Chapter 22 the Lymphatic System and Immunity
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SAHLGRENSKA AKADEMIN Thymic Studies
Göteborg, 2019 Thymic studies Investigations into the effects of childhood thymectomy, and characterization of thymic B cells and Hassall's corpuscles Akademisk avhandling Som för avläggande av medicine doktorsexamen vid Sahlgrenska akademin, Göteborgs universitet kommer att offentligen försvaras i föreläsningssalen våning 3, Guldhedsgatan 10A, Göteborg Tisdagen den 14e maj, klockan 13.00 av Christina Lundqvist Fakultetsopponent: Professor Ludger Klein Ludwig-Maximilians-Universität, Tyskland Avhandlingen baseras på följande delarbeten I. Gudmundsdottir J*, Lundqvist C*, Ijspeert H, van der Slik E, Óskarsdóttir S, Lindgren S, Lundberg V, Berglund M, Lingman-Framme J, Telemo E, van der Burg M, Ekwall O. T-cell receptor sequencing reveals decreased diversity 18 years after early thymectomy. J Allergy Clin Immunol. 2017 Dec;140(6):1743- 1746.e7. doi: 10.1016/j.jaci.2017.08.002. Epub 2017 Sep 1. * These authors contributed equally to this work. II. Lundqvist C*, Camponeschi A*, Visentini M, Telemo E, Ekwall O‡, Mårtensson IL‡. Switched CD21-/low B cells with an antigen-presenting phenotype in the infant thymus. J Allergy Clin Immunol. 2018 Nov 30. pii: S0091-6749(18)31721- 4. doi: 10.1016/j.jaci.2018.11.019. * These authors contributed equally to this work. ‡ These authors contributed equally to this work. III. Lundqvist C, Lindgren S, Cheuk S, Lundberg V, Berglund M, Thörn K, Telemo E, Ekwall O. Characterization of Hassall's corpuscles in the human thymus. Manuscript SAHLGRENSKA AKADEMIN INSTITUTIONEN FÖR MEDICIN Göteborg, 2019 Thymic studies Investigations into the effects of childhood thymectomy, and characterization of thymic B cells and Hassall's corpuscles Christina Lundqvist Avdelningen för reumatologi och inflammationsforskning, Institutionen för medicin, Sahlgrenska akademin, Göteborgs universitet Abstract This thesis focuses on the human thymus, a primary lymphoid organ responsible for the maturation of T cells. -
USC 591.4: 591.441: 597/599 MORPHOLOGICAL FEATURES of the SPLENIC RED PULP Ph.D. in Biological Sciences, Associate Professor, Du
INNOVATIVE SOLUTIONS IN MODERN SCIENCE № 4 (4), 2016 USC 591.4: 591.441: 597/599 MORPHOLOGICAL FEATURES OF THE SPLENIC RED PULP Ph.D. in Biological Sciences, associate professor, Dunaievska O. F. Zhytomyr National Agroecological University, Ukraine, Zhytomyr The spleen is an important peripheral organ of the sanguification and immune defense. In vertebrates and humans, it is formed by the support- contractile apparatus, as well as by the white and red pulps. The red pulp consists of the soft splenic cords, reticular stromal systems, and sinuses, including vascular structures. The relative area of red pulp is an important test criterion of the organ. It takes from 48,95% to 84,3% in the vertebrates, and from 71,4% to 83,6% in humans. It depends on the class, type, race, sex, breed, the age of animals, or the person's age and physiological state. The indicator of red pulp’s relative area is used as a biomarker in the environment bioindication. Any change of its values indicates the changes of the environmental conditions. Determination of the morphological standards in the organs and tissues according to the animals’ age, species, and breed aspects is used in the prevention of diseases, effective treatment, and getting the high-quality food. The test criteria of the spleen are important while studying the effect of pharmacological drugs, conditions of animal sustentation and feeding. Determination of splenic morphometric parameters is of the great practical importance, particularly in surgery, laboratory diagnostics, and development of the medical measures. Keywords: spleen, morphology, fish, frogs, birds, mammals, human. Spleen belongs to the peripheral organ of the sanguification and immune protection; it is presented in all vertebrates. -
B Cells + Interaction
Human B Cell Activation by Autologous NK Cells Is Regulated by CD40-CD40 Ligand Interaction: Role of Memory B Cells and CD5 + B Cells This information is current as of October 2, 2021. Isaac R. Blanca, Earl W. Bere, Howard A. Young and John R. Ortaldo J Immunol 2001; 167:6132-6139; ; doi: 10.4049/jimmunol.167.11.6132 http://www.jimmunol.org/content/167/11/6132 Downloaded from References This article cites 45 articles, 17 of which you can access for free at: http://www.jimmunol.org/content/167/11/6132.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 October 2, 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 © 2001 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. Human B Cell Activation by Autologous NK Cells Is Regulated by CD40-CD40 Ligand Interaction: Role of Memory B Cells and CD5؉ B Cells Isaac R. Blanca,*† Earl W. Bere,* Howard A. -
Advanced Laboratory Studies for Primary Immunodeficiency Disorders
