B6 - Preventing And Treating Disease (Y10 - Spring 2) Flashcards

1
Q

๐ŸŸข How do Antigens and White Blood Cells Work

A

Every cell has unique proteins on itโ€™s surface called antigens on the microorganisms that get into your body are different to the ones on your own cells. Your immune system recognises that they are different.

Your white blood cells then make specific antibodies, which join up with the antigens and inactivate or destroy that particular pathogen.

Some of your white blood cells (the memory cells) rememeber the right antibod needed to destroy a particular pathogen. If you meet tnat pathigen again, these memory cells can make that same antibody very quickly to kill the pathogen, so you become immune to the disease.

The first time you meet a new pathogen you get ill because there ie a delay while your body sorts out the right antibody neded. The next time, your immune system destroys the invaders they can make you feel unwell.

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2
Q

๐ŸŸข What are Vaccines and How Do They Work

A

You can be protected against many of these serious diseases by the vaccination (also known as immunisation).

Immunisation involves giving you a vaccine made of a dead or inactivated form of a disease causing microorganism. It stimulates your bodyโ€™s natural immune response to invading pathogen.

A small amount of dead or inactive forms of a pathogen is introduced into your body. This sitimulates the white blood cell to produce the antibodies needed to fight the pathogen and prevent you from getting ill. Then, if you meet the same, live pathogen, your white blood cells can respond rapidly. They can make the right antibodies just as if you had already had the diease, so that you are protected against it.

Doctors use vaccines to protect us both against bacterial diseases, such as tetaus and diphthetia, and viral diseases such as pilio, measles and mumps. For example, the MMR vaccine protects aginst measles, mumps, and rubella. Binccines have saved millions of lives around the world. One disease - smallpox - has been completely wiped out by vaccinations. Doctors hope polio will also disappear in the next year.

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3
Q

๐ŸŸข What is Herd Immunity and how does it Work

A

If a large proportion of the population is immune to a disease, the spread of the pathogen is the populatiom is very much reduced and the disease may even disappear. This is known as herd immunity. If, for any reason, the number of people taking up a vaccine fall, the herd immunity is lost and the disease can reappear. This is what happened in the UK in the 1970โ€™s when there was a scare about the safety of the whooping cough vaccine. Vaccination rates fell from over 80% to around 30%. In the following years, thousands of children got whooping cough again and a substantial number died. Yet the vaccine was as safe as any medicine. Eventually people realised this and enough children were vaccinated for herd immunity to be effective again. There are gloabl vaccination programmes to control a number diseases, including tetanus in mothers and new-born babies, polio, and measles. The World Health Organisation want 95% children to have two doses of measles vaccine to give global herd immunity. Current global figures show that 85% of children get the first dose and 56% get the second. It will take money and determination to get global herd immunity against a range ofdifferent diseases, but advantages both to individuals and to global economies are huge.

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4
Q

๐ŸŸข How Vaccination protects you against dangerous infectious diseases

A

Firstly, small amounts of dead or inactive pathogen are put into your body, often by injection.

Then, the antigens in the vaccines stimulate your white blood cells into making antibodies. The antibodies destroy the antigens without any risk of you getting the disease.

You are immune to future infections by the pathogen. Thatโ€™s because your body can respond rapidly and make the correct antibody as if you had already had the disease. Also, in future infections a lot more antibodies will be created in a lot quicker period of time.

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5
Q

๐ŸŸข What happens when a B-Cell is 1st Infected, and when itโ€™s secondly infected

A

B-Cell upon 1st Infection:

  • The B-Cell will bind to the specific antigen on the surface.
  • This means that masses of antibodies will be produced, which will go on to eliminate the infection.
  • After this, memory B-Cells are formed and circulate around the body. This will alow the antibodies to produce quicker in future.

B-Cell upon 2nd Infection:
-The memory B-Cells will divide into antibodies quicker than the first time and will eliminate the pathogen faster.

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6
Q

โŒ How can Painkillers help, but what are their limitations too?

