Transport of Passive Immunity to the Calf
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THE IMMUNE SYSTEM Blood Cells Cells of the Immune System
THE IMMUNE SYSTEM Blood Cells Cells of the Immune System White Blood Cells • Phagocytes - Neutrophils - Macrophages • Lymphocytes Phagocytes • Produced throughout life by the bone marrow. • Scavengers – remove dead cells and microorganisms. Neutrophils • 60% of WBCs • ‘Patrol tissues’ as they squeeze out of the capillaries. • Large numbers are released during infections • Short lived – die after digesting bacteria • Dead neutrophils make up a large proportion of puss. Macrophages • Larger than neutrophils. • Found in the organs, not the blood. • Made in bone marrow as monocytes, called macrophages once they reach organs. • Long lived • Initiate immune responses as they display antigens from the pathogens to the lymphocytes. Macrophages Phagocytosis Phagocytosis • If cells are under attack they release histamine. • Histamine plus chemicals from pathogens mean neutrophils are attracted to the site of attack. • Pathogens are attached to antibodies and neutrophils have antibody receptors. • Enodcytosis of neutrophil membrane phagocytic vacuole. • Lysosomes attach to phagocytic vacuole pathogen digested by proteases Lymphocytes • Produce antibodies • B-cells mature in bone marrow then concentrate in lymph nodes and spleen • T-cells mature in thymus • B and T cells mature then circulate in the blood and lymph • Circulation ensures they come into contact with pathogens and each other B -Lymphocytes • There are c.10 million different B- lymphocytes, each of which make a different antibody. • The huge variety is caused by genes coding for abs changing slightly during development. • There are a small group of clones of each type of B-lymphocyte B -Lymphocytes • At the clone stage antibodies do not leave the B- cells. • The abs are embedded in the plasma membrane of the cell and are called antibody receptors. -
Clotting Phenomena at the Blood-Polymer Interface and Development of Blood Compatible Polymeric Surfaces
Clotting Phenomena at the Blood-Polymer Interface and Development of Blood Compatible Polymeric Surfaces Adriaan Bantjes In the past two decades many attempts have been made to relate surface and interfacial parameters with the blood compatibility of polymeric surfaces. It is however doubtful if by a single parameter the behaviour of blood on a surface can be predicted. Two major aspects of blood compatibility -- the prevention of platelet adhesion and the deactivation of the intrinsic coagulation system are determined by the measure and nature of competi- tive blood protein adsorption on the foreign surface. The adhesion of blood platelets is promoted by adsorbed fibrinogen and gamma globulin, while adsorbed albumin inhibits platelct adhesion. Heparinised surfaces do not adsorb fibrin and consequently no adhesion of platelets takes place. Othcr surfaces with low platelct adhesion are the hydrogels, certain block copolyetherurethanes, polyelectrolyte complexes and biolised proteins. Heparinised surfaces of the cationically bonded type inhibit the intrinsic coagulation as well, however this may be due to unstable coatings and heparin leakage. In the authors laboratory a synthetic heparinoid was prepared with the structure - [CH, - C(CH3) NHS03Na ~ C(H) COONa ~ CH2 --] with h, = (7.5 5 1 .O) x lo5 and an in vivo anticoagulant activity of 50% of heparin. Its coatings on PVC, using tridodecyltiietliyl-ammoniuni chloridc as a coupling agent, are stable in plasma and salt solutions and provide surfaces which show negligible platelet adhesion and a strong inhibition 01 the intrinsic coagulation on contact with blood. Similar results were found with polydimethylsiloxane surfaces coated with this heparinoid. 1. INTRODUCTION new blood compatible materials may be developed it is necessary to explain sotne of the mechanisms of blood co- The clinical use of blood contacting devices and prosthcses is agulation on intcraction with a foreign surface. -
The Effect of Gamma Globulin in Pustular Acne*
PRELIMINARY AND SHORT REPORT THE EFFECT OF GAMMA GLOBULIN IN PUSTULAR ACNE* LOREN W.SHAFFER,M.D., BENJAMIN SdHWIMMER, M.D. AND RENATO J.STANICCO,M.D. One of us (LWS) bad occasion to treat a young Clinical Response: Patient 1: New lesions ceased white man with gamma globulin for prophylaxisappearing immediately after the first injection. after exposure to infectious hepatitis. He wasBy the third week most of the cystic and pustular given two injections, 10 cc. each, of human Polio-lesions had dried up, and no new ones had ap- myelitis Immune Globulin, one week apart. Itpeared. Comedones were not decreased in number. was observed that shortly after the second injec-The patient maintained his improvement through tion, his severe pustular and indurated acnethe fifth week when the cystic and pustular lesions improved considerably. This observation led tobegan to recur. the present