Infection and immune system overview Flashcards

1
Q

What infections make up the big 3 ?

A

tuberculosis, HIV/AIDS, Malaria

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2
Q

What are the impacts to infectious diseases ?

A

Co-infections (multiple species of pathogen infect), healthcare resources, wider impacts (socio-economic, quality of life, morbidity (illness), mortality (death))

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3
Q

What are ways to acquire infection ?

A
  • Environmental – soil and water
  • Other hosts
  • Physical: contact, ingestion, inhalation or a vector
  • Mucosal sites
  • Abrasions, cuts
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4
Q

How can microbes be beneficial ?

A

Beneficial functions include digestion of food, protection of pathogenic bacteria, synthesis of nutrients and vitamins

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5
Q

What makes microorganisms harmful ?

A
  • Microbe-specific (virulence factors)
  • Host-specific (inflammation)
  • Microorganisms can adapt to their host or vica-versa (high pathogenicity is not a good survival strategy)
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6
Q

How can a microorganism adapt ?

A

o Adaptations can be site-specific or host specific (intra-host or inter-host)
 Intra-host: different microbiome in different sites in one host
 Inter-host: difference between people

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7
Q

Zoonoses and reverse zoonoses ?

A
  • Zoonoses: disease spread from animals to humans
  • Reverse zoonoses: humans to animals
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8
Q

Host-pathogens adaptations

A
  • Innate immunity: fruit bats suppress viral infections
  • Adaptive immunity: antibody repertoires are large in bats, meaning they don’t require rapid affinity maturation for limiting viral replication
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9
Q

What can mutations do to a microorganism ?

A

Virus mutations are random and can enhance transmission, virulence or immune evasion, depending on selective pressures and opportunities (including human behaviour)

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10
Q

What are some zoonotic pandemics ?

A

Zoonotic pandemics: H1N1 (1918-20), HIV (1981-), SARS CoV-1 (2002-04), H1N1 (2009), MERS CoV (2012-), Ebola (2014-16), Zika virus (2016-17), SARS CoV-2 (2020-)

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11
Q

What is CFR ?

A

Case fatality rate (CFR): proportion of deaths in a population of cases

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12
Q

How have we co-evolved with pathogens ?

A

We have co-evolved with microorganisms: our immune system expects challenges and may become dysregulated if not exposed to microorganisms, the absence of microorganisms may cause more disease than the presence (we can be too clean)
- Immunotherapy and probiotics

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13
Q

What are the key functions of the immune system ?

A

Immune system functions: controlling infections, killing tumours, immune pathology (allergies, autoimmunity), graft rejection (barriers to transplantation), metabolic diseases (obesity), mental health

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14
Q

What is SCID ?

A

SCID (Severe-combined immunodeficiency) – individuals born with a defect in T and B cells have severely impaired immune responses, and if untreated with die within a year

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15
Q

What are some mechanical barriers ?

A
  • Skin: epithelial cells joined by a tight junction, longitudinal flow of air or fluid.
  • Gut: epithelial cells joined by a tight junction, longitudinal flow of air or fluid.
  • Lungs: epithelial cells joined by a tight junction, movement of mucus by cilia
  • Eyes/nose/oral cavity: epithelial cells joined by a tight junction, tears nasal cilia
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16
Q

What are some chemical barriers ?

A
  • Skin: fatty acids, beta-defensins lamellar bodies cathelicidin
  • Gut: Low pH, enzymes (pepsin), alpha-defensins (cryptdins), regll (lecticidins), cathelicidin
  • Lungs: pulmonary surfactant, alpha-defensins cathelicidin
  • Eyes/nose/oral cavity:lysozymes in tears and saliva, histatins, beta-defensins
17
Q

What is an example of microbiological barriers ?

A

Normal microbiota

18
Q

What is the mucosal barrier ?

A

respiratory tract (sinus, trachea, lungs), gastrointestinal tract (oral cavity, esophagus, stomach, pancreas,intestine), urogenital (uterus, bladder, vagina), lacrimal glands (tears), salivary glands, mammary glands, reproductive tracts
- Pathogens that can evade the mucosal tract: Placenta (HIV), Lungs (influenza), STD (herpesvirus), tapeworms (food)

19
Q

Match these to either innate or adaptive ?
Mast cells
B cells
macrophages
T cells
Dendritic cells
basophil
natural killer cells
eosinophil
neutrophil
CD4+ cells
granulocytes
complement proteins
CD8 cells

A

INNATE:
Mast cells
macrophages
Dendritic cells
basophil
natural killer cells
eosinophil
neutrophil
granulocytes
complement proteins

ADAPTIVE:
B cells
T cells
CD4 cells
CD8 cells

20
Q

What does the graph look like for duration of infection against number of microorganisms for lack of innate and adaptive vs normal ?

A

Lack of innate: sudden and severe increase in microorganisms

Lack of adaptive: normal number of microorganisms to a normal infection but then starts to increase rather than decreases

Normal: increase then decrease

Innate gives a chance for adaptive to develop

21
Q

Functions of innate immunity ?

A

Sense and responds to danger signals (infection and damage)
Always on, always ready to responds instantly
Communicates danger to other cells of innate and adaptive immunity
Recruits immune cells to infection site (inflammation)
Tells adaptive immune cells when to respond
Cellular and biochemical killing mechanisms

22
Q

Innate killing mechanisms

A

phagocytosis (macrophages, neutrophils), secretion of cytotoxic granules (destructive chemicals), killing of infected cells, complement proteins

23
Q

Functions of the adaptive immune system ?

A
  • adaptive immunity consists of T cells and B cells
  • T and B cells can recognise a huge range of proteins and molecules (called antigens) with a degree of specificity)
  • Their specificity for the pathogen makes the immune response more effective
  • Identifying and expanding the T and B cells that recognise the pathogen takes time, which is why adaptive immunity is slow
  • T and B cells can remember previous encounters with pathogens (immune memory)
24
Q

What are the 3 main types of T cells ?

A
  • Helper T cells (Th cells); talks to other cells, co-ordinate immune responses, amplify innate immunity
  • Regulatory T cells (Treg cell): Turn-off immune responses
  • Cytotoxic T cells (CTL): kill infected cells
25
What are some functions of the antibody ?
- Are highly specific to individual pathogens - Neutralise pathogen molecules, e.g., toxins - Mark pathogens for destruction by other immune cells - Link innate and adaptive killing mechanisms
26
What are some features of immunological memory ?
- Specific to the original pathogen - Responds faster and bigger - Combines specificity with speed
27
What are cytokines ?
Cytokines: chemical messages like hormones, Many different cytokines with different Functions, Target any cell with relevant receptor, allow one cell to signal to many other cells, cells don’t need to be in contact, can act locally or systemically.
28
How does activated macrophages and Th cells interact ?
Receptor/ ligand o Many different receptors and ligands with different functions o Cells have to be in contact and have correct receptor/ligand pairs o Allows very precise communication between individual cells
29
What is the importance of the lymph nodes and the spleen ?
- specialised sites where the immune response is co-ordinated - Focal points for immune cell communication - Play a role in initiating adaptive immune response