Antibodies, Epigenetics, and a Bit of Hay

Total Page:16

File Type:pdf, Size:1020Kb

Antibodies, Epigenetics, and a Bit of Hay Antibodies, Epigenetics, Rebecca Tallmadge, PhD and a Bit of Hay Maria Julia Bevilaqua Felippe, MV, MS, PhD ‘The overall focus of our work is to gain insight into the development and function of the immune system, then applying that knowledge to the benefit of immunodeficient horses and young foals during that period of time where they are especially susceptible to pathogens.’ – Dr Tallmadge ANTIBODIES, EPIGENETICS, AND A BIT OF HAY Dr Julia Felippe and Dr Rebecca Tallmadge of Cornell University’s College of Veterinary Medicine are attempting to understand the complex world of the equine immune system. We talk to them about their discoveries and plans. Imagine a gingerbread house, tall as a the womb, babies tend to be born in an is newer to the field than Dr Felippe, but mountain, warm and cosy, full of all the immunologically ‘naïve’ state – they have not nonetheless brings an exceptionally broad proteins and nutrients which you could yet had any exposure to the outside world, array of knowledge and experience derived possibly need to grow, reproduce, and start full of bacteria and other antigens. This from both equine immunology and genetics. a giant family. Sounds tempting, doesn’t means that the intrinsic protection provided As she comments, her current role allows it? This is you, from the point of view of the by exposure has not yet been developed and her to ‘provide insight from my training in millions of microbes swarming over your so newborn mammals have a much higher equine immunogenetics – combining data skin, your hair, in your gut and in your nose. risk of catching disease than those just a we obtain in the lab with genome sequences A delicious mountain of food protected only few months older. To offset this window to characterise the strength or limitations by the tireless defence offered by the bodies’ of vulnerability, the newborn receives the of an immune system, whether it be an own immune system. Small wonder then that antibodies produced by its mother – these immunodeficient horse or a young foal.’ those who lose this vital protection rapidly antibodies continue to circulate for a succumb to diseases which would barely while after birth and so effectively act as a Their studies focus on the role of the even irritate a healthy individual. borrowed immune system. Borrowed, but developing immune system in diseases such not as effective as it could be; newborns as those caused by pathogenic infections There are many ways in which we can be ranging from human babies through to horse or developmental difficulties. The two have The trick, then, is to develop a way to target body, this leads to a rapid drop in circulating be modified at a later stage, changing the left without a functioning immune system. foals are highly susceptible to pathogenic been, in Dr Tallmadge’s words, ‘gaining a bacterium which can hijack and kill the antibodies and thus significantly weakens expression of the genes involved without Perhaps the most famous is AIDS, in which attack. insight into the development and function very immune cells which are meant to be the ability of the affected horse to resist modifying their basic code. The study of infection with HIV leads to a progressive loss of the immune system, then applying that killing it. This sounds difficult, and indeed it disease. CVID is a disease found both in these secondary genetic factors is known as of immune capability and eventual death Something old, something new, something knowledge to the benefit of immunodeficient is – despite many different approaches the horses and humans, though the origins of epigenetics, and this is the field in which Dr from minor secondary infections. Otherwise borrowed horses and young foals during that period of only sure-fire way to induce a robust immune the symptoms often remain mysterious, as Felippe found herself. known as immunodeficiencies, these time where they are especially susceptible to response in foals is to infect them with the Dr Felippe explains: ‘though known in human situations are also brought about by cancer, A cavalcade of complexity is thus occurring pathogens.’ microbe itself. As part of the road to better patients for the last 6 decades, only about Because CVID involves epigenetic by chemotherapy, by infections with various in a newborn, mixing new-developing with understand how the pathogen deceives the 10% of patients have been described with a mechanisms, can epigenetic factors also help pathogens, even just by being born. decaying-borrowed immune systems, all These pathogens include particularly nasty immune system, the group demonstrated genetic mutation, and the cause of disease is to provide a cure? Bone marrow transplants reacting to the colonisation of bacteria which examples such as R. equi, a dust-borne the ability to make a miniature lung segment unknown for 90% of patients.’ The lack of a are rarely used in humans with CVID to Just by being born? occurs moments after being born. Sounds bacterium which, like the agent responsible – complete with the ability to clean itself of genetic source led her group to follow other provide a fresh source of the precursor impossible to untangle? Even more complex for Tuberculosis, is able to avoid destruction inhaled dust, and then used this to watch in possibilities, with the eventual discovery that, cells which can differentiate into B-cells – Though we don’t often think about it, an when your subject is up and running around by hiding within the lungs’ own immune detail the manner in which R. equi infected in her words ‘target gene expressions were essentially overwriting the patients’ immune immune system develops – it expands in within hours of being born – as is the case cells. By hijacking these cells, known as macrophages. Knowledge of these processes downregulated in affected equine patients, system with one from a healthy donor. Dr capabilities over time. Infections trigger with those who study the immunology of macrophages, R. equi is able to grow without allows the further development of targeted and aberrant epigenetic mechanisms were Felippe’s group is studying a novel approach, expansions in antibody-producing cells horses. fear of detection and thus can rapidly treatments, and indeed Dr Felippe has associated with gene silencing, with the attempting to take the patient’s own derived which can target those pathogens, a spread throughout the lungs, causing an collaborated with other groups assessing resulting halt in B cell production.’ bone marrow and reactivate the affected memory of sorts which remains long after Untangling this complexity is the lofty often severe pneumonia. The bacterium is effective non-infectious vaccines. B-cell precursors using epigenetic modifiers. the infection is gone, protecting against the goal of Dr Julia Felippe and Dr Rebecca exclusively dangerous to newborn horses Fine words, I hear you say, but what does These cells can then be retransplanted into next infection (this, of course, is the basis of Tallmadge, both of Cornell University. Dr and foals, as (despite their loaned set of Epidemics of epigenetic this actually mean? The traditional view of the affected horse, essentially allowing them immunisation). The flip side of this, however, Julia Felippe is one of the top researchers antibodies), they have yet to develop the genetics was that each trait held by a person to be the healthy donor for themselves. is that an immune system which has not yet in the field of equine immunology, innate immunity which would otherwise Another major focus of their work is known or animal (strong legs, black hair, brown had time to develop is also far weaker than it having spent the last 27 years either protect them from infection – this same as common variable immunodeficiency eyes) was the product of one or more genes, Epigenetics are also involved in mediating could otherwise be. as a practicing equine veterinarian, effect can be seen in immunocompromised (CVID for short). One mechanism involved passed down from parents to children and the overall effect of other diseases such studying equine clinical medicine, or human or adult horse patients, who can be is the sudden halt in the production of B set in stone from the moment of conception. as equine herpesvirus-1 (EHV-1), a highly Although a large portion of the bodies’ researching equine immunodeficiencies susceptible to the same disease. cells within the bone marrow. As B-cells are This view turns out to be incomplete. There contagious virus which not only leads to immune system is developed while in and immunodevelopment. Dr Tallmadge the major source of antibodies within the are a number of ways in which DNA can neurologic damage but remains latent – WWW.SCIENTIAPUBLICATIONS.COM WWW.SCIENTIAPUBLICATIONS.COM Meet the researchers Rebecca Tallmadge, PhD Maria Julia Bevilaqua Felippe, MV, MS, PhD Department of Clinical Sciences Department of Clinical Sciences College of Veterinary Medicine College of Veterinary Medicine Cornell University Cornell University USA USA CONTACT CONTACT E: [email protected] E: [email protected] T: (+1) 607 253 3493 T: (+1) 607 253 3100 Dr Tallmadge has been in the field of equine research for many Dr Felippe is a veterinary internist and immunologist, and faculty years, beginning with her first scientific employment as a technician at Cornell University College of Veterinary Medicine. She oversees taking part in the horse genome project. This quickly led to other the Equine Clinical Immunology Laboratory, and has served as the roles in equine science: a PhD project examining immunological editor of the Equine Clinical Immunology book. Inspired by her proteins, postdoctoral work studying infectious diseases and horse patients, she has dedicated the last 27 years of her career immunodeficiencies, and her current role investigating CVID.
