SLE Flashcards

1
Q

What is the definition of autoimmunity?

A

An immune reaction against self-antigens secondary to a loss of self-tolerance

  • Can be isolated single organ disease or multi-organ systemic dysfunction
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2
Q

What are the possible mechanisms of injury for autoimmunity?

A
  • *B-cells - Autoantibodies**:
  • Ab dependent cellular cytoxicity (Type II)
  • Complement (Type II)
  • Anti-receptor antibody (Type II)
  • Immune complexes (Type III)
  • *Cell-mediated (type IV)**
  • T cells and macrophages
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3
Q

How is self-tolerance prevented in the immune system?

A
  • Clonal Deletion: Receptors strongly bind to self antigen, these cells are killed early on
  • Clonal anergy: If, in periphery, there are self-reactive lymphocytes, they are made anergic
  • Suppression: Tregulatory cells (CD3+CD4+CD25+FOXP3)
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4
Q

What is Systemic Lupus Erythematosus?

A
  • Multisystem autoimmune disease of Connective Tissue Disorder (CTD) type
  • CD4+ Tcell dependent B Cell hyperactivity
  • Cell type-specific autoantibodies (type II) and immune complexes (type III) induce tissue injury
  • interplay of multiple genes, hormones, and environmental influences
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5
Q

What are the Lupus Classification Criteria?

A

RASH ON MAIDS

  • *R**enal
  • *A**rthritis
  • *S**erositis
  • *H**ematologic (hemolytic anemia, leukopenia, thrombocytopenia)
  • *O**ral ulcers
  • *N**eurologic (psychosis, seizures)
  • *M**alar rash
  • *A**NA+
  • *I**mmunologic (anti-dsDNA Ab, anti-Sm Ab, anti-phospholipid Ab)
  • *D**iscoid rash
  • *S**un sensitivity
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6
Q

What are the seronegative arthritises?

A

Ankylosing spondylitis

Reactive arthritis

Psoriatic arthritis

IBD-associated arthritis

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7
Q

What are environmental triggers of SLE?

A

UV light

Infection

Emotional stress

Surgery

Pregnancy, post-partum, and abortion

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8
Q

What is the immunologic pathophysiology for SLE?

A

Humoral Immunity:
- B cell hyperactiity and hypergammaglobulinemia
- Auto Abs

(ANA - Immune complexes)
(Antibodies to phospholipid-bound proteins)
(Antibodies to membrane proteins of specific cell types - hematologic and neuronal cell injury)
- Complement activation and decrease in serum complement (consumption)

  • Cell-Mediated Immunity*:
  • *- Excessive or poorly controlled CD4+ Th cell activity**
  • Viruses implicated as triggers in genetically susceptible hosts
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9
Q

What specific anti-nuclear antibodies are present in SLE?

A

Anti-dsDNA and anti-Sm –> virtually diagnostic

Anti-histone (drug induced SLE)

Anti-SS-A [Ro] and Anti-SS-B [La] - subacute cutaneous lupus and congenital heart block (also Abs present in majority of Sjogren’s syndrome patients)

Anti-phospholipid Antibodies

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10
Q

What is the significance of anti-phospholipid antibody presence?

A

May lead to Antiphospholipid Syndrome:

Autoimmune hypercoagulable state caused by:
Anti-phospholipid-ß2 glycoprotein
Anti-cardiolipin
(also causes false + syphilis)
Lupus anticoagulant (may show false + PPT elongation)

May lead to:
Venous and arterial thromboses
Spontaneous miscarriage
Focal cerebral ischemia
Ocular ischemia

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11
Q

What are the most characteristic SLE lesions secondary to immune complexes?

A

Skin (rash)

Kidneys (glomerulonephritis)

Blood vessels

Connective Tissue

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12
Q

What are the histological features of skin involvement in SLE?

A

Ig/complement complexes at dermal-epidermal junction

  • lymphocytic infiltration at DEJ
  • Liquefaction of basal layer of epidermis
  • Edema and perivascular lymphocytes in dermis

Complex deposition made visible by “Lupus band test”
–> immunofluorescence of complex deposition

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13
Q

What skin involvement is seen in SLE?

A

- Erythema: Butterfly rash; similar rash on extremities and trunk

- Accentuation by sunlight

- Ulcerations (oral, vaginal, nasal)

- Alopecia

- Raynaud’s (arterial vasospasm in digits of hands and feet in response to cold or emotional stress)

- Vasculitis (majority-cutaneous and small vessel involvement)

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14
Q

What is subacute cutaneous lupus erythematosus?

A

- Multiple skin lesions with reddened raised borders, cenntral clearing, and light scale

  • Present in sun-exposed areas (but not on face)
  • Most patients have mild SLE symptoms
  • Association with Anti-SS-A and Anti-SS-B, and HL-DR3 genotype
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15
Q

What is chronic discoid Lupus Erythematosus?

A

- Discoid rash present on face and scalp (occassionaly wide dissemination)

- Thick scales, atrophy, scarring, edema, erythema

  • Only 5-10% develop multisystem features of SLE after many years
  • 35% ANA+ (anti-dsDNA rare)
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16
Q

What renal involvement is seen in SLE?

A

Lupus Nephritis

- Immune complex-mediated

- High titers anti-dsDNA associated with active renal disease

  • Glomerular tubulointerstitial, and vascular involvement
  • Proteinuria and hematuria in Urinalysis
  • Serum creatinine increased with renal insufficiency
  • Important source of morbidity and mortality
17
Q

What musculoskelatal involvement is seen in SLE?

A
  • *Arthralgias and/or Arthritis**
  • Small joints
  • Symmetric
  • Non-erosive synovitis
  • Swelling and pain
  • *Myopathy**
  • Muscle pain and weakness
18
Q

What neuropsychiatric involvment is seen in SLE?

A
  • *Neurologic**
  • headache
  • SEIZURES
  • cranial/peripheral neuropathy
  • stroke
  • chorea
  • retinopathy (vasculitis)
  • *Psychiatric**
  • PSYCHOSIS
  • Depression
  • Organic brain syndrome

Anti-phospholipid Ab-mediated damage of endothelium (occulsion of small vessels)

Antibodies against synaptic membrane protein

19
Q

What are the most common causes of death in SLE?

A
  • renal failure
  • intercurrent infections
  • coronary artery disease (atherosclerosis)
20
Q

What are characteristics of Drug induced lupus?

A

Fever, arthritis, and serositis (Pleuritis, pericarditis)

–> NO renal or CNS involvment

  • ANA+, but no anti-dsDNA –> anti-histone instead
  • Normal serum complement

–> STOP DRUG, disease resolves