Immunology Flashcards

1
Q

Lymphoma

A

Location: lymph tissue
Increased: mature naive T-cells and B-cells

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2
Q

Multiple myeloma

A

Location: bone marrow
Increased: plasma cells

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3
Q

Myeloproliferative disorders

A

Location: bone marrow
Increased: thrombocytes, erythrocytes, granulocytes, monocytes

Includes CML

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4
Q

Primary lymphoid organs

A

Bone marrow: all immune cells originate here, B-cell maturation

Thymus: T-cell maturation

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5
Q

Secondary lymphoid organs

A

Lymph nodes: site of dendritic cell (bringing the foreign antigen), B-cell and T-cell interaction

Spleen: site of removal of RBCs and AB-coated bacteria, storage of cells (RBCs, lymphocytes, platelets)

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6
Q

Tertiary lymphoid organs

A

Lymph node like ectopic structures that form during chronic inflammation

E.g. in MS, focal TLOs form in the brain which produce anti-myelin antibodies

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7
Q

Mucosa associated lymphoid tissue (MALT)

A

Network of lymphoid tissue distributed in submucosal layers of the GI, genital, respiratory and urinalysis tracts as well as the eyes, skin, thyroid, breasts

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8
Q

Innate immunity

A

Short duration (days)
No memory or recognition of specific antigens
Local and generalised
Cells: macrophages, neutrophils, NK cells

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9
Q

Recognition in innate immunity

A

Macrophages have toll-like receptors (TLRs) that recognise pathogen-associated molecular patterns (PAMPs) on foreign invaders

Response: phagocytosis, cytokine release, interferon release

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10
Q

Cells responsible for phagocytosis

A

Macrophages and neutrophils

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11
Q

Four stages of phagocytosis

A
Attachment e.g. bacterium to macrophage 
Engulfment 
Phagosome formation 
Lysosomal fusion and digestion
Antigen presentation (MHC II)
Secretion of waste products
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12
Q

Cytokines

A
Interleukins 
Colony-stimulating factor
Tumour necrosis factor
Growth factor
Chemokine
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13
Q

Cytokine roles in innate immunity inflammation

A
Activate more macrophages 
Recruiting monocytes 
Recruiting and activating neutrophils 
Recruiting and activating NK cells
Bring opsonins (help macrophages and neutrophils recognise and phagocytosis pathogens)
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14
Q

Interferons

A

Cytokines produced by macrophages, NK cells, endothelial and epithelial cells

  • Block viral entry into cells and block viral replication inside cells (interfere with viruses)
  • Activate macrophages and NK cells
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15
Q

NK functions

A

Spray target with cytokines causing apoptosis

Secrete interferon gamma (IFN-y) which further activates macrophages

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16
Q

C3b role in the complement system

A

Acts as an opsonin for phagocytosis of the attached cells

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17
Q

Specific/adaptive immunity

A
Highly specific 
Slow (days to weeks) with long duration (months to years)
Immune memory 
T helper cells
Production of antibodies
Production of cytotoxic T cells
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18
Q

T cell receptors

A

Recognise antigens with their variable domain

Antigen needs to be presented to them by major histocompatibility complex (MHC) molecules on the surface of other cells

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19
Q

Human form of MHC

A

Human leukocyte antigen (HLA)

Specific variants found in various diseases e.g. HLA B27 in ankylosing spondylitis

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20
Q

Two types of MHC molecules

A

Class 1: present antigens that come from within the cells (i.e. from a virus that is replicating within the cell); recognised exclusively by CD8 T-cells (leads to destruction of the cell)

Class 2: found mostly on dendritic cells, macrophages, monocytes and B-cells; present antigens that come from outside the cell; recognised exclusively by CD4 T-cells (leads to differentiation into T helper cells)

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21
Q

T helper (CD4+) 1 cells

A

Cell mediated immunity
Secrete IL-2: CD4 and CD8 cells
Delayed type (IV) hypersensitivity reaction: travel to site of infection and release cytokines (macrophage recruitment)
Stimulate B cells to produce IgG

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22
Q

T helper (CD4+) 2 cells role

A

Humoral immunity
Stimulate B cells to produce all antibodies but notably more IgE
Travel to site of infection and release cytokines: (mast cell and eosinophil recruitment)
Important in parasitic infections and type 1 hypersensitivity reactions (allergy) and asthma

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23
Q

CD8 cells

A
Have TcRs specific to antigens displayed on MHC class 1 molecules on dendritic cells 
Undergo dramatic proliferation and differentiation into cytotoxic T cells specific to the antigen
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24
Q

Cytotoxic T cell mechanisms

A

Granule exocytosis

Activate Fas molecule (apoptosis)

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25
Q

Antibody heavily secreted in mucous to protect mucous membranes from infection e.g. saliva, breast milk

A

IgA

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26
Q

IgD antibody

A

Found on the surface of B cells

27
Q

IgE antibodies

A

Least abundant in the blood
Important in asthma and allergy
Bound to mast cells and basophils by FcR

28
Q

IgG antibodies

A

Most abundant in the blood
Highly specific
Important in secondary response (second exposure to antigen)
Useful in measuring a patients immunity (vaccine or previous infection)

29
Q

IgM

A

First antibody produced in acute infection
Tends to disappear once the infection is going (unlike IgG)
Most antibodies on B-cells are IgM