Recommended publications
  • Single Nucleotide Polymorphism (SNP)
    Aquaculture Genome Technologies Zhanjiang (John) Liu Copyright © 2007 by Blackwell Publishing Chapter 6 Single Nucleotide Polymorphism (SNP) Zhanjiang Liu Single nucleotide polymorphism (SNP) describes polymorphisms caused by point mutations that give rise to different alleles containing alternative bases at a given nucleotide position within a locus. Such sequence differences due to base substitu- tions have been well characterized since the beginning of DNA sequencing in 1977, but the ability to genotype SNPs rapidly in large numbers of samples was not possible until several major technological advances in the late 1990s. With the development of the TaqMan technology, gene chip technology, pyrosequencing, and MALDI-TOF, which is matrix-assisted laser desorption ionization-time of flight mass spectrometry (Haff et al. 1997, Tost et al. 2005), SNPs are again becoming a focal point in molecular marker development because they are the most abundant polymorphism in any organ- ism (as shown in Table 6.1), adaptable to automation, and reveal hidden polymor- phism not detected with other markers and methods. SNP markers are regarded by many as the projected markers of choice for the future. In this chapter, I will summa- rize methods for SNP discovery, review the traditional approaches for SNP genotyp- ing and their principles, present several major platforms for SNP genotyping using recently developed technologies, and discuss the pros and cons of SNP markers for aquaculture genome research. What Are SNP Markers and Why Are They the Future Markers of Choice? SNP can be defined as base variation at any site of the genome among individuals, or an alternative base at a given DNA site (Figure 6.1).
    [Show full text]
  • Genetic, Epidemiological and Biological Analysis of Interleukin-10
    Genes and Immunity (2009) 10, 174–180 & 2009 Macmillan Publishers Limited All rights reserved 1466-4879/09 $32.00 www.nature.com/gene ORIGINAL ARTICLE Genetic, epidemiological and biological analysis of interleukin-10 promoter single-nucleotide polymorphisms suggests a definitive role for À819C/T in leprosy susceptibility AC Pereira1,5, VN Brito-de-Souza1,5, CC Cardoso2, IMF Dias-Baptista1, FPC Parelli1,3, J Venturini1,3, FR Villani-Moreno1, AG Pacheco4 and MO Moraes2 1Instituto Lauro de Souza Lima, Bauru, Sa˜o Paulo, Brazil; 2Laborato´rio de Hansenı´ase, Departamento de Micobacterioses, Instituto Oswaldo Cruz, Rio de Janeiro, Brazil; 3Tropical Diseases Area, Botucatu Medical School, Sao Paulo State University, UNESP, Botucatu, Sa˜o Paulo, Brazil and 4Departamento de Epidemiologia e Me´todos Quantitativos em Sau´de (DEMQS), Escola Nacional de Sau´de Pu´blica (ENSP)/PROCC, FIOCRUZ, Rio de Janeiro, Brazil Leprosy is a complex infectious disease influenced by genetic and environmental factors. The genetic contributing factors are considered heterogeneous and several genes have been consistently associated with susceptibility like PARK2, tumor necrosis factor (TNF), lymphotoxin-a (LTA) and vitamin-D receptor (VDR). Here, we combined a case–control study (374 patients and 380 controls), with meta-analysis (5 studies; 2702 individuals) and biological study to test the epidemiological and physiological relevance of the interleukin-10 (IL-10) genetic markers in leprosy. We observed that the À819T allele is associated with leprosy susceptibility either in the case–control or in the meta-analysis studies. Haplotypes combining promoter single-nucleotide polymorphisms also implicated a haplotype carrying the À819T allele in leprosy susceptibility (odds ratio (OR) ¼ 1.40; P ¼ 0.01).
