FOCUS SAS Training Day Leeds Dr. Joanna Sheldon Protein Reference Unit, St

Total Page:16

File Type:pdf, Size:1020Kb

FOCUS SAS Training Day Leeds Dr. Joanna Sheldon Protein Reference Unit, St FOCUS SAS Training Day Leeds Dr. Joanna Sheldon Protein Reference Unit, St. George’s 1 Questions and Cases 1 List five disorders that are associated with the presence of monoclonal immunoglobulins? 2 What is the electrophoretic mobility of haemoglobin and fibrinogen on agarose pH 8.6 or comparable CZE? 3 What are the two major sites of production of the plasma proteins? 4 What are the half-lives of IgG, IgA and IgM. What is special about IgG? 5 What results need urgent action? 6 Which antibody is the most important and why? 7 What is the approx. % of BJP myeloma? 8 Where are the genes controlling immunoglobulin production, what is the order or rearrangement and what is the order of heavy chains? 9 What concentrations of fibrinogen and alpha-1 antitrypsin can be seen in inflammation? 10 What factors determine the concentration of an analyte? 11 List the main proteins in each zone on the 2 electrophoresis. 12 Which EP patterns should you immunofix? 13 What is di-thio-threitol and why do we use it? 14 What are the main proteins seen in a glomerular proteinuria? 15 Where can paraproteins or BJP appear on the serum or urine protein electrophoresis? 16 What are the possible reasons for finding monoclonal light chain only on serum immunofixation? 17 What are the possible reasons for finding heavy chain only on serum immunofixation? 18 What electrophoresis pattern would you expect in acute inflammation? 19 Are measurements of IgG, IgA and IgM traceable and if they are, what to? 20 Which is the most common antibody deficiency? 3 Write interpretative comments for the following CZE separations from adult patients. Some also show the serum immunofixations. 21. TP = 93g/L, IgG = 38.0 IgA = 0.7 IgM =1.6 22. IgG = 4.9 IgA = 0.9 IgM =0.5 23. IgG = 21.4 IgA = 6.9 IgM =2.5 24. IgG = 21.3 IgA = 3.1 IgM =0.5 4 25. IgG = 8.0 IgA = 0.8 IgM =0.5 26. IgG = 9.5 IgA = 6.3 IgM =1.9 27. IgG = 17.6 IgA = 2.6 IgM =0.8 28. Total protein = 111g/L (60-80) IgG = 72.5g/L (6-16) IgA = 1.0g/L (0.8-4) IgM = 9.8g/L (0.5-2.0) 5 29. 44 year old woman complaining of tiredness IgG = 8.0, IgA = 0.8 IgM =0.5 Urine total protein 0.4g/L Your comments and actions 6 30. The patient is a 54 year old man. Pulmonary oedema, AKI Immunoglobulin G 7.0 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 3.8 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 0.1 g/l ( 0.5 to 2.0 ) Auth Your comments and actions 7 31. The patient is a 49 year old woman post PBSCT. Total Protein 78 g/L ( 60 to 80 ) Auth Immunoglobulin G 14.3 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 3.5 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 1.7 g/l ( 0.5 to 2.0 ) Auth Your comments and actions 8 32. 72 year old female, known myeloma on treatment. No obvious paraprotein detected 35g/L IgA lambda paraprotein. Small IgG kappa paraprotein (seen since previous November) What are the possible causes of these patterns and the changes if pattern and what actions will you take? 9 33. 68 year old man – stroke investigation Total Protein 68 g/L ( 60 to 80 ) Auth Immunoglobulin G 11.3 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 2.2 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 0.6 g/l ( 0.5 to 2.0 ) Auth CZE and immunoglobulins double checked from primary tube Serum Agarose gel Serum protein electrophoresis immunofixation electrophoresis on CZE 72 hours later Your comments 10 34. Look at the results below for a patient with an IgG paraprotein. The graph shows the concentration of paraprotein for each serum sample received. Indicate at which points you would have contacted the requesting clinician and why. Your comments 11 35. 75 year old man - ? myeloma Total Protein 72 g/L ( 60 to 80 ) Auth Immunoglobulin G 7.5 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 0.9 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 0.4 g/l ( 0.5 to 2.0 ) Auth Paraprotein 4g/L Your comments and actions. What is the technique shown on the right and how does it work? 12 36. 