L6_Immunodeficiency & Infection Flashcards

1
Q

What is the difference between primary and secondary immunodeficiency?

A
  • primary = an inherited developmental or genetic defect affecting the immune system.
  • secondary = the loss of the immune function that results from exposure to external agents.
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2
Q

Define severe combined immunodeficiency (SCID).

A
  • genetic defect causing dysfunctional or attenuated T cell and B cell function in the peripheral blood.
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3
Q

What causes SCID?

A
  • a mutation in the genes transcribing the cytokines released by the cells or a mutation in the cytokine receptors.
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4
Q

What is the most common cause of SCID?

A
  • IL-2 receptor defect.

- most commonly in the gamma chain of the IL-2 receptor.

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5
Q

Which three cell types would be affected in an IL-2 receptor defect caused by a genetic mutation?

A
  • T cells, B cells and NK cells.
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6
Q

What can delayed umbilical cord separation lead to?

A
  • neutrophil adhesion defect.
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7
Q

Why is family history significant in immunodeficiency investigations?

A
  • bc history of early infant death is linked with ID.
  • consanguinity is also linked with ID.
  • ID can be x-linked inherited.
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8
Q

What is the most common cause of acquired immune deficiency?

A
  • HIV.
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9
Q

What test is used to detect the presence of antibodies directed against proteins of HIV-1?

A
  • ELISA.
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10
Q

Which test is used to detect the presence of antibodies directed against protein of HIV-1 in infants? And why?

A
  • PCR.
  • Bc the maternal antibody still lingers in the infants blood which may confuse diagnosis.
  • to prevent this, the actual viral particles will be detected using PCR.
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11
Q

Name 4 features of AIDS?

A
  • HIV high viral load in blood.
  • CD4 cells <200 cells / microL of blood.
  • impaired/delayed-type hypersensitivity reaction.
  • occurrence of OI.
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