    [Show full text]
  • Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases
    Journal of Clinical Medicine Review Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases Anna Wajda 1 , Larysa Sivitskaya 2,* and Agnieszka Paradowska-Gorycka 1 1 Department of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637 Warsaw, Poland; [email protected] (A.W.); [email protected] (A.P.-G.) 2 Institute of Genetics and Cytology, National Academy of Sciences of Belarus, 220072 Minsk, Belarus * Correspondence: [email protected] Abstract: NGS technologies have transformed clinical diagnostics and broadly used from neonatal emergencies to adult conditions where the diagnosis cannot be made based on clinical symptoms. Autoimmune diseases reveal complicate molecular background and traditional methods could not fully capture them. Certainly, NGS technologies meet the needs of modern exploratory research, diagnostic and pharmacotherapy. Therefore, the main purpose of this review was to briefly present the application of NGS technology used in recent years in the understanding of autoimmune diseases paying particular attention to autoimmune connective tissue diseases. The main issues are presented in four parts: (a) panels, whole-genome and -exome sequencing (WGS and WES) in diagnostic, (b) Human leukocyte antigens (HLA) as a diagnostic tool, (c) RNAseq, (d) microRNA and (f) microbiome. Although all these areas of research are extensive, it seems that epigenetic impact on the development of systemic autoimmune diseases will set trends for future studies on this area. Citation: Wajda, A.; Sivitskaya, L.; Keywords: next-generation sequencing; autoimmune diseases; autoimmune connective tissue dis- Paradowska-Gorycka, A. Application eases; HLA; microRNA; microbiome of NGS Technology in Understanding the Pathology of Autoimmune Diseases. J. Clin.
    [Show full text]
  • IMGT-Choreography for Immunogenetics and Immunoinformatics
    In Silico Biology 5 (2005) 45–60 45 IOS Press IMGT-Choreography for Immunogenetics and Immunoinformatics Marie-Paule Lefranc∗, Oliver Clement,´ Quentin Kaas, Elodie Duprat, Patrick Chastellan, Isabelle Coelho, Kora Combres, Chantal Ginestoux, Veronique´ Giudicelli, Denys Chaume and Gerard´ Lefranc IMGT, the international ImMunoGeneTics information system , Universite´ Montpellier II, Laboratoire d’ImmunoGen´ etique´ Moleculaire´ LIGM, UPR CNRS 1142, Institut de Gen´ etique´ Humaine IGH, 141 rue de la Cardonille, 34396 Montpellier Cedex 5, France Tel.: +33 4 99 61 99 65; Fax: +33 4 99 61 99 01 Edited by H. Michael; received 11 September 2004; revised and accepted 14 December 2004; published 24 December 2004 ABSTRACT: IMGT, the international ImMunoGeneTics information system (http://imgt.cines.fr), was created in 1989 at Montpellier, France. IMGT is a high quality integrated knowledge resource specialized in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC) of human and other vertebrates, and related proteins of the immune system (RPI) which belong to the immunoglobulin superfamily (IgSF) and MHC superfamily (MhcSF). IMGT provides a common access to standardized data from genome, proteome, genetics and three-dimensional structures. The accuracy and the consistency of IMGT data are based on IMGT-ONTOLOGY, a semantic specification of terms to be used in immunogenetics and immunoinformatics. IMGT-ONTOLOGY has been formalized using XML Schema (IMGT-ML) for interoperability with other information systems. We are developing Web services to automatically query IMGT databases and tools. This is the first step towards IMGT-Choreography which will trigger and coordinate dynamic interactions between IMGT Web services to process complex significant biological and clinical requests.
    [Show full text]
  • Multiple Sclerosis: Shall We Target CD33?
