Lc8 - virology Flashcards

1
Q

HIV - general

A
  • Retrovirus –> ssRNA –> reverse transcriptase –> DNA
  • HIV-1 clades:
    o M (major) has subtypes (CRFs)
     C – 50%
     CRFs – 18%
     A – 12%
     B – 10% (western world)
    o O (outlier)
    o N (new)
    o P
  • HIV-2
    o A-H
    o Only A and B are epidemic (west Africa and portugal)
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2
Q

HIV replication

A

Early phase:
1. VAP: gp41 and gp120
Target: CD4 and CCR5
o Later stage the coreceptor is CXCR4
2. penetration
3. uncoating
4. reverse transcription (error prone)
5. nuclear import of preintegration complex DNA
6. DNA integration

Late phase
1. transcription viral genes
2. translation
3. gal polyprotein etc.
4. assembly
5. budding
6. maturation

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3
Q

new HIV staging

A

based on:
- absolute CD4 count per uL
- CD4%
- presentation of AIDS defining diseases

AIDS: <200 c/uL / <14% / yes

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4
Q

acute HIV infection

A
  1. Infection via sex or needles etc.
  2. Attaches to DC
  3. DC goes to lymph node
  4. Infects macrophages, active CD4 and inactive CD4 cells
  5. Once the CD4 cells is active it starts to produce virions
  6. Virions are released and infect other cells  normally initially in the GALT
    - During this period PreP can work
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5
Q

Biomarker profile HIV infection (feibig stages)

A

1.viral RNA
2. p24 protein
3. anti-HIV env protein antibodies
4. anti-p31 antibodies

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5
Q

CD4 loss - HIV

A
  • Gut CD4 cells are lost within months which leads to mucosal infections and high bacterial load
    o This high bacterial load leads to inflammation (systemic) which causes a high turnover rate of CD4 cells in the blood leading to their slower decline than GALT CD4 cells
  • After 6 months a steady state is reached – this includes a set viral load
    o Low viral load leads to low CD4 loss and slower progression
    o High load –> fast progression
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6
Q

quasispecies

A
  • Since replication of retroviruses is very fast and sloppy approx. one mutation per replicative cycle occurs
  • This leads to large differences between virions of an individual host (quasispecies) –> contributes to immune evasion
  • During sexual transmission only the fittest particles can leave the genital tract meaning that upon infection an individual receives a very ‘strong’ quasispecies from the previous individual –> sexual transmission bottleneck
  • Quasispecies development is faster than production of antibodies –> immune evasion
    o Some individuals will after 3 years finally have developed broadly neutralising antibodies
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7
Q

chronic HIV - dynamics

A
  • CD4 cells in HIV patients have a high turnover rate  every 2 days they replicate which contributes to 93-99% of viral production
  • Memory cells –> 1-7%
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8
Q

CD4 cytotoxicity

A

o Direct cytotoxic effect
o Indirect (only 1:1000 cells are infected but more die)
 Hyperimmune activation (due to GALT destruction)

And reduced production by thymus

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9
Q

lymphoid damage

A
  • Due to HIV sustained inflammation causes fibrosis of LNs
  • This impairs the interaction between APCs and lymphocytes
  • Also the structure of the reticular network is worsened over time
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10
Q

cART

A
  • Aims to reduce the viral load and prevent loss of CD4 cells by inhibiting viral replication
  • Blood plasma virus concentration <50 RNA copies per mL
  • cART: 3 drugs combined
    o 2 NRTI + INSTI/PI/NNRTI +pharmacokinetic enhancer (CYP inhibitor)
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11
Q

clinical features - COVID

A
  • Lung: pneumonia and cytokine storm
  • Heart: myocarditis
  • NS: encephalopathy, anosmia, dysgeusia
  • GI: nausea, vomiting, diarrhoea
  • Kidney: renal failure
  • Blood vessels: thrombi, emboli
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12
Q

general virology - COVID

A
  • Enveloped
  • VAP: spike glycoprotein
  • Hemagluttinin-acetylestrase glycoprotein
  • Membrane glycoprotein
  • Small envelope glycoprotein
  • (+)ssRNA
  • nucleocapsid phosphoprotein
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13
Q

variants - COVID

A
  • Changes in the receptor binding domain of the spike protein leads to higher or lower transmission and immune evasion
  • Delta was crazy transmissible –> all parts of the world had slightly different variants at different timepoints until delta hit
    o Higher binding affinity
    o Higher viral production
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14
Q

replication - COVID

A
  1. spike-ACE2
  2. cleavage TMPRSS2
  3. uncoating
  4. translation of RNA replication proteins (nsps)
  5. RNA replication
  6. translation of structural proteins
  7. assembly in ER vesicles
  8. release by fusion
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15
Q

mRNA - vax

A

lipid nanoparticles with spike protein mRNA
fast short lived humoral response (4-6 it drops of fast)
cellular response is longer lived >8months

16
Q

adjuvanted protein - vax

A

spike protein subunit (produced by yeast of bacteria) with an adjuvant
injected and presented by muscle cell

17
Q

vax platforms

A
  1. mRNA
  2. inactivated virus
  3. adjuvanted protein
  4. adenovirus vector
18
Q

adenovirus vector

A

non-pathogenic virus is used to deliver covid spike gene
longer lastig humoral immunity but slower initial response