Cell Recognition & the Immune System Flashcards

1
Q

Pathogen def + eg

A

A disease causing microorganism e.g. bacteria, virus, fungi, parasite

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2
Q

Infection def

A

The interaction between a pathogen and the body’s defence mechanisms (an invasion of pathogens in the body)

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3
Q

Immunity def

A

The means by which he body protects itself from infection

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4
Q

Antigen def + eg

A

(Antibody generator) a foreign protein on the surface of pathogens or other non-self cells that causes an immune response by lymphocytes e.g. bacteria, viruses, fungi, parasites, cancerous abnormal body cells, toxins, transplanted cells

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5
Q

Clonal selection def

A

When an antigen binds to the cell of a specific T cell clone or when a lymphocyte recognises a foreign molecule and is stimulated to divide

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6
Q

Clonal expansion def

A

When a T cell clone has the ability to generate into many different cells

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7
Q

Antibody structure

A

Light chains, heavy chains, hinge region, two antigen binding sites at the ends, variable regions, constant regions

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8
Q

How do antibodies demonstrate the different protein structures?

A

Tertiary - disulfide bridge

Quaternary - made of more than one (four) polypeptide chains

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9
Q

Passive immunity

A

Produced by the introduction of antibodies. No direct contact with a pathogen is necessary (eg anti-venom). Immunity is acquired immediately. Antibodies are not produced by the individuals themselves - immunity acquired by by the foetus from the mother when antibodies pass across the placenta to the womb. Antibodies are not replaced when they are broken down, no memory cells are formed, no lasting immunity

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10
Q

Active immunity

A

Produced by stimulating the production of antibodies by the individual’s own immune system. Direct contact with the pathogen is necessary. Takes time to develop, but generally long lasting. Two types: natural or artificial

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11
Q

Natural active immunity

A

Individual is infected under normal circumstances

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12
Q

Artificial active immunity

A

Vaccinations immunisation programme). Induces an immune response without them suffering the symptoms

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13
Q

Vaccination def

A

Small doses of dead or inactive pathogens or its antigens injected or taken by mouth to induce an immune response and produce memory cells without experiencing symptoms of the disease

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14
Q

Features if a successful vaccination programme

A

Must be economically available in sufficient quantities to most vulnerable population. Must be few side-effects. Must have available means of producing, storing and transporting the vaccine (technologically advanced equipment, refrigerated transport, hygienic conditions). Must be means of administering the vaccine properly at the appropriate time. Produces herd immunity

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15
Q

Why might vaccinations not eliminate a disease?

A

People have defective immune systems. Antigen variability (antigen change frequently so antibodies produced no longer match). Too many varieties of a pathogen. Some pathogens hide from the immune system (viruses in the lysogenjc cycle). Individuals object due to ethical, medical or religious reasons.

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16
Q

How are monoclonal antibodies produced?

A

Mouse is vaccinated to produce antibodies. Antibody-forming cells taken from spleen. Tumour cells grown in tissue culture. Form hybridomas by fusing antibody-forming cells with cultivated tumour cells to stimulate growth. Hybridomas screened for antibody production. Cloned. Monoclonal antibodies isolated for cultivation

17
Q

Uses of monoclonal antibodies

A

Pregnancy testing, targeting medication, indirect monoclonal antibody therapy, medical diagnosis

18
Q

How does phagocytosis lead to presentation of the virus’ antigens?

A

The vesicle (phagosome) fuses with a lysosome. The virus is hydrolysed by lysozymes. The broken down antigen are then presented on the cell-surface membrane

19
Q

Why do antibodies only attack certain cells/antigens?

A

Antibodies have specific tertiary structures. The binding sites and variable regions are complementary to the antigen. The antigen is found on specific cells. Therefore the antibody only binds with these cells

20
Q

Why can’t ELIZA tests be used to find out if a person has AIDS?

A

The ELIZA test only shows the number of helper T cells. A person can be HIV-positive but not have AIDS as it doesn’t show the symptoms of the patient

21
Q

In an ELIZA test what are the reasons for having a control well?

A

To show the enzyme is causing a colour change. To show that the washing is effective.

22
Q

If a HIV positive mother gives birth to a baby, explain why the positive result does not prove that they are infected?

A

Passive immunity would’ve taken place so the solution would have turned blue

23
Q

How do vaccines lead to the production of antibodies?

A

A macrophage present antigens on its surface. T cells with complementary receptor proteins binds to the antigen. This stimulates B cells. The B cell divides to form clones or secrete antibodies or presents antibodies on the cell surface membrane

24
Q

How is HIV replicated after into the human cell?

A

HIV joins to the host DNA. Reverse transcriptase turns the viral RNA to DNA. HIV proteins are therefore copied in protein synthesis. This is made at ribosomes.

25
Q

How does the destruction of T cells by HIV lead to death?

A

There are not enough T cells to activate B cells. The person will be unable to fight infections such as TB

26
Q

Structure of HIV

A

Lips envelope on the outside, attachment proteins embedded in, capsid protein layer inside the envelope, encloses two single strands of RNA and enzymes eg reverse transcriptase, matrix

27
Q

Reverse transcriptase function

A

Catalyses the production of DNA from RNA

28
Q

Retroviruses def

A

Contain reverse transcriptase and have the ability to make DNA from RNA

29
Q

How does HIV replicate it self?

A

HIV enters the bloodstream and circulates around the body. A protein on HIV readily binds to a protein called CD4. This protein occurs on a number of different cells but HIV most frequently attaches to helper T cells. The protein capsid fuses with the cell-surface membrane. The RNA and enzymes of HIV enter the T-cell. HIV reverse transcriptase converts the viruses RNA into DNA. The newly made DNA is moved to the helper T cell’s nucleus where it is inserted into the host cells DNA. Here it creates mRNA which contains the instructions for making new viral proteins and the RNA to go into new HIV. The mRNA passes out of the nucleus through nuclear pore and uses the cells protein synthesis mechanisms to make HIV particles. These break away from the helper T-cell with a piece of its cell-surface membrane to form a lipid envelope.

30
Q

How does HIV cause symptoms of AIDS?

A

It’s a tax helper T cells by killing or interfering with the normal functioning of them. Without a sufficient number of helper T cells, the immune system can’t stimulate B cells to produce antibodies or cytotoxic T cells that kill cells infected by pathogens. Memory cells can also be infected and destroyed. This means that the body is unable to produce an adequate immune response and becomes susceptible to other infections and cancers. These secondary diseases caused death