30
Q

B cells

A

Sit in lymph nodes, spleen or MALT
IgM surface antibodies recognise specific antigens
Present the antigen on MHC class II molecules
Stimulate T helper cells to release cytokines that activate the B cell
Differentiation into plasma cells or memory B cells (happens in the germinal centre of lymph tissue)

31
Q

Differentiation into plasma cells

A

Make the antibody more specific to the antigen (affinity maturation)
Antibody class switch: chooses whether to produce IgA, IgE, IgG, IgM or IgD e.g. IL-4 promotes IgE class switching
Start to produce vast amounts of antibodies

32
Q

Four functions of antibodies

A

Ab-Ag complexes: Activation of the complement system

Neutralisation of toxin effects

Agglutination (attach to pathogen and clump together to slow the spread)

Act as opsonins

Antibody-dependent cell mediated cytotoxicity (attach to cells and recognised by NK cells, neutrophils, macrophages and eosinophils)

33
Q

Cell mediated immunity

A

Immune response not involving antibodies

Phagocytes, antigen specific cytotoxic T cells, release of cytokines

34
Q

Humoral immunity

A

Immunity mediated by the secretion of antibodies and the complement system

35
Q

Mature B cell marker

A

CD20

36
Q

Target of rituximab

A

CD20

37
Q

Toll like receptor 4 (TLR4)

A

Sense gram-negative lipopolysaccarides

38
Q

Antigen presenting cells

A

Dendritic cells
Macrophages
B cells

39
Q

Mast cells

A

Involved in anaphylaxis and asthma

IgE binds to the allergen, which binds to mast cells, causes them to release histamines

40
Q

Type I hypersensitivity reaction

A

Anaphylaxis
Atopy (e.g. asthma, eczema, hay fever)

IgE mediated:
CD4+ cells recognise allergen 
T helper 2 cells release IL-4 which stimulates IgE production by B cells 
IgE binds to mast cells and basophils 
Degranulation: histamine and TNF-a
41
Q

Type 2 hypersensitivity reaction

A

Autoimmune haemolytic anaemia
Goodpastures syndrome
Pernicious anaemia
Rheumatic fever

IgG and IgM binds to self antigens on cell surface leading to damage

42
Q

Type 3 hypersensitivity reaction

A

Systemic lupus erythematous (SLE)
Post streptococcal glomerulonephritis
Rheumatoid arthritis (RF = IgM that recognises IgG as an antigen)

Antibody-Antigen complexes deposited in tissues
Activate complement system and cause inflammation

43
Q

Type 4 hypersensitivity reaction

A

TB
Multiple sclerosis
Guillain-Barré syndrome

Delayed type (24-72 hours)
T helper 1 cells activated by dendritic cell
T helper cells travel to site
Macrophage recruitment and cytokine release

44
Q

First line treatment for anaphylaxis

A

ABCDE

IM adrenaline

45
Q

Four examples of live attenuated vaccines

A

Contain a weakened version of the virus (avoid in immunosuppressed patients)

MMR
BCG (TB)
Shingles (varicella zoster)
Nasal influenza vaccine

46
Q

Passive immunity

A

Antibodies introduced from outside the body

Takes effect immediately
Short term

Maternal (passed from mother to child through breast milk or the placenta)
Injected antibodies

47
Q

Active immunity

A

Antibodies produced inside the body

Takes effect over time (several weeks)
Long term

Direct infection (natural active) 
Vaccination (artificial active)
48
Q

HLA DR4

A

T1DM
Rheumatoid arthritis

‘HLA DIABETES RHEUMATOID 4’

49
Q

Macrophage cell surface markers

A

CD14

CD40

50
Q

Cytokine primarily responsible for activating macrophages

A

INF-y

51
Q

Key cytokine in type 1 hypersensitivity

A
IL-4 
Causes class switching to IgE
52
Q

Markers of disease progression in HIV+ patients

A

CD4 cell count (HIV uses CD4 to enter CD4+ cells)
AIDS: <200

HIV viral load

53
Q

Name 3 risk groups for HIV

A

Men who have sex with men
Intravenous drug users
Commercial sex workers

54
Q

Age group for which 50% of all new HIV infections occur worldwide

A

19-24 years old

55
Q

Different types of polymorphonuclear leukocytes

A

Neutrophils (most abundant)
Basophil
Eosinophil

56
Q

Fever, rash and non-specific symptoms

A

Ask about sexual history

Think of HIV seroconversion

57
Q

Most common opportunistic infection in HIV

A

PCP

58
Q

Treatment of HIV

A
Antiretroviral treatment (ART) 
HAART
59
Q

CA-125 biomarker

A

Ovarian cancer

60
Q

CA 19-9 biomarker

A

Pancreatic cancer

61
Q

HER-2 biomarker

A

Breast cancer

62
Q

Lifecycle of malaria parasite

A

Sporozoites introduced by a mosquito bite > migrate to the liver > multiply into thousands of merozoites > merozoites infect red blood cells and replicate > parasites form gametocytes, which are taken up by a mosquito, continuing the life cycle

63
Q

Malaria causative microorganism

A

Plasmodium species

Many of the symptoms associated with severe malaria are caused by the tendency of P. falciparum to bind to blood vessel walls and cause damage