2. Immune System - phagocytes, B cells and T cells Flashcards
Antigen Presentation
Macrophage to Death`
Explain the increase in specific plasma cells and antibody in people infected with the Ebola virus
1.Antigen/glycoprotein on Ebola binds to/stimulates (a specific) B cell;
Accept correct reference to stimulation of B cells by T cells
2.(Binding causes) replication/cloning of B cell
;Accept replication/cloning of plasma cell
;3.Plasma cells/B cells release/produce antibodies;
Explain how a blood transfusion from a patient recently recovered from Ebola may be an effective trea
1.Lots of antibodies (against Ebola) in recovered patient
;2.Transfusion/plasma contains antibodies;Ignore reference to cells
3.Antibodies (specific so) will bind with (Ebola) antigen;
4.(In recipient) virus destroyed/cannot
A high mutation rate makes it difficult to develop a vaccine (line 11).Explain why
1.(High mutation rate leads to) antigens change/antigenic variability;Accept (high mutation rate leads to) changes in base sequence coding for antigen;
2.Vaccine contains specific antigen;
3.Antibodies not complementary to (changed) antigen / won’t bind to (changed) antig
Using your knowledge of the structure of the cell-surface membrane, suggest how LDL enters the cell
- Lipid soluble / hydrophobic2. Enters through (phospholipid) b
Explain how the monoclonal antibody would prevent the regulator protein from working
Any two from:
- (Monoclonal antibody) has a specific tertiary structure / variable region / is complementary to regulator protein
Do not award MP1 if reference to active site. - Binds to / forms complex with (regulator protein)
“It” refers to monoclonal antibody in MP1 and MP2 - (So regulator protein) would not fit / bind to the receptor / is not complementary to receptor
When a vaccine is given to a person, it leads to the production of antibodies against a disease-causing organism. Describe how
- Vaccine contains antigen from pathogen;
2.Macrophage presents antigen on its surface;
3.T cell with complementary receptor protein binds to antigen;
4.T cell stimulates B cell;
5.(With) complementary antibody on its surface;
6.B cell secretes large amounts of antibody;
7.B cell divides to form clone all secreting / producing same antibody
Differences between B cells and T cells
B Cells and the Humoral Immune System
The body contains millions of different B-lymphocytes (another type of white blood cell)
Each one is covered in antibodies
When antigens enter the body there will be a B- cell with complementary antibodies.
This B cell will combine with the antigen.
This binding, together with substances from T cells activates the B cells
They divide rapidly by mitosis to form daughter cells- clonal selection
Some will form plasma cells which release antibodies
A small number will remain as memory cells
Primary Response
Occurs when antigen enters body for the first time
It is slow as there aren’t many B cells initially that can make the antibody
Person will show symptoms until there are sufficient antibodies to overcome the infection
After exposure to an antigen both T and B cells produce memory cells
Memory cells are retained in the body for a long time
The person is now immune and has the ability to respond quickly to a second infection
Secondary Response
If the same pathogen enters the immune system will produce a quicker, stronger immune response
Clonal selection happens faster
Memory B cells divide to form plasma cells which produce the right antibody
Memory T cells are activated to kill the cell carrying the antigen
Secondary response often gets rid of pathogen before the person shows any symptoms
Phagocytosis
Carried out by neutrophils and macrophages
Shortly after engulfing bacteria neutrophils die as they have used up a lot of energy
Macrophages are longer lasting. After they have engulfed a bacteria they present some of the foreign antigens on their own membrane. They become antigen presenting cells (=APC)
Cells infected by viruses can also be APCs- this sends a signal to other cells that it should be destroyed.
Phagocytes are able to attack and destroy almost any foreign cell or material that enters the body
The response is non- specific
Clonal Selection
Active immunity vs Passive
Active -Your immune system makes antibodies in response to an antigen
It can be natural- you become immune after catching a disease
Or artificial- you become immune after being vaccinated
Passive - You are given antibodies from a different organism
It can be natural- via placenta/breast milk
Or artificial- you are injected with antibodies directly e.g. rabies/ tetanus