    G C A T T A C G G C A T genes Article Multiple Sclerosis: Shall We Target CD33? Vasileios Siokas 1, Zisis Tsouris 1, Athina-Maria Aloizou 1 , Christos Bakirtzis 2, Ioannis Liampas 1 , Georgios Koutsis 3 , Maria Anagnostouli 4 , Dimitrios P. Bogdanos 5, Nikolaos Grigoriadis 2, Georgios M. Hadjigeorgiou 1,6 and Efthimios Dardiotis 1,* 1 Laboratory of Neurogenetics, Department of Neurology, University Hospital of Larissa, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41110 Larissa, Greece; [email protected] (V.S.); [email protected] (Z.T.); [email protected] (A.-M.A.); [email protected] (I.L.); [email protected] (G.M.H.) 2 Multiple Sclerosis Center, B’ Department of Neurology, AHEPA University Hospital, Aristotle University of Thessaloniki, GR54636 Thessaloniki, Greece; [email protected] (C.B.); [email protected] (N.G.) 3 Neurogenetics Unit, 1st Department of Neurology, Eginition Hospital, School of Medicine, National and Kapodistrian University of Athens, Vassilissis Sofias 72-74 Ave, 11528 Athens, Greece; [email protected] 4 Multiple Sclerosis and Demyelinating Diseases Unit and Immunogenetics Laboratory, 1st Department of Neurology, Eginition Hospital, School of Medicine, National and Kapodistrian University of Athens, 115 28 Athens, Greece; [email protected] 5 Department of Rheumatology and Clinical Immunology, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41110 Larissa, Greece; [email protected] 6 Department of Neurology, Medical School, University of Cyprus, 1678 Nicosia, Cyprus * Correspondence: [email protected]; Tel.: +30-241-350-1137 Received: 23 September 2020; Accepted: 5 November 2020; Published: 12 November 2020 Abstract: Background: Multiple sclerosis (MS) is a chronic disease of the central nervous system (CNS).
    [Show full text]
  • Course of Study M. Sc. in Molecular & Human Genetics
    Course of Study M. Sc. in Molecular & Human Genetics DISTRIBUTION OF DIFFERENT COURSES AND CREDITS IN VARIOUS SEMESTERS Semester-I Course Code Title Credits MGM101 Transmission Genetics 2 MGM102 Molecular Genetics 3 MGM103 Basic Human Genetics 3 MGM104 Cytogenetics 2 MGM105 Biochemistry 3 MGM106 Cell Biology 3 MGM107 Lab work based on courses MGM101 &MGM102 2 MGM108 Lab work based on courses MGM103 & MGM104 2 MGM109 Lab work based on courses MGM105 & MGM106 2 Total 22 Semester-II Course Code Title Credits MGM201 DNA Technology & Genetic Engineering 3 MGM202 Bioinformatics and Biotechniques 3 MGM203 Model Genetic Systems 2 MGM204 Genomic Instability and Cancer 3 MGM205 Human Genome 3 MGM206 Reproductive Genetics 2 MGM207 Lab work based on courses MGM201 & MGM202 2 MGM208 Lab work based on courses MGM203 & MGM204 2 MGM209 SWAYAM Course 2 Total 22 Semester-III Course Code Title Credits MGM301 Human Molecular Genetics 3 MGM302 Clinical Genetics 3 MGM303 Developmental Genetics 3 MGM304 Immunogenetics 3 MGM305 Population & Evolutionary Genetics 2 MGM306 Lab work based on courses MGM301 & MGM302 2 MGM307 Lab work based on courses MGM303 & MGM304 2 MGM308 SWAYAM Course 2 Total 20 Semester-IV Course Code Title Credits MGM401 Neurogenetics 3 MGM402 Genetic Counseling and Intellectual Property Rights 2 MGM403 Lab work based on course MGM401 1 MGM404 Seminar & Formulation of Research Project 2 MGM405 Comprehensive Viva-voce 2 MGM406 Dissertation 6 Total 16 Grand Total 80 SEMESTER - I MGM101: Transmission Genetics Credits: 2 Lecture hours 1. Introduction to Genetics 1 2.Mendelism 5 2.1.Mendel and his experiments 2.2.Law of segregation 2.3.Law of independent assortment 2.4.Application of laws of probability (product rule, sum rule) 2.5.
