Science of Rheumatic arthritis Flashcards

1
Q

What are the functions of the synovial membrane (Synovium)?

A

Functions of synovium:
> Maintenance of intact tissue surface

> Lubrication of cartilage

> Control of synovial fluid volume and composition (hyaluronan, lubricin)

> Nutrition of chondrocytes within joints

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2
Q

Which cell types are there in the synovium?

A

Two cell types:

  • Macrophage
  • Fibroblast = Produce the components of synovial fluid
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3
Q

In Rheumatoid arthritis what does the synovium thicken to form?

A

The pannus

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4
Q

What is Rheumatic arthritis?

A

Rheumatoid arthritis is a chronic symmetric polyarticular inflammatory joint disease, which primarily affects the small joints of the hands and feet

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5
Q

What is rheumatoid synovitis (Pannus) characterised by?

A

The rheumatoid synovitis (pannus) is characterised by inflammatory cell infiltration, synoviocyte proliferation and neoangiogenesis

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6
Q

What does the synovial fluid in the joint cavity contain during Rheumatoid arthritis?

A

The synovial fluid in the joint cavity contains neutrophils, particularly during acute flares of RA

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7
Q

What does the pannus causes?

A

Bone and cartilage destruction (Deformities)

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8
Q

Which autoantibodies are usually present in RA?

A

Autoantibodies, such as RFs and anti-citrullinated protein antibodies, are commonly associated with RA (Most Common)

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9
Q

Which secondary autoantibodies are usually present in RA?

A

Autoantibodies occur in RA that recognise either joint antigens, such as type II collagen, or systemic antigens, such as glucose phosphate isomerase (Secondary Aa)

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10
Q

Seropositive rheumatoid arthritis?

A

Seropositive rheumatoid arthritis:
> Rheumatoid factor

> Anti-citrullinated protein antibody (ACPA)

> Diagnostic anti-CCP assays recognise citrullinated self-proteins
- α-enolase, keratin, fibrinogen, fibronectin, collagen, vimentin

> Patients with ACPA+ disease have a less favourable prognosis

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11
Q

Which serotype is associated with genetic factors leading to RA?

A

Alleles containing a common amino acid motif (QKRAA – shared epitope) in the HLA-DRB1 region (HLA-DR4 serotype) confer susceptibility:

  • Role in promoting autoimmunity (e.g. altered antigen presentation)
  • Molecular mimicry (e.g. with microbial proteins)

Other associations = PTPN22, CTLA4, c-REL etc

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12
Q

Environmental factors leading to RA?

A

> Smoking and bronchial stress (exposure to silica)

> Infectious agents have been associated with RA:
Viruses (EBV, CMV)
- E. Coli
- Mycoplasma
- Periodontal disease (Porphyromonas gingivalis)
- Microbiome (gut microbes)

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13
Q

What occurs in individuals who are highly susceptible to RA and receive repeated insults of environmental factors?

A

> Formation of immune complexes and rheumatoid factor (high-affinity autoAb against the Fc portion of Ig)

> Altered citrullination of proteins and breakdown of tolerance, with resulting ACPA response

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14
Q

What is synovitis?

A

Inflammation of the synovium

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15
Q

Pathogenesis of RA?

A

> Villous hyperplasia
Infiltration of T cells, B cells, macrophages and plasma cells
Intimal cell proliferation (fibroblasts)
Production of cytokines and proteases
Increased vascularity
Self-amplifying process

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16
Q

How is pathogenicity of CD20+ cells confirmed in RA?

A

Efficacy of rituximab

17
Q

Role of B cells in RA?

A

Role of B cells goes beyond production of autoAb
> Autoantigen presentation
> Cytokines (IL-6, TNF-α)

18
Q

What do inflammatory cytokines activate in RA?

A

> Activate synovial fibroblasts, chondrocytes, osteoclasts

> Promote angiogenesis

> Suppress T-regs

> Activate leukocytes

> Promote autoAb production

> IL-6 mediates systemic effects

19
Q

Which interleukin mediates the systemic effects in RA?

A
IL-6 mediates systemic effects:
> Acute-phase response
> Anaemia
> Cognitive dysfunction
> Lipid metabolism dysregulation
20
Q

Which interleukin mediates the systemic effects in RA?

A
IL-6 mediates systemic effects:
> Acute-phase response
> Anaemia
> Cognitive dysfunction
> Lipid metabolism dysregulation
21
Q

Bone destruction in RA?

A

Bone destruction is mediated by osteoclasts that are activated under the influence of RANKL produced by RA synovium

22
Q

Cartilage destruction in RA?

A

> Several classes of proteases, including metalloproteinases and aggrecanases are produced by FLS in the intimal lining layer

> Synovial lining cells, especially FLS, can attach to and invade cartilage in RA

23
Q

Key cytokines in RA?

A
Key cytokines:
TNF-a*
IL-1
IL-6*
RANKL M-CSF
24
Q

Systemic consequences of RA?

A

> Vasculitis, nodules, scleritis, amyloidosis = secondary to uncontrolled chronic inflammation

> Cardiovascular disease

  • Altered lipid metabolism
  • Elevated acute-phase reactants
  • Increased endothelial activation

> Fatigue and reduced cognitive function (secondary fibromyalgia)
- Dysregulation of the HPA axis

> Liver

  • Elevated acute-phase response
  • Anaemia of chronic disease (IL-6 increases hepatocyte production of hepcidin, an iron-regulatory hormone)

> Lungs (interstitial lung disease, fibrosis)

> Muscles (sarcopoenia)

> Bone (osteoporosis)

> Secondary Sjogren’s syndrome