6.7 Response to infection

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What is a pathogen?

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1

What is a pathogen?

Organisms cause harm by invading and destroying host tissues and producing toxins

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2

What are examples of pathogens?

  • Lamda phage

  • RNA viruses

  • TMV

  • Ebola

  • Staphylococcus Aureus

  • Stem rust fungus

  • Myobacterium

  • Influenza

  • Plasmodium

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3

What are some barriers to non-specific infection?

  • Skin

  • Blood clotting

  • Stomach acid

  • Mucus and cilia

  • Antibacterial chemicals in sweat and tears

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4

Skin

Physical and waterproof (keratin)

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5

Blood clotting

Quick seal any breaks in skin

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6

Stomach acid

Destroys ingested pathogens

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7

Mucus and cilia

Trap + remove pathogens

Cilia waft mucus to stomach

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8

Antibacterial chems

Lysozymes (digestive enzymes) found in sweat and tears

Kill bacteria

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9

What are eosinophils

Parasitic function

Regulate allergic responses

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10

What are monocytes?

Type of phagocytic cell

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11

Macrophages

  • Phagocytic cells

  • Kidney chased nucleus

  • Mature from monocytes

  • Produced in bone marrow

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12

Macrophage function

Engulf foreign cells, particles and infectious agents

Process them + present to lymphocytes

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13

What cells are found in bone marrow?

WBCs and RBCs

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14

Neutrophils

  • Phagocytic

  • lobed nucleus

  • Short live, large quant in bone marrow

  • Found in all tissues at site of injury

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15

Neutrophil function

Engulf and destroy foreign cells, particles and infectious agents by phagocytosis

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16

Lymphocytes

  • Non phagocytic cells

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17

What do lymphocytes do?

Mature in bone marrow B for bone

or migrate to and mature in thymus gland T for thymus gland

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18

Lymphocytes function

  • Differentiate into many different types of cells

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19

Lymphocytes functions

  • Killing infected cells

  • Producing antibodies = providing immunity

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20

Outline non-specific immune response

  • Offers protection against all pathogens encountered without any specificity

  • Lacks immunological mem, so rs are at same each time patho is encountered

  • Quicker than specific I r

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21

What components of non-s defences are always present?

Barriers to infection - phagocytic less

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22

How is non specific i r activated?

Histamine, complement and interferons

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23

Where is histamine found?

Amine stored in granules of basophils

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24

What happens when histamine is released from its granules?

Histamine = arterioles dilate + increase in permeability of capillaries

= plasma, leukocytes + blood plasma, proteins leak from bloodstream

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25

Where do they leak from the bloodstream to?

Vessel walls + migrate to site of tissue injury of infection

Fight infection and help heal injured tissue

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26

What is apoptosis?

Cell death

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27

Complement

Complex system of more than 30 proteins

Eliminate infectious microorganisms

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28

Where are the complement proteins produced?

Liver

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29

What activates the complement?

Histamine

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30

What happens to complement once activated?

Proteins = lysis of foreign and infected cells

Phagocytes of foreign particles, cell debris + inflammatory of surround tiss

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31

What are interferons?

  • Group of proteins released by nucleus in response to presence of viruses

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32

What do interferons do?

Virus infected cell will release interferons

= nearby cells heighten anti-viral defences

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33

Are interferons cytokine?

Yes, used for communication bet cells to = protective defences of immune s

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34

What is cytokine?

Cell signalling molecule

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35

What do interferons do?

Infected cells = apoptosis = make infected cells = more obvs to killer cells = production of anti-viral enzymes in nearby cells

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36

What are the anti-viral enzymes called?

Ribonuclease

Protein kinase

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37

What are pseudopodia?

Fake feet

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38

What type of reaction is digestion?

Hydrolysis as it requires water

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39

Process of phagocytosis

  1. Phagocyte extends its cell surf mem (forming pseudopodia) + pathogen

  2. Cell surf mem meets + fuses = phagocytic vesicle

  3. Lysosomes (containing lysozyme) move to + fuse w phagocytic vesicles

  4. Hydrolytic enzymes from lysosomes digest pathogens

  5. Products of digestion absorbed by cell

  6. Undigested material is released by exocytosis

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40

What can be antigens?

Glycoprotein, glycolipid and protein

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41

What are antigens

Mols, usually on surface of a cell = immune r

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42

How does a cell surface identify antigens?

Each cell has specific antigens on its surface

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43

What do antigens enable immune s to do?

identify

  • pathogens

  • Cells from other organisms of same species

  • Abnormal body cells (infected or cancerous cells)

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44

What is antigen variability?

Change antigens through mutation

= immunity + disease protection diffi

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45

Would an MHC be similiar to family members

Yes

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46

What does MHC stand for

Major histocompatibility complex

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47

What is MHC

Collection of glycoproteins on surf of cell that identifies it as self

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48

Why is MHC unique to individual

Gen determined and inherited f

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49

Where are genes for MHC found

Found on chromosome 6

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50

What is role of MHC?

  • prevents immune s attacking its own cells

  • Used in antigen presentation

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51

What do lymphocytes have antigen receptors that can…

  • recognise MHC antigens

  • Differentiate bet these + foreign antigens

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52
<p>(A) (I) For antibody A, compare increase in mean level after vaccination with mean level after infection of <em>Bortella pertussis</em></p><p>B) (I) Explain the changes in mean level of antibody A after infection with Bordtella pertussis </p><p>B (ii) Suggest why antibody B was not present in blood of these rats until after infection with Bordetella pertussis </p><p>C) Comment on reliability </p>

(A) (I) For antibody A, compare increase in mean level after vaccination with mean level after infection of Bortella pertussis

B) (I) Explain the changes in mean level of antibody A after infection with Bordtella pertussis

B (ii) Suggest why antibody B was not present in blood of these rats until after infection with Bordetella pertussis

C) Comment on reliability

(A) Levels of antibody rise sooner higher and faster after infection

(A) (I) sec I. R memory cells, 2nd exposure mem cells stimulated, sec r antibodies produced from plasma cells

B I) antibodies present if antigen is present antigen is not present in vaccine

C) no error bars, no control variables, stats analysis

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