The Gut Microbiome and the Big Eight
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Bacterial Exposure and Immune Homeostasis: A
BACTERIAL EXPOSURE AND IMMUNE HOMEOSTASIS: A MECHANISTIC VIEW OF THE HYGIENE HYPOTHESIS By JENNY LYNN JOHNSON Submitted in fulfillment of the requirements for the Degree of Doctor of Philosophy Thesis Advisor: Dr. Brian A. Cobb, Ph.D. Department of Pathology CASE WESTERN RESERVE UNIVERSITY May 2015 CASE WESTERN RESERVE UNIVERSITY SCHOOL OF GRADUATE STUDIES We hereby approve the dissertation of Jenny Lynn Johnson Candidate for the degree of Doctor of Philosophy* Committee Chair Eric Pearlman Committee Member George Dubyak Committee Member Kristie Ross Committee Member Brian Cobb Committee Member Clive Hamlin Date of Defense March 16, 2015 *We also certify that written approval has been obtained for any proprietary material contained therein 2 Dedication I would like to dedicate this work to those who have supported me through the six years I have spent at CWRU, and in particular my parents, Mark and Sharon Johnson, and my cousins, Janice, David and Henry Graves. 3 Table of Contents List of Tables .................................................................................................................................... 7 List of Figures ................................................................................................................................... 8 Acknowledgements........................................................................................................................ 10 List of Abbreviations ..................................................................................................................... -
WO 2018/064165 A2 (.Pdf)
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2018/064165 A2 05 April 2018 (05.04.2018) W !P O PCT (51) International Patent Classification: Published: A61K 35/74 (20 15.0 1) C12N 1/21 (2006 .01) — without international search report and to be republished (21) International Application Number: upon receipt of that report (Rule 48.2(g)) PCT/US2017/053717 — with sequence listing part of description (Rule 5.2(a)) (22) International Filing Date: 27 September 2017 (27.09.2017) (25) Filing Language: English (26) Publication Langi English (30) Priority Data: 62/400,372 27 September 2016 (27.09.2016) US 62/508,885 19 May 2017 (19.05.2017) US 62/557,566 12 September 2017 (12.09.2017) US (71) Applicant: BOARD OF REGENTS, THE UNIVERSI¬ TY OF TEXAS SYSTEM [US/US]; 210 West 7th St., Austin, TX 78701 (US). (72) Inventors: WARGO, Jennifer; 1814 Bissonnet St., Hous ton, TX 77005 (US). GOPALAKRISHNAN, Vanch- eswaran; 7900 Cambridge, Apt. 10-lb, Houston, TX 77054 (US). (74) Agent: BYRD, Marshall, P.; Parker Highlander PLLC, 1120 S. Capital Of Texas Highway, Bldg. One, Suite 200, Austin, TX 78746 (US). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. -
Rhoa and ROCK Mediate Histamine-Induced Vascular Leakage and Anaphylactic Shock
ARTICLE Received 24 Nov 2014 | Accepted 22 Feb 2015 | Published 10 Apr 2015 DOI: 10.1038/ncomms7725 RhoA and ROCK mediate histamine-induced vascular leakage and anaphylactic shock Constantinos M. Mikelis1, May Simaan1, Koji Ando2, Shigetomo Fukuhara2, Atsuko Sakurai1, Panomwat Amornphimoltham3, Andrius Masedunskas3, Roberto Weigert3, Triantafyllos Chavakis4, Ralf H. Adams5,6, Stefan Offermanns7, Naoki Mochizuki2, Yi Zheng8 & J. Silvio Gutkind1 Histamine-induced vascular leakage is an integral component of many highly prevalent human diseases, including allergies, asthma and anaphylaxis. Yet, how histamine induces the disruption of the endothelial barrier is not well defined. By using genetically modified animal models, pharmacologic inhibitors and a synthetic biology approach, here we show that the small GTPase RhoA mediates histamine-induced vascular leakage. Histamine causes the rapid formation of focal adherens junctions, disrupting the endothelial barrier by acting on H1R Gaq-coupled receptors, which is blunted in endothelial Gaq/11 KO mice. Interfering with RhoA and ROCK function abolishes endothelial permeability, while phospholipase Cb plays a limited role. Moreover, endothelial-specific RhoA gene deletion prevents vascular leakage and passive cutaneous anaphylaxis in vivo, and ROCK inhibitors protect from lethal systemic anaphylaxis. This study supports a key role for the RhoA signalling circuitry in vascular permeability, thereby identifying novel pharmacological targets for many human diseases characterized by aberrant vascular leakage. 1 Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892, USA. 2 Department of Cell Biology, CREST-JST, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka 565-8565, Japan. 3 Intracellular Membrane Trafficking Unit, Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892, USA. -
