T1 Immune Dysfunction Flashcards

1
Q

Define hypersensitivity

A

Immune system occurs when the normal immune mechanisims produce an exaggerated response to an antigen, or an inappropriate response to self-antigens.

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2
Q

Define alloimmunity

A

Alloimmunity is a type of delayed hypersensitivity (type IV) reaction cause by a reaction of immune system to antigens on transplanted cells from the same species.

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3
Q

Define autoimmune disorder

A

Disease occurrs with the loss of the immune systems ability to distinguish self from non-self.

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4
Q

Define immunodeficiency

A

Is the state where the immune system is unable to response appropriately because apart of the system is defective, missing or has been compromised by disease.

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5
Q

Define B and T cells

A

B cells: responsible for humoral immunity

T cells: are involved in cell-mediated immunity.

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6
Q

Define Plasma cell

A

B lymphocytes which have been turned into plasma cells. Which are antibody producing factories.

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7
Q

Describe the four types of hypersensitivity disorders.

A

ABCD

  1. Allergic anaphylaxis and atropy
  2. Cytotoxic (antiBody)
  3. Complex mediated (immune Complex)
  4. Cell mediated (Delayed)
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8
Q

Explain the function of different types of cells involved in humoral and cell-mediated immunity

A

Macrophages: detection, phagocytosis and destruction of bacteria
NK cells: cytotoxic contain proteins such as perforin and proteases in their cytoplasm
Cytotoxic T-lymphocytes: bind infected cells and induce apoptosis

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9
Q

Explain how B and T cells of the adapted immune system become activated in response to an antigen.

A

ResearchMHC Proteins?

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10
Q

Compare the difference between the primary and secondary humoral response

A

Primary: several days to produce antibodies and they are rarely enough.

Secondary humoral response: Only takes several hours to evoke a response and produces massive amounts of antibodies

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11
Q

Contrast the difference between natural and acquired immunity

A

Naturally acquired - Active: infection contact with a pathogen.
Passive: antibodies pass from moth to fetus via placenta or via breast milk.
Artificially acquired - Active: Vaccine; dead or attenuated pathogen. Passive: Injection of immune serum.

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12
Q

Provide examples of active and passive ways of acquiring immunity. (natural and acquired immunity).

A

Naturally acquired - Active: Flu, contact with pathogen via droplet.
Passive: Placental transfer of IgG from other to fetus during pregnancy.
Artificially acquired - Active: Immunisations
Passive: Antivenom from a snake transferred to a humam

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13
Q

Providing an example of each, describe the four types of hypersensitivity disorders.

A

Type I - allergic response: histamin
Type II - Hemolytic diease of a new born, allergy to anaesthetics
Type III Immune complex: Rheumatoid arthritis

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14
Q

What is an auto immune disease?

A

Loss of the immune systems ability to distinguish self from non-self.

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15
Q

How does adrenaline reduce the signs and symptoms in patients suffering from anaphylactic shock?

A

Epipen = epinephrine. Adrenaline decreases ↑ vascular permeability and the vasodilation that occurs during anaphylaxis.
Adrenaline activates receptors in lings whihc relax bronchial smooth muscle. thereby relieving bronchospasm, increasing vital capacity.

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16
Q

Contrast between primary and secondary immunodeficiencies.

A

Primary immunodeficiencies - genetic

Secondary immunodeficiencies - acquired extrinsicly.

17
Q

Outline the pathogenesis of HIV infection to the development of AIDS. In your answer be sure to include the critical cellular changes that occur following HIV infection

A
  1. Acute HIV infection
  2. Chronic HIV infection
  3. Acquired immunodeficiency syndrome (AIDS).

HIV is a RNA virus, AIDS is a condition cause from chronic overuse of antiviral medications. HIV targets helper T (Th) cells, Other cells
bearing CD41 receptors, such as macrophages and dendritic
cells, also become infected by HIV. Attachment to the CD41
receptor and a co-receptor of the integral membrane protein
family, called C-chemokine receptor 5 (CCR5), is the means by
which the virus infects cells.
After infection, cellular and humoral immune processes
become progressively weakened, leaving the affected person
vulnerable to opportunistic infections,