41 year old woman in neurology being investigated for back pain. Total Protein 92 g/L ( 60 to 80 ) Auth Immunoglobulin G 37.5 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 0.2 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 0.2 g/l ( 0.5 to 2.0 ) Auth Paraprotein 24g/L Urine total protein = 1.1g/L Serum immunofixation Urine immunofixation Your comments and actions 13 37. 83 year old man with proteinuria (0.4g/L) and slight polyclonally raised IgG and IgA in the serum Your comments and actions 14 15 38. 54 year old female with a rash – complex medical and social history. Total Protein 92 g/L ( 60 to 80 ) Auth Immunoglobulin G 39.1 g/l ( 6.0 to 16.0 ) Auth Immunoglobulin A 1.1 g/L ( 0.8 to 4.0 ) Auth Immunoglobulin M 0.1 g/l ( 0.5 to 2.0 ) Auth Your comments and actions Paraprotein 21g/L 16 17 39. 37 year old man with spleonmegaly Immunoglobulin G 11.5 g/l ( 6.0 to 16.0) Auth Immunoglobulin A 0.7 g/L ( 0.8 to 4.0) Auth Immunoglobulin M 13.3 g/l ( 0.5 to 2.0) Auth IgM kappa paraprotein 6g/L. Your comments and actions 18 19 .
Recommended publications
  • Immunoglobulin G Is a Platelet Alpha Granule-Secreted Protein
    Immunoglobulin G is a platelet alpha granule-secreted protein. J N George, … , L K Knieriem, D F Bainton J Clin Invest. 1985;76(5):2020-2025. https://doi.org/10.1172/JCI112203. Research Article It has been known for 27 yr that blood platelets contain IgG, yet its subcellular location and significance have never been clearly determined. In these studies, the location of IgG within human platelets was investigated by immunocytochemical techniques and by the response of platelet IgG to agents that cause platelet secretion. Using frozen thin-sections of platelets and an immunogold probe, IgG was located within the alpha-granules. Thrombin stimulation caused parallel secretion of platelet IgG and two known alpha-granule proteins, platelet factor 4 and beta-thromboglobulin, beginning at 0.02 U/ml and reaching 100% at 0.5 U/ml. Thrombin-induced secretion of all three proteins was inhibited by prostaglandin E1 and dibutyryl-cyclic AMP. Calcium ionophore A23187 also caused parallel secretion of all three proteins, whereas ADP caused virtually no secretion of any of the three. From these data and a review of the literature, we hypothesize that plasma IgG is taken up by megakaryocytes and delivered to the alpha-granules, where it is stored for later secretion by mature platelets. Find the latest version: https://jci.me/112203/pdf Rapid Publication Immunoglobulin G Is a Platelet Alpha Granule-secreted Protein James N. George, Sherry Saucerman, Shirley P. Levine, and Linda K. Knieriem Division ofHematology, Department ofMedicine, University of Texas Health Science Center, and Audie L. Murphy Veterans Hospital, San Antonio, Texas 78284 Dorothy F.
    [Show full text]
  • What Are Immunoglobulins? by Michelle Greer, RN
    CLINICAL BRIEF What Are Immunoglobulins? By Michelle Greer, RN THE IMMUNE SYSTEM is a complex the body such as bacteria or a virus, or in antigen, it gives rise to many large cells network of cells, tissues and organs that cases of transplant, another person’s known as plasma cells. Every plasma cell protect the body from bacteria, virus, organ, tissue or cells. Antigens are identi - is essentially a factory for producing an fungi and other foreign organisms. The fied by the immune system by a marker antibody. 1 Antibodies are also known as primary functions of the immune system molecule, which enables the immune immunoglobulins. Antibodies, or immuno- are to recognize self (the body’s own system to differentiate self from nonself. globulins, are glycoproteins made up of healthy cells) from nonself (anything Lymphocytes (natural killer cells, T cells light chains and heavy chains shaped like foreign), keep self healthy and destroy and B cells) are one of the subtypes of a Y (Figure 1). The different areas on and eliminate nonself. Immunoglobulins white blood cells in the immune system. these chains have different functions and take the lead in this process. B cells secrete antibodies that attach to roles in an immune response. antigens to mark them for destruction. A Review of Terminology Antibodies are antigen-specific, meaning Types of Immunoglobulins Understanding a few related terms and one antibody works against a specific There are several types of immunoglob - their function can provide a better appre - type of bacteria, virus or other foreign ulins and each has a different role in an ciation of immunoglobulins and how substance.
