ageing and immunity Flashcards

1
Q

list diseases associated with ageing

A
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2
Q

name the 3 hallmarks of ageing

A
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3
Q

What are the four interdependent hallmarks of the senescence phenotype?

A
  1. Cell-cycle withdrawal: Cells stop dividing.
  2. Macromolecular damage: Accumulation of damage to biomolecules like proteins and DNA.
  3. Secretory phenotype (SASP): Senescent cells release inflammatory molecules.
  4. Deregulated metabolism: Altered energy and metabolic pathways.
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4
Q

What is SASP, and why is it significant in ageing?

A

SASP (Senescence-Associated Secretory Phenotype) involves the release of inflammatory molecules by senescent cells, contributing to tissue damage and ageing.

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5
Q

What happens during cell-cycle withdrawal in senescence?

A

Cells permanently stop dividing, marked by a halt in the cell cycle.

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6
Q

How does macromolecular damage contribute to senescence?

A

Damage to DNA, proteins, and lipids disrupts cellular function.

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7
Q

What does deregulated metabolism mean in senescent cells?

A

Abnormal energy production and inefficient metabolic processes.

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8
Q

What happens to phagocytosis in ageing?

A

decreases

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9
Q

what is immunosenescence

A

Immunosenescence, defined as the changes in the immune system associated with age

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10
Q

What changes occur in macrophages during immunosenescence?

A

Increased production of inflammatory cytokines.

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11
Q

How do neutrophil functions change with age?

A

Reduced NETs and oxidative burst.

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12
Q

What happens to NK (natural killer) cells in ageing?

A

Decreased IFN-γ production.

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13
Q

What is inflammaging?

A

Chronic, low-grade inflammation due to ageing.

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14
Q

What contributes to inflammaging?

A

Hormones, metabolites, PAMPs/DAMPs, and cellular debris.

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15
Q

What key pathway is activated in inflammaging?

A

NF-κB.

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16
Q

What are the consequences of inflammaging?

A

Increased inflammatory cytokines, impaired autophagy, proteostasis changes, mitochondrial dysfunction, microbiota dysbiosis, and cell senescence.

17
Q

What happens to B cells during immunosenescence?

A

Decreased AID activity and BCR repertoire, reduced antibody levels, and diversity.

18
Q

How are T cells affected by immunosenescence?

A

Reduced naïve T cell signalling and increased memory T cells (CD28-, PD-1+, Tim3+, Th2).

19
Q

What happens to naïve and memory immune cells?

A

Naïve cells decrease; memory cells become exhausted.

20
Q

What happens to T cells during immunosenescence?

A
  • Naïve T cells: Decrease.
  • Memory T cells: Increase.
  • TCR diversity: Decreases.
  • Effector T cells: Decline.
  • Antigen recognition repertoire: Decreases.
21
Q

What changes occur in NK cells during ageing?

A
22
Q

How are dendritic cells affected by immunosenescence?

A

Reduced antigen presentation.
Decreased endocytosis.
Lower IFN production.

23
Q

What happens to macrophages with ageing?

A

Decreased number and function.
Reduced antigen presentation.
Impaired phagocytosis.

24
Q

How are B cells affected by immunosenescence?

A

Naïve B cells: Decrease.
Memory B cells: Decline in function.
Antibody production: Decreases in diversity and effectiveness.

25
Q

what happens to Myeloid-Derived Suppressor Cells (MDSCs) during ageing?

A

Number and function: Both increase.

26
Q

What are the overarching consequences of immunosenescence?

A

Reduced immune response effectiveness.
Increased susceptibility to infections and chronic diseases.

27
Q
A