Autoimmune Dx Flashcards

(49 cards)

1
Q

What are the different types of autoimmune diseases students should identify?

A

Organ-specific and systemic autoimmune diseases.

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2
Q

What are common symptoms students should recognize in autoimmune diseases?

A

The most common symptoms evident in each autoimmune disease.

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3
Q

What is autoimmunity?

A

A breakdown in self-tolerance leading to the immune system responding to self-molecules as if they were foreign.

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4
Q

What triggers the autoimmune response?

A

Sequestered antigens, foreign antigens, altered antigens, mutation of immunocompetent cells, and dysfunction of T cells.

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5
Q

What occurs in autoimmune diseases?

A

An individual produces antibody or T cell response to his/her own antigens, resulting in a loss of self-tolerance.

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6
Q

What are the mechanisms involved in autoimmune diseases?

A

Antibody-cell surface component interaction, formation of autoantigen-autoantibody complexes, sensitization of T cells, and genetic factors.

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7
Q

What is Hashimoto’s disease?

A

An organ-specific autoimmune disease where humoral and cellular immunity lead to the destruction of normal thyroid tissue, causing hypothyroidism.

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8
Q

What antibodies are detected in Hashimoto’s disease?

A

Antithyroid antibodies including antithyroglobulin, antithyroid peroxidase, and second colloid antigen.

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9
Q

What characterizes Graves’ disease?

A

Hyperplasia and diffuse goiter caused by an autoantibody reacting with thyroid receptors, overstimulating the thyroid gland.

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10
Q

What results from the overstimulation in Graves’ disease?

A

Thyrotoxicosis, with elevated free and total T3 and T4, and decreased TSH.

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11
Q

What are common findings in Graves’ disease?

A

Exophthalmos and infiltrative dermopathy, including pretibial myxedema.

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12
Q

What is Myasthenia Gravis?

A

A neuromuscular disease in which the nerve muscles do not function normally. Most patients exhibit antibodies to acetylcholine receptors that block nerve impulses and can damage neurons.

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13
Q

What is Multiple Sclerosis?

A

A chronic progressive inflammatory disease characterized by demyelination of the nerves. Studies suggest certain viruses, especially Epstein-Barr virus and human herpes virus 6, are associated with MS.

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14
Q

What are the laboratory findings in Multiple Sclerosis?

A

Active lesions contain CTLs, T helper cells, and macrophages. Most patients have increased IgG concentrations in the cerebrospinal fluid (CSF).

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15
Q

What does the IgG index indicate?

A

It differentiates true increases in IgG production from increases due to blood-brain barrier permeability.

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16
Q

What are the laboratory findings in Sjogren Syndrome?

A

Findings include polyclonal hypergammaglobulinemia, autoantibodies against the salivary glands, positive RF, ANA (speckled or diffuse pattern), anti-SSA, and anti-SSB.

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17
Q

What is Pernicious Anemia?

A

A condition associated with autoimmune processes affecting the absorption of vitamin B12, leading to anemia.

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18
Q

What are Oligoclonal Bands in CSF?

A

They are indicative of Multiple Sclerosis but can also appear in other conditions like SLE, viral meningitis, and neurosyphilis.

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19
Q

What is Autoimmune Rheumatoid Arthritis?

A

A chronic, noninfectious, systemic inflammatory disease primarily affecting women, characterized by abnormal circulating IgM autoantibodies known as rheumatoid factor (RF).

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20
Q

What are the symptoms of Autoimmune Rheumatoid Arthritis?

A

Symptoms include fatigue, weight loss, weakness, mild fever, anorexia, morning stiffness, joint pain (improves during the day), vasculitis, and rheumatoid nodules.

21
Q

What causes Type 1 Diabetes Mellitus?

A

Islet cell destruction in the pancreas results in insulin-dependent diabetes. Autoantibodies and CTLs react against pancreatic beta cells, causing insulin deficiency.

22
Q

What viruses can trigger Type 1 Diabetes Mellitus?

A

Viruses like mumps, measles, rubella, Coxsackie B virus, and infectious mononucleosis can trigger autoantibody production leading to new cases of diabetes.

23
Q

What is the role of HLA-DQ1.2 and HLA-DR2 in Type 1 Diabetes?

A

These HLA types decrease the risk of developing diabetes.

24
Q

What is the pathophysiology of Sjogren Syndrome?