    [Show full text]
  • The Immunoglobulin G Subclass Composition of Immune Complexes in Cystic Fibrosis
    The immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesion. D B Hornick, R B Fick Jr J Clin Invest. 1990;86(4):1285-1292. https://doi.org/10.1172/JCI114836. Research Article It has been shown that pulmonary macrophage (PM) phagocytosis of Pseudomonas aeruginosa (PA) is inhibited in the presence of serum from cystic fibrosis (CF) patients colonized by Pseudomonas, and that these sera contain high concentrations of IgG2 antibodies. The goal of these studies was to investigate the role that IgG2-containing immune complexes (IC) play in this inhibition of both PM and neutrophil phagocytosis. We found that serum IgG2 concentrations were elevated significantly in CF patients with chronic PA colonization and that in selected sera from CF patients with chronic PA colonization (CF + IC, n = 10), the mean IC level was significantly elevated (2.90 +/- 0.22 mg/dl [SEM]). IgG2 comprised 74.5% of IgG precipitated in IC from CF + IC sera. An invitro phagocytic assay of [14C]PA uptake using CF + IC whole-sera opsonins confirmed that endocytosis by normal PM and neutrophils was significantly depressed. Removal of IC from CF + IC sera resulted in significantly decreased serum IgG2 concentrations without a significant change in the other subclass concentrations, and enhanced [14C]PA uptake by PM (26.6% uptake increased to 47.3%) and neutrophils (16.9% increased to 52.6%). Return of the soluble IgG2 IC to the original CF sera supernatants and the positive control sera resulted in return of the inhibitory capacity of the CF + IC sera.
    [Show full text]
  • Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
    Journal of Patient-Centered Research and Reviews Volume 4 Issue 3 Article 5 8-10-2017 Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response Michael A. Thompson Martin K. Oaks Maharaj Singh Karen M. Michel Michael P. Mullane Husam S. Tarawneh Angi Kraut Kayla J. Hamm Follow this and additional works at: https://aurora.org/jpcrr Part of the Immune System Diseases Commons, Medical Immunology Commons, Neoplasms Commons, Oncology Commons, Public Health Education and Promotion Commons, and the Respiratory Tract Diseases Commons Recommended Citation Thompson MA, Oaks MK, Singh M, Michel KM, Mullane MP, Tarawneh HS, Kraut A, Hamm KJ. Multiple myeloma baseline immunoglobulin G level and pneumococcal vaccination antibody response. J Patient Cent Res Rev. 2017;4:131-5. doi: 10.17294/2330-0698.1453 Published quarterly by Midwest-based health system Advocate Aurora Health and indexed in PubMed Central, the Journal of Patient-Centered Research and Reviews (JPCRR) is an open access, peer-reviewed medical journal focused on disseminating scholarly works devoted to improving patient-centered care practices, health outcomes, and the patient experience. BRIEF REPORT Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response Michael A. Thompson, MD, PhD,1,3 Martin K. Oaks, PhD,2 Maharaj Singh, PhD,1 Karen M. Michel, BS,1 Michael P. Mullane,3 MD, Husam S. Tarawneh, MD,3 Angi Kraut, RN, BSN, OCN,1 Kayla J. Hamm, BSN3 1Aurora Research Institute, Aurora Health Care, Milwaukee, WI; 2Transplant Research Laboratory, Aurora St. Luke’s Medical Center, Aurora Health Care, Milwaukee, WI; 3Aurora Cancer Care, Aurora Health Care, Milwaukee, WI Abstract Infections are a major cause of morbidity and mortality in multiple myeloma (MM), a cancer of the immune system.