    [Show full text]
  • GENETICS of LIVER DISEASE: IMMUNOGENETICS and DISEASE Gut: First Published As 10.1136/Gut.2003.031732 on 11 March 2004
    RECENT ADVANCES IN CLINICAL PRACTICE GENETICS OF LIVER DISEASE: IMMUNOGENETICS AND DISEASE Gut: first published as 10.1136/gut.2003.031732 on 11 March 2004. Downloaded from PATHOGENESIS 599 PTDonaldson Gut 2004;53:599–608. doi: 10.1136/gut.2003.031732 nderstanding the genetic basis of ‘‘complex disease’’ has been heralded as one of the major challenges of the post genome era.1 However what are ‘‘complex diseases’’ and how will understanding the genetics of such diseases advance medical science? There has been a U 2 great deal of ‘‘hype’’ about the potential of the human genome mapping project. The three major claims are that this information will: (a) be used in diagnosis; (b) provide useful prognostic indices for disease management (including the development of individualised treatment regimens, based on the findings of both immunogenetic and pharmacogenetic studies); and (c) provide insight into the pathogenesis of these diseases. Of these three objectives the last has the greatest potential and is the least exaggerated claim. In this review I shall highlight major associations, discuss some of the practical issues that arise, and outline how current knowledge of the immunogenetic basis of chronic liver disease is beginning to inform the debate about disease pathogenesis. c AN INTRODUCTION TO COMPLEX TRAITS Complex traits are defined as those where inheritance does not follow a Mendelian (that is, simple) pattern. This is not a new science; studies of complex traits were first performed in the mid-20th century. However, in the 21st century, the prevailing language has changed. Previously complex traits were called ‘‘polygenic’’ (involving more than one gene), multifactorial (depending on the interaction of the host genome and one or more environmental factors), or oligogenic (whereby individual mutations in several different genes in one or more common pathways lead to the same clinical syndrome but each patient with the disease may possess a single disease causing mutation only) (see box 1).
    [Show full text]
  • Combatting Disease Using Genetics
    WHAT IS PIRBRIGHT DOING? Traditional methods for performing such modifications are time consuming and unreliable. At Pirbright, COMBATTING Mosquito-borne diseases researchers are now using the CRISPR/Cas9 system for vaccine development which makes the process Mosquitoes have the ability to carry and transmit quick, simple and efficient. This technique also allows DISEASE many deadly diseases that are responsible for millions multiple genes from different viruses to be inserted of deaths and billions of pounds of economic losses into a single vaccine to provide protection against every year, particularly in developing countries. USING GENETICS multiple diseases. Pirbright carries out research to understand how genetically Immunogenetics modified mosquitoes can Immunogenetics explores the link between the be used for the control of immune system and an animal’s genes. Understanding mosquito populations to the genes that control livestock immune responses can prevent diseases of both help us improve their resistance to disease. livestock and people. Experts at Pirbright have been working to understand One of the most promising Female Aedes aegypti the genes that control natural killer (NK) cells; one control techniques is known mosquito feeding of the first lines of defence against viral infection. as a gene drive. This is where the mosquito genome NK cells detect the presence of a virus using special is modified to decrease their ability to breed or receptor proteins on their surface. These attach to carry infections, and this modification is favourably signalling proteins on cells that have become infected, spread into a population at a faster rate than normal triggering the NK cell to kill the infected cell and inheritance.