Targeting the Gut Microbiome in Allogeneic Hematopoietic Stem Cell Transplantation
medRxiv preprint doi: https://doi.org/10.1101/2020.04.08.20058198; this version posted June 9, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license . Targeting the gut microbiome in allogeneic hematopoietic stem cell transplantation Marcel A. de Leeuw & Manuel X. Duval, GeneCreek List of Figures Contents 1 GM composition evolution across allo-HSCT . 2 I 2 Baseline GM composition and conditioning level . 3 NTRODUCTION 1 3 Top 10 variable importances estimated by the ran- dom survival forest models .............. 3 MATERIALS & METHODS 2 4 Biological safety level and aGvHD at onset . 3 DATA ANALYSIS .................. 2 5 Relative importance of regressors explaining the RESULTS 2 aGvHD status ...................... 3 OVERALL GM COMPOSITION EVOLUTION ACROSS 6 Co-exclusion by and co-occurrence with QPS species 4 ALLO-HSCT ................. 2 List of Tables CORRELATION BETWEEN CONDITIONING AND THE GM 2 BASELINE GM COMPOSITION AND SURVIVAL . 3 1 Prospective data sets used in the study . 1 AGVHD CASES, CONTROLS AND GM COMPOSITION 3 IMMUNO-MODULATING METABOLITES . 4 IN SILICO SCREENING OF THE ALLO-HSCT GM . 4 DISCUSSION 4 CONCLUSIONS 6 SUMMARY 6 DECLARATIONS 6 BIBLIOGRAPHY 7 NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice. Revised manuscript medRxiv preprint doi: https://doi.org/10.1101/2020.04.08.20058198; this version posted June 9, 2020. -
Chapter 34 • Drugs Used to Treat Nausea and Vomiting
• Chapter 34 • Drugs Used to Treat Nausea and Vomiting • Learning Objectives • Compare the purposes of using antiemetic products • State the therapeutic classes of antiemetics • Discuss scheduling of antiemetics for maximum benefit • Nausea and Vomiting • Nausea : the sensation of abdominal discomfort that is intermittently accompanied by a desire to vomit • Vomiting (emesis): the forceful expulsion of gastric contents up the esophagus and out of the mouth • Regurgitation : the rising of gastric or esophageal contents to the pharynx as a result of stomach pressure • Common Causes of Nausea and Vomiting • Postoperative nausea and vomiting • Motion sickness • Pregnancy Hyperemesis gravidarum: a condition in pregnancy in which starvation, dehydration, and acidosis are superimposed on the vomiting syndrome • Common Causes of Nausea and Vomiting (cont’d) • Psychogenic vomiting: self-induced or involuntary vomiting in response to threatening or distasteful situations • Chemotherapy-induced emesis (CIE) Anticipatory nausea and vomiting: triggered by sight and smell associated with treatment Acute CIE: stimulated directly by chemotherapy 1 to 6 hours after treatment Delayed emesis: occurs 24 to 120 hours after treatment; may be induced by metabolic by-products of chemotherapy • Drug Therapy for Selected Causes of Nausea and Vomiting • Postoperative nausea and vomiting (PONV) • Antiemetics include: Dopamine antagonists Anticholinergic agents Serotonin antagonists H2 antagonists (cimetidine, ranitidine) • Nursing Process for Nausea and Vomiting -
Child Fatalities in Tennessee 2009
CHILD FATALITIES IN TENNESSEE 2009 Tennessee Department of Health Bureau of Health Services Maternal and Child Health Section Acknowledgements The Tennessee Department of Health, Maternal and Child Health (MCH) Section, expresses its gratitude to the agencies and individuals who have contributed to this report and the investigations that preceded it. Thank you to the Tennessee Department of Health, Division of Health Statistics, and to The University of Tennessee Extension, both of whom meticulously manage the data represented in these pages. Thank you to the Child Fatality Review Teams in the 31 judicial districts across the state who treat each case with reverence and compassion, working with a stalwart commit- ment to preventing future fatalities. Thank you to the State Child Fatality Prevention Review Team members who find ways to put the recommendations in this report to work in saving lives. Their efforts, and ours, are reinforced immeasurably by the support and cooperation of the following Tennessee agencies: the Department of Health, the Commission on Children and Youth, the Department of Children’s Services, the Center for Forensic Medicine, the Office of the Attorney General, the Tennessee Bureau of Investigation, the Department of Mental Health, the Tennessee Medical Association, the Department of Education, the General Assembly, the State Supreme Court, the Tennessee Suicide Prevention Network, Tennessee local and regional health departments, and the National Center for Child Death Review. It is with deepest sympathy and respect that we dedicate this report to the memory of those children and families represented within these pages. This report may be accessed online at http://health.state.tn.us/MCH/CFR.htm 2 Table of Contents EXECUTIVE SUMMARY ............................................................................................... -
Malnutrition Topic 5
Malnutrition Topic 5 Module 5.1 Undernutrition – Simple and Stress Starvation Lubos Sobotka Peter Soeters Remy Meier Yitshal Berner Learning Objectives • To know how the body reacts to short-term and long-term starvation during non-stress conditions; • To understand the difference between simple and stress starvation; • To know the consequences of stress on metabolic pathways related to starvation. Contents 1. Definition and classification of malnutrition 2. Undernutrition 3. Aetiology of undernutrition 4. Adaptation to undernutrition – non stress starvation 5. Stress starvation 6. Summary Key Messages • Humans adapt well to short or a longer-term starvation, using their reserve stores of carbohydrates, fat and protein; • Reduction of energy expenditure and conservation of body protein are further reaction to starvation. Energy stores are replenished during feeding period; • Long-term partial or total cessation of energy intake leads to marasmic wasting; • With the addition of the stress response, catabolism and wasting are accelerated and the normal adaptive responses to simple starvation are overridden; • Weight loss in either situation results in impaired mental and physical function, as well as poorer clinical outcome. Copyright © 2006 by ESPEN 1. Definition and classification of malnutrition Malnutrition can be defined as a state of nutrition in which a deficiency or excess (or imbalance) of energy, protein and other nutrients causes measurable adverse effects on tissue/body form (body shape, size, composition), body function and clinical outcome. In broad term, malnutrition includes not only protein-energy malnutrition (both over- and under- Classification of energy and protein malnutrition nutrition) but also malnutrition of other nutrients, such as micronutrients. Malnutrition Malnutrition of micronutrients can cause deficiency states or toxic symptoms - these are discussed in Overnutrition Undernutrition particular modules related to vitamins and trace elements. -
Hypothermia Hyperthermia Normothemic
Means normal body temperature. Normal body core temperature ranges from 99.7ºF to 99.5ºF. A fever is a Normothemic body temperature of 99.5 to 100.9ºF and above. Humans are warm-blooded mammals who maintain a constant body temperature (euthermia). Temperature regulation is controlled by the hypothalamus in the base of the brain. The hypothalamus functions as a thermostat for the body. Temperature receptors (thermoreceptors) are located in the skin, certain mucous membranes, and in the deeper tissues of the body. When an increase in body temperature is detected, the hypothalamus shuts off body mechanisms that generate heat (for example, shivering). When a decrease in body temperature is detected, the hypothalamus shuts off body mechanisms designed