Which of the following cells responds first when a person receives the MMR vaccination?
- helper \( \text{T} \) cells
- memory \( \text{T} \) cells
- cytotoxic \( \text{T} \) cells
- antigen-presenting cells
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Which of the following cells responds first when a person receives the MMR vaccination?
\(D\)
→ As the MMR vaccine contains a weakened version of the Measles, Mumps and Rubella viruses, it is the antigen-presenting cells which first respond.
\(\Rightarrow D\)
Tetanus vaccines were introduced in 1953 resulting in reduced case numbers. The majority of recorded cases occurred in people aged 65 and over. The graph shows the vaccination schedule for tetanus. Assess the use of vaccinations and the vaccination schedule. Use the data provided to support your answer. (5 marks) → Vaccines are an excellent tool to reduce the severity and spread of certain infectious diseases. → This is because vaccines contain dead or inactive versions of a pathogen, which then stimulates the body to fight it and store memory B cells with the associated antibodies. → This can be clearly seen on the graph after the first and second injections of the vaccine, where the first injection is the initial exposure while the second injection has a much larger production of antibodies due to the memory B cells being activated. This is the basis of immunity. → This effect is compounded each time with the the length of immunity increasing after each dose. → The vaccination schedule is designed so that a new dose is scheduled at the time a person following the recommended schedule would become non-immune. → The general trend in the graph/data suggest that the increase in cases of people over 65 is likely due to a long period elapsing since their last booster. → In summary, if an individual on the recommended vaccination schedule is exposed to the tetanus virus after 6 months of age, they would have already built up an adequate immunity to be able to fight the tetanus bacteria. → This effect makes vaccines especially effective in stopping the spread and severity of infectious diseases such as tetanus. → Vaccines are an excellent tool to reduce the severity and spread of certain infectious diseases. → This is because vaccines contain dead or inactive versions of a pathogen, which then stimulates the body to fight it and store memory B cells with the associated antibodies. → This can be clearly seen on the graph after the first and second injections of the vaccine, where the first injection is the initial exposure while the second injection has a much larger production of antibodies due to the memory B cells being activated. This is the basis of immunity. → This effect is compounded each time with the the length of immunity increasing after each dose. → The vaccination schedule is designed so that a new dose is scheduled at the time a person following the recommended schedule would become non-immune. → The general trend in the graph/data suggest that the increase in cases of people over 65 is likely due to a long period elapsing since their last booster. → In summary, if an individual on the recommended vaccination schedule is exposed to the tetanus virus after 6 months of age, they would have already built up an adequate immunity to be able to fight the tetanus bacteria. → This effect makes vaccines especially effective in stopping the spread and severity of infectious diseases such as tetanus.
How do vaccinations prevent disease?
`C`
→ Vaccines stimulate the immune response, encouraging the division of B cells and therefore producing more antibodies.
`=>C`
The graph shows the expected life span (the age to which people are expected to live in years) for people of different ages during the 20th century in one country.
There have been many biological developments that have contributed to our understanding of the identification, treatment and prevention of disease.
Evaluate the impact of these developments on the expected life span. In your answer, include reference to trends in the data provided. (8 marks)
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→ For all ages listed in the graph, life expectancy increased during the 20th century.
→ The lifespan from birth has increased more significantly than other ages ~ 48 to 74 years.
→ The smallest increase being for 60 year olds at ~ 5 years.
→ The ability to understand pathogens and the causes of infectious disease (Koch and Pasteur) has led to early identification and treatment of childhood illnesses such as rubella, polio and whooping cough.
→ Koch and Pasteur established germ theory, culture techniques and a set of postulates to follow in order to create the link between a particular pathogen and disease.
→ Vaccines to combat childhood illnesses were developed through a knowledge of germ theory.
→ The infant/childhood mortality rate has improved significantly, and hence life expectancy, due to the immunity provided by vaccines.
→ An understanding of inherited disorders has also improved lifespans with early diagnosis and prenatal genetic screening for genetic disorders and illnesses.
→ Antibiotic remedies were developed to combat bacterial diseases such as Staphylococcus aureus, due to an understanding of the difference between prokaryotic and eukaryotic cells.
→ With the use of antibiotics many diseases were then no longer life threatening, leading to improved mortality rates across all ages.
→ However, bacterial resistance has resulted with the overuse of antibiotics, so some diseases are now unresponsive to antibiotic treatment.
