collection
https://read.qxmd.com/read/21853842/does-this-patient-with-urticaria-angioedema-have-anaphylaxis
#21
REVIEW
G P Spickett, C Stroud
No abstract text is available yet for this article.
August 2011: Clinical Medicine: Journal of the Royal College of Physicians of London
https://read.qxmd.com/read/23374261/atopic-dermatitis-a-practice-parameter-update-2012
#22
REVIEW
Lynda Schneider, Stephen Tilles, Peter Lio, Mark Boguniewicz, Lisa Beck, Jennifer LeBovidge, Natalija Novak, David Bernstein, Joann Blessing-Moore, David Khan, David Lang, Richard Nicklas, John Oppenheimer, Jay Portnoy, Christopher Randolph, Diane Schuller, Sheldon Spector, Stephen Tilles, Dana Wallace
This parameter was developed by the Joint Task Force on Practice Parameters, representing the American Academy of Allergy, Asthma & Immunology (AAAAI); the American College of Allergy, Asthma & Immunology (ACAAI); and the Joint Council of Allergy, Asthma and Immunology. The AAAAI and the ACAAI have jointly accepted responsibility for establishing "Atopic dermatitis: a practice parameter update 2012." This is a complete and comprehensive document at the current time. The medical environment is a changing environment, and not all recommendations will be appropriate for all patients...
February 2013: Journal of Allergy and Clinical Immunology
https://read.qxmd.com/read/26634783/the-role-of-immune-mechanisms-in-alcoholic-and-nonalcoholic-steatohepatitis-a-2015-update
#23
REVIEW
Salvatore Sutti, Stefania Bruzzì, Emanuele Albano
So far, innate immune mechanisms have been recognized as the main responsible for the evolution of both alcoholic steatohepatitis (ASH) and nonalcoholic steatohepatitis (NASH). However, increasing evidence points toward the possible role of adaptive immune responses, as an additional factor in promoting hepatic inflammation in steatohepatitis. In this article, we discuss recent data involving circulating antibodies and lymphocyte-mediated responses in sustaining the progression of ASH and NASH to fibrosis, as well as the possible mechanisms implicated in favoring the onset of adaptive immunity in the setting of steatohepatitis...
2016: Expert Review of Gastroenterology & Hepatology
https://read.qxmd.com/read/26568190/innate-immunity-in-diabetes-and-diabetic-nephropathy
#24
REVIEW
Jun Wada, Hirofumi Makino
The innate immune system includes several classes of pattern recognition receptors (PRRs), including membrane-bound Toll-like receptors (TLRs) and nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs). These receptors detect pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs) in the extracellular and intracellular space. Intracellular NLRs constitute inflammasomes, which activate and release caspase-1, IL-1β, and IL-18 thereby initiating an inflammatory response...
January 2016: Nature Reviews. Nephrology
https://read.qxmd.com/read/18695702/mucosal-immunology-down-under-special-interest-group-in-mucosal-immunology-workshop-australasian-society-for-immunology-sydney-australia-2-december-2007
#25
Allan W Cripps, Philip Sutton, Ken Beagley, Sarah Robertson, Margaret Dunkley
The Mucosal Immunology Special Interest Group (SIG-MI) of the Australasian Society of Immunology was formed 14 years ago and has run regular symposia and workshops in conjunction with the Australasian Society of Immunology since that time. In December 2007 the Mucosal Immunology Special Interest Group held a 1-day satellite workshop in conjunction with the annual Australasian Society of Immunology scientific meeting in Sydney to celebrate the decade since hosting the 9th International Congress of Mucosal Immunology (9-ICMI) in 1997, which was also held in Sydney...
October 2008: Immunology and Cell Biology
https://read.qxmd.com/read/22447352/mucosal-immunology-of-tolerance-and-allergy-in-the-gastrointestinal-tract
#26
REVIEW
Lauren Steele, Lloyd Mayer, M Cecilia Berin
The mucosal immune system typically exists in a state of active tolerance to food antigens and commensal bacteria. Tolerance to food proteins is induced in part by dendritic cells residing in the intestinal mucosa and implemented by regulatory T cells. Food allergy occurs when immune tolerance is disrupted and a sensitizing immune response characterized by food-specific IgE production occurs instead. Experimental food allergy in mice requires use of adjuvant or exploitation of alternate routes of sensitization to induce allergic sensitization, and can aid in understanding the mechanisms of sensitization to food allergens and the pathophysiology of gastrointestinal manifestations of food allergy...
December 2012: Immunologic Research
https://read.qxmd.com/read/17452477/am3-modulates-dendritic-cell-pathogen-recognition-capabilities-by-targeting-dc-sign
#27
JOURNAL ARTICLE
Diego Serrano-Gómez, Rocío T Martínez-Nuñez, Elena Sierra-Filardi, Nuria Izquierdo, María Colmenares, Jesús Pla, Luis Rivas, Javier Martinez-Picado, Jesús Jimenez-Barbero, José Luis Alonso-Lebrero, Salvador González, Angel L Corbí
AM3 (Inmunoferon) is an orally effective immunomodulator that influences the regulatory and effector functions of the immune system whose molecular mechanisms of action are mostly unknown. We hypothesized that the polysaccharide moiety of AM3 (IF-S) might affect immune responses by modulating the lectin-dependent pathogen recognition abilities of human dendritic cells. IF-S inhibited binding of viral, fungal, and parasite pathogens by human monocyte-derived dendritic cells in a dose-dependent manner. IF-S specifically impaired the pathogen recognition capabilities of DC-SIGN, as it reduced the attachment of Candida, Aspergillus, and Leishmania to DC-SIGN transfectants...