to cool the body (for example, sweating). The body continuously adjusts the metabolic rate in order to maintain a constant CORE Hypothermia Core body temperatures of 95ºF and lower is considered hypothermic can cause the heart and nervous system to begin to malfunction and can, in many instances, lead to severe heart, respiratory and other problems that can result in organ damage and death.Hannibal lost nearly half of his troops while crossing the Pyrenees Alps in 218 B.C. from hypothermia; and only 4,000 of Napoleon Bonaparte’s 100,000 men survived the march back from Russia in the winter of 1812 - most dying of starvation and hypothermia. During the sinking of the Titanic most people who entered the 28°F water died within 15–30 minutes. Symptoms: First Aid : Mild hypothermia: As the body temperature drops below 97°F there is Call 911 or emergency medical assistance. -
Acute Radiation Syndrome Clinical Picture, Diagnosis and Treatment
ACUTE RADIATION SYNDROME CLINICAL PICTURE, DIAGNOSIS AND TREATMENT Module XI Lecture organization Introduction ARS manifestations Haematological syndrome Gastrointestinal syndrome Neurovascular syndrome Triage of injured persons Medical management Summary Module Medical XI. 2 Introduction Acute radiation syndrome (ARS): Combination of clinical syndromes occuring in stages hours to weeks after exposure as injury to various tissues and organs is expressed ARS threat Discharged medical irradiators Industrial radiography units Commercial irradiators Terrorist detonation Nuclear fuel processing Nuclear reactors Module Medical XI. 3 Early deterministic effects <0.1 Gy, whole body - No detectable difference in exposed vs non-exposed patients 0.1-0.2 Gy, whole body - Detectable increase in chromosome aberrations. No clinical signs or symptoms >0.12 Gy, whole body - Sperm count decreases to minimum about day 45 0.5 Gy, whole body - Detectable bone marrow depression with lymphopenia Module Medical XI. 4 Exposure levels at which healthy adults are affected _________________________________________________________________ _________________________________________________________________ Health effects Acute dose (Gy) Blood count changes 0.50 Vomiting (threshold) 1.00 Mortality (threshold) 1.50 LD50/60 (minimal supportive care) 3.2-3.6 LD50/60 (supportive medical treatment) 4.8-5.4 LD50/60 (autologous bone marrow or ____________________________________stem cell transplant)___________________________ ______ >5.4 Source: NCRP Report 98 "Guidance on Radiation Received in Space Activities", NCRP, Bethesda (MD) (1989). Module Medical XI. 5 Factors decreasing LD50/60 Coexisting trauma combined injury Chronic nutritional deficit Coexisting infection Contribution of high LET radiation Module Medical XI. 6 Phases of ARS Initial or prodromal phase Latent phase Manifest illness phase Recovery phase Module Medical XI. 7 Manifestations of ARS Haematopoietic syndrome (HPS) Gastrointestinal syndrome (GIS) Neurovascular syndrome (NVS) Module Medical XI. -
Healthy Infants Harbor Intestinal Bacteria That Protect Against Food Allergy
LETTERS https://doi.org/10.1038/s41591-018-0324-z Healthy infants harbor intestinal bacteria that protect against food allergy Taylor Feehley1,9, Catherine H. Plunkett1,9, Riyue Bao 2,3,9, Sung Min Choi Hong1, Elliot Culleen1, Pedro Belda-Ferre 1, Evelyn Campbell1, Rosita Aitoro4, Rita Nocerino4, Lorella Paparo4, Jorge Andrade 2,3, Dionysios A. Antonopoulos5,6, Roberto Berni Canani4,7,8 and Cathryn R. Nagler 1* There has been a striking generational increase in life-threat- formula to manage ongoing allergic symptoms, whereas the healthy ening food allergies in Westernized societies1,2. One hypoth- donors received a standard cow’s milk-based formula5. Initial trans- esis to explain this rising prevalence is that twenty-first fer recipients were used as living repositories for subsequent experi- century lifestyle practices, including misuse of antibiotics, ments (see Online Methods). dietary changes, and higher rates of Caesarean birth and for- Groups of germ-free mice and mice colonized with either the mula feeding have altered intestinal bacterial communities; healthy or CMA infant microbiota were sensitized with BLG and early-life alterations may be particularly detrimental3,4. the mucosal adjuvant cholera toxin. Consistent with previous To better understand how commensal bacteria regulate food reports7,11, germ-free mice, devoid of any bacterial colonization, allergy in humans, we colonized germ-free mice with feces were highly susceptible to anaphylactic responses to food, as evi- from healthy or cow’s milk allergic (CMA) infants5. We found denced by a drop in core body temperature (Fig. 1a) and production that germ-free mice colonized with bacteria from healthy, of BLG-specific IgE and IgG1 (Fig. -