→ Epidemiology studies involving intricate planning and design, control groups and large scale analysis of data have lead to improvements in the treatment of non-infectious diseases such as cancer.
→ For example the discovery of links between smoking and lung cancer, sun exposure and melanoma, obesity and type II diabetes, has lead to widespread public health campaigns to inform people of the health risks and lowered the associated mortality rates.
→ Improved hygiene, food storage and preservation, and water filtration also occurred in the 20th century leading to fewer preventable diseases and hence increased life spans for all age groups.
→ Improved quarantine requirements have helped prevent the spread of plant, animal and human diseases via international travel.
→In conclusion, developments in biology have lead to increased life expectancy across all age groups, with the biggest improvements for babies and children.
→ These benefits are not necessarily a worldwide phenomenon as poor living conditions and access to medical treatment is not available in many poor socioeconomic communities.
→ For all ages listed in the graph, life expectancy increased during the 20th century.
→ The lifespan from birth has increased more significantly than other ages ~ 48 to 74 years.
→ The smallest increase being for 60 year olds at ~ 5 years.
→ The ability to understand pathogens and the causes of infectious disease (Koch and Pasteur) has led to early identification and treatment of childhood illnesses such as rubella, polio and whooping cough.
→ Koch and Pasteur established germ theory, culture techniques and a set of postulates to follow in order to create the link between a particular pathogen and disease.
→ Vaccines to combat childhood illnesses were developed through a knowledge of germ theory.
→ The infant/childhood mortality rate has improved significantly, and hence life expectancy, due to the immunity provided by vaccines.
→ An understanding of inherited disorders has also improved lifespans with early diagnosis and prenatal genetic screening for genetic disorders and illnesses.
→ Antibiotic remedies were developed to combat bacterial diseases such as Staphylococcus aureus, due to an understanding of the difference between prokaryotic and eukaryotic cells.
→ With the use of antibiotics many diseases were then no longer life threatening, leading to improved mortality rates across all ages.
→ However, bacterial resistance has resulted with the overuse of antibiotics, so some diseases are now unresponsive to antibiotic treatment.
→ Epidemiology studies involving intricate planning and design, control groups and large scale analysis of data have lead to improvements in the treatment of non-infectious diseases such as cancer.
→ For example the discovery of links between smoking and lung cancer, sun exposure and melanoma, obesity and type II diabetes, has lead to widespread public health campaigns to inform people of the health risks and lowered the associated mortality rates.
→ Improved hygiene, food storage and preservation, and water filtration also occurred in the 20th century leading to fewer preventable diseases and hence increased life spans for all age groups.
→ Improved quarantine requirements have helped prevent the spread of plant, animal and human diseases via international travel.
→In conclusion, developments in biology have lead to increased life expectancy across all age groups, with the biggest improvements for babies and children.
→ These benefits are not necessarily a worldwide phenomenon as poor living conditions and access to medical treatment is not available in many poor socioeconomic communities.
The diagram shows the life cycle of the malaria parasite, Plasmodium sp. Five stages in this life cycle are numbered on the diagram.
To prevent malaria, the following four strategies have been used:
Which row in the table shows the stage in the life cycle in which each of these strategies would be most effective?
`D`
→ Vaccines are most effective when administered before the parasite enters the cell (1).
→ Mosquito nets are only useful if utilised prior to the injection of the parasite into a human (5).
→ Insecticides help prevent the vectors from breeding (3).
→ Anti-malarial drugs may be useful once the disease is present (2).
`=>D`
Explain why the combined use of quarantine and vaccination programs is a more effective way of controlling disease than using only one of these strategies. (5 marks)
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→ Quarantine alone does not provide any immunity from disease, so outbreaks can still occur if exposure occurs.
→ Vaccination can prevent infection, however, immunity takes time to build up, so infection can occur before the vaccine takes effect.
→ Effective vaccination programs can create herd immunity.
→ If this is backed up with isolation of containable outbreaks of the disease, a combined approach can be more effective.
→ Quarantine alone does not provide any immunity from disease, so outbreaks can still occur if exposure occurs.
→ Vaccination can prevent infection, however, immunity takes time to build up, so infection can occur before the vaccine takes effect.
→ Effective vaccination programs can create herd immunity.
→ If this is backed up with isolation of containable outbreaks of the disease, a combined approach can be more effective.