    [Show full text]
  • ©Ferrata Storti Foundation
    Stem Cell Transplantation • Research Paper Rabbit-immunoglobulin G levels in patients receiving thymoglobulin as part of conditioning before unrelated donor stem cell transplantation Mats Remberger Background and Objectives. The role of serum concentrations of rabbit antithymoglob- Berit Sundberg ulin (ATG) in the development of acute graft-versus-host disease (GVHD) after allogene- ic hematopoietic stem cell transplantation (HSCT) with unrelated donors is unknown. Design and Methods. We determined the serum concentration of rabbit immunoglobu- lin-G (IgG) using an enzyme linked immunosorbent assay in 61 patients after unrelat- ed donor HSCT. The doses of ATG ranged between 4 and 10 mg/kg. The conditioning consisted mainly of cyclophosphamide and total body irradiation or busulfan. Most patients received GVHD prophylaxis with cyclosporine and methotrexate. Results. The rabbit IgG levels varied widely in each dose group. The levels of rabbit IgG gradually declined and could still be detected up to five weeks after HSCT. We found a correlation between the grade of acute GVHD and the concentration of rabbit IgG in serum before the transplantation (p=0.017). Patients with serum levels of rabbit IgG >70 mg/mL before HSCT ran a very low risk of developing acute GVHD grades II-IV, as compared to those with levels <70 mg/mL (11% vs. 48%, p=0.006). Interpretations and Conclusions. The measurement of rabbit IgG levels in patients receiving ATG as prophylaxis against GVHD after HSCT may be of value in lowering the risk of severe GVHD. Key words: ATG, GVHD, BMT, thymoglobulin, rabbit-IgG. Haematologica 2005; 90:931-938 ©2005 Ferrata Storti Foundation From the Department of Clinical he outcomes of unrelated donor and rate of T-cell depletion.
    [Show full text]
  • 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.
    [Show full text]
  • Activation of Human Complement by Immunoglobulin G Antigranulocyte Antibody
    Activation of human complement by immunoglobulin G antigranulocyte antibody. P K Rustagi, … , M S Currie, G L Logue J Clin Invest. 1982;70(6):1137-1147. https://doi.org/10.1172/JCI110712. Research Article The ability of antigranulocyte antibody to fix the third component of complement (C3) to the granulocyte surface was investigated by an assay that quantitates the binding of monoclonal anti-C3 antibody to paraformaldehyde-fixed cells preincubated with Felty's syndrome serum in the presence of human complement. The sera from 7 of 13 patients with Felty's syndrome bound two to three times as much C3 to granulocytes as sera from patients with uncomplicated rheumatoid arthritis. The complement-activating ability of Felty's syndrome serum seemed to reside in the monomeric IgG-containing serum fraction. For those sera capable of activating complement, the amount of C3 fixed to granulocytes was proportional to the amount of granulocyte-binding IgG present in the serum. Thus, complement fixation appeared to be a consequence of the binding of antigranulocyte antibody to the cell surface. These studies suggest a role for complement-mediated injury in the pathophysiology of immune granulocytopenia, as has been demonstrated for immune hemolytic anemia and immune thrombocytopenia. Find the latest version: https://jci.me/110712/pdf Activation of Human Complement by Immunoglobulin G Antigranulocyte Antibody PRADIP K. RUSTAGI, MARK S. CURRIE, and GERALD L. LOGUE, Departments of Medicine, Duke University and Durham Veterans Administration Medical Centers,
    [Show full text]
  • Theranostics Sialylated Immunoglobulin G: a Promising
    Theranostics 2021, Vol. 11, Issue 11 5430 Ivyspring International Publisher Theranostics 2021; 11(11): 5430-5446. doi: 10.7150/thno.53961 Review Sialylated immunoglobulin G: a promising diagnostic and therapeutic strategy for autoimmune diseases Danqi Li1,2*, Yuchen Lou1,2*, Yamin Zhang1,2, Si Liu3, Jun Li4 and Juan Tao1,2 1. Department of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. 2. Hubei Engineering Research Center for Skin Repair and Theranostics, Wuhan, China. 3. Britton Chance Center for Biomedical Photonics at Wuhan National Laboratory for Optoelectronics-Hubei Bioinformatics & Molecular Imaging Key Laboratory, Systems Biology Theme, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China. 4. Department of Dermatology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology (HUST), Wuhan, China. *These authors contributed equally to this work. Corresponding authors: E-mail address: [email protected] (J. Li), [email protected] (J. Tao). © The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. Received: 2020.09.30; Accepted: 2021.03.04; Published: 2021.03.13 Abstract Human immunoglobulin G (IgG), especially autoantibodies, has major implications for the diagnosis and management of a wide range of autoimmune diseases. However, some healthy individuals also have autoantibodies, while a portion of patients with autoimmune diseases test negative for serologic autoantibodies. Recent advances in glycomics have shown that IgG Fc N-glycosylations are more reliable diagnostic and monitoring biomarkers than total IgG autoantibodies in a wide variety of autoimmune diseases.