    [Show full text]
  • Genetics and Epigenetics of Atopic Dermatitis: an Updated Systematic Review
    G C A T T A C G G C A T genes Review Genetics and Epigenetics of Atopic Dermatitis: An Updated Systematic Review 1,2, 1,2,3, 1,2,3, Maria J Martin y, Miguel Estravís y , Asunción García-Sánchez * , Ignacio Dávila 1,2,4 , María Isidoro-García 1,2,5,6 and Catalina Sanz 1,2,7 1 Institute for Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain; [email protected] (M.J.M.); [email protected] (M.E.); [email protected] (I.D.); [email protected] (M.I-G.); [email protected] (C.S.) 2 Network for Cooperative Research in Health–RETICS ARADyAL, 37007 Salamanca, Spain 3 Department of Biomedical and Diagnostics Sciences, University of Salamanca, 37007 Salamanca, Spain 4 Department of Immunoallergy, Salamanca University Hospital, 37007 Salamanca, Spain 5 Department of Clinical Biochemistry, University Hospital of Salamanca, 37007 Salamanca, Spain 6 Department of Medicine, University of Salamanca, 37007 Salamanca, Spain 7 Department of Microbiology and Genetics, University of Salamanca, 37007 Salamanca, Spain * Correspondence: [email protected]; Tel.: +3-492-329-1100 These authors equally contribute to the manuscript. y Received: 12 March 2020; Accepted: 15 April 2020; Published: 18 April 2020 Abstract: Background: Atopic dermatitis is a common inflammatory skin disorder that affects up to 15–20% of the population and is characterized by recurrent eczematous lesions with intense itching. As a heterogeneous disease, multiple factors have been suggested to explain the nature of atopic dermatitis (AD), and its high prevalence makes it necessary to periodically compile and update the new information available. In this systematic review, the focus is set at the genetic and epigenetic studies carried out in the last years.
    [Show full text]
  • Single Nucleotide Polymorphisms of Immunity-Related Genes and Their Effects on Immunophenotypes in Different Pig Breeds
    G C A T T A C G G C A T genes Article Single Nucleotide Polymorphisms of Immunity-Related Genes and Their Effects on Immunophenotypes in Different Pig Breeds Ann Ying-An Chen 1,2 , Chao-Wei Huang 3, Shyh-Hwa Liu 4, An-Chi Liu 1 and Hso-Chi Chaung 1,2,* 1 Research Center for Animal Biologics, National Pingtung University of Science and Technology, Neipu, Pingtung 912, Taiwan; [email protected] (A.Y.-A.C.); [email protected] (A.-C.L.) 2 Department of Veterinary Medicine, National Pingtung University of Science and Technology, Neipu, Pingtung 912, Taiwan 3 Department of Tropical Agriculture and International Cooperation, National Pingtung University of Science and Technology, Neipu, Pingtung 912, Taiwan; [email protected] 4 Department of Animal Science, National Pingtung University of Science and Technology, Neipu, Pingtung 912, Taiwan; [email protected] * Correspondence: [email protected] Abstract: Enhancing resistance and tolerance to pathogens remains an important selection objective in the production of livestock animals. Single nucleotide polymorphisms (SNPs) vary gene expression at the transcriptional level, influencing an individual’s immune regulation and susceptibility to diseases. In this study, we investigated the distribution of SNP sites in immune-related genes and their correlations with cell surface markers of immune cells within purebred (Taiwan black, Duroc, Landrace and Yorkshire) and crossbred (Landrace-Yorkshire) pigs. Thirty-nine SNPs of immune- related genes, including 11 cytokines, 5 chemokines and 23 Toll-like receptors (TLRs) (interferon-α Citation: Chen, A.Y.-A.; Huang, and γ (IFN-α, γ), tumor necrosis factor-α (TNF-α), granulocyte-macrophage colony-stimulating C.-W.; Liu, S.-H.; Liu, A.-C.; Chaung, factor (GM-CSF), Monocyte chemoattractant protein-1 (MCP-1) and TLR3, TLR4, TLR7, TLR8, and H.-C.
