Humoral immune responses Flashcards

1
Q

Why do mammal’s immune systems need to be complex?

A

Because we have lots of body compartments and have babies that grow inside us whom need protection after birth

  • body compartments
  • fetus and neonate
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2
Q

What are acute phase proteins? What can they be used for in the lab?

A
  • Proteins produced by the liver under the influence of interleukin-6 from mast cells of innate immune system
  • CRP, fibrinogen and mannose binding lectin
  • basically function to opsonise bact and activate the complement pathway
  • test for CRP - indicates infection (non specific)
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3
Q

What are the outcomes of the complement system?

A
  1. MAC - punches bad cells causing them to lyse
  2. Tag - opsonisation for recognition by macrophages and engulfing by phagocytosis
  3. Activate inflam response by triggering mast cells to release histamine - recruit cells from bv
  4. Enhance clearance of AG-AB complexes
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4
Q

What are the microbial strategies used to evade complement activity?

A
  1. Inhib alternate activity by making the bact cell surface acidic (sialylation) e.g. Neisseria sp.
  2. Inactivate complement components by producing elastases e.g. Pseudomonas
  3. Interfere w rec for complement components (C3b) which interferes w opsonisation and phagocytosis e.g. Steptococcus
  4. Bind plasma proteins that negatively regulate complement activity (remember antibodies need to bind to bact antigens for the classical pathway to occur) - done by expressing Pra1 on cell surface e.g. Candida
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5
Q

Describe structure of immunoglobulins (antibodies)

A
  • antigen binding site
  • binding to Fc receptors (receptors for immunoglobulins)
  • complement binding site
  • placental transfer
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6
Q

What are the main immunoglobulins?

A

IgM = B cell rec, agglutination and opsonisation
IgG = complement and cell activation in tissues
IgA = mucosal antibodies
IgE = activation of eosinophils and mast cells
(more functions and subtypes but these are the main ones to remember)

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7
Q

What do immunoglobulins/antibodies do?

A
  • neutralise bact toxins and viruses
  • opsonisation
  • activate complement pathway
  • activate NK cells (ADCC)
  • activate basophils/mast cells
  • activate eosinophils
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8
Q

What are 3 ways antibodies can neutralise influenza virus?

How does the flu virus evade these mechanisms?

A
  1. antibodies for HA1 blocks binding to sialic acid on host CM
  2. antibodies for HA2 blocks fusion of endosome membrane w virus membrane therefore preventing release of virus into cytoplasm
  3. antibodies for neuraminidase prevents sialic acid from being cleaved off the new viruses and therefore prevents new viruses being released
  • basically, haemaglutination (HA) inhibiting antibodies are protective of the flu

Flu virus evades neutralising antibodies by changing ANTIGENETICITY by RECOMBINATION of diff strains of virus = variation

Esp true for HIV

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9
Q

What’s interesting about rotavirus?

A

It is neutralised in the mucosal surfaces, therefore by IgA (mucosal protection), stimulated by vaccine and breast milk

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10
Q

What popn is more susceptible to pneumococcal disease and why?

A

Elderly.
Low opsonophagocytic antibody response to pneumococcal polysaccharide vaccine

  • Basically, when elderly ppl are vaccinated the produce insufficient antibodies for phagocytosis to occur and therefore for immunity to develop
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