    [Show full text]
  • Dietary Whey Protein Supplementation Increases Immunoglobulin G Production by Affecting Helper T Cell Populations After Antigen Exposure
    foods Article Dietary Whey Protein Supplementation Increases Immunoglobulin G Production by Affecting Helper T Cell Populations after Antigen Exposure Dong Jin Ha 1, Jonggun Kim 1 , Saehun Kim 2, Gwang-Woong Go 3,* and Kwang-Youn Whang 1,* 1 Division of Biotechnology, Korea University, Seoul 02841, Korea; [email protected] (D.J.H.); [email protected] (J.K.) 2 Division of Food Bioscience and Technology, Korea University, Seoul 02841, Korea; [email protected] 3 Department of Food and Nutrition, Hanyang University, Seoul 04763, Korea * Correspondence: [email protected] (G.-W.G.); [email protected] (K.-Y.W.) Abstract: Whey protein is a by-product of cheese and casein manufacturing processes. It contains highly bioactive molecules, such as epidermal growth factor, colony-stimulating factor, transforming growth factor-α and -β, insulin-like growth factor, and fibroblast growth factor. Effects of whey protein on immune responses after antigen (hemagglutinin peptide) injection were evaluated in rats. Experimental diets were formulated based on NIH-31M and supplemented with 1% amino acids mixture (CON) or 1% whey protein concentrate (WPC) to generate isocaloric and isonitrogenous diets. Rats were fed the experimental diets for two weeks and then exposed to antigen two times (Days 0 and 14). Blood was collected on Days 0, 7, 14, and 21 for hematological analysis. The WPC group showed decreased IgA and cytotoxic T cells before the antigen injection (Day 0) but increased IgG, IL-2, and IL-4 after antigen injection due to increased B cells and T cells. Helper T cells were increased at Days 14 and 21, but cytotoxic T cells were not affected by WPC.
    [Show full text]
  • Understanding the Immune System and Lymphoma
    Understanding the Immune System and Lymphoma The body’s immune system is comprised of a network of cells, tissues, and organs. This network operates together to eliminate harmful pathogens, like bacteria and viruses, as well as cancer cells from the body. The immune system provides two different types of immunity: • Innate (meaning “inborn” or “natural”) immunity — This type of immunity is provided by natural barriers in the body, substances in the blood, and specific cells that attack and kill foreign cells. Examples of natural barriers include skin,mucous membranes, stomach acid, and the cough reflex. These barriers keep germs (bacteria or viruses) and other harmful substances from entering the body. Inflammation (redness and swelling) is also a type of innate immunity. Blood cells that are part of the innate immune system include neutrophils, macrophages, eosinophils, and basophils. • Adaptive (meaning adapting to external forces or threats) immunity — This type of immunity is provided by the thymus gland, spleen, tonsils, bone marrow, circulatory system, and lymphatic system. B cells and T cells, the two main types of lymphocytes, carry out the adaptive immune response by recognizing and either inactivating or killing specific invading organisms. The adaptive immune system can then “remember” the identity of the invader, so that the next time the body is infected by the same invader, the immune response will develop more quickly and strongly. All normal cells have a limited lifespan. A self-destruct mechanism called apoptosis is triggered when cells become senescent (too old) or get damaged; this natural process is called apoptosis or programmed sequence of events that lead to the cell’s death.