A

Drugs such as asprin and paracetomol are very useful painkillers. When you have a cold, they will help relive your headache and sore throat. On the other hand, they will have no effect on the viruses that have entered your tissues and that have made your feel ill. Many of the medicines you can buy at chemists or a supermarket relieve your symptoms but do not kill the pathogens, so they do not cure you any faster. You have to wait for your immune system to overcome the pathogens before you actually get well again.

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7
Q

โŒ What are Antibiotics

A

Drugs that make you feel better are useful, but in some cases what you really need are drugs that can cure you. You can use antiseptics and disinfectants to kill bacteria outside of your body, but they are far too poisonous to use inside your body. They will kill you, along with the pathogens at the same time.

The drugs that have really changed the treatment of communicable diseases are antibiotics. These are medicines that can work inside your body to kill bacterial pathogens. The impact of antibiotics on deaths from communicable diseases have been enormous.

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8
Q

โŒ How Do Antibiotics Work

A

Antibiotics, such as penicillin, work by killing the bacteria that cause disease whilsit they are inside your body. They damage the bacterial cells without harming your own cells. Bacterial diseases that killed millions of people in the past can now be cured using antibiotics. They have had an enormous effect on our society.

If you need antibiotics, you usually take a pill, or syrup, but if you are very ill antibiotics may be put straight into your bloodstream. This makes sure that they reach the pathogens in your cells as quickly as possible. Some antibiotics kill a wide range of bacteria. Others are very specific and only work against particular bacteria. It is importamt that the right antibiotic is chosen and used. Specific bacteria be treated with the specifc antibiotic that is effective against them.

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9
Q

โŒ Why/How do Bacteria become Antibiotic Resistant

A

The antibiotics become resistant overtime, after the bacteria evolve over the years. This means that certain antibiotics are changing faster than new antibiotics are able to be created. This can lead to certain โ€˜superbugsโ€™ that cannot be treated by antibiotics, as the bacteria that has made the โ€˜superbugโ€™ has resistance.

Bacteria can randomly mutate at times, but can sometimes lead to their characteristics being changed before it forms a new colony of resistant bacteria. This process can happen again and again with different types of antibiotics, leading one type of bacteria being resistant to very many different types of antibiotics. Around 1,000 tonnes of bacteria are given out per year, but 2/3 of this is given to animals to try to make them stay strong and healthy, even if they are not unwell. This creates a breeding ground for bacteria to become immune to lots of different types of antibiotics.

It is very important that you finish your course of antibiotics even when you feel better, to make sure that all of the bacteria is killed off, meaning there are no left over bacterias when can evolve and become resistant.

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10
Q

โŒ Whatโ€™s leading more Bacteria to become Antibiotic Resistant?

A

Unfortunately, antibiotics are not the complete answer to the problem of infectious diseases:

  • Antibodies cannot kill viral pathogens so they have no effect on diseases caused by viruses. Viruses reproduce inside the cells of your body. It is extremely difficult to develop drugs that will kill the viruses without damaging the cells and tissues of your body at the same time.
  • Strains of bacteria that are resistant to antibiotics are evolving. This means that antibiotics which used to kill a particular type of bacteria no longer have an effect, so they cannot cure the disease. There are some types of bacteria that are resistant to all known antibiotics. The emergence of antibiotic strains is a matter of great concern. Unless scientists can discover new antibiotics soon, we may no longer be able to cure bacterial diseases. This means that many millions of people in the future will die of bacterial diseases that we can currently cure.
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11
Q

๐ŸŸ  How Do You Reduce the Rate of Bacteria becoming Antibiotic Resistant?

A

Bacteria can eveolve rapidly because they reproduce at a fast rate. Mutations of bacterial pathogens produce new strains. Some strains might be resistant to antibiotics, and so are not killed. They survive and reproduce, so the population of the resistant strain rises. The resistant strain will then spread because people are not immune to it and there is no effective treatment.