study, of which this is a preliminary Patient 2: New lesions continued to develop report. throughout the period of treatment and the one This study of the therapeutic effect of gammamonth follow up. globulin in pustular acne is coupled with a study Patient 3: There was no observable effect of of the serum protein and C-reactive protein levelstreatment. before and after treatment. Patient 4: The first improvement was seen in Method: Four patients in their late teens, other-the second week and by the third, all cystic and wise healthy, but with severe pustular and cysticpustular lesions were dry. The improvement acne that had been resistant to conventionallasted for two weeks after which the lesions methods of treatment were selected for the study.began to return. -
The Relationship Between Maternal Postpartum Psychological State and Breast Milk Secretory Immunoglobulin a Level
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Tsukuba Repository The Relationship Between Maternal Postpartum Psychological State and Breast Milk Secretory Immunoglobulin A Level 著者 Kawano Atsuko, Emori Yoko journal or Journal of the American Psychiatric Nurses publication title Association volume 21 number 1 page range 23-30 year 2015-01 権利 Authors URL http://hdl.handle.net/2241/00124572 doi: 10.1177/1078390314566882 The relationship between maternal postpartum psychological state and breast milk secretory immunoglobulin A level. Kawano A, Emori Y. J Am Psychiatr Nurses Assoc. 2015 Jan-Feb;21(1):23-30. doi: 10.1177/1078390314566882. Epub 2015 Jan 14. PMID:25589451 Abstract BACKGROUND: Maternal psychological state may influence the passive transfer of immune factors (e.g., immunoglobulin) via the mother’s breast milk. OBJECTIVE: The aim of this study was to determine whether a correlation exists between mothers’ postpartum psychological state and their breast milk secretory immunoglobulin A (SIgA) levels. STUDY DESIGN: Eighty-one mothers who delivered at an urban general hospital were included in our analysis. Two weeks after delivery, we measured their breast milk SIgA levels and simultaneously documented their psychological state using the Profile of Mood States (POMS), General Health Questionnaire (GHQ), and State-Trait Anxiety Inventory (STAI) scales. RESULTS: Breast milk SIgA levels were negatively correlated with negative POMS states (tension-anxiety, depression-dejection, anger-hostility, fatigue, and confusion). A negative correlation was also observed between SIgA levels and GHQ mental health (r = −.625, P = .000), and a similar negative correlation was observed with STAI trait and state anxieties. -
Gamma Globulin”
CLINICAL APPLICATION OF A SIMPLE METHOD FOR ESTIMATING “GAMMA GLOBULIN” B. V. Jager, Margaret Nickerson J Clin Invest. 1948;27(2):231-238. https://doi.org/10.1172/JCI101938. Research Article Find the latest version: https://jci.me/101938/pdf CLINICAL APPLICATION OF A SIMPLE METHOD FOR ESTIMATING "GAMMA GLOBULIN" 1 By B. V. JAGER AND MARGARET NICKERSON (From the Department of Medicine, School of Medicine, University of Utah, Salt Lake City) (Received for publication August 11, 1947) The electrophoretic technique offers the most cipitate is finely emulsified in 3.0 ml. of 33.3 per cent accurate method for serum fractionation. This saturated ammonium sulfate. The tube is recentrifuged for 30 minutes and the supernatant fluid is discarded. permits a quantitative separation of serum into The precipitate is dissolved in 10 ml. of saline and an albumin and into three major globulin fractions aliquot is employed to determine its protein content, using which are designated as alpha, beta and gamma a biuret method such as that of Weichselbaum (2). components. In recent years electrophoretic anal- Triplicate determinations may be made with an *yses of serum proteins have been performed by accuracy of + 2 per cent. Electrophoretic studies many investigators in a variety of diseases. The indicate that 73 to 83 per cent of this protein accumulated data from these studies have now at- fraction consists of gamma globulin, the remainder tained sufficient size and agreement that they may consisting of alpha and beta globulins. From 70 to be of value as an aid in the differential diagnosis 82 per cent of the total gamma globulin present of certain diseases or for following the course of in the serum is recovered in this fraction. -
Modeling to Understand Plant Protein Structure-Function Relationships—Implications for Seed Storage Proteins
