lecture7 Flashcards

1
Q

What are the types of vaccines??

A

Live attenuated
-virulent in a diff species—> like cox pow, caused disease in cows but did not cause in human but still replicated
-infectious but not disease
-loss of virulence mutants
-adapted to the cold
-genitcally manipulated

Inactivated

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2
Q

What is the goal of vaccination?
What is sterilizing immunity?

A

Establish protective immune response without causing disease
-effective provide disease protection

Rendered someone functionally resistant to infection—- some vaccines do this and some do not

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3
Q

What is the duration of immunity, thermostability, breath of immunity, reversion to virulence, cost between live and inactivated

A

Live:
Long term
Low temps
Good
Occasional
Low

Inactivated:
Shorter
Higher
Poor
None
Low

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4
Q

What is the IPV vaccine ?
What did it give?
What does it protect against?

A

Inactivated polio vaccine

Trivalent—> given via injection

Serological immunity

Protects against disease, not infection

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5
Q

What is the OPV vaccine?
What immunity did it give?
Protects against?

A

Oral polio vaccine—> live attenuated

Trivalent

Mucosal immunity

Protects against infection

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6
Q

What are problems with vaccine use??
What is an example of this?
What is difficult to control with vaccines?

A

-Live vaccine can revert to virulent form
-Vaccines in immunocompromised person can be threatening
-side effects
-expensive

Live polio vaccine no longer used in US bc strains can cause vaccine reversion

-organisms with many serotypes are diff to control w vaccine
-don’t know what responses are required for immunity

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7
Q

What are subunit vaccines?
Ex?

What are recombinant viruse vaccines, HPV & J&J Covid ?

A

Immune response to single protein confers immunity

-hep B surface antigen

HPV—virus like particles , viral protein coat but not genomes

Covid vaccine—chimeric
-includes gene for Cov2 spike, delivers DNA but does not replicated

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8
Q

What are nucleic acid vector vaccines?

A

DNA, RNA Vaccine

Covid- stabilized spike protein

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9
Q

What are viral vectors ?
Adv and dis?

A

Harmless virus which is altered to contain part of COVID-19 genetic code

Adv: less expensive, more stable than RNA

dis: immunity to vaccine virus, may limit repeated used

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10
Q

What are mRNA vaccines ?
Advantages?
Dis??

Improvements ?

A

Contains synthetic version of part of COVID19 genetic code

Adv:
translated in cells so can stimulate production of antibodies and T cell responses
-easy to change sequence

Dis: expensive
Needs cold

Improvements:
Lipid nanoparticles for RNA devliery
Generation of modified RNA that do not trigger innate immune response —>pseudouridine mod

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11
Q

What is herd immunity?
What vaccines are less effective or at causing herdimmunity?

A

Lack of susceptibility / possession of immunity in most people in a population greatly reduces the probability that individuals will be infected

This is why even if small set of the population is

Those that do not cause sterilizing immunity —> COVID

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12
Q

what are 8 factors that contribute to success or failure of vaccination campaigns?

A

1) human as sole reservoir — small pox

2) rate of asymptotic infection

3) modes of transmission

4) number of strains:
-few for polio so only have to add a few serotypes
-rate of evolution for flue is really high

5) virus replication properties

6) immune reponse to viral antigens that do not achieve goals of vaccination—ex: RSV

7: economics of vaccine development

8: immune compliance

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13
Q

why can people be successfully vaccinated after contact with rabies?

A

–rabies is slow replicating,

–people that get vaccine initiated acquired immune responses can develop rapidly enough to prevent disease even when immunization is after infection

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13
Q

why would smallpox be easier to eliminate vaccination than influenza?

A

–smallpox replicates only in humans and has a low inapparnt/ asymptomatic rate

–influenze has a lot serotypes

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14
Q

what is a confounding factor?
how do they complicate the dengue infection?
what is ADE mechanism?

A

other factors than appear to be incommon between groups and appear to cause something, but actually don’t

-dengue people who get infected again get the disease worse the second time

-appears to be due to ADE

-antibody binding to virions allows target cell binding via antibodies constant region
&
- the virus initiations replication cycles more efficiently in presence of the antibodies

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15
Q

why isn’t ART good enough?

A

viral suppression does not cure

can lead to CMV/ EBV tumors

neurological effects— HAND happens in about half of patients (HIV associated neurocognitive disorders)

16
Q

what are 2 proposed HIV cure strategies:
transplanting
and shock and kill, what are they?

A

HIV-resistant cell transplantation or gene editing:
-Based on patients cured using CCR5-Δ32 mutant bone marrow transplants.
-Promising but not broadly applicable due to the risks and complexity of bone marrow transplants.

“Shock and kill” strategy:
-Use of latency-reversing agents to reactivate hidden virus so immune system can destroy infected cells.
-Experimental, still being tested in trials.

17
Q

what is the difference between herpes latency, untreated HIV latency and latent reservoirs of HIV?

A

-Herpesvirus latency: No active replication; virus remains as unintegrated DNA in long-lived cells with minimal/no gene expression.

-Untreated HIV clinical latency: Misleading term—it’s a chronic phase with ongoing active replication, but at low levels due to immune suppression.

HIV latent reservoirs: In patients on ART, HIV persists as integrated, transcriptionally silent proviruses in a small number of cells, capable of reactivation.

18
Q

what is the likelihood of developing AIDS after stopping HAART?

A

Very high: Virus replication almost always resumes after stopping HAART.

HIV is not eradicated by HAART, so stopping treatment typically leads to progression toward AIDS

19
Q

what are 2 components to HIV persistence?

A

Chronic replication (in untreated individuals): Active replication with continuous cell death.

Latent infection (in ART-treated individuals): Silent, integrated proviruses remain in some cells. These can reactivate and reignite infection, requiring lifelong treatment.

20
Q

what is PrEP ( pre exposure prophylaxis?

A

-preventative using low does antivirals in high risk HIV negative individuals

-effective when consistent

-Lenacapvir show great promise