Refer to the following information to answer Questions 19 and 20.
Question 19
What can be inferred from the scientists' discovery?
Question 20
The effect of the melanoma vaccine is to stimulate
Q19. `A`
Q20. `C`
Q19.
→ The vaccine can create an immune response against the cancer cells if self-antigens are not present in the cells.
`=>A`
Q20.
→ Lymphocyte development would be promoted by the vaccine.
`=>C`
The steps below show the preparation and use of blood products in the treatment of Ebola Virus Disease. This disease is characterised by significant blood loss.
Explain why this protocol produces an effective treatment for Ebola Virus Disease. (3 marks)
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→ The plasma has been taken from a person who has survived the Ebola Virus and as a result, it will contain antibodies for the disease.
→ This will assist in the immobilisation of the pathogen in the blood stream of the recipient.
→ The spread of blood-borne diseases such as Ebola from donor to recipient can be prevented through blood screening.
→ The plasma has been taken from a person who has survived the Ebola Virus and as a result, it will contain antibodies for the disease.
→ This will assist in the immobilisation of the pathogen in the blood stream of the recipient.
→ The spread of blood-borne diseases such as Ebola from donor to recipient can be prevented through blood screening.
What does the body produce in response to a vaccine?
`C`
→ The vaccine promotes an immune response, thus producing antibodies.
`=>C`
A new vaccine against an infectious disease was developed. The effectiveness of the vaccine in preventing infection in humans was plotted over time in three different age groups.
Which of the following is a valid conclusion that can be drawn from the data in the graph?
`D`
The graph shows that the vaccine has a lower effectiveness against infection for people aged over 65 than for the younger age groups over the whole period.
`=>D`
Rabies is a disease that can affect all mammals and is caused by the rabies virus. It is transmitted by the bite of an infected animal. Without treatment it almost always results in death.
The rabies virus is a single-stranded RNA virus. It contains and codes for only five proteins. The diagrams show the structure and reproduction of the virus.
Post exposure prophylaxis (PEP) is given to patients who have been bitten by a rabid animal.
PEP includes an injection of human rabies antibodies (HRIG) as well as injections of a rabies vaccine at 0, 3, 7 and 14 days after exposure to the virus.
The following graphs show a generalised response to rabies infection without and with PEP.
Explain how PEP prevents rabies developing after infection with the virus. Support your answer with reference to the information and data provided above. (8 marks)
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Once the rabies virus has entered the wound:
→ It will use the patient’s cells to replicate and the viral concentration will increase (as seen in the first five days).
→ Without PEP the virus will continue to replicate, migrate to the CNS (in the first graph this occurs by day 7), and eventually cause rabies and death.
→ Initially, the infected individual will not have the antibodies required to inactivate the virus.
→ A HRIG injection provides the required antibodies to inactivate the virus, through inhibiting replication or enhancing phagocytosis.
→ The PEP graph shows that these antibodies will only last up to 21 days, but are essential in inactivating the initial virus, as seen by a reduction in viral concentration after 6-8 days.
The rabies vaccine works by:
→ containing an inactivated or weakened version of the rabies virus, which stimulates an immune response by the individual.
→ Initially, macrophages will display an MHC-antigen complex on its surface which helper T lymphocytes will bind to.
→ This then stimulates specific plasma B cells which can produce complementary antibodies, and memory B cells, which stay dormant and can rapidly differentiate into plasma B cells when exposed to the same virus.
→ The PEP graph shows the rapid production of antibodies on day 7, which coincides with rapid decrease in the virus concentration over the next few days.
→ The antibodies then remain in the bloodstream and slowly decline over months, which allows quick diffusion if the virus is encountered within that timeframe.
Once the rabies virus has entered the wound:
→ It will use the patient’s cells to replicate and the viral concentration will increase (as seen in the first five days).
→ Without PEP the virus will continue to replicate, migrate to the CNS (in the first graph this occurs by day 7), and eventually cause rabies and death.
→ Initially, the infected individual will not have the antibodies required to inactivate the virus.
→ A HRIG injection provides the required antibodies to inactivate the virus, through inhibiting replication or enhancing phagocytosis.
→ The PEP graph shows that these antibodies will only last up to 21 days, but are essential in inactivating the initial virus, as seen by a reduction in viral concentration after 6-8 days.
The rabies vaccine works by:
→ containing an inactivated or weakened version of the rabies virus, which stimulates an immune response by the individual.