July 2007: Antimicrobial Agents and Chemotherapy
https://read.qxmd.com/read/26445701/an-update-on-immunopathogenesis-diagnosis-and-treatment-of-multiple-sclerosis
#28
REVIEW
Neeta Garg, Thomas W Smith
BACKGROUND: Multiple sclerosis is an acquired demyelinating disease of the central nervous system. It is the second most common cause of disability in adults in United States after head trauma. DISCUSSION: The etiology of MS is probably multifactorial, related to genetic, environmental, and several other factors. The pathogenesis is not fully understood but is believed to involve T-cell-mediated inflammation directed against myelin and other related proteins with a possible role for B cells...
September 2015: Brain and Behavior
https://read.qxmd.com/read/26441488/guidelines-for-the-use-and-interpretation-of-diagnostic-methods-in-adult-food-allergy
#29
REVIEW
Donatella Macchia, Giovanni Melioli, Valerio Pravettoni, Eleonora Nucera, Marta Piantanida, Marco Caminati, Corrado Campochiaro, Mona-Rita Yacoub, Domenico Schiavino, Roberto Paganelli, Mario Di Gioacchino
Food allergy has an increasing prevalence in the general population and in Italy concerns 8 % of people with allergies. The spectrum of its clinical manifestations ranges from mild symptoms up to potentially fatal anaphylactic shock. A number of patients can be diagnosed easily by the use of first- and second-level procedures (history, skin tests and allergen specific IgE). Patients with complex presentation, such as multiple sensitizations and pollen-food syndromes, frequently require a third-level approach including molecular diagnostics, which enables the design of a component-resolved sensitization profile for each patient...
2015: Clinical and Molecular Allergy: CMA
https://read.qxmd.com/read/23749606/recent-advances-in-autoimmune-pancreatitis-type-1-and-type-2
#30
REVIEW
Terumi Kamisawa, Suresh T Chari, Markus M Lerch, Myung-Hwan Kim, Thomas M Gress, Tooru Shimosegawa
Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis characterised clinically by frequent presentation with obstructive jaundice, histologically by a lymphoplasmacytic infiltrate with fibrosis, and therapeutically by a dramatic response to steroids. When so defined, AIP can be sub-classified into two subtypes, 1 and 2. Recent international consensus diagnostic criteria for AIP have been developed for diagnosis of both forms of AIP. Type 1 AIP is the pancreatic manifestation of a multiorgan disease, recently named IgG4-related disease...
September 2013: Gut
https://read.qxmd.com/read/25289722/oral-immunotherapy-for-allergic-conjunctivitis
#31
REVIEW
Waka Ishida, Ken Fukuda, Yosuke Harada, Hideo Yagita, Atsuki Fukushima
Antigen-specific immunotherapy is expected to be a desirable treatment for allergic diseases. Currently, antigen-specific immunotherapy is performed by administering disease-causing antigens subcutaneously or sublingually. These approaches induce long-term remission in patients with allergic rhinitis or asthma. The oral route is an alternative to subcutaneous and sublingual routes, and can also induce long-term remission, a phenomenon known as "oral tolerance." The effectiveness of oral tolerance has been reported in the context of autoimmune diseases, food allergies, asthma, atopic dermatitis, and allergic rhinitis in both human patients and animal models...
November 2014: Cornea
https://read.qxmd.com/read/26221205/thyroid-dysfunction-an-autoimmune-aspect
#32
REVIEW
Farah Aziz Khan, Noura Al-Jameil, Mohammad Fareed Khan, May Al-Rashid, Hajera Tabassum
Auto immune thyroid disease (AITD) is the common organ specific autoimmune disorder, Hashimoto thyroiditis (HT) and Grave's disease (GD) are its well-known sequelae. It occurs due to loss of tolerance to autoantigens thyroid peroxidase (TPO), thyroglobulin (Tg), thyroid stimulating hormone receptor (TSH-R) which leads to the infiltration of the gland. T cells in chronic autoimmune thyroiditis (cAIT) induce apoptosis in thyroid follicular cells and cause destruction of the gland. Presences of TPO antibodies are common in HT and GD, while Tg has been reported as an independent predictor of thyroid malignancy...
2015: International Journal of Clinical and Experimental Medicine
https://read.qxmd.com/read/26233425/autoimmunity-and-immune-dysregulation-in-primary-immune-deficiency-disorders
#33
REVIEW
Heather K Lehman
Primary immune deficiencies are often associated with autoimmune disease due to the dysregulation of the immune system as a whole. In many immune deficiencies, lymphocytes may be present but dysfunctional, allowing for the development of excessive autoreactivity and resultant autoimmune disease. Autoimmune polyendocrinopathy candidiasis and ectodermal dystrophy, autoimmune lymphoproliferative syndrome, immunodyregulation polyendocrinopathy enteropathy X-linked, IL-10/IL-10 receptor deficiencies, and PLCG2-associated antibody deficiency and immune dysregulation are disorders in which autoimmunity is a hallmark of the clinical disease presentation...
September 2015: Current Allergy and Asthma Reports
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