Immuno Final Flashcards

1
Q

What is the function of Th17 cells in the immune defense?

A

Th17 cells produce IL-17 to recruit neutrophils for the destruction of fungi and some bacteria. Th17 releases IL-17, IL-21 (for GF of Th17), IL-23 (for B cell class switching to IgA and IgG3).

without IL-17 = devasting fungi infection

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2
Q

What is the significance of regulatory T cells (Tregs) in immune homeostasis?

A

Tregs suppress unwanted immune responses and maintain tolerance to self-antigens.

-Subset of CD4s
-Intermediate binding during self-recongition phase.
-Happens in Thymus
-Foxp3 expression for transcription factor (peripherals)

Natural: Inhibit naive T cell activation
Inducable Treg: inhibit APC to bind to T cells for activation and reduces hypersresonse to invaders

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3
Q

How is tolerance established during T and B cell development?

A

Through positive selection for functional receptors and negative selection against self-reactivity.

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4
Q

What is the significance of CD28 and CTLA-4 in T cell signaling?

A

CD28 provides necessary co-stimulatory signals for activation, while CTLA-4 inhibits T cell activation by outcompeting CD28 for B7.

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5
Q

How do IgE antibodies mediate hypersensitivity reactions?

A

IgE binds to allergens and activates mast cells and basophils, leading to the release of mediators during an allergic response.

Type 1 with basophil, mast cells and eosinophils. IgE will bind to FceRI on mast cells and basophils, if enough binds it will activate the cells.

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6
Q

What role do APCs play in the activation of naive T and B cells?

A

APCs present antigens and provide co-stimulatory signals necessary to activate naive T and B cells.

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7
Q

How do MHC I and MHC II differ in terms of structure and function?

A

MHC I presents to CD8+ T cells (cytotoxic), while MHC II presents to CD4+ T cells (helper).

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8
Q

What happens to T cells during activation-induced cell death (AICD)?

A

AICD eliminates T cells that have been repeatedly activated, making space for new naive T cells.

Fas-FasL -> suicide or homicide (NTK)

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9
Q

What mechanisms do T cells employ to avoid attacking self-antigens?

A

T cells undergo negative selection and require additional co-stimulation to become activated against pathogens.

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10
Q

What is the significance of co-receptors in T cell activation?

A

Co-receptors like CD4 and CD8 determine the type of T cell and help in recognizing peptide-MHC complexes.

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11
Q

What is the role of Th cells in orchestrating the immune response?

A

Th cells orchestrate the immune response by releasing cytokines that activate and direct other immune cells.

  • Activate B cells to prodice Ab and Plasma cells
  • Growth factor release
  • Cyokines to recuit other immune cells
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12
Q

What is the role of CD40 and CD40L in B cell activation?

A

CD40 on B cells interacts with CD40L on T helper cells, facilitating B cell activation and antibody production.

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13
Q

How does molecular mimicry contribute to autoimmune diseases?

A

TCR/BCR may recognize pathogens but also cross-react with self-antigens, leading to autoimmunity. Since immune system may still be active, it will attack self angtigens that look like the pathogen that is dead.

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14
Q

Why is a co-stimulatory signal required in T cell-dependent activation?

A

To ensure both the B cell and T cell recognize danger and agree on the need for an immune response.

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15
Q

What are the main types of T cell memory and where do they reside?

A

Tissue-resident memory T cells remain in tissues, effector memory T cells circulate, and central memory T cells reside in secondary lymphoid organs.

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16
Q

What are the three types of antigen presenting cells (APCs)?

A

Activated dendritic cells, activated macrophages, and activated B cells.

17
Q

What are the two ways a naive B cell can be activated?

A

T cell-dependent activation and T cell-independent activation.

18
Q

How does PD-1 contribute to T cell lethargy in inflamed tissues?

A

PD-1 binding to PD-L1 in inflamed tissues results in reduced T cell activity and promotes exhaustion.

19
Q

What is the difference between T cell-dependent and T cell-independent activation?

A

T cell-dependent activation requires help from T cells and co-stimulatory signals, while T cell-independent activation can occur without T cell involvement.

20
Q

How do Th2 helper T cells contribute to the immune response against parasites?

A

They release IL-4, IL-5, and IL-13 to stimulate class switching in B cells to IgE for parasite defense.

21
Q

What is the role of CD4 and CD8 co-receptors in T cell function?

A

CD4 is involved in helper T cell function (MHC II), while CD8 is involved in CTL function (MHC I).

22
Q

How do B cells undergo somatic hypermutation during maturation?

A

B cells mutate their antibody genes to increase affinity for antigens, allowing for improved immune responses.

23
Q

What is the process of receptor editing in B cells?

A

B cells with self-reactive BCRs can rearrange their light chain genes to avoid self-binding.

24
Q

How do encapsulated organisms affect B cell activation in the spleen?

A

Spleen can activate B cells independently of T cells via marginal zone B cells in response to polysaccharide antigens.

25
Q

What are the primary functions of Th1 helper T cells?

A

They promote cell-mediated immunity, activate macrophages, and stimulate B cell class switching to IgG3.

DC releases IL-12
Th1 realeases:
- TNF
- IFN-gramma
- IL-2

26
Q

Why is co-stimulation necessary for T cell activation?

A

Co-stimulation activates naive T cells and amplifies TCR signaling.
-CD40 and CD40L

27
Q

How do cytotoxic T lymphocytes (CTLs) recognize and kill infected cells?

A

CTLs recognize infected cells via MHC I presenting foreign peptides and kