affinity Maturation of B Lymphocytes in the Germinal Centre By ADAM THOMAS REYNOLDS A thesis submitted to The University of Birmingham for the degree of MASTER OF PHILOSOPHY School of Biosciences The University of Birmingham June 2010 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. To my Mum and Dad Acknowledgments I would like to thank all the people who have helped me directly and indirectly during this research project and helped me make this a memorable experience. I would like to thank Francesco Falciani, Kai Tollener, Mike Salmon, Micheal Hermann and Dov Stekel for technical support and guidance. I would also like to thank the BBSRC for providing funding for this thesis and thank Illogic for providing a licence to use the Rhapsody tool. I would also like to thank Antony Pemberton for help and support in the use of the Birmingham Biosciences High Performance Computer Cluster to perform the many computer simulations and to thank Ruth Harrison and the student support services who where invaluable in providing support and help with this thesis. -
Does Recycling in Germinal Centers Exist?
Does Recycling in Germinal Centers Exist? Michael Meyer-Hermann Institut f¨ur Theoretische Physik, TU Dresden, D-01062 Dresden, Germany E-Mail: [email protected] Abstract: A general criterion is formulated in order to decide if recycling of B-cells exists in GC reactions. The criterion is independent of the selection and affinity maturation process and based solely on total centroblast population arguments. An experimental test is proposed to verify whether the criterion is fulfilled. arXiv:physics/0102062v2 [physics.bio-ph] 6 Mar 2002 1 1 Introduction The affinity maturation process in germinal center (GC) reactions has been well charac- terized in the last decade. Despite a lot of progress concerning the morphology of GCs and the stages of the selection process, a fundamental question remains unsolved: Does recycling exist? Recycling means a back differentiation of antibody presenting centrocytes (which undergo the selection process and interact with antigen fragments or T-cells) to centroblasts (which do not present antibodies and therefore do not interact with antigen fragments but proliferate and mutate). The existence of recycling in the GC has important consequences for the structure of the affinity maturation process in GC reactions. The centroblasts proliferate and mutate with high rates in the environment of follicular dendritic cells. During the GC reaction they differentiate to antibody presenting centrocytes which may then be selected by inter- action with antigen fragments and T-cells. If the positively selected centrocytes recycle to (proliferating and mutating) centroblasts the antibody-optimization process in GCs may be compatible with random mutations of the centroblasts. -
In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response
J Clin Exp Hematopathol Vol. 46, No. 2, Nov 2006 Original Article In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response Hito-aki Saitoh, Kunihiko Maeda, and Mitsunori Yamakawa Germinal centers are highly organized anatomic structures essential for the clonal expansion of germinal center (GC) B- cells and associated somatic hypermutation, isotype switching, selection of the high-affinity B-cells (affinity maturation), and elimination of irrelevant or autoreactive clones. The identification of cellular interactions and regulatory mechanisms controlling apoptosis within GCs is essential for a complete understanding of the cellular and molecular dynamics of the GC reaction. We performed a kinetic analysis of the apoptotic activity occurring within GCs of draining lymph nodes of mice immunized with sheep red blood cells (SRBC) after secondary stimulation. The apoptotic activity of GC cells can be divided into three distinct phases : 1) initial phase (within the first days after immunization), 2) reactive phase (from the 5th day to 15th day after secondary immunization), and 3) late phase (after the 15th day). Apoptosis decreased shortly after secondary immunization followed by an increase to peak after an additional 10 days. Finally, apoptosis of GC cells decreased to basal levels. Administration of apoptosis inhibitors decreased the amount of apoptosis during the reactive phase. These results suggest that the reactive phase may be the critical period in which clonal selection and cellular differentiation -
MUM1: a Step Ahead Toward the Understanding of Lymphoma Histogenesis G Gaidano1 and a Carbone2
Leukemia (2000) 14, 563–566 2000 Macmillan Publishers Ltd All rights reserved 0887-6924/00 $15.00 www.nature.com/leu EDITORIAL MUM1: a step ahead toward the understanding of lymphoma histogenesis G Gaidano1 and A Carbone2 1Division of Internal Medicine, Department of Medical Sciences, Amedeo Avogadro University of Eastern Piedmont, Novara, and 2Division of Pathology, Centro di Riferimento Oncologico, IRCCS, Istituto Nazionale Tumori, Aviano, Italy In recent times, the field of B cell lymphoma histogenesis has togenesis has progressed rapidly due to the increasing avail- progressed rapidly due to the increasing availability of histo- ability of histogenetic markers of lymphoid cells.2 In normal genetic markers. Genotypic markers of B cell histogenesis are represented by mutations of IgV and BCL-6 genes, which are B cell physiology, the presence, or absence, of these histogen- somatically acquired at the time of B cell transit through the etic markers denotes different stages of lymphoid differen- germinal