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Defense Against Infections Disease Topic 11.1 (and 6.3)

Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

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Page 1: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Defense Against Infections Disease

Topic 11.1 (and 6.3)

Page 2: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood ClottingWhen blood vessels get broken, blood is able

to escape from the closed circulatory system and pathogens have a way to enter the body.

To prevent excessive blood loss and the entry of pathogens, a clot will form to seal the damaged blood vessels.

Page 3: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood ClottingThere are a few components in your blood

that are important for blood clotting:

1)Prothrombin and Fibrinogen These are plasma proteins Always present in blood but inactive unless

you start to bleed

Page 4: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood Clotting

2. Platelets Small, irregularly shaped blood cells made in

bone marrow They start as large cells, and then break into

many smaller fragments No nucleus Live only 8-10 days

Page 5: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood Clot1) A cut occurs damaging a small blood vessel

2) Blood (including rbc, wbc, plasma proteins and platelets) will ooze out of the cut.

3) The damaged tissues will release chemicals that will cause platelets to adhere to each other and the damaged area causing a plug.

Page 6: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood Clot4) The platelets and damaged tissue will release

clotting factors which include the enzyme thrombokinase.

5) Thrombokinase will catalyze the conversion of prothrombin (a plasma protein) into the enzyme thrombin

6) Thrombin will catalyze the conversion of soluble fibrinogen (a plasma protein) into insoluble fibrin

Page 7: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Blood ClotFIBRIN:

A fibrous protein which forms a mesh-like network that helps to stabilize the platelet plug

7.More cellular debris will become trapped in the fibrin mesh and a stable clot will form preventing further blood loss or the entry of pathogens

http://www.pennmedicine.org/encyclopedia/em_DisplayAnimation.aspx?gcid=000011&ptid=17

Page 8: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way
Page 9: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Lymphatic SystemThe lymphatic system transports a watery,

clear fluid known called lymphThe lymph distributes leucocytes (wbc) and

other factors throughout the body. It also interacts with the circulatory system

to drain fluid from cells and tissues and remove foreign invaders and microorganisms.

It contains lymphocytes that protect the body against antigens by producing antibodies

Page 10: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Lymph nodes are small ball-shaped organs throughout the body, and part of the lymphatic system.

They become enlarged when there is an infection because an increase in T and B lymphocytes.

http://www.pennmedicine.org/encyclopedia/em_DisplayAnimation.aspx?gcid=000083&ptid=17

Page 11: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way
Page 12: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

The Immune Response & Antibody ProductionWhen a pathogen enters your body, the

immune system will try to get rid of it.

Remember, your leukocytes recognize cell surface proteins (antigens) and can determine if a cell is “self” or “not self

“self”= body cell“not-self” = a foreign cell

Page 13: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way
Page 14: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

(Remember, there are lots of different types of leukocytes.)

The first type of leukocyte that will encounter a pathogen is usually a macrophage.

The macrophage will ingest the pathogen through phagocytosis and partially digests it.

The macrophage will take the antigens of the pathogen and display on its own cell membrane

This is known as antigen presentation

The macrophage will then go to the lymph nodes

Page 15: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

In the lymph node, the macrophage will present the antigens to various types of helper-T cells (TH)

Helper-T cells are a types of lymphocytes

A helper-T cell with receptors on its membrane that are complementary to the antigen will be selected. (They basically take an imprint of the antigen)

These helper-T cells will undergo mitosis to make clones of itself.

Page 16: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

The helper-T cells will then go to a B lymphocyte (also called a B cell)

B lymphocytes make antibodies

The B cell will identify the blueprint of the antigen and make antibodies against the antigen that can be released and attach to the antigens of the pathogen

When a B cell is activated, it will also undergo mitosis to make clones of itself

It will make plasma cells and memory cells

Page 17: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Types of B LymphocytesPlasma cells (Plasma B cells):

these cells will make antibodies immediately to fight off the infection

Memory Cell (Memory B Cells):These cells do not secrete antibodies during the 1st

infection.They are long-lived cells which will remain

circulating in the bloodstream If the individual becomes infected with the same

pathogen, the memory B cells will be ready to release antibodies against the pathogen

Page 18: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way
Page 20: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

NoteWhen the macrophage displays the antigens

on its cell membrane, the antigens are attached to MHC proteins (major histocompatability complex proteins)

Helper T-cells will only respond to antigens attached to MHC proteins

Cytotoxic T-cells or Killer T-Cells are another type of lymphocyteThey recognize cells that have been invaded by

pathogens and will destroy these cells.