    [Show full text]
  • Poster Group 9
    Abstracts S32 124 125 HLA ALLELES IN ISOLATED POPULATIONS FROM NORTH HLA-DPB1* POLYMORPHISMS IN GREEK POPULATION SPAIN: ORIGIN OF THE BASQUES AND THE ANCIENT IBERIANS. Katerina E. Tarassi, Diamanto I. Kouniaki, Theophilos I. Athanassiades, Chryssa A. Papasteriades. Pablo Sánchez-Velasco2, Eduardo Gómez-Casado1, Jorge Martínez-Laso1, Immunology - Histocompatibility Dept, Evangelismos Hospital, Juan Moscoso1, Jorge Zamora1, Ernesto Lowy1, Carlos Silvera-Redondo1, Athens, Greece. Alberto Cemborain2, Francisco Leyva-Cobián2, and Antonio Arnaiz-Villena1. 1Department of Immunology and Molecular Biology, Hosp. 12 de Octubre, Since the number of HLA-DPB1 identified alleles is continuously increasing Universidad Complutense, Madrid, Spain. E-mail: [email protected]. and their clinical relevance, particularly in Bone Marrow Transplantation, is 2Department of Immunology. Hospital Universitario Marqués de established, the aim of this work is to present the HLA-DPB1 polymorphism in Valdecilla. 39008 Santander, Spain. Greeks. The population studied consisted of 140 unrelated, unselected healthy individuals of Greek origin. Sixty-eight (68) of them were typed for HLA-A, -B, -DRB1, -DQA1 and -DQB1 alleles have been studied in three DPB1*0101-1901 using oligonucleotide typing, whereas 72 were typed for all relatively isolated populations of northern Spain from Cantabria (Pas Valleys known DPB1 alleles by PCR-SSOP and/or PCR-SSP. inhabitants or Pasiegos and Cabuernigos) and from the Basque Country (Arratia The DPB1* alleles detected are presented in the following table: Valley inhabitants). These populations have been compared to other neighbouring ones and other Mediterraneans by using neighbor-joining DPB1 Freq % DPB1 Freq % DPB1 Freq % dendrograms, plane genetic distances, correspondence and HLA haplotype (N=140) (N=140) (N=72) analyses.
    [Show full text]
  • Division of Immunogenetics Division of Immunogenetics
    DIVISION OF IMMUNOGENETICS diVision of ImmunoGenetics Mission The Division of Immunogenetics is committed to providing basic science support aimed at better understanding the etio-pathogenesis of pediatric diseases to more efficiently and correctly diagnose, prevent, and possibly 136 better treat them. 137 DEPARTMENT OF PEDIATRICS 2012 ANNUAL REPORT DEPARTMENT OF PEDIATRICS 2012 ANNUAL REPORT DIVISION OF IMMUNOGENETICS DIVISION OF IMMUNOGENETICS facultY AND staff To block auto-immunity, without the use of immunosuppressant, Nick Giannoukakis and Massimo Trucco have success- fully completed a National Institutes of Health (NIH)-funded, U.S. Food and Drug Administration (FDA)-approved Massimo Trucco, MD Yong Fan, PhD Steven Ringquist, PhD phase I clinical trial that was designed to test the safety of a treatment in which autologous DC—rendered functionally Hillman Professor of Research Assistant Professor Research Assistant Professor immature by exposing them to CD40, CD80, and CD86 antisense oligodeoxyribonucleotides (AS-ODN) to reduce Pediatric Immunology costimulatory molecule levels at their surface—were administered to T1D patients with established disease. Leukocytes Nick Giannoukakis, PhD William Rudert, MD, PhD of the patient were obtained by apheresis, and DCs were then isolated and expanded. DC engineered in GMP facilities Suzanne Bertera, PhD Associate Professor Research Associate Professor to express low levels of CD40, CD80, and CD86 were then injected into the patient by intradermal administration at an Research Assistant Professor Jing He, MD, PhD Tatyana Votyakova, MD, PhD anatomical site proximal to the pancreas. DCs then migrate to the nearest (i.e., pancreatic) lymph nodes, where they are Rita Bottino, PhD Research Assistant Professor Research Assistant Professor able to interrupt the vicious circle that maintains islet-specific inflammation (i.e., insulitis).
    [Show full text]