Lecture 17- Immune System Flashcards

1
Q

Phagocytes

A

destroy pathogens by engulfing them, acidifying the phagolysosome and digesting the contents.

When phagocytes cannot ingest their targets, they may release chemicals that are lethal to pathoge

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2
Q

Natural killer cells

A

function like T lymphocytes but are part of innate immunity.

They lyse and kill cancer cells and virus-infected cells before the adaptive immune response is activated.

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3
Q

Inflammation

A

Occurs when body tissues are injured

Limits the spread of damage, disposes of debris and pathogens, alerts the adaptive immune system, and sets up repair.

four main signs of acute inflammation are:
redness
heat
swelling
pain.

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4
Q

Pro inflammatory chemicals

A

Causes vasodilation and increased capillary permeability

Allows fluid containing clotting factors and antibodies to enter the tissues followed by neutrophils and macrophages

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5
Q

Antimicrobial proteins

A

Enhance innate defences by attacking microorganisms directly or by hindering their ability to reproduce

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6
Q

Interferons (IFNs)

A

small proteins produces by virus infected cells that help protect surrounding heathy cells by telling the tot make proteins that interfere with viral replication

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7
Q

Complement cascade

A

Group of plasma proteins that Can assemble a membrane attack complex to kill a cell by punching a hole int he plasma membrane, making the cell leak

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8
Q

Microbe associated molecular patterns

A

Often indicate something is trying to infect yo

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9
Q

Adaptive defences

A

Recognize and destroy the specific antigen that initiated the response

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10
Q

What does Adaptive immune response include?

A

Systemic response
Has memory
Includes both cellular immunity and humoral immunity

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11
Q

Cellular immunity

A

Based on direct attack of microorganisms by T lymphocytes and has living cells as its protective factor

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12
Q

Humoral immunity

A

Provided by antibodies present int he body’s “humours” or fluids produced by B lymphocytes

Antibodies are proteins that target and bind to extracellular antigens.

Clonal expansion ( mitosis) develops clones into plasma cells and the remaining cells into memory B cells.

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13
Q

Clonal selection

A

Antigen binding with a particular lymphocyte selects that lymphocyte for further development

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14
Q

Colonal expansion

A

producing a group of cells with an identical ability to bind this antigen.

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15
Q

Effector cells

A

actively fight the infection.

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16
Q

Memory cells

A

Respond quickly to future encounters with this antigen

17
Q

Antigen presenting cells (APCs)

A

phagocytose pathogens and present antigen fragments in major histocompatibility complex II (MHC II) molecules on their surfaces, where they can activate T cells.

18
Q

Dendritic cells

A

Located near external body surfaces (skin) phagocytose antigens and migrate to lymphoid organs to present antigens to T cells

19
Q

Macrophages

A

Found in lymphoid organs and connective tissues and present antigens to T cells

20
Q

B lymphocytes

A

Present antigens to T cells in order to become more fully activates B cells

21
Q

What are the two major groups of T cells based on cluster of differentiation?

A

CD4+ cells

CD8+ cells

22
Q

CD4+ cells

A

Helper T cells that activate B cells, T cells and macrophages, some are regulatory T cells hat inhibit overly aggressive responses

Activated by Class II MHC ( 2 X 4 = 8)

23
Q

CD8+ cells

A

Cytotoxic T lymphocytes that destroy cells or foreign substances

Activated by Class I MHC ( 1 X 8 = 8)

24
Q

Class I MHCs

A

found on all body cells except RBCs and display antigens synthesized from within the cell

if infected, may also include fragments of foreign antigens.

If cells mutate so they no longer produce MHC I, they will be destroyed by NK cells.

25
Q

Class II MHCs

A

only on antigen-presenting cells (dendritic cells, macrophages and B cells) and display antigen fragments from phagocytosis.

26
Q

Helper T cells

A

TH1cells- work with macrophages and CD8+ cytotoxic T lymphocytes to activate cell-mediated immune responses against intracellular threats.

TH2 cells- work with B cells, eosinophils and mast cells to stimulate B cell proliferation and increase antibody production against extracellular threats.

27
Q

What are the ways antibodies help fight off infection?

A

Neutralization

Opsonization

Complement fixation and activation

28
Q

Neutralization

A

occurs when antibodies block specific sites on viruses or toxins, causing them to lose their infectious or toxic effects.

29
Q

Opsonization

A

occurs when antibodies stick to antigens and make it easier for phagocytes to engulf pathogens.

30
Q

Complement fixation and activation

A

occur when complement proteins bind to antibodies attached to antigens and lead to lysis of the cell.

31
Q

Primary immune response

A

occurs on first exposure to a particular antigen, with a lag time of about 3-6 days.

The antibody titre in the blood rises, peaking in about 10 days, and then declines.

32
Q

Secondary immune response

A

occurs when someone is exposed to the same antigen for a second time.

Mobilization of B cells takes only a few hours and rises to a much higher peak concentration after only 2-3 days, producing antibodies with a higher binding affinity for the antigen, and can persist for weeks or months.