A

It involves the production of IgG or IgM antibodies against IgG in the synovium, leading to immune complex formation, complement activation, and tissue destruction.

25
What are the laboratory diagnosis indicators for autoimmune diseases?
Elevated erythrocytic sedimentation rate (ESR), elevated CRP, positive RF, cryoglobulins, and sometimes ANAs. Synovial fluid is cloudy, with a WBC count between 5000 and 20,000/uL, elevated protein, poor mucin clot development, and decreased complement.
26
What characterizes polymyositis?
Characterized by inflammation and degeneration of muscle tissue. ## Footnote Autoantibodies include Antinuclear antibodies (ANA), RF, and anti-Jo-1 antibodies.
27
What is Systemic Lupus Erythematosus (SLE)?
A chronic, noninfectious inflammatory disease involving many organs, characterized by the presence of circulating immune complexes.
28
What causes tissue injury in SLE?
Tissue injury is caused by autoantibodies and immune complexes deposited in the tissues. Depressed suppressor T cell function allows the production of antibodies against the 'self.'
29
Who is more likely to develop SLE?
The disease is more likely to occur in women than men and in blacks than whites.
30
What are common symptoms of SLE?
Fever, weight loss, malaise, weakness, arthritis, skin lesions, photosensitivity, butterfly rash, renal disease, pericarditis, seizures, ocular changes, pancreatitis, and small-vessel vasculitis.
31
What are the techniques used to detect ANA?
1. Immunohistochemistry: Human epithelial cells are used as substrate cells. HRP binds to any ANA that has bound to the nuclei of the cells. 2. Fluorescent antinuclear antibody test (FANA): An indirect immunofluorescence technique used for ANA screening.
32
What is the interpretation of FANA results?
Results can be interpreted as diffuse or homogenous, speckled, nucleolar, or centromere.
33
What causes SLE?
SLE may be idiopathic or drug-induced.
34
What is the pathophysiology of SLE?
Antibodies to native or altered self-antigens are produced and form circulating immune complexes with the antigens, typically involving DNA. These complexes are deposited in various organs and cause inflammation, leading to tissue injury.
35
What are the diagnostic tests for SLE?
ANA testing, which includes Antinuclear antibodies (ANAs), Anti-ds DNA, Anti-ss DNA, Anti-RNA, Anti-extractable nuclear antigen, and Anti-Smith antigen.
36
What is the LE cell test?
The LE cell test detects the presence of LE factor/ANA in a patient's serum, which interacts with leukocyte nuclear material to form LE bodies that attract phagocytic cells.
37
What is the principle behind the LE cell phenomenon?
The patient's serum containing LE factor/ANA is directed towards the nuclear material of leukocytes, transforming it into an LE body that is ingested by phagocytic cells.
38
What is the LE Latex agglutination test?
The LE Latex agglutination test is based on the agglutination reaction between latex particles coated with DNP and serum containing antinuclear antibodies, where agglutination indicates a positive reaction.
39
What is autoimmune hemolytic anemia?
Autoimmune hemolytic anemia is characterized by an increased rate of RBC destruction, resulting in normocytic, normochromic anemia.
40
What are the laboratory findings in autoimmune hemolytic anemia?
Laboratory findings include a positive direct antiglobulin test and sometimes the presence of cold agglutinins.
41
What is the role of autoantibodies in autoimmune hemolytic anemia?
In autoimmune hemolytic anemia, autoantibodies are directed against RBC antigens.
42
HLA allele associated with high risk of Myasthenia Gravis
HLA-B8
43
HLA Allele Associated with high risk of developing Type 1 DM
HLA-DR3 and HLA-DR4
44
HLA Alleles associated with decreased risk of having Type 1 DM
HLA-DQ1.2 and HLA-DR2
45
HLA Allele associated with high risk of developing Scleroderma
HLA-DR3
46
Medication for Hashimoto’s Disease
Levothyroxine
47
Type of B12 deficiency anemian caused by the body’s inability to absorb vitamin B12 properly. An autoimmune disorder that primarily results from the destruction of gastric parietal cells, leading to a deficiency in intrinsic factor, which is essential for vitamin B12 absorption in the terminal ileum
Pernicious Anemia
48
Characterized by inflammation and degeneration of skeletal muscles
Polymyositis
49
A chronic autoimmune connective tissue disorder characterized by excessive fibrosis of the skin and internal organs die to abnormal collagen deposition
Scleroderma