To reduce the rate of development of antibiotic resistant strains (like MRSA):

  • Doctors should not prescribe antibiotic inappropriately, such as treating non-serious or vial infections
  • Patients should complete their course of antibiotics so all bacteria are killed and none survive to mutate and form resistant strains
  • The agricultural use of antibiotics should be restricted

The development of new antibotics is costly and slow. It is unlikely to keep up with the emergence of new resistant strain.

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12
Q

โŒ Where Do Drugs Come From?

A

Traditionally, drugs were extracted from plants or microorganisms such as moulds. In ancient Egypt, mouldy bread was used on septic wounds. Other examples include the heart drug digitalis (comes from foxgloves), the painkiller asprin (comes from willow), and penicillin (which was discovered by Alexander Flemming from the Penicillium mould).

However nowadays, scientists often adapt chemicals from microorganisms, plants, and animals to make more effective drugs. Most new drugs are synthesised by chemists in the pharmaceutical industry. However, the starting point may still be a chemical extracted from a plant.

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13
Q

โŒ How did Flemming Discover Penicillin?

A

In 1928, while studying influenza, Fleming noticed that mould had developed accidentally on a set of culture dishes being used to grow a certain type of germ he was testing on (staphylococci germ). The mould had created a bacteria-free circle around itself. Fleming experimented further and named the active substance penicillin.

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14
Q

โŒ What Needs To Happen For A New Medical Drug To Be Released?

A

New Medicinal drugs have to be tested and trialled before being used to check tnat they are safe and effective.

New drugs are extensively tested for toxicity, efficacy and dose.

Preclinical testing is done in a laboratory using cells, tissues and live animals. Clinical trials use healthy volunteers and patients. In clinical trials:

  • Very low doses of the drug are given at the start of the clinical trial
  • If the drug is found to be safe, further clinical trials are carried out to find the optimum dose for the drug
  • In double blond trials, some patients are given a placebo.
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15
Q

โŒ What Drugs Originate From Plants

A

There are a number of drugs used today that are based on traditional medicines extracted from plants. Digitalis is one of several drugs extracted from foxgloves, and the drug digoxin is another. They have been used since the 18th century to help strengthen the heartbeat. There are many more modern drugs, but doctors still use digoxin, especially for older patients with heart problems. Large amounts of these chemicals can instead act as poisons.

The painkiller aspirin originates from a compound found in the bark of willow trees. The anti-inflammatory and pain-relieving properties were first recorded in 400BC. In 1897, Felix Hoffman synthesised acetyl salicylic acid (aspirin) which not only relieves pain and inflammation better than willow bark, but has fewer side affects. Aspirin is still commonly used to treat a wide range of health problems.

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16
Q

โŒ How Was Penicillin Made And What Proved That It Would Work

A

In the early 20th century, scientists were looking for chemicals that might kill bacteria and infectious diseases. In 1928, Alexander Flemming was growing bacteria for study purposes. He was rather careless, often leaving the lids iff his culture plates - health and safety procedures were not as good in thise days.

Afyer one holiday, Flemming saw that lots of his culture plates had mould growing on them. Henoticed a clear ring in thejelley around some of the spots of mould and realiser something had killed the bacteria โ€˜penicillinโ€™ after the Penicillium mould that produced it. He tried unsuccessfully for several years to extract an active juice from the mould befire giving up and moving onto other work.

About 10 years after Flemmingโ€™s discovery, Ernst Chain and Howard Florey set about trying to extract penicillin, and they succeeded. They gave some penicillin to a man dying of blood infection, and he recovered almost miraculously - until the penicillin ran out. Even though he eventually died, it was demonstrated that penicillin could cure bacterial infections in people. Eventually, working with the company Pfizer in the USA, Florey and Chain mad penicillin on an industrial scale, peoducing enough to supply the demands of WW2, and itโ€™s still used today.

17
Q

โŒ What Possible Future Medicines Are There?

A

There is a continuing drive to find new medicines, but it is difficult. For example, it is not easy to find chemicals that kill bacteria wothout damaging human cells. Most drugs are now synthesised by research chemists working in the pharmaceutical industry using chemical banks and computer models. However, tne starting pount may still be chemicals extracted from a plant or microorganism. Compounds showing peomise as antibiotics can be modified to produce more powerful molecules that can be synthesised easily and cheaply.