center (GC). Phenotypic markers are represented by tiation, allowing the distinction of mature B cells into virgin BCL-6 and CD138/syndecan-1 protein expression and allow the (ie pre-germinal center) B cells, germinal center B cells, and distinction between GC and post-GC B cells. On this basis, lym- post-germinal center (ie either memory B cells or plasmacells) phomas may be histogenetically distinguished into: (1) lym- B cells2 (Figure 2). Because these histogenetic markers are also phomas devoid of somatic IgV and BCL-6 hypermutation, which derive from pre-germinal center B cells; (2) lymphomas retained upon neoplastic transformation, the origin and differ- associated with somatic IgV and/or BCL-6 hypermutation and entiation stage of a given lymphoma may be temptatively BCL-6 expression, which closely reflect germinal center B assigned based on the combination of histogenetic markers cells; and (3) lymphomas associated with somatic IgV and/or associated with the tumor clone (Figure 2). -
The Broad Landscape of Follicular Lymphoma: Part I
PATHOLOGICA 2020;112:1-16; DOI: 10.32074/1591-951X-35-19 Review The broad landscape of follicular lymphoma: Part I Stefano Fratoni1, Magda Zanelli2, Maurizio Zizzo3,4, Francesca Sanguedolce5, Valentina Aimola6, Giulia Cerrone6, Linda Ricci7, Alessandra Filosa8, Giovanni Martino9, Stefano Ascani10 1 Department of Anatomic Pathology, St. Eugenio Hospital of Rome, Rome, Italy; 2 Pathology Unit, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Italy; 3 Surgical Oncology Unit, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Italy; 4 Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Modena, Italy; 5 Pathology Unit, Azienda Ospedaliero-Universitaria - Ospedali Riuniti di Foggia, Italy; 6 Pathology Unit, University of Cagliari, Italy; 7 Pathology Unit, University of Siena, Italy; 8 Pathology Unit, Ospedale di Ascoli Piceno, Ascoli, Italy; 9 Hematology Unit, CREO, Azienda Ospedaliera di Perugia, University of Perugia, Italy; 10 Pathology Unit, Azienda Ospedaliera Santa Maria Terni, University of Perugia, Terni, Italy Summary Follicular lymphoma is a neoplasm derived from follicle center B cells, typically both cen- trocytes and centroblasts, in variable proportions according to the lymphoma grading. The pattern of growth may be entirely follicular, follicular and diffuse, and rarely completely dif- fuse. It represents the second most common non-Hodgkin lymphoma, after diffuse large B-cell lymphoma and is the most common low-grade mature B-cell lymphoma in western countries. In the majority of cases, follicular lymphoma is a nodal tumor, occurring in adults and frequently associated with the translocation t(14;18)(q32;q21)/IGH-BCL2. However, in recent years the spectrum of follicular lymphoma has expanded and small subsets of follicular lymphoma, which differ from common follicular lymphoma, have been identified Received and accepted: December 8, 2019 and included in the current 2017 WHO classification. -
B Cell–Intrinsic Mtorc1 Promotes Germinal Center–Defining
B Cell−Intrinsic mTORC1 Promotes Germinal Center−Defining Transcription Factor Gene Expression, Somatic Hypermutation, and Memory B Cell This information is current as Generation in Humoral Immunity of September 26, 2021. Ariel L. Raybuck, Sung Hoon Cho, Jingxin Li, Meredith C. Rogers, Keunwook Lee, Christopher L. Williams, Mark Shlomchik, James W. Thomas, Jin Chen, John V. Williams and Mark R. Boothby Downloaded from J Immunol published online 12 March 2018 http://www.jimmunol.org/content/early/2018/03/11/jimmun ol.1701321 http://www.jimmunol.org/ Supplementary http://www.jimmunol.org/content/suppl/2018/03/11/jimmunol.170132 Material 1.DCSupplemental Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision by guest on September 26, 2021 • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication *average Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2018 by The American Association of Immunologists, Inc. All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. Published March 12, 2018, doi:10.4049/jimmunol.1701321 The Journal of Immunology B Cell–Intrinsic mTORC1 Promotes Germinal Center–Defining Transcription Factor Gene Expression, Somatic Hypermutation, and Memory B Cell Generation in Humoral Immunity Ariel L. -
Hematopathology
320A ANNUAL MEETING ABSTRACTS expression of ALDH1 was analyzed using mouse monoclonal ALDH1 antibody (BD Conclusions: Based on the present results we conclude that miR29ab1 ko’s have Biosciences, San Jose, CA). Correlations between ALDH1 expression and clinical and decreased hematopoietic stem cell population compared to the wild types and that histological parameters were assessed by Pearson’s Chi-square and M-L Chi-square miR29ab1 might have an important role in the maintenance of this cell population. tests. Survival curves were generated using the Kaplan-Meier method and statistical Also, miR29 genes might regulate immunity and life span, since both miR29ab1 and differences by log rank test. miR29ab1/b2c ko’s seem to have markedly decreased life spans. Results: Majority of the tumors (116, 63%) showed stromal staining only, 21 (11%) tumors showed both epithelial and stromal expression, 47 (26%) tumors did not show 1347 The Majority of Immunohistochemically BCL2 Negative FL Grade either epithelial or stromal staining. The normal salivary gland showed epithelial I/II Carry A t(14;18) with Mutations in Exon 1 of the BCL2 Gene and Can expression only. Statistical analyses did not show any correlation between tumor pattern, Be Identifi ed with the BCL2 E17 Antibody tumor size, the presence of perineural invasion and the patterns of ALDH1 expression. P Adam, R Baumann, I Bonzheim, F Fend, L Quintanilla-Martinez. Eberhard-Karls- The survival analysis using Kaplan-Meier method and log rank test did not show any University, Tubingen, Baden-Wurttemberg, Germany. signifi cant differences among the three patterns of ALDH1 expression with survival. -
