Infectious diseases and vaccines Flashcards

1
Q

Describe the main immune modules induced by the innate lymphoid cells.

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

Some pathogens use Vectors

A

Intermediate hosts
* carry infections
* often blodsucking
* Tics, Fleas, Flies, Mosquitos

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

Antibodies

A

Antibodies are protective proteins produced by your immune system. They attach to antigens (foreign substances) — such as bacteria, fungi, viruses and toxins — and remove them from your body.

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

Viral infections

A

binds to a surface receptor to infect a cell
– DNA or RNA (ds or ss) -Replicate within host cell
– Genome replication may be error-prone =>mutations – Protein or lipoprotein coat
– Lipid-envelope when extra-cellular (some)

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

Antibody (especially secretory IgA)

A

Blocks binding of virus to host cells; preventing infection or reinfection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

IgG, IgM, and IgA

A

Block fusion of viral envelope with host cell’s plasma membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

IgG and IgM

A

Enhance phagocytosis of viral particles (opsonization)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

IgM

A

Agglutinates viral particles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Complement activated by IgG or IgM antibody

A

Mediates opsonization by C3b and lysis of enveloped viral particles by membrane-attack
complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

IFN-g secreted by TH or TC cells

A

Direct antiviral activity

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

Cytotoxic T lymphocytes (CTLs)

A

Kill virus-infected self cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

NK cells and macrophages

A

Kill virus-infected cells by antibody-dependent cell-mediated cytotoxicity (ADCC)

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

Hepatitis C

A

overcomes interferon antiviral effects by blocking/inhibiting PKR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

HSV

A

inhibits TAP activity => shutting down MHC class I presentation to CD8+ T-cells

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

Influenza and HIV

A

change their surface Ag

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Virus -Evasion strategies

A

Type I and III interferon pathways
* Peptide processing and presentation in MHC class I
* Cytotoxic T lymphocyte and NK-cell response
* Modulation immunresponse by producing or blocking cytokines, chemokines or receptors
* Latency – ceasing to replicate until immunity wanes
* Survival within Macrophages
* Antigen variation

17
Q

Intracellular bacteria

A

Type1andcytotoxicimmune response
– Macrophages
– NKcells

18
Q

Extracellular bacteria

A

Type3 immune response
– Neutrophils
– Antibodies
* Neutralization & opsonization
– Complement
* opsonization & lysis

19
Q

Mycobacterium Tuberculosis

A

Intracellular bacteria
* Survive in macrophages
* Hard to eliminate – although often contained
* Th1 type immune response
* Recruits&acitvates
macrophages
* Granulomas

20
Q

Parasitic infections

A

Very broad category
Giardia lamblia
SEM 8698 lores.jpg.
(2019 Wikimedia Commons.
* From small unicellular (protozoan) to large macroscopic worms
* Ways of infection
– Water–Giardia
– Vectors–Malaria
– throughintestinaltract(food,water,feces) – Somethroughskin(egSchistosomas)
* Immune response depends on
* Mode of immune detection
* Paracitic stage * Location

21
Q

Parasitic infections - Helminths

A

Enter hosts- intestinal tracts
* Exclusively extracellular
* Type 2 immune response
– ILC2s
– IL-4, IL-5, IL13
– Mucosa
– Smooth muscle contraction
– induction of IgE
– mast cells, eosinophils
– M2 Macrophages -Alternatively activated
* Evasion:
– decrease external Ag expression
– wrap themselves in host proteins to limit immunity

22
Q

Fungal infections

A

Type 3 Immune response
* Commensal fungal organisms
– May be pathogenic if dominant
– Ie:antibacterial medications–oral candidosis (oral thrush) or vulvovaginal candidiasis (yeast infections)
* Opportunistic infections – Not normally pathogenic – Immunodeficient patients
* Neutropenia, Immunesuppression, HIV/AIDS – Candidosis
* Pneumocystis Carini * Evasion:
Candidiasis
Shankargouda et al, Fron Microbiol 2015
– –
Capsules that prevent PRRbinding
Fungi-induced expulsion from macrophages

23
Q

Vaccination

A

Aim:
– to generate protective immunity without having to go through the disease
* Active immunization
– Induce adaptive response by exposure to nonpathogenic or parts of a microbe
– Effectors:
* Antibodies
* ProtectiveTcells

24
Q

Vaccines adjuvants

A

Adjuvants are included to enhance the immune response to a vaccine
– Alum — good at stimulating TH2 but not TH1 responses
– AS04 — alum plus a TLR4 agonist
* Encourages TH1 responses
– Virosome — reconstituted viral envelope with no genetic information

25
Q

Vaccines – conjugate

A

Conjugate or multivalent vaccines can improve immunogenicity – Linking with something immunogenic

26
Q

Passive immunisation

A

Passive immunity is provided when a person is given antibodies to a disease rather than producing them through his or her own immune system.

27
Q

Influenza vaccines

A

Antigens form 4 different virus – 2 A and 2 B
* 3 forms approved in Norway:
– Inactivated virus (most)
– Inactivated with virus (for patients >65 yrs)
– Live attenuated virus (nosespray) (children 2-17 yrs)