HS III Flashcards

1
Q

What type of reaction is a type III hypersensitivity reaction?

A

Immune complex deposition, targeting soluble antigens

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2
Q

How long does a type III hypersensitivity reaction take to develop?

A

3-8 hours

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3
Q

Which immunoglobulin is involved in type III hypersensitivity reactions and how does it cause a reaction?

A

IgG/IgM antibodies
React with soluble antigens to form immune complexes that are deposited in tissue and release toxins that damage the tissue

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4
Q

What factors affect immune complex pathogenesis?

A

Size of immune complex (big/small easily cleared)
Haemodynamic factors, clearance
Host response, low affinity antibodies less likely to form immune complexes
Complement deficiency, clearance

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5
Q

Describe the immune mechanism of type III hypersensitivity reactions

A

IgG/IgM antibodies bind with soluble antigens to form medium sized immune complexes that are deposited in tissue
Complement is activated
Neutrophil chemotaxis
Neutrophil binds to tissue and releases toxins

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6
Q

What antibodies are tested for in rheumatoid arthritis?

A

Autoantibody to rheumatoid factor (IgG)
Anti-cyclic citrullinated peptide (Anti-CCP)
Anti-citrullinated protein antibody (ACPA)

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7
Q

Describe the pathophysiology of rheumatoid arthritis

A

Chemoattractants in joints recruit B and T lymphocytes
Lymphocytes interact and drive overproduction of tumour necrosis factor, which causes synovitis and joint destruction
TNF also stimulates overproduction of IL 6 and other cytokines, recruiting more inflammatory cells

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8
Q

Describe how the lungs can be affected by rheumatoid arthritis

A

Nodules
Pleural effusion
Interstitial lung disease

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9
Q

Name non-articular manifestations of rheumatoid arthritis

A
Pericarditis 
Nodules 
Pleural effusion
Interstitial lung disease
Ankle oedema
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10
Q

Describe the articular manifestations of rheumatoid arthritis

A

Progressive, symmetrical, peripheral, polyarthritis with persistent synovitis and systemic inflammation

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11
Q

Describe the typical presentation of rheumatoid arthritis

A

30-50 years old
More likely female
Smoking risk factor
Chronic, symmetrical joint pain in the small joints
Morning stiffness lasting longer than 30 mins
Inflammed joints, hot and tender
Rheumatoid nodules

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12
Q

Which specific joints are typically affected?

A

Proximal interphalangeal joints and metacarpophalangeal

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13
Q

How is rheumatoid arthritis treated?

A

Corticosteroid: Prednisolone

+DMARD: Methotrexate/hydroxychloroquine

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14
Q

Describe the pathophysiology of glomerulonephritis

A

Infection with Hep B or bacterial endocarditis, IgG immune complex deposition in GBM, kidney damage

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15
Q

Describe typical X ray findings for rheumatoid arthritis

A

Narrowing of joint space
Osteoperosis localised to metacarpopharangeal joints
Small erosions at proximal phalanges
Soft tissue swelling involving all fingers

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16
Q

Name a monoclonal antibody used to treat rheumatoid arthritis

A

Tumour necrosis factor antibody

17
Q

Describe how monoclonal antibodies can work in autoimmune disease

A

Bind to cell surface receptor to activate or inhibit signalling within cell
Bind to and be internalised by cancer cells to deliver toxins
Block inhibitory effects on T cells

18
Q

Describe how monoclonal antibodies can be used to treat breast cancer

A

Trastuzumab

Inhibits HER-2 signalling (oncogene)

19
Q

Describe how monoclonal antibodies can be used to treat lymphoma

A

Rituximab

CD 20 is expressed on all B cell surfaces, and rituximab is an antibody against CD20

20
Q

Describe the pathophysiology of systemic lupus erythematosus

A

Self antigens form and the immune system fails to inactivate the B and T lymphocytes that recognise the self antigens - breakdown of tolerance
Autoantibodies form immune complexes that are deposited in tissues
Complement is activated
Influx of neutrophils, causing inflammation
Abnormal cytokine production

21
Q

What features indicate systemic lupus erythematosus?

A
Antinuclear antibody present
Renal abnormalities 
Arthritis 
Photosensitive 
Oral ulcers 
Malar rash 
Arthralga
22
Q

How is systemic lupus erythematosus treated?

A

Corticosteriods: Prednisolone
DMARDs: Hydroxychloroquine/Azathioprine
Lifestyle modification and use of suncream

23
Q

What antibodies are tested for in systemic lupus erythematosus?

A

Antinuclear antibodies (dsDNA)
Anti-Sm antibodies
Antiphospholipid antibodies

24
Q

Describe the features of skin involvement in systemic lupus erythematosus

A
Butterfly/malar rash on face
Photosensitivity 
Urticaria
Vasculitis 
Purpura
25
Describe the findings of a full blood count in a patient with systemic lupus erythematosus
Anaemia Low white cell count Low platelet count
26
If haemolytic anaemia is present, which test confirms it as autoimmune?
Coombs test