COVID-19 Puts 'Hygiene Hypothesis' to Test 2 November 2020
COVID-19 puts 'hygiene hypothesis' to test 2 November 2020 That might seem to be a blow for the hygiene hypothesis, which holds that as the incidence of infections decreases in developed and developing countries there is a corresponding rise in allergies and autoimmune diseases. However, the study hastens to warn against pursuing weak hygiene as a strategy in dealing with COVID-19 or other diseases. "Although we provide a possible explanation based on sanitation practices on the CFR (death rate) differences among economically stronger and weaker countries, this should not be inferred as our A town pool in Bihar, which is used for bathing, laundry, advocating a move towards weaker hygiene and for other domestic uses. The new study associates practices for handling future pandemics." low COVID-19 mortality rate with poor access to water, sanitation, and hygiene. Credit: Melissa So, what are the researchers pushing? They are Cooperman/IFPRI (https://www.flickr.com/photos/ifpri/34 looking at new possibilities for "immune training" 989936695/in/album-72157684454567045/) (CC BY-NC- and at microbiome therapies that may supplement SA 2.0, https://creativecommons.org/licenses/by-nc- conventional hygiene and sanitation practices. sa/2.0/) Earlier studies have also suggested that exposure to pathogens boost the immune system against infections, but this is still to stand up to close Indian researchers from the formidable Council of scientific scrutiny. Indeed, research in Sub-Saharan Scientific and Industrial Research (CSIR) and two Africa, again awaiting peer-review, associates other institutes have put to test the "hygiene higher COVID-19 death rates with poor access to hypothesis" with a study suggesting that areas with WASH, acronym for Water, Sanitation and high prevalence of infectious diseases are likely to Hygiene. -
Butyrate Production in Phylogenetically Diverse Firmicutes
mbt_244 Microbial Biotechnology (2011) doi:10.1111/j.1751-7915.2010.00244.x 1 Butyrate production in phylogenetically diverse 2 Firmicutes isolated from the chicken caecummbt_244 1..11 3 4 Venessa Eeckhaut,1* Filip Van Immerseel,1 present study indicates that butyrate producers 50 5 Siska Croubels,2 Siegrid De Baere,2 related to cluster XVI may play a more important role 51 6 Freddy Haesebrouck,1 Richard Ducatelle,1 in the chicken gut than in the human gut. 52 3 4 7 Petra Louis and Peter Vandamme 53 8 1Department of Pathology, Bacteriology and Avian Introduction 54 9 Diseases, Research Group Veterinary Public Health and 10 Zoonoses, and 2Department of Pharmacology, In the chicken gastrointestinal tract, the main sites of 55 11 Toxicology, Biochemistry and Organ Physiology, Faculty bacterial activity are the crop and the caeca and, to a 56 12 of Veterinary Medicine, Ghent University, Salisburylaan lesser extent, the small intestine. Lactobacillus spp. domi- 57 131 1 133, B-9820 Merelbeke, Belgium. nate the crop (Barnes et al., 1972; Watkins and Kratzer, 58 14 3Microbial Ecology Group, Rowett Institute of Nutrition 1983) and small intestinal tract (Lu et al., 2003), while the 59 15 and Health, University of Aberdeen, Greenburn Road, caecal microbiota are dominated by species of the 60 16 Bucksburn, Aberdeen AB219SB, UK. Clostridiales order, followed by Lactobacillales and Bacte- 61 17 4Laboratory of Microbiology, Faculty of Sciences, Ghent roidales (Dumonceaux et al., 2006). A molecular, culture- 62 18 University, K. L. Ledeganckstraat 35, B-9000 Ghent, independent study from Zhu and colleagues (2002) on the 63 19 Belgium.