Another example is the noni fruit, which is widely used in traditional medicine in Costa Rica and many other countries to treat both infections are non-communicable diseases. People have also used it for food and drink for centuries eith no apparent problems. Recent research shows that it has antibiotic properties. More research is taking place to see if this traditional healing plant might be the source of new antibiotics or other medicines.

Scientists are also collecting soil samples globally and searching for microorganisms to produce a ne antibiotic against antibiotic-resistant bacteria. Only about 1% of soil microorganisms can be cultured in the lab. Scientists have developed a special unit that enables the, to grow microorganisms in the soul in a controlled way. Usi g this technology, in 2015, they announced a completely new type of antibiotic from some soil bacteria. In tests so far, this antibiotic has detroyed all bacteria including MRSA and other antibiotic resistant pathogens.

18
Q

โŒ What Makes A Good Medicine?

A

A good medicine is:
Effective - it must prevent or cure a disease or at least make you feel better

Safe - the drug must not be too toxic (poisonous) or have unacceptable side affects for the patients

Stable - you must be able to use the medicine under normal conditions and store it for some time.

Successfully taken and remove from your body - it must reach itโ€™s target and be cleared from your system once it has done itโ€™s work.

19
Q

โŒ How and What Does It Take To Develop and Test A New Drug For Manufacturing? (+ What are the Stages It Goes Through)

A

When scientists research a new medicine, they have to make sure all the conditions to have a good medicine are met. It can take up to 12 years to bring a new medicine into you dictorโ€™s surgery amd costs around ยฃ1,700 million, includimg failures and capital costs.

Researchers target a disease and make lots of possible new drugs. These are tested in the laboratory to find out if they are toxic and if they seem to do their job effectively. In the lab, they are tested on cell tissues, and even who organs. Many chemicals fail at this stage.

The small numbers of chemicals which do pass up to this stage, are the laboratory tested on animals, to find out how they work in a whole living organism. It also gives information about possible doses and side affects. The tissues and animals are used to predict how the drugs may behave in humans.

Up to this point the chemicals are undergoing preclinical testing. This always takes places in the laboratory using cells, tissues and live animals.

Drugs that pass animal testing move on to clinical trials. Clinical trials use healthy volunteers and patients. First, very low doses are given to healthy people to check for side effects. If the drug is found to be safe, it is tried on a small number of patients to see if it treats the disease. If it seems to he safe and effective, bigger clinical trials take place to find the optimum dose for the drug.

If the medicine passes all the legal tests, it is licenced so your doctor can prescribe it. Itโ€™ safety will be monitired for as long as it is used.

20
Q

โŒ What are Double Blind Trials and What Are They Used For?

A

In human trials, scientists use a double blind trial to see just how effective the new medicine is. A grouo of patients witj the target disease agree to take part in the trials. Some are given a placebo that does not contain the drug and some are given the new medicine. Patients are randomly allocated to different groups. Then neither the doctor nor the oatients know who has recieved the real drug or the placebo intil the trial is complete. The patientsโ€™ health is monitored carefully after this.

Often the placebo will contain a different drug that is already used to treat the disease. This means the patient is not deprived of treatment whilst taking part.

21
Q

โŒ How are the Results Checked

A

The results of drug tests and trials, like all scientific research, are publisjed in journals after they have been scrutinised in a process of peer review. This means other scientists working in tne same area can check the results over, helping to prevent false claims. National bodies such as the National Insititute for Health and Care Excellence (NICE) look at the published results of drugs trials and decide which drugs give good value for money and should be prescribed by the NHS.

22
Q

โŒ What are the seperate stages of Developing a new Medicine

A

Developing the Drug - Computer models are used to create a new drug and then it is created in a lab

Preclinical Trials - Then it will be tested in the lab in cell cultures to see if the drug is toxic. It will also be tested on live animals to find the correct dose.