molecules Review Modeling to Understand Plant Protein Structure-Function Relationships—Implications for Seed Storage Proteins 1,2, 1, 2 1, Faiza Rasheed y, Joel Markgren y , Mikael Hedenqvist and Eva Johansson * 1 Department of Plant Breeding, The Swedish University of Agricultural Sciences, Box 101, SE-230 53 Alnarp, Sweden; [email protected] (F.R.); [email protected] (J.M.) 2 School of Chemical Science and Engineering, Fibre and Polymer Technology, KTH Royal Institute of Technology, SE–100 44 Stockholm, Sweden; [email protected] * Correspondence: [email protected] These authors contributed equally to this work. y Received: 2 January 2020; Accepted: 14 February 2020; Published: 17 February 2020 Abstract: Proteins are among the most important molecules on Earth. Their structure and aggregation behavior are key to their functionality in living organisms and in protein-rich products. Innovations, such as increased computer size and power, together with novel simulation tools have improved our understanding of protein structure-function relationships. This review focuses on various proteins present in plants and modeling tools that can be applied to better understand protein structures and their relationship to functionality, with particular emphasis on plant storage proteins. Modeling of plant proteins is increasing, but less than 9% of deposits in the Research Collaboratory for Structural Bioinformatics Protein Data Bank come from plant proteins. Although, similar tools are applied as in other proteins, modeling of plant proteins is lagging behind and innovative methods are rarely used. Molecular dynamics and molecular docking are commonly used to evaluate differences in forms or mutants, and the impact on functionality. -
Current Trends in Research on Human Milk Exchange for Infant Feeding
Current trends in research on human milk exchange for infant feeding By: Aunchalee E. L. Palmquist, Maryanne T. Perrin, Diana Cassar-Uhl, Karleen D. Gribble, Angela B. Bond, and Tanya Cassidy Palmquist AEL, Perrin MT, Cassar-Uhl D, Gribble KD, Bond AB, Cassidy T. Current Trends in Research on Human Milk Exchange for Infant Feeding. Journal of Human Lactation. 2019;35(3):453-477. doi:10.1177/0890334419850820 Made available courtesy of SAGE publications: https://doi.org/10.1177/0890334419850820 ***© 2019 The Authors. Reprinted with permission. No further reproduction is authorized without written permission from SAGE. This version of the document is not the version of record. *** Abstract: Breastfeeding is critical for the healthy growth and development of infants. A diverse range of infant-feeding methods are used around the world today. Many methods involve feeding infants with expressed human milk obtained through human milk exchange. Human milk exchange includes human milk banking, human milk sharing, and markets in which human milk may be purchased or sold by individuals or commercial entities. In this review, we examine peer- reviewed scholarly literature pertaining to human milk exchange in the social sciences and basic human milk sciences. We also examine current position and policy statements for human milk sharing. Our review highlights areas in need of future research. This review is a valuable resource for healthcare professionals and others who provide evidence-based care to families about infant feeding. Keywords: human milk | human milk expression | infant-feeding patterns | lactation | milk banking | breastfeeding Article: Key Messages • Breastfeeding is critical for the healthy growth and development of infants, but it is not always possible or desired. -
Greenbook Chapter 1
Chapter 1: Immunity and how vaccines work December 2018 1 Immunity and how vaccines work vaccines work Introduction Immunity and how Immunity is the ability of the human body to protect itself from infectious disease. The defence mechanisms of the body are complex and include innate (non-specific, non-adaptive) mechanisms and acquired (specific, adaptive) systems. Innate or non-specific immunity is present from birth and includes physical barriers (e.g. intact skin and mucous membranes), chemical barriers (e.g. gastric acid, digestive enzymes and bacteriostatic fatty acids of the skin), phagocytic cells and the complement system. Acquired immunity is generally specific to a single organism or to a group of closely related organisms. There are two basic mechanisms for acquiring immunity – active and passive. Active immunity Active immunity is protection that is produced by an individual’s own immune system and is usually long-lasting. Such immunity generally involves cellular responses, serum antibodies or a combination acting against one or more antigens on the infecting organism. Active immunity can be acquired by natural disease or by vaccination. Vaccines generally provide immunity similar to that provided by the natural infection, but without the risk from the disease or its complications. Active immunity can be divided into antibody- mediated and cell-mediated components. Antibody-mediated immunity Antibody-mediated responses are produced by B lymphocytes (or B cells), and their direct descendants, known as plasma cells. When a B cell encounters an antigen that it recognises, the B cell is stimulated to proliferate and produce large numbers of lymphocytes secreting an antibody to this antigen. -
I M M U N O L O G Y Core Notes