4813: Problem-based Learning Workshop Advanced Laboratory studies for Primary Immunodeficiency Disorders Moderator: Richard Wasserman, MD, PhD Discussion Leader: Roshini Abraham, PhD ● Understand B cell flow analysis in CVID (PBL case) HUMAN PERIPHERAL B CELL DIFFERENTIATION Marginal zone B cells Bone marrow Immature B cells Transitional B cells Naïve B cells Memory B cells Plasmablasts Periphery MARKERS FOR PERIPHERAL B CELL SUBSETS - CURRENT Total B cells: CD19 and/or CD20 Transitional B cells: CD19+CD38+IgM+ Total IgM+ B cells: CD19+IgM+ (includes naïve B cells) Memory B cells: CD19+CD27+ switched memory B cells: CD19+CD27+IgM-IgD- marginal zone B cells: CD19+CD27+IgM+IgD+ IgM-only memory B cells: CD19+CD27+IgM+IgD- Plasmablasts: CD19+CD38+IgM- CD21+ B cells: CD19+CD21+ CD21- B cells: CD19+CD21- ● With newer information, more suitable cellular markers are available for accurate identification of transitional B cells and plasmablasts, in particular, but also for naïve B cells NEWER B CELL MARKERS FOR B CELL SUBSET QUANTITATION Total B cells and B cell subsets can be quantitated in blood using multicolor flow cytometry: Total B cells: CD45+CD19+20+ For B cell subset analysis, the gating strategy uses CD45+19+20+/- (depending on the subset being studied), thus these markers are not specifically repeated in the panel below:- Transitional B cells: T1: CD24hi38hi10+27-21lowIgM+++ T2: CD24hi38hi10+27-21int IgM+++ Naïve B cells: IgM+IgD+27-38-21+++ Memory B cells: Marginal zone B cells: CD27+IgM+IgD+ IgM-only memory: CD27+IgM+IgD- IgD-only -
B-Chapter 2.P65
1 2 3 4 CHAPTER 2 / MICROANATOMY OF MAMMALIAN SPLEEN 11 5 6 7 8 9 10 11 2 The Microanatomy 12 13 of the Mammalian Spleen 14 15 Mechanisms of Splenic Clearance 16 17 18 19 FERN TABLIN, VMD, PhD, JACK K. CHAMBERLAIN, MD, FACP, 20 AND LEON WEISS, MD 21 22 23 2.1. INTRODUCTION 2.2.1. CAPSULE AND TRABECULAE The human spleen 24 weighs approx 150 g, in adults, and is enclosed by a capsule com- The spleen is a uniquely adapted lymphoid organ that is dedi- 25 posed of dense connective tissue, with little smooth muscle (Faller, cated to the clearance of blood cells, microorganisms, and other 26 1985; Weiss, 1983, 1985). This arrangement reflects the minimal particles from the blood. This chapter deals with the microanatomy 27 contractile role of the capsule and trabeculae in altering the blood of the spleen, its highly specialized extracellular matrix compo- volume of the human spleen, under normal circumstances. The 28 nents, distinctive vascular endothelial cell receptors, and the extra- capsule measures 1.1–1.5 mm thick, and is covered by a serosa, 29 ordinary organization of the venous vasculature. We also address except at the hilus, where blood vessels, nerves, and lymphatics 30 the cellular mechanisms of splenic clearance, which are typified by enter the organ. There are two layers of the capsule: This can be 31 the vascular organization of the spleen; mechanisms and regula- determined by the orientation of collagen fibers (Faller, 1985), 32 tion of clearance, and the development of a unique component; which are moderately thick and uniform, but which become finer 33 specialized barrier cells, which may be essential to the spleen’s in the deeper regions, where the transition to pulp fibers occurs. -
Vaccine Immunology Claire-Anne Siegrist
2 Vaccine Immunology Claire-Anne Siegrist To generate vaccine-mediated protection is a complex chal- non–antigen-specifc responses possibly leading to allergy, lenge. Currently available vaccines have largely been devel- autoimmunity, or even premature death—are being raised. oped empirically, with little or no understanding of how they Certain “off-targets effects” of vaccines have also been recog- activate the immune system. Their early protective effcacy is nized and call for studies to quantify their impact and identify primarily conferred by the induction of antigen-specifc anti- the mechanisms at play. The objective of this chapter is to bodies (Box 2.1). However, there is more to antibody- extract from the complex and rapidly evolving feld of immu- mediated protection than the peak of vaccine-induced nology the main concepts that are useful to better address antibody titers. The quality of such antibodies (e.g., their these important questions. avidity, specifcity, or neutralizing capacity) has been identi- fed as a determining factor in effcacy. Long-term protection HOW DO VACCINES MEDIATE PROTECTION? requires the persistence of vaccine antibodies above protective thresholds and/or the maintenance of immune memory cells Vaccines protect by inducing effector mechanisms (cells or capable of rapid and effective reactivation with subsequent molecules) capable of rapidly controlling replicating patho- microbial exposure. The determinants of immune memory gens or inactivating their toxic components. Vaccine-induced induction, as well as the relative contribution of persisting immune effectors (Table 2.1) are essentially antibodies— antibodies and of immune memory to protection against spe- produced by B lymphocytes—capable of binding specifcally cifc diseases, are essential parameters of long-term vaccine to a toxin or a pathogen.2 Other potential effectors are cyto- effcacy. -