Immune response to microbial challenge Flashcards

1
Q

Pathogens that infect via the respiratory tract

A

Influenza, RSV, M. Tuberculosis (TB), S. Pneumoniae, Cryptococcus

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2
Q

Pathogens that infect via the faecal oral route

A

Hepatitis A, V. Cholerae, Shigella, E. coli

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3
Q

Pathogens that infect via the sexually transmitted route

A

HIV, HPV, T. pallidum (Syphilis) N. gonorrhoeae, Candida albicans

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4
Q

Pathogens that require a vector to infect

A

Rabies Virus, Plasmodium (Malaria), Schistosoma, Trypanosoma

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5
Q

Mechanical mechanisms for preventing infection at Mucosal surfaces

A

Epithelial tight junctions

Longitudinal flow of air or fluid

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6
Q

Chemical mechanisms for preventing infection at mucosal surfaces

A
Fatty acids (skin)
Enzymes: lysozyme, pepsin
Low pH
Antibacterial peptides
Mucus
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7
Q

Microbiological mechanisms for preventing infection at Mucosal surfaces

A

Normal flora compete for nutrients/attachment sites

Production of antibacterial substances (colicins, E. coli)

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8
Q

Examples of antimicrobial molecules

A

Lactoferrin
Lysozyme
Defensins

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9
Q

Defence against pathogens in the lower respiratory tract

A
Mucosal surfaces
Lysozyme
‘Sweeping’ movement upward by ciliated epithelium
Antimicrobial peptides
Alveolar macrophages
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10
Q

Defence against pathogens in the digestive system

A

Oral route – competition with well - adapted normal flora of mouth, intestine
Stomach - acid and secretions
Lower intestine – alkaline pH
Intestine - peristaltic action of intestine flushes out organisms
Pancreatic enzymes - bile salts, lysozyme

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11
Q

Defence against pathogens in the genito-urinary system

A
Male system kept sterile
Female system colonised
Flushing mechanisms of urine
Acidity of urine
Vaginal epithelium – Lactobacillus acidophilus – acidic end products prevent colonisation
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12
Q

How does MHC class I antigen presentation occur?

A
Peptides cleaved by proteasome
TAP transporter to ER
Assembled with MHC class I
Sent to Golgi complex
Sent to cell surface
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13
Q

How do CD8+ lymphocytes kill infected cells?

A

Releasing granzymes and perforin or by engagement of Fas on target cells by Fas Ligand (FasL)
Secrete IFNy and TNFa

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14
Q

Functions of antibodies

A
Lysis of membrane bound virus particles
Opsonisation of particles
Lysis of infected cells or pathogens 
Triggering of inflammation and immune cells
These functions often involve complement
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15
Q

What does the membrane attack complex act upon?

A

Gram positive bacteria

Enveloped viruses

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16
Q

Methods of passive immune evasion

A

Antigenic shift and drift leading to epitope escape
Anatomical seclusion/ hiding
Infection of immune cells

17
Q

Define antigenic drift

A

Small mutations in viral DNA accumulate over multiple replications, producing a closely related virus similar to the original

18
Q

Define antigenic shift

A

An abrupt, major change due to exchange of DNA between viral strains, producing a novel viral protein which the host has little protection against

19
Q

Methods of active immune invasion

A

Interference with innate system (e.g. affecting cytokines, Type I IFN, complement)
Interference with NK cells
Interference with the adaptive system (e.g. affecting MHC or antibodies)

20
Q

How HIV evades the immune system

A

Targets a key cell in adaptive immunity (CD4) and able to infect via APCs
Coat Proteins are covered in carbohydrates to evade recognition
Epitopes in gp41 are masked
RNA genome undergoes rapid change both CTL and antibody are evaded
Vaccination increases CD4 T cell infiltration to infected area, therefore increasing target cells

21
Q

What is most important in control of viruses?

A

Type I IFN, NK cells, CD8 cells

22
Q

What is most important in control of bacteria?

A

Antibody, Neutrophils, CD4 Cells

23
Q

What is most important in control of fungi?

A

CD4 Cells, Neutrophils

24
Q

What is most important in control of parasites?

A

Mast Cells, Eosinophils