Case studies- key info Flashcards

1
Q

POLIO- transmission route

A

faecal-oral, but moves to the CNS

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2
Q

POLIO- name when virus gets into CNS

A

paralytic polio myelitis

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3
Q

POLIO- 2 vaccine types

A

Salk- inactivated, injected, expensive (cold chains and inactivation)
Sabin- live attenuated, oral, cheaper- mostly used

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4
Q

POLIO- subtype which still exists and where

A

WPV1- Afghanistan, Pakistan

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5
Q

POLIO- new vax in development

A

nOPV2

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6
Q

PLAGUE- pPst virulence factors

A

pla- facilitates adhesion by cleaving fibrin clots

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7
Q

PLAGUE- pFra plasmid virulence factors

A

caf1, capsule, antiphagocytic

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8
Q

PLAGUE- pLct VFs

A

yopH- interfere w intercellular signalling and immune responses

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9
Q

chromosome VFs

A

irp2- iron uptake, important for growth

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10
Q

SCHISTOSOMES- life cycle

A

via snails, gets back into water via people

bloodstream > gut > can get caught in liver also

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11
Q

SCHISTOSOMES- drug

A

praziquantel

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12
Q

SCHISTOSOMES- how many infected

A

250 mil

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13
Q

CHOLERA- antigen determining phenotype

A

O antigen

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14
Q

CHOLERA- important toxins

A

Ctx and Tcp

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15
Q

CHOLERA- how do toxins influence pathogenesis

A

toxins affect ion efflux, so ions move out, water follows into the gut

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16
Q

CHOLERA- vaccine effectiveness

17
Q

TRYPANOSOMES- T. brucei immune avoidance strategy

A

VSG coat

some other important potential targets are in a ‘flagellar pocket’

18
Q

TRYPANOSOMES- what % of the genome are VSGs

A

1500 genes, 10% of total genome

19
Q

HIV- how many people living with

A

39 million

20
Q

HIV- PrEP and PEP effectiveness

A

PrEP- 99% for sex, 74 for drugs
PEP- 80%

21
Q

HIV- 3 protein types and total number

A

9 genes encoding 15 proteins
structural (env, pol, gag)
essential regulatory (tat, rev)
accessory (nef, vpu)

22
Q

HIV- immune evasion mechanisms megalist (should maybe make a set of just these)

A

-PAMP modification
-blocking of IFN production
-Vpu inhubiting cellular mechanisms which block release of virus particles
-MHC1 degradation through endomembrane system or exocytosis
-CTL escape (mutation, up to 42% variation in just Env between HIV subtypes and 30% variation within)
-glycan shields

23
Q

HIV- vaccine examples which have been trialed

A

vaccines like AIDSVAX and ALVAC have been tried in various regimens, generally with limited success

e.g. Uhambo trial (nothing, SA), RV144 (Thailand, 30%)

24
Q

HIV- vaccine development avenues

A

targeting broadly neutralising antibodies, combinatorial design to try and target multiple bits of the immune system, mRNA vaccines

25
Q

MENINGITIS- how many capsule types, and howmany are pathogenic

26
Q

MENINGITIS- disease process

A

bacteria is normally just vibing, but canget into brain capillaries, inflammation

27
Q

MENINGITIS- 2 vax types

A

plain polysaccharide- not good for infants and ineffective against carriage
conjugate polysaccharide- developed later, more effective in infants, shown to be strongly effective

28
Q

MENINGITIS- vax programs

A

MCC 1999
MenAfriVac 2010
MenACWY 2015

29
Q

MENINGITIS- current issues

A

group B, showing low immunogenicity so need to be a bit creative
outer-membrane vesicles? fHbp as a candidate protein? decent efficacy when using this