Immunodeficiency Flashcards

1
Q

Name 3 mechanisms by which antibodies bind to antigens to enhance phagocytosis

A

Neutralisation
Agglutination
Precipitation

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2
Q

Name the mechanism direceted by antibodies that enables cell lysis

A

Activation of complement system

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3
Q

How to cytotoxic T cells act?

A

Bind to infected cells and perforin makes holes in infected cell’s membrane and enzyme enters. Infected cell is destroyed.

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4
Q

What are the cytokines released by innate cells that direct the immune system to carry out more appropriate response

A

Pathogen associated molecular patterns (PAMP) e.g. directs T cells to develop into Th1, Th2 or Treg

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5
Q

Primary immunodeficiencies

A

Genetic defect in component of immune system

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6
Q

Secondary immunodeficiencies

A

Secondary to the effects of external factors

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7
Q

IRAK4 deficiency -PRR activation defect

A

TLRs become activated and trigger a cascade of cytokine release- IRAK is essential in the production of an inflmmatory response- as adaptive immune system develops, other pathways offer protection-most severe in early life.

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8
Q

Chronic granulomatous disease

A

Defect in phagocytosis affecting primarily males. AR. Neutrophils are unable activate proteolytic enzymes in phagosome. Defect in NADPH-oxidase complex-transports H+ across phagosome membrane.

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9
Q

Diagnosis of chronic granulomatous disease

A

Nitroblue tetrazolium test- normally neutrophils release oxygen radicals which converts blue dye to black. Defect = no chance in colour

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10
Q

Clinical presentation of CGD

A

Osteomyelitis, pneumonia, swollen lymph nodes, ginigivitis-gum disease, non malignant granuloma, inflammatory bowel disease

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11
Q

Which complement pathways activate C5 to form pores in bacterial cell wall?

A

All 3

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12
Q

Diagnosis of complement deficiency

A

Sheep RBCs incubated in patient’s serum-in competent terminal pathway- lysis of RBCs.

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13
Q

Clinical presentation of complement deficiency

A

Meningococcal infections

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14
Q

Treatment for people with complement deficiencies

A

Vaccines for meningococcal e.g. penicillin prophylaxis

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15
Q

X linked agammaglobinaemia

A

Defect in B cells- antibody deficiency. Recurrent bacterial infections e.g. sino pulmonary infections. Usually diagnosed 1-2 yr, since maternal IgG protects.

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16
Q

Treatment for X linked agammaglobinaemia

A

Treat with antibodies, then IgG for life

17
Q

Sever combined immunodeficiency (SCID)

A

Absent/reduced T cells and reduced B cells. Usually more severe than B cell defects, as B cells also need T cell help.

18
Q

Clinical presentation of SCID

A

Recurrent infections with opportunistic infections

19
Q

Treatment for SCID

A

Bone marrow transplant, gene therapy

20
Q

Infections caused in PRR activation defects

A

Pneumococcus, HSV

21
Q

Infections caused in phagocyte defects

A

CGD, staphylococcus aspergicillus

22
Q

Infections caused in complement defects

A

Meningococcus

23
Q

Infections caused in B cell defects

A

Recurrent sino-pulmonary infections

24
Q

Infections caused in T cell defects

A

SCID, opportunistic infections