Clinical Trials - It will then go through the 3 Phases:

  • Phase 1: Phase 1 clinical trials are carried out on healthy people. This stage is checking for the safety of the drug and looks for the side affects.
  • Phase 2: Phase 2 clinical trials are carried out on a small group of patients. This is the stage where scientists can begin to see if the drug is effective (the efficacy is tested).
  • Phase 3: If the drug gets to phase 3, it will be given to many more people, and some of those people will be given a dummy treatment (a placebo). This is so doctors can compare the effect of the drug with the already avaliable medicine. In this phase, they will be able to find the optimum dose and if the drug is effective for a wide range of different people, e.g old and young.

Licencing: By the end of a successful phase 3, the drug company will submit itโ€™s research to the government to ask for a licence to sell their new drug.

23
Q

โŒ Why are Drugs Clinically tested like this (link to Thalidomide)

A
  • Thalidomide was a drug taken to help people sleep, and during trials in animals, it was said that it was completely safe for everyone as there wasnโ€™t a high enough dose to kill a rat.
  • Because of this it was then prescribed to pregnant women as a cure for morning sickness
  • Many women who had taken the drug had babies born with birth defects.
  • This is why nowadays, a drug must be trialled on people before it is deemed safe, and they should also be tested on those who are intended to take it.
24
Q

๐ŸŸข What Are Monoclonal Antibodies?

A

Moncolonal antobidies (like vaccinations) are a form of medical treatment that relies on the immune system. Monoclonal antibodies are proteins that are produced to target particular cells or chemicals in the body. Some white blood cells known as lymphocytes make antibodies but cannot divide. Tumour cells do not usually make antibodies, but they can divide rapidly to make a clone of cells.

25
Q

๐ŸŸข How Are Monoclonal Antibodies made?

A

All mammals, including mice, produce lymphocytes. Scientists combine mice lymphocytes (that have been stimulated to make a particular antibody) with a type of tumour cell to make a cell called a hybridoma. Single hybridoma cell divide to make a larger number of identical cells that produce the same antibodies. These antibodies are collected and purified. They are monoclonal antibodies - antibodies peoduced from a single clone of cells. More recently, scientists have combined mice cells with human cells as well to produced monoclonal antibodies that are less likely to be rejected by human cells.

26
Q

๐ŸŸข Method For How Monoclonal Antibodies Are Made?

A

-If you were to inject a lab mouse with an antigen, then lymphocytes will produce antibodies against the antigen.
-After some time, you can collect the lymphocytes from the mouse
-However, there is a problem that these lymphocytes will not divide by mitosis
-This means in the next stage, you fuse the lymphocytes with a tumour cell.
-The cell that is produced from this, is a hybridoma cell
-Hydrbidoma cells can produce antibodies and divide by mitosis
-In the next stage you select a single hybridoma cell producing the antibody you want
-You now allow this hybridoma cell to divide by mitosis to form a clone
of identical hybridoma cells (the antibodies produced from this clone of hybridoma cells are identical
-We call these monoclonal antibodies because they all come from a
single hybridoma clone
-A large amount of our monoclonal antibody can then be collected and purified

27
Q

๐ŸŸข How Can Monoclonal Antibodies Be Used? (+ What are they used in)

A

Antigens are protein molecules that are often found on the surface of cells, although free protein molecules can also act as antigens. The monoclonal antibodies produced from a single clome of cells are specific to one binding site on one specific antigen. The antigen might be found on specific types of cell in the body, or it might be a specific chemical. Because the monoclonal antibodies only target and bind to one specific antigen, they can then be used in a number of ways. These include:

  • Pregnancy Tests
  • Diagnosis of disease
  • Studying Cells (e.g Microscopy, Fluorscent Materials)
  • Measuring and monitoring
  • Research
  • Treating Disease
28
Q

๐ŸŸข How are Monoclonal Antibodies used in Pregnancy Tests?

A

These rely on monoclonal antibodies that bind to the hormone human chorionic gonadotropin (HCG) that is made in the early stages of pregnancy. Tiny amounts of the hormone ate passed out of the body in urine. Monoclonal antibodies in the pregnancy test bind to the hormone if it is present, and this is used to produce the colour change that signals a positive result.

