immune protection Flashcards

1
Q

true or false:
the goal of vaccination is to reduce the risk and/or severity of vaccine-preventable illnesses
true or false:
the people we vaccinate are:
* Children  schedule of immunisations for vaccine-preventable illnesses
* Vulnerable groups  eg. pregnant women: Pertussis vaccine, flu vaccine…
 eg. immunocompromised patients: meningitis, pneumococcal, flu vaccines…
 eg. elderly patients: pneumococcal, flu vaccine…
* Occupational risk  eg. healthcare workers: MMR, Hepatitis, influenza, pertussis, varicella, (BCG)…
 eg. prison, security workers: Hepatitis B, (BCG)…
* Travel vaccines  location-dependent; eg. yellow fever, cholera…
Goal: to reduce the risk and/or severity of vaccine-preventable illnesses
Also: Ad hoc public health vaccinations – eg. COVID, monkeypox…

A

true

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

vaccination is the inducing a protective immune response by exposure to — or their components and vaccination can be —- or —-

A

microbes
active and passive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

1-active antigen:
exposure the body to an —
an adaptive immune response is developed after —-
the protection is usually —-
2- passive antigen :
provides — to protect against infection
protection is — but —-
usually classified as — or —

A

antigen
7-14 days
long lasting or lifelong
antibodies
immediate but short lived ( few weeks)
natural or acquired

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

passive immunisation - principle:
1- transfers —- against disease-causing protein or pathogen to patient
2- has an —- effect/protection
3- —- : - transfer of maternal IgG to foetus across the placenta; transfer
of IgA to newborn in breast milk.
4- — : introduce antibodies from other individuals or animals
( CAVEATS: Generates no memory cells; protection is transient)
passive immunisation- external antibodies used for — toxins , and for — to treat high risk groups as pre-term babies, the immunocompromised.
sources:
* Individuals recovering from the disease – measles, chickenpox, hepatitis B, CMV
* Animals injected with —
Eg. snake venom, spider venom
* ——

A

antibodies
immediate
natural
artificial
neutralise toxins
for infection
with toxins
monoclonal antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

active immunisation - principle:
1- introduces — to individuals for immune response
2- an — humoral immune response is critical (antibodies)
3- the — humeral immune response is quicker and more effective than — humeral response
* The more similar a vaccine is to the disease-causing form of the
organism, the better the immune response to the vaccine

A
  • antigen
  • adaptive
  • 2ndary
  • primary
    ( check slide 10 for graph )
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

the requirements for effective active immunisation :
1-Induce adaptive — immune response with antibody secretion and
the generation of long-lasting —- and —
2- Requires cooperation with — ( which needs – presenting to — and — ) and—- ( by which cd4+ and T cells differentiate into — and secrete —– to help b cells ) cellular immune response
- info: The longest-lasting humoral immune response has help from—

A
  • humoral
  • innate which needs APCs presenting to CD4+ T cells
  • cellular which differentiates into Th-4 ad IL-5
  • T cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

types of vaccines :
1- live attenuated vaccines:
- attenuated/weakened from – microbes
- must — to be effective
- immune response similar to – infection
- usually effective w – dose
- disadvantage : may cause the — they are designed to protect against as it could be revert back to virelcne or be insfuufienctly attenuated for high risk patient.
- example: MMR , MCG , rotavirus vaccines
2- killed / inactivated vaccines:
- kills the microbe using —
- used mostly for — but since it cant replicate it gets — immune response
- need — asdmisntration
- advantage: safer and cant be mutated back to vurelnt type , stable and easily stored
example: Polio, hepatitis A, rabies, influenza (viral pathogens)
Pertussis, typhoid, cholera, plague (bacterial pathogens)
3- subunit vaccines :
- only includes – of the pathogens that best induce an immune response
- examples:
* Toxins– diphtheria and tetanus
* Bacterial coat polysaccharides - Neisseria
meningitidis or Haemophilus influenzae
4- virus like particle ( VLP) vaccines :
- protein shell made to look like – without —-
- elicits a strong — and —- response
- examples:
* Hepatitis B vaccine
Developed against surface antigens on virus
* HPV vaccine (GardasilTM)
Developed against surface antigens on the most common HPV strains that cause cervical cancer

A
  • wild
  • replicare
  • natural
  • one dose
  • illness
  • heat chemicals irradiation
  • bacteria
  • weaker immune response
  • parts
  • virus without genetic material
  • strong t and b cell response
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

how to make mRNA vaccines :
1- prepare antigenic sequence as part of SARS-CoV-2 spike protein as — or —
2- encapsulate in — for delivery into cells
3- – gets exposed
4- induces robust — and — immune response
5- cheap , – used , and have — properties

A
  • modified or synthetic mRNA
  • lipid nanoparticles
  • proteins
  • innate and adaptive
  • rapidly
  • adjuvant
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

adjuvants - vaccination dirty little secret lol:
1- promotes a —- immune respinse
2- inclusion of contaminates in early vaccines — response
3- aid —-
4- usually component will activate —
5- examples:

A
  • strong innate
  • increased
  • antigen presentation
  • TLR
  • examples:
  • Bacterial particles like dried, inactivated Mycobacteria (in Freund’s Adjuvant)
  • Viral DNA
  • Alum (aluminium hydroxide)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

adverse effects of vaccines :
1- —- carry risk of infecting immunocompromised individuals as young ppl elderly immodfienct transplant patients etc
2- cutaneous reactions at injection site, mostly —-
3- some systemic effects as :
4- hypersentistivites as:
5- excipient effects as egg protein and preservatives are rare but often manageable ( examples: patient with severe egg allergy should get flu vaccine under medical supervision)
6- passive vaccination: most IVIG side effects are — and —- as:

