HC28: Pathology of allergy
Classification
Classification is the act of forming a distribution into groups, classes, orders and families according to some common relations or attributes. A classification system is used to:
- Enhanced the quality of communication
- Especially between experts involved in the field
- Provide a logical structure for categorization
- For epidemiologic, prognostic or interventional studies
- Assist in the management of individual patients
- To this extent, categories should be mutually exclusive and predictive of the subsequent behavior of the disease
Conjunctivitis
Conjunctivitis is a type I hypersensitivity reaction. In case of direct hypersensitivity reactions, there is a fast immunological reaction in a sensitive individual, often called an allergy.
Morphology:
Histological images of conjunctivitis are different from most images of type I hypersensitivity reactions:
- Eosinophils are strongly present
- IgE is hard to find in a histological image
- Mast cells are present, but are hard to distinguish
Symptoms:
Conjunctivitis is an ocular allergy caused by pollen release spores. Symptoms are:
- Itching
- Watery discharge
- Redness
The upper ENT may also be involved.
Therapy:
Therapy consists of:
- Antihistamines
- Mast cell stabilizers
- Non-steroidal anti-inflammatory agents
Anti-GBM nephritis
Anti-GBM nephritis is an example of Type II hypersensitivity. GBM stands for glomerular basal membrane. Type II hypersensitivity reactions are mediated by antibodies directed to antigens on the cell-surface in the extracellular matrix. It is caused by cell destruction, an inflammatory reaction or intervention with the normal function. Deposited IgG-antibodies activate the complement system → inflammatory reaction.
Process:
In case of anti-GBM nephritis, the following happens:
- Anti-GBM antibodies bind to the basal membrane of capillaries
- Leukocytes (such as neutrophils) are activated and attack the vessel walls → the basal membrane breaks
- The vessel walls become infected → glomerulonephritis and alveolar capillaritis
- Capillary loops are destroyed
- Inflammatory mediators come into Bowman’s space → lining epithelium starts to proliferate → crescent formation
- Histological images of glomerulonephritis show a crescent
The IgG antibodies work against the alpha-3 chain of collagen type IV, a complement of GBM. The alpha-3 chain is part of the basement membrane in the kidney and the lung. This causes leukocytes to attack the membrane with antigens. Anti-GBM nephritis typically occurs in the kidneys and lungs.
Goodpasture syndrome:
About 50% of anti-GBM nephritis cases occurs without the lungs being involved. In case of Goodpasture-syndrome, both kidneys and lungs are involved. This usually is paired with hemorrhagia (bleeding). The alveolar walls are inflamed and pneumocytes are clearly visible.
Smokers:
Glomerulonephritis typically occurs in smokers → smoking destroys the alveolar epithelia → antibodies travel from the lungs to the kidneys. This can be diagnosed with serology for anti-GBM antibodies.
Fibrinoid necrosis
Fibrinoid necrosis is a type III hypersensitivity reaction. An important difference between type II and III hypersensitivity is that in case of type III the antibodies bind to solubles.
Morphology:
Histological images of fibrinoid necrosis show:
- Fibrine
- Necrosis
- Inflammation
Process:
Fibrinoid necrosis is vasculitis at the level of the glomerular capillary:
- The capillaries are destroyed → inflammatory mediators are released
- Fibrin and cytokines leak into Bowman’s space
- Epithelial cells lining Bowman’s capsule start to proliferate
Asthma
Asthma is a type I hypersensitivity reaction. This reaction is triggered by the binding of an antigen to IgE on the surface of mast cells.
Morphology:
A morphological image of asthma shows:
- Eosinophils
- Lymphocytes
- Whether they are B- or T-lymphocytes isn’t distinguishable
- Prominent muscle tissue
- Caused by hyperplasia of smooth muscle cells
- Many mucus producing cells
- Small lumen
In case of allergic rhinitis (hayfever) an infiltrate with granulocytes can be visible → edema. Eosinophils can be distinguishing for the diagnosis of asthma.