II MM MM UU NN OO LL OO GG YY CCOORREE NNOOTTEESS MEDICAL IMMUNOLOGY 544 FALL 2011 Dr. George A. Gutman SCHOOL OF MEDICINE UNIVERSITY OF CALIFORNIA, IRVINE (Copyright) 2011 Regents of the University of California TABLE OF CONTENTS CHAPTER 1 INTRODUCTION...................................................................................... 3 CHAPTER 2 ANTIGEN/ANTIBODY INTERACTIONS ..............................................9 CHAPTER 3 ANTIBODY STRUCTURE I..................................................................17 CHAPTER 4 ANTIBODY STRUCTURE II.................................................................23 CHAPTER 5 COMPLEMENT...................................................................................... 33 CHAPTER 6 ANTIBODY GENETICS, ISOTYPES, ALLOTYPES, IDIOTYPES.....45 CHAPTER 7 CELLULAR BASIS OF ANTIBODY DIVERSITY: CLONAL SELECTION..................................................................53 CHAPTER 8 GENETIC BASIS OF ANTIBODY DIVERSITY...................................61 CHAPTER 9 IMMUNOGLOBULIN BIOSYNTHESIS ...............................................69 CHAPTER 10 BLOOD GROUPS: ABO AND Rh .........................................................77 CHAPTER 11 CELL-MEDIATED IMMUNITY AND MHC ........................................83 CHAPTER 12 CELL INTERACTIONS IN CELL MEDIATED IMMUNITY ..............91 CHAPTER 13 T-CELL/B-CELL COOPERATION IN HUMORAL IMMUNITY......105 CHAPTER 14 CELL SURFACE MARKERS OF T-CELLS, B-CELLS AND MACROPHAGES...............................................................111 -
Vaccines Why Use Passive Immunity?
Vaccines n Active vs Passive Immunization n Active is longer acting and makes memory and effector cells n Passive is shorter acting, no memory and no effector cells n Both can be obtained through natural processes: n Getting antibodies from mother n Directly getting the disease n Or by unnatural processes n Being given pre-formed antibodies (gamma globulin shot) n Altered (attenuated) vaccines, toxoids n Immunity elicited in one animal can be transferred to another animal by injecting the recipient animal with serum from the immune animal n Passive immunization= pre-formed antibodies given from one individual to another (across placenta, gamma globulin injection) Why use passive immunity? n Deficiency in synthesis of Ig because of congenital or acquired defects n When a susceptible person is likely to be exposed to disease n When time does not permit adequate protection through active immunization n When a disease is already present and Ig may help to ameliorate or help to suppress the effects of toxin (tetanus, diphtheria or botulism) n Passive Immunity- n Natural maternal Ab & Immune globulin & Antitoxin n Active Immunity- n Natural Infection n Vaccines (attenuated & inactivated organisms & purified microbial proteins, cloned microbial antigens & toxoids) 1 n Tetanus- horse serum (horses do NOT get tetanus and can be injected with tetanus toxin) n Horse produces antibodies to toxin and when injected into person they act to neutralize toxin to prevent binding (serum sickness to horse albumin possible) n People can be given a toxoid (altered -
1. Introduction to Immunology Professor Charles Bangham ([email protected])
MCD Immunology Alexandra Burke-Smith 1. Introduction to Immunology Professor Charles Bangham ([email protected]) 1. Explain the importance of immunology for human health. The immune system What happens when it goes wrong? persistent or fatal infections allergy autoimmune disease transplant rejection What is it for? To identify and eliminate harmful “non-self” microorganisms and harmful substances such as toxins, by distinguishing ‘self’ from ‘non-self’ proteins or by identifying ‘danger’ signals (e.g. from inflammation) The immune system has to strike a balance between clearing the pathogen and causing accidental damage to the host (immunopathology). Basic Principles The innate immune system works rapidly (within minutes) and has broad specificity The adaptive immune system takes longer (days) and has exisite specificity Generation Times and Evolution Bacteria- minutes Viruses- hours Host- years The pathogen replicates and hence evolves millions of times faster than the host, therefore the host relies on a flexible and rapid immune response Out most polymorphic (variable) genes, such as HLA and KIR, are those that control the immune system, and these have been selected for by infectious diseases 2. Outline the basic principles of immune responses and the timescales in which they occur. IFN: Interferon (innate immunity) NK: Natural Killer cells (innate immunity) CTL: Cytotoxic T lymphocytes (acquired immunity) 1 MCD Immunology Alexandra Burke-Smith Innate Immunity Acquired immunity Depends of pre-formed cells and molecules Depends on clonal selection, i.e. growth of T/B cells, release of antibodies selected for antigen specifity Fast (starts in mins/hrs) Slow (starts in days) Limited specifity- pathogen associated, i.e. -
ISO 9001:2000 Certified
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