A

live
local mild inflammation
fever malaise headaches fatigue
type iii arthus reactions and type I anaphylaxic which is rare
- mild and transient as: Eg. headache, chills, myalgia, nausea, tachycardia, hypotension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

the 2 types of antibodies as therapeutic agents are:

A

polyclonal antibodies ( many antibodies recognised by one antigen )
monoclonal antobdoeis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • Diphtheria antitoxin;
    tetanus anti-toxin; anti-venom for certain snake bites are examples of
A

polyclonal antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

another examples of polyclonal antibodies:
1- ATG - anti thymocyte globulin
- source from :
- used to deplete — and prevent organ — for post transplant in moderate/severe cases of aplastic anemia
2- Anti-D (RhD) immunoglobulin, pooled human polyclonal blood product:
- sources: female RhD- – blood donors naturally immunised during pregansty w RhD– fetouse , RhD negative males volunteers immunised w RhD antigen
-used in 000 patients and decoy ro prevent — diseases of the newborn

A
  • polyclonal antibodies from course or rabbit serum
  • T cells and prevent organ rejection
  • female Red -ve and the baby is +ve
  • in autoimmne thromocytepernia patients and prevents haemolytic disease due to rheas incompatibility
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

polyclonal antibodies advantage and limiation :

A

Advantages
- Better immunity?? The endogenous immune response is polyclonal in nature!
- Cheaper than monoclonal antibodies
Limitations
- Theoretical risk of infection from pooled blood products
Eg. Hepatitis C contamination of Anti-D from Irish blood products in 1970s
- May confound results in serological testing
- Possibility of local inflammation at injection site, possibility of systemic side effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Purified, pooled, sterilised IgG from the plasma of >1,000 donors is known as –
propose: —- to reduce/prevent infection , — in autoimmne or inflammatory disease
- specific indication includes:
- advantages :
- drawbacks:

A
  • IVIG aka intravenous immunoglobulin
  • antibody replacement
  • immonodulator
  • indications include:
  • Primary immunodeficiencies eg. CVID, humoral immunodeficiency
  • Chronic lymphocytic leukaemia
  • Immune-mediated thrombocytopenia
  • Neurological conditions – Guillain-Barré Syndrome, some neuropathies
  • Kawasaki disease
  • Toxic epidermal necrolysis
  • advantages: life-saving or at least life-enabling
  • drawback:
  • Side effects incl. headache, chills, myalgia, nausea, tachycardia, hypotension… usually mild, transient
    and reversible;
  • Thrombotic complications (rare), acute renal failure (rare);
  • Theoretical risk of transmitting infection (eg. cases of Hepatitis C, human parovirus);
  • May confound recent vaccination and serological testing;
  • Not indicated in patients with IgA deficiency, often develop anaphylaxis.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

monoclonal antibodies used for;

A

To increase the immune response
(checkpoint inhibitors in cancer)
To reduce the immune response
(CK or immune cell signalling)
To block infection
To block signalling in cancer cells
( check slide 27)

17
Q

antibodies targeting immune cells and cytokines;
- when the goal is to — the immune response:
* Checkpoint inhibitors – “taking the
brakes off immune cells”
- when the goal is to – immune response:
- — to reduce inflammation
- —- to prevent transplant rejection
-Eg. Basiliximab– Simulect (Novartis)
* Anti-IL-2 receptor antibody
* IL-2 drives T cell proliferation – important in organ transplant rejection
* Anti-rejection drugs target T cell activation

A

increase
decrease
anti cytokines
antagonise T cells
( check slide 29,30)

18
Q

monoclonal antibodies against cancer- how do they work :
1- targets growth factors —- :
- use MAbs as receptor —- –>. reduces the GFR signalling and activates — in tumours
example : Gefitinib for lung cancers targets EGFR and Trastuzumab (Herceptin) in breast and gastric
cancers – HER2
2- targets GFR — :
- MABs against GFR ligands —> antibody bound ligands is too — to bind and activate GFR example: Bevacizumab in brain and other cancers targets VEGF to
block angiogenesis
3- targets the — response:
— inhibitors MAbs blocks the pathway that tumor use to turn off T cells activation which restores the immune response against tumour cells as:
Atezolimab
Pembrolizumab

A
  • receptors
  • antagonists
    -apoptosis
  • ligands
    -bulky
  • immune response
  • checkpoint inhibtor
    ( check slide 32 33)
19
Q

checkpoint inhibitors - poster drugs:

A
  • Anti CTLA-4: Ipilimumab approved for advanced melanoma,
    mesothelioma, colorectal, some lung cancers…
    Works by inhibiting CTLA-4 and by depleting regulatory T cells (Treg)
  • Anti-PD1: Nivolumab and Pembrolizumab approved for melanoma,
    lung, renal, bladder, colorectal, gastric cancer…;
  • Anti-PD-L1: Atezolizumab approved for melanoma, urothelial, breast,
    some lung cancers…
  • More effective and less toxic than anti-CTLA-4
  • Can be used combined: but more side effects
20
Q

1-immunogenicity can be:
2- antibodies can be used as – not only for infections

A

1
-Rodent monoclonal
-Chimeric monoclonal
-Humanised monoclonal
2- drug