Diabetes
Diabetes is an example of type IV hypersensitivity. Cytotoxic T-cells destroy insulin-producing cells in the islets of Langerhans. In a histological image, this is visible as brown spots. There also are infection cells colored for CD8.
Auto-antibodies also are present at one point, but later disappear again.
Systemic Lupus Erythematosus
An example of type III hypersensitivity is Systemic Lupus Erythematosus. SLE is a prototype of a multisystemic disease of autoimmune origin. It is characterized by production of many antibodies by the B-cells. On the face, erythema and butterfly-looking rash is visible.
Lupus nephritis:
60% of SLE patients develop renal involvement during the course of their disease → lupus nephritis. Lupus nephritis is linked with high morbidity rates, especially in case of ESRD. There is a complex relation between diagnosis, pathogenesis and treatment of lupus nephritis.
Classification:
Histopathological characteristics of lupus nephritis can vary considerably → classification of lupus is important for the choice of treatment. The classification system of lupus nephritis is based on the percentage available in the glomeruli:
- If less than 50% of glomeruli are present the classification is acute or chronic
- If more than 50% of glomeruli are present the classification is segmental or global
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Mechanisms of Disease 1 2020/2021 UL
- Mechanisms of Disease 1 HC1: Introduction to G2MD1
- Mechanisms of Disease 1 HC2: Introduction to the immune system
- Mechanisms of Disease 1 HC3: Innate and adaptive immune responses & key cytokines
- Mechanisms of Disease 1 HC4: Pathology of normal immune response
- Mechanisms of Disease 1 HC5: B- and T-cell generation and diversity
- Mechanisms of Disease 1 HC6: Mechanisms of adaptive immunity
- Mechanisms of Disease 1 HC7: Effector mechanisms of antibodies
- Mechanisms of Disease 1 HC8: B-cell development and antibodies
- Mechanisms of Disease 1 HC9: Tissue injury and repair
- Mechanisms of Disease 1 HC10: Repair mechanism
- Mechanisms of Disease 1 HC11: Pathology of inflammatory reactions
- Mechanisms of Disease 1 HC12: Introduction to infectious diseases
- Mechanisms of Disease 1 HC13: Bacteria
- Mechanisms of Disease 1 HC14: Viruses
- Mechanisms of Disease 1 HC15: Fungi and parasites
- Mechanisms of Disease 1 HC16: Invaders
- Mechanisms of Disease 1 HC17: Host versus invader
- Mechanisms of Disease 1 HC18: Immune deficiencies and infection risk
- Mechanisms of Disease 1 HC19: Pathology of infectious diseases
- Mechanisms of Disease 1 HC20: Diagnostics of infectious diseases
- Mechanisms of Disease 1 HC21: Essential microorganisms
- Mechanisms of Disease 1 HC extra: Mycobacterial infections (tuberculosis)
- Mechanisms of Disease 1 HC22: Antimicrobial therapy
- Mechanisms of Disease 1 HC23: Principles of antibiotic pharmacotherapy
- Mechanisms of Disease 1 HC24: Introduction MOOC
- Mechanisms of Disease 1 HC25: Epidemiology
- Mechanisms of Disease 1 HC26: Prevention and control
- Mechanisms of Disease 1 HC extra: COVID-19
- Mechanisms of Disease 1 HC27: Mechanisms of hypersensitivity reactions
- Mechanisms of disease 1 HC28: Pathology of allergy
- Mechanisms of Disease 1 HC29: Asthma
- Mechanisms of Disease 1 HC30: Pathology of autoimmunity
- Mechanisms of Disease 1 HC31: HLA and autoimmunity
- Mechanisms of Disease 1 HC32: Vasculitis
- Mechanisms of Disease 1 HC33: Systemic Lupus Erythematosus
- Mechanisms of Disease 1 HC35: Infections and autoimmunity
- Mechanisms of Disease 1 HC36: Immune cells in rheumatoid arthritis
- Mechanisms of Disease 1 HC37+38: Pharmacology: immunosuppression
- Mechanisms of Disease 1 HC39: Pathology of transplantation
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Mechanisms of Disease 1 2020/2021 UL
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