    [Show full text]
  • Seroprevalence of Immunoglobulin G Antibodies Against Mycobacterium Avium Subsp
    veterinary sciences Communication Seroprevalence of Immunoglobulin G Antibodies Against Mycobacterium avium subsp. paratuberculosis in Dogs Bred in Japan Takashi Kuribayashi 1,*, Davide Cossu 2 and Eiichi Momotani 3 1 Laboratory of Immunology, School Life and Environmental Science, Azabu University, Kanagawa 252-5201, Japan 2 Department of Neurology, School of Medicine, Juntendo University, Tokyo 113-8431, Japan; [email protected] 3 Comparative Medical Research Institute, Ibaraki 305-0856, Japan; [email protected] * Correspondence: [email protected] Received: 27 May 2020; Accepted: 13 July 2020; Published: 17 July 2020 Abstract: In this study, the seroprevalence of immunoglobulin G (IgG) antibodies against Mycobacterium avium subsp. paratuberculosis (MAP) in dogs bred in Japan was evaluated. Ninety-two non-clinical samples were obtained from three institutes and fifty-seven clinical samples were obtained from a veterinary hospital in Japan. Serum titers of total IgG, IgG1 and IgG2 isotype antibodies against MAP were measured using an indirect enzyme-linked immunosorbent assay (ELISA). The IgG antibodies against MAP in non-clinical serum obtained from three institutes was observed to be 2.4%, 20% and 9.0%. Similarly, the IgG1 antibodies titers against MAP were observed to be 7%, 20% and 0%. Lastly, the IgG2 antibodies against MAP were observed to be 7%, 20% and 4.4%. No significance differences in these titers were observed among the three institutes. The IgG, IgG1 and IgG2 antibodies in serum obtained from a veterinary hospital were observed to be 55.3%, 42% and 42%, respectively. Significant differences were found between the non-clinical and clinical samples. The titers in the clinical samples showed a high degree of variance, whereas low variance was found in the non-clinical samples.
    [Show full text]
  • Sweet but Dangerous – the Role of Immunoglobulin G Glycosylation in Autoimmunity and Inflammation
    Lupus (2016) 25, 934–942 http://lup.sagepub.com SPECIAL ARTICLE Sweet but dangerous – the role of immunoglobulin G glycosylation in autoimmunity and inflammation MHC Biermann1, G Griffante1, MJ Podolska1, S Boeltz1, J Stu¨rmer1, LE Mun˜ oz1, R Bilyy1,2 and M Herrmann1 1Friedrich-Alexander-University Erlangen-Nu¨rnberg (FAU), Department of Internal Medicine 3 – Rheumatology and Immunology, Universita¨tsklinikum Erlangen, Erlangen, Germany; and 2Danylo Halytsky Lviv National Medical University, Lviv, Ukraine Glycosylation is well-known to modulate the functional capabilities of immunoglobulin G (IgG)-mediated cellular and humoral responses. Indeed, highly sialylated and desialylated IgG is endowed with anti- and pro-inflammatory activities, respectively, whereas fully deglycosy- lated IgG is a rather lame duck, with no effector function besides toxin neutralization. Recently, several studies revealed the impact of different glycosylation patterns on the Fc part and Fab fragment of IgG in several autoimmune diseases, including systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). Here, we provide a synoptic update summarizing the most important aspects of antibody glycosylation, and the current progress in this field. We also discuss the therapeutic options generated by the modification of the glycosylation of IgG in a potential treatment for chronic inflammatory diseases. Lupus (2016) 25, 934–942. Key words: Glycosylation; sialylation; fucosylation; galactosylation; Fc fragment; autoanti- body; autoimmunity; inflammation Introduction and recruit inflammatory effector cells expressing Fcg receptors (FcgRs), which ultimately contrib- 5 One of the mechanisms fostering the development ute to tissue damage. The glycosylation pattern of of immunoglobulin G (IgG)-mediated inflamma- an antibody crucially influences its conformation, tory autoimmune diseases is the impaired clearance if it binds to FcgRs and complement, as well as of cell-derived remnants, which results in a break- its aggregation behaviour.
    [Show full text]