→ Initially, macrophages will display an MHC-antigen complex on its surface which helper T lymphocytes will bind to.
→ This then stimulates specific plasma B cells which can produce complementary antibodies, and memory B cells, which stay dormant and can rapidly differentiate into plasma B cells when exposed to the same virus.
→ The PEP graph shows the rapid production of antibodies on day 7, which coincides with rapid decrease in the virus concentration over the next few days.
→ The antibodies then remain in the bloodstream and slowly decline over months, which allows quick diffusion if the virus is encountered within that timeframe.
A study compared the incidence of disease and survival of 8134 children who had received the measles vaccine with 8134 children from a neighbouring area who remained unvaccinated against measles. Children in each group were matched for age, sex, size of dwelling, number of siblings and maternal education. The graphs show the number of measles cases among the two groups over three years.
The table compares the cause of death and number of deaths of the two groups over the same three years.
'A vaccine only protects the community against a specific disease.'
Analyse the data with reference to this statement. (7 marks)
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→ These two studies show proof that the vaccine protects against measles.
→ The graphs show the incidence of measles in vaccinated children is extremely low, occasionally zero, compared to unvaccinated children. Since these children are matched for age and other sociocultural/socioeconomic factors, it is highly likely the vaccine is responsible for this difference.
→ The table also supports this conclusion, where 40 children who were unvaccinated died due to measles compared to the 2 who died who were vaccinated.
→ The table also provides evidence that the vaccine may protect children from dying from other diseases, contradicting the statement.
→ The table also uses the same groups as the graph, again, keeping cultural/socioeconomic factors similar. It shows that children vaccinated against measles died at half the rate of unvaccinated children due to diarrhoea and dysentery, and at about a quarter of the rate for oedema.
→ However, the small differences between groups with respect to fever and the small sample size for oedema mean that further research is required.
→ In general, the vaccinated group had less than half the mortality of the unvaccinated group, supporting the conclusion that the vaccine provides a wider protection.
→ However, this statement needs qualification as the data is only with respect to the measles vaccine.
→ These two studies show proof that the vaccine protects against measles.
→ The graphs show the incidence of measles in vaccinated children is extremely low, occasionally zero, compared to unvaccinated children. Since these children are matched for age and other sociocultural/socioeconomic factors, it is highly likely the vaccine is responsible for this difference.
→ The table also supports this conclusion, where 40 children who were unvaccinated died due to measles compared to the 2 who died who were vaccinated.
→ The table also provides evidence that the vaccine may protect children from dying from other diseases, contradicting the statement.
→ The table also uses the same groups as the graph, again, keeping cultural/socioeconomic factors similar. It shows that children vaccinated against measles died at half the rate of unvaccinated children due to diarrhoea and dysentery, and at about a quarter of the rate for oedema.
→ However, the small differences between groups with respect to fever and the small sample size for oedema mean that further research is required.
→ In general, the vaccinated group had less than half the mortality of the unvaccinated group, supporting the conclusion that the vaccine provides a wider protection.
→ However, this statement needs qualification as the data is only with respect to the measles vaccine.
An mRNA vaccine has been developed in order to immunise people against a virus. The vaccine contains modified mRNA which codes for the spike protein on the surface of the virus.
Explain how this vaccine can lead to active immunity to the virus. (5 marks)
→ The modified mRNA enters the individuals cells and is translated at the ribosomes to form the viral spike protein, which is then released into the body.
→ The protein will be rendered as an antigen, and will trigger a specific immune response by B and T lymphocytes that match the antigen.
→ Once the viral protein has been removed, memory B and T lymphocytes specific to the protein remain, providing active immunity that allows for a rapid future response.
→ If the individual is later exposed to the virus, the same spike proteins present on the virus’ surface will trigger a rapid and large response by the memory cells. This is the basis for providing active immunity.
→ The modified mRNA enters the individuals cells and is translated at the ribosomes to form the viral spike protein, which is then released into the body.
→ The protein will be rendered as an antigen, and will trigger a specific immune response by B and T lymphocytes that match the antigen.
→ Once the viral protein has been removed, memory B and T lymphocytes specific to the protein remain, providing active immunity that allows for a rapid future response.
→ If the individual is later exposed to the virus, the same spike proteins present on the virus’ surface will trigger a rapid and large response by the memory cells. This is the basis for providing active immunity.