Immunity to Viruses Flashcards

1
Q

Immunity to Viruses
Mechanisms:
Soluble extracellular factors

A

– neutralizing antibody and complement (opsonin)

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2
Q

Immunity to Viruses
Mechanisms:
Inhibition of intracellular replication

A

– interferons, host cell

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3
Q

Immunity to Viruses
Mechanisms:
Immune-mediated lysis of infected cells

A

– CTL (CD8) and NK cells

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4
Q

Innate immune system:

Pattern recognition

A

– C-type lectins, membrane TLRs, cytosol sensors (Nod-like receptor), NK cells (viral surface products)

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5
Q

Innate immune system:

Soluble

A

– complement, interferons, cytokines recognize and neutralize free virons

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6
Q

Innate immune system:
Soluble
Interferons

A

– induced by TLRs → act via Jak/Stat → ↑transcription of MHC-1 for better viral antigen presentation

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7
Q

Innate immune system:
Soluble
Complement

A

– C3b opsonin → phagocytes, blocks viral attachment, enveloped viruses, EBV uses C3b to facilitate binding

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8
Q

Innate immune system:
Soluble
NK cells

A

– activated by ↓ MHC-1 → granzymes, perforin → apoptosis of infected cells, produce IFN, recognize Ab coated cells

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9
Q

Innate immune system: Importance

A

– newborns, early infection, pattern recognition, no memory, unaffected by vaccine

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10
Q

Adaptive immune system:

Antibody

A

– mucosal secretory IgA, protective Ab to epitopes, IgG/M clearance, block attachment/uncoating, target infected cells

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11
Q

Adaptive immune system:

Seroconversion

A

Seroconversion – rise in serum antibody titer, 4-fold increase indicates acute/chronic infection

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12
Q

Adaptive immune system:

CTLs

A

CTLs – resolving infection, latent and persistent infection, facilitate apoptosis, impaired with T cells deficiency

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13
Q

Adaptive Immune System:

T helper

A

T helper – regulate Ab production (class switching), CTL differentiation, NK activation, IFN-γ production

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14
Q

Adaptive immune system:

Importance

A

Importance – extracellular and intracellular elimination, induced by vaccines, low function in infants/immunocompromised

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15
Q

Microbial immune evasion:

A

co-evolves with immune mechanisms

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16
Q

Microbial immune evasion:

Cell-to-cell spread

A

Cell-to-cell spread – avoids extracellular environment, latency and avoidance of detection

17
Q

Microbial immune evasion:

Antigenic variation

A

Antigenic variation – Abs can recognize, shift and drift allows for reinfection of a new strain, seasonal vaccines

18
Q

Microbial immune evasion:

MHC

A

MHC – downregulation of MCH inhibits antigen presentation and recognition of infected cells, HSV, CMV, EBV

19
Q

Microbial immune evasion:

Cytokines

A

Cytokines - production of mimic cytokines, soluble receptors

20
Q

Microbial immune evasion:

Apoptosis

A

Apoptosis – blocked by viruses, promotes immortalization and chances for mutation

21
Q

Types of vaccines:

Subunit

A
  • recombinant antigen protein → Ab production – Hep B
22
Q

Types of vaccines:

Inactivated

A

Inactivated – dead whole virus → no mucosal immunity – Polio, HAV, rabies

23
Q

Types of vaccines:

Attenuated live

A

Attenuated live – whole weakened virus → mucosal immunity, CD8 cells

24
Q

Vaccine Schedule

A

Schedule – certain vaccines interfere with maternal IgG, blood products, other vaccines, etc.

25
Q

Immune globulin:

Uses

A

vaccine does not exist, progression is rapid, viral load reduction is critical, or viremia is common

26
Q

Immune globulin:

IVIG

A

IVIG - some neutralizing antibodies, pathogen-specific IG, post-exposure, ex: rabies, HBV

27
Q

Risks for viral infections:

Marrow transplant

A

– cyclosporine, GVH → herpes infections are common, CMV

28
Q

Risks for viral infections:

Antibody deficiency

A

Antibody deficiency – enteroviruses, respiratory viruses

29
Q

Risks for viral infections:

T cell deficiency

A

T cell deficiency – herpes viruses