29
Q

๐ŸŸข How are Monoclonal Antibodies used in Diagnosis of Disease?

A

Monocolonal antibodies are made to bind to specific antigens found on pathogens, or on blood clots, or on cancer cells. The monoclonal antibodies may also cary markers that make it easy for doctors to see where they have built up. This allows doctors to detect problems before they are seriously affecting a patientโ€™s health. For example, the blood test for prostate cancer uses monoclonal antibodies to bind to prostate-specific antigens. Monoclonal antibodies are becoming increasingly important in the detection of plant, animal, and human diseases.

30
Q

๐ŸŸข How are Monoclonal Antibodies used in Measuring and Monitoring?

A

Monoclonal antibodies are used in hospitals and laboratories to measure or monitor the levels of hormones and other chemicals in the blood. For example, screening donate blood for HIV infection, detecting drugs that have been used illigally by athletes, and detecting infections such as syphilis.

31
Q

๐ŸŸข How are Monoclonal Antibodies used in Research?

A

Research scientists use monoclonal antibodies to locate or identify specific molecules in a cell or tissue. Scientists produce the monoclonal antibodies bind to the desired molecules, scientists can see what has happened by observing the build-up of fluorescence.

32
Q

๐ŸŸข How are Monoclonal Antibodies used in Treatment of Disease (e.g Cancer)?

A

Currently there are three different ways of using monoclonal antibodies to cancers, for example. Each has produced some cancer treatments that are being used and many more are in clinical trials. They include:

  • Direct use of monoclonal antibodies to trigger the immune system to recognise, attack, and destroy cancer cells.
  • Using monoclonal antibodies to block receptors on the surface cancer cells and so stop the cells growing and dividing.
  • Monoclonal antibodies can be used to carry toxic drugs or radioactive substances for radiation therapy, or chemicals that stop cells growing and dividing to attack the cancer cells directly, without harming other cells in the body.
33
Q

๐ŸŸข How Does A Pregnancy Test Work?

A

A pregnancy test has a Reaction Zone (when the liquid passes through the start), a Test Zone/Window (which is where the first red line would be found), and Control Zone/Window (which is the second read line which confirms the first red line is correct). All these zones look for the HCG and the monoclonal antibodies specifically created then bind to the HCG hormone when it is present, which sets off the dye to give a line at a time.

34
Q

๐ŸŸข Advantages Involving Monoclonal Antibodies (Compared To Other Treatments)

A

One of the biggest potential advatages of using monoclonal antibodies is that they only bind to specific diseased or damaged cells that need treatment. Healthy cells are not affected at all, while conventional drug treatment can have devastating effects on cells as well, for example, cancer cells. Radiotherapy treatment for cancer is targted on the area of the body affected by the tumour, but still usually affects the healthy tissue in that area as well.

Another advantage is that the specificity of monoclonal antibodies means that they could be used to treat a wide range of conditions. Although, at the moment monoclonal antibodies are fery expensive to develop, potentially they could become cheaper to develop than coventinal drugs, because all the trestments will be based on tested technology.

35
Q

๐ŸŸข Disadvantages Involving Monoclonal Antibodies (Compared To Other Treatments)

A

Monoclonal antibody treatments are not yet widely used or as successful as it was first hoped 40 years ago. Initially, they created more side effects that expected, which was partly fue to to the use of mouse cells only in the formation of hybridoma cells. The monoclonal antibodies produced were mouse antibodies, and they triggered an immune response in humans (this held back some of the research). Now defelopments such as the production of mouse - human hybrid cells and the use of fractions of antibodies to carry drugs to target cells are reducing side effects. Also, doctors are now prepared for side effects and treat the symptoms.

36
Q

๐ŸŸข Difficulties Involving Monoclonal Antibodies?

A

Producing the right monoclonal antibodies and attaching them to drugs and other compounds provide more difficult than expected. The development of more skills and technologies now means monoclonal antibodies are being used in more different ways. They may yet end up being one of the greatest medicinal technologies.