Color Atlas of Hematology
i ii iii Color Atlas of Hematology Practical Microscopic and Clinical Diagnosis Harald Theml, M.D. Professor, Private Practice Hematology/Oncology Munich, Germany Heinz Diem, M.D. Klinikum Grosshadern Institute of Clinical Chemistry Munich, Germany Torsten Haferlach, M.D. Professor, Klinikum Grosshadern Laboratory for Leukemia Diagnostics Munich, Germany 2nd revised edition 262 color illustrations 32 tables Thieme Stuttgart · New York iv Library of Congress Cataloging-in-Publica- Important note: Medicine is an ever- tion Data is available from the publisher changing science undergoing continual development. Research and clinical ex- perience are continually expanding our knowledge, in particular our knowledge of This book is an authorized revised proper treatment and drug therapy. Insofar translation of the 5th German edition as this book mentions any dosage or appli- published and copyrighted 2002 by cation, readers may rest assured that the Thieme Verlag, Stuttgart, Germany. authors, editors, and publishers have made Title of the German edition: every effort to ensure that such references Taschenatlas der Hämatologie are in accordance with the state of knowl- edge at the time of production of the book. Translator: Ursula Peter-Czichi PhD, Nevertheless, this does not involve, imply, Atlanta, GA, USA or express any guarantee or responsibility on the part of the publishers in respect to any dosage instructions and forms of appli- 1st German edition 1983 cations stated in the book. Every user is re- 2nd German edition 1986 quested to examine carefully the manu- 3rd German edition 1991 facturers’ leaflets accompanying each drug 4th German edition 1998 and to check, if necessary in consultation 5th German edition 2002 with a physician or specialist, whether the 1st English edition 1985 dosage schedules mentioned therein or the 1st French edition 1985 contraindications stated by the manufac- 2nd French edition 2000 turers differ from the statements made in 1st Indonesion edition 1989 the present book. -
A Mathematical Model for the Germinal Center Morphology and Affinity
A mathematical model for the germinal center morphology and affinity maturation Michael Meyer-Hermann Institut f¨ur Theoretische Physik, TU Dresden, D-01062 Dresden, Germany E-Mail: [email protected] Abstract: During germinal center reactions the appearance of two specific zones is ob- served: the dark and the light zone. Up to now, the origin and function of these zones are poorly understood. In the framework of a stochastic and discrete model several possi- ble pathways of zone development during germinal center reactions are investigated. The importance of the zones in the germinal center for affinity maturation, i.e. the process of antibody optimization is discussed. arXiv:physics/0203021v1 [physics.bio-ph] 7 Mar 2002 1 1 Introduction Germinal centers (GC) are an important part of the humoral immune response. They develop after the activation of B-cells by antigens. Such activated B-cells migrate into the follicular system where they begin a monoclonal expansion in the environment of follicular dendritic cells (FDC). This phase of pure centroblast multiplication is followed by a phase of intense hypermutation and proliferation which leads to a larger repertoire of different centroblast types. This seems to be the basis of the affinity maturation process, i.e. the optimization process of the antibodies with respect to a given antigen during germinal center reactions. Antigen fragments are presented on the surface of the FDCs which enables antibody presenting cells to interact with them. It is widely believed that centroblasts do not present antibodies (Han et al., 1997). Accordingly, the selection process must begin after the differentiation of centroblasts to centrocytes (the initiation of this differentiation process is still unclear) which do neither proliferate nor mutate but which present antibodies. -
7432.Full.Pdf
CD27 Is Acquired by Primed B Cells at the Centroblast Stage and Promotes Germinal Center Formation This information is current as Yanling Xiao, Jenny Hendriks, Petra Langerak, Heinz Jacobs of September 29, 2021. and Jannie Borst J Immunol 2004; 172:7432-7441; ; doi: 10.4049/jimmunol.172.12.7432 http://www.jimmunol.org/content/172/12/7432 Downloaded from References This article cites 43 articles, 23 of which you can access for free at: http://www.jimmunol.org/content/172/12/7432.full#ref-list-1 http://www.jimmunol.org/ Why The JI? Submit online. • Rapid Reviews! 30 days* from submission to initial decision • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication by guest on September 29, 2021 *average Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2004 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. The Journal of Immunology CD27 Is Acquired by Primed B Cells at the Centroblast Stage and Promotes Germinal Center Formation1 Yanling Xiao, Jenny Hendriks, Petra Langerak, Heinz Jacobs, and Jannie Borst2 Studies on human B cells have featured CD27 as a marker and mediator of the B cell response.