week 1-5 Flashcards

1
Q

What cells are the first responders to infection

A

Myeloid cells

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2
Q

first line of defence?

A

innate immune cells

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3
Q

Cellular Bridge btw innate and Adaptive immunity?

A

APCs- Antigen presenting cells
(DCs, B-cells, mf)

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4
Q

——— is the process by which Hematopoietic stem cells (HSC) differentiate into mature RBCs (and leukocytes)

A

Hematopoiesis

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5
Q

HSCs are directed to differentiate into two major types of progenitors ———— or ——— progenitor cell

A

HSCs are directed to differentiate into two major types of progenitors lymphoid progenitor cell or myeloid progenitor cell

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6
Q

Failure of Hematopoietic regulatory mechanisms can have seroious consequences such as?

A

Leukemia

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7
Q

Myeloid progenitor cells diffrentiate into?

A

mf, DCs, neutrophils, Basophils, Monocytes, Mast cells, WBCs, RBCs

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8
Q

Lymphoid Progenitor cells diffrentiate into?

A

T-cells, B-cells, NK cells and DCs

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9
Q

Fxn of Myeloid cells

A

1) detection of pathogens via PRRs
2) phagocytosis
3) escalate imune responses through cytokine and chemokine secretion

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10
Q

——– presence in tissue indicates an active immune response

A

Granulocytes (neurtorphils, eosinophil, basophils, mast cells)

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11
Q

Provide the major defense against pus-forming (pyogenic) bacteria such as streptococci and staphylococci and fungi?

A

Neutrophils

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12
Q

cells that make up APCs ?

A

DCs , macrophages, B-cells, monocytes

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13
Q

fxn of APCs

A

part of the first line defence against pathogens
* Act as cellular bridges btw innate and Adaptive immunity

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14
Q

fxn of Macrophages

A

Regulation of the immune response through production of pro-inflammatory (IL-1, TNF, IL-6) and anti-inflammatory (TGFβ, ΙL-10) cytokines

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15
Q

Pro -inflammatory cytokines

A

IL-1, TNF, IL-6

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16
Q

Anti-inflammatory Cytokines

A

TGFβ, ΙL-10

17
Q

Mutation in signaling molecules affecting TLRs will cause?

A

Recurrent, severe bacterial infections (pneumonia)

18
Q

Gain of function mutations in inflammasome will cause?

A

1)Gout
2)Atherosclerosis
3)Type II diabetes
4)Familial Mediterranean Fever (FMF)

19
Q

NOD2 mutations are associated with enhanced susceptibility to ———-

A

Crohn’s disease

20
Q

IL-12 and IFN-γ receptor deficiency will cause?

A

Increased susceptibility to intracellular infections (mycobacterium tuberculosis)

21
Q

Fxn of IL-8

A

neutrophil chemoatractant

22
Q

———— are released by the liver in resposne to inflammation?

A

Acute-phase proteins are released by the liver in response to inflammation (IL-6, TNF, IL-1β pro-inflammatory cytokines)

23
Q

examples of acute-phase proteins released by the liver

A

CRPs, MBL

24
Q

Cytokines that maintain granuloma

A

IFN-γ (produced by the activation of Th cells)

* Also maintains macrophage activation

25
Q

Cytokine that aids the formation of granulomas

A

TNF

26
Q

why is IL-2 given to AIDS patients in combo w/ antiretrovirals

A

To restore the decreased levels of CD4+ T cells

27
Q

Fxn of IL-12

A

1) Promotes the development of CD4+ T cells
2) induces the production of IFN-γ (by activating TH cells)

* Pro-inflammatory cytokine

28
Q

—- inhibitis Th and Tc activation

A

anti-CD25 (Ab against IL-2 receptor)

CD25–> IL-12

29
Q

State the difference in fxn btw granulation tissue and Granulomas

A
  • Granulation tissue : part of the repair response, fxn -> healing of injured tissue
  • Granuloms : a form of chronic inflammation, fxn –> phgocytosis
30
Q

Histology of Granulation tissue

A

1) Newly formed blood vessles (angiogenesis)
2) Fibroblasts
3) mononuclear cells in extracelluar matrix
(does not surround an indigestible particle like granulomas)

31
Q

Histology of Granulomas

A

1) Macrophages (circumsrcibed aggregates of epithelioid cells)
2) surrounded by lymphocytes
3) Giant cells and dead material

32
Q

Which of the following is a caseating granuloma ; TB or Sarcoidosis

A

TB

33
Q

patines w/ severly reduced C3 levels tend to have?

A

increased numbers of sever Bacterial infection

34
Q

Diganosis: -
- low CD4+ levels on flow Cytometry
- normal levels of CD8+ cells and B cells
- Hypogammaglobulinemia

  • Presenting symtpoms: numerous, severe infections requiring IV antibiotic, diarrhea and oral candidiasis

disroder?

A

Bare lymphocyte syndrome type 2 aka MHC class II deficiency

  • Lack of MHC II due to mutations of regulators of MHC-II transcription (CIITA, RFXANK, RFX5, RFXAP)
  • Epi: death at around 4 yrs

* similar diganosis to SCID

35
Q

Clues in the diagnosis of SCID

A

1) presents in first few weeks/months of life
2) Infections are often viral/ fungal rather than bacterial
3) Chronic diarrheais common (“Gastroenteritis”)
4) Repiratory infections and oral thrush are common
5) faliure to thrive
6) Lymphopenia (low WBCs)

36
Q

Diagnosis:
- low CD8+ levels
- Activated NK cells
- normal CD4+ levels
- normal antibody production

Presenting symptoms:
- characteristic mark “necrotizing skin lesions” on the extremities and midface
- Frequent, Bacterial infections of the upper respiratory tract

diagnosis?

A

Βare lymphocyte syndrome type 1: MHC class I deficiency

cause: lack of expression of TAP1 and TAP2

37
Q

Cause of Βare lymphocyte syndrome type 1: MHC class I deficiency

A

lack of expression of TAP1 and TAP2