Title: Practical Immunity
1Practical Immunity
- Some diseases and how we are fighting them.
2Principal Vaccines Used in the United States to
Prevent Bacterial Diseases in Humans
- DtaP
- Diphtheria Purified diphtheria toxoid
- Pertussis Acellular fragments of B. pertussis
- Tetanus Purified tetanus toxoid
- Meningococcal meningitis Purified polysaccharide
from N. meningitidis - Haemophilus influenzae type b meningitis
Polysaccharides conjugated with protein - Pneumococcal conjugate vaccine S. pneumoniae
antigens conjugated with protein
3Principal Vaccines Used in the United States to
Prevent Viral Diseases in Humans
- Smallpox Live vaccinia virus
- Poliomyelitis Inactivated virus
- Rabies Inactivated virus
- Hepatitis A Inactivated virus
- Influenza Inactivated or attenuated virus
- Measles Attenuated virus
- Mumps Attenuated virus
- Rubella Attenuated virus
- Chickenpox Attenuated virus
- Hepatitis B Antigenic fragments (recombinant
vaccine)
4Enzyme-Linked Immunosorbent Assay(Direct ELISA)
Figure 18.12a
5Enzyme-Linked Immunosorbent Assay (Indirect
ELISA)
Figure 18.12b
6Serological Tests
Figure 18.13
7We will look at a number of things and how they
deal with our immunity.
- Malaria
- HIV
- HepB a subunit vaccine.
- Tissue Transplant
- Asthma
- Leishmaniasis
- Botfly Larvae MYIASIS
8Malaria
- Kills 1-3 million people a year.
- Hundreds of millions of clinical infections
- Mostly in sub-Saharan Africa
- Anopheles control is the major way.
- What happens if we loose this control?
- In 1985 the mortality rate for Malaria increased
to almost 15 from 5 of hospitalized cases in
Zaire
9The Biology of Malaria
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11Outline of Infection.
- Organism Apicomplexan genus of Plasmodium
- Infective stage is sporozoite moves from mosquito
to human blood. - Carried to liver, move into cells change to
merozoites that move into blood stream and become
merozoites (form ring structure in RBC, how can
be identified)
12- Cyclically rupture RBCs and release more
infective particles as well as waste products
that cause fever. - Merozoites change into gametocytes where they can
be picked up by Mosquitoes. - Gametocytes unite in the mosquito and can produce
sporozoites.
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14- Why do these species usually rupture and cause
fever in 24 hr cycles??? - Why are humans considered an intermediate host?
15Problems with Vaccination
- Many diseases do not occur in the US for 1999
- 0 rabies
- 8 plague
- 58 botulism
- 0 Yellow fever
- 0 small pox
- Is the risk and the expense worth the effort?
16Why does the US not Vaccinate for TB, if a
vaccine exists?
- Risk
- Variable result
- Interferes with testing
17What are we trying to induce with vaccination?
18Recent studies
- 1993 Childhood Immunization Initiative (CII)
increase coverage levels to 90. - 1997 best year with 78 1 million children under
the age of 2 still have not received
immunizations. - Other countries?
- Measles still accounts for 10 mortality among
children aged less than 5 years
19Why does the rest of the world not have the same
vaccination rate as we do?
- Record keeping
- Cannot afford even minimal treatments
- Immunocompramized
- No refrigeration
- No system of distribution
- No profit for drug companies.
20Do you think that Malaria can be cured by only
one type of vaccine?
- No
- We are in the process of developing different
antigens that will lead to protective immunity at
each state
21- Vaccine against the sporozoites must produce
antibodies that work within 30 minutes to block
invasion of hepatocites. - CD4 and CD8 cells must be trained to kill cells
with the intrahepatic parasites - A vaccine against merozoites will block the
cyclical invasion of RBCs - Antibodies must be created against the malaria
toxins to reduce the cyclical fever cause by the
release of merozoites
22- Antibodies to parasite antigens expressed on
RBCs block adherence to endothelium and
rupturing. - Cell mediated immunity can be stimulated to kills
RBCs containing the parasite. - Antibodies to gametocytes can block structures
involved in fertilization which would prevent
zygote formation in the mosquito.
23Is a malarial Vaccine possible?
24Humoral response to vaccination
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28Cell mediated response.
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30HIV
- Lentivirus (retrovirus)
- Genome is RNA
- Particle contains the Enzyme Reverse
transcriptase - Envelope of cytoplasm has viral protein gp120 and
others
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32- Spikes allow virus to attaches to CD4 receptor on
host cells. - Receptor is found on Helper T cells, Macrophages
and dendritic cells - Following attachment is absorption and infection
- Infection can be latent or active
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34Stages of HIV infection
- Clinical stages include
- Category A. Asymptomatic
- Category B. persistent infections of Candida
albicans denote early indication of immune
failure infections that one does not normally get
but one gets over it. - Category C. C.a. of esophagus and lung other more
serious infections typical AIDS indicator
condition. CD4 Tcellsgt200/mm3
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36HIV vaccine
- Probably most realistic way to control epidemic
- Problems because we lack an animal test model.
How do we know this works? - Rapid mutation rate of GP120 makes it difficult
to target. - Why does HIV have a rapid mutation rate?
37Tissue Transplants
- symptoms
- Biology
- problems
38Asthma
- Symptoms.
- Biology
- Problems
39Leishmaniasis
- 20 different forms of protozoan pathogens.
- Transmitted by bite of female sand flies found in
the tropics and deserts. - Unaffected reservoir of small mammals
- Promastigote in salvia of insect from vector
- Amastigote in phagocyticic cells to vector
40treatments
- 4 weeks of toxic metal antimony
- Amphotericin B
- Fluconazole
41Look at the change of Promastigote to Amastigote
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43Is a vaccine worth making?
- Cost to US?
- Cost world wide.
- Current treatment is toxic.
- How Could we go about making a vaccine?
- Would it necessarily work?
44One method
- Rather than target the pathogen, scientists at
the U.S. National Institute of Allergy and
Infectious Diseases (NIAID) use fly slava. - Isolated saliva protein 15 and cloned the gene.
- Made a DNA vaccine
- Provided some protection
- Is this T cell or antibody mediated?
45- Used antibody knock out mice and found that the
method still worked. - Is a T cell mediated response.
46MYIASISIs this a problem?How is damage done?
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48Practical vaccination
- Making product that will produce an immune
response. - Administering product
- Making sure that product is effective and has low
side effects.