Page 21: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

http://www.pennmedicine.org/encyclopedia/em_DisplayAnimation.aspx?gcid=000073&ptid=17

http://highered.mheducation.com/sites/0072943696/student_view0/chapter14/animation__t-cell_dependent_antigens__quiz_1_.html

http://highered.mheducation.com/sites/0072943696/student_view0/chapter14/animation__the_immune_response.html

Antigen formation (advanced) http://highered.mheducation.com/sites/0072943696/student_view0/chapter

14/animation__antigen_processing.html

Page 22: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

ImmunityACTIVE IMMUNITY:

Due to the production of antibodies by the organism itself after the introduction of antigens

PASSIVE IMMUNITY:Due to the acquisition of antibodies from another

organisms in which active immunity has be stimulated

Ex: from mother to fetus via the placenta or breast milk

Ex: the injection of antibodies (often used as treatment after a snake or spider bite)

Page 23: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Active Immunity can be…..

NATURAL IMMUNITY:Antibodies are present because the individual

naturally came into contact with the pathogen

ARTIFICIAL IMMUNITYAntibodies are present because the individual

was given a vaccine and introduced to a weak or dead form of the virus

Page 24: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Monoclonal Antibody ProductionThe primary immune response of an

organism is called a polyclonal response.This is because the pathogen will have many

type of antigens on its cells surface , not just one.

So several kinds of plasma B cells will go under clonal selection to produce several kinds of antibodies

After a polyclonal immune response, it is difficult to separate the different kinds of antibodies

Page 25: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Monoclonal Antibody ProductionHow are monoclonal antibodies obtained?

1)A mammal (i.e. a mouse) is injected with a particular antigen

2)The mouse’s plasma B cells will produce antibodies against the antigen

3)The plasma B cells are extracted and fused with a B-cell tumour cell (a rapidly dividing B-Cell) to create a hybrid called “hybridoma cells”

4)Hybridoma cells grow in culture producing identical antibodies that can be collected

Page 26: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way
Page 27: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Use of This TechnologyBlood Type TestsPregnancy TestsTests for diseases and infections

Page 28: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Ex: Pregnancy TestsRemember, when a woman is pregnant she

secretes the (protein) hormone HCG (human chorionic gonadotropin) in her urine

The antibodies for HCG can be fixed to a testing strip

If a woman is pregnant, the HCG in her urine will attach to the antibodies on the testing strip

The test is designed to produce a specific colour (or shape) to indicate a positive test

Page 29: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Monoclonal Antibodies as Treatments

When body cells become cancerous, they begin to produce specific antigens on their cell membrane

A possible treatment for cancer is to produce monoclonal antibodies that target the cancer-cell antigens

The antibodies could be modified to carry a toxin to those cells or a radioisotope to mark the cells for radiation therapy

Page 30: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

VaccinationThe secondary response to an antigen is must

faster than the first response

Vaccinations deliberately expose an individual to a weakened/dead/similar pathogen

In this way, the individual can create memory B cells against the antigens of the pathogen and be prepared for an infection

If the individual comes into contact with the pathogen after vaccination, they will have a faster immune response and will likely avoid illness

Page 32: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Benefits of VaccinationsEradication of some diseases (e.g. small pox)Fewer people get the diseases (because

already have the antibodies)Prevents disability and other effects of the

pathogenEx: polio can cause paralysis (no polio, no polio

related paralysis)Herd immunity

If many people in the population are vaccinated, the disease will not spread and there will be a decreased chance that someone who did not get the vaccine will contract it anyway

Page 33: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Dangers of VaccinationOverloading the immune system with

antigens will reduce the ability to handle other infections

Other pathogens could grow in the solution with the vaccine

The vaccine could have other harmful substances (often added to increase shelf life of vaccine)

Page 34: Topic 11.1 (and 6.3). Blood Clotting When blood vessels get broken, blood is able to escape from the closed circulatory system and pathogens have a way

Artificial immunity is less effectiveDiseases avoided as a child are more serious as

an adultEx: chicken pox in adults can result in shingles

Side AffectsEx: Suggested an increase chance of autism

(not confirmed)Can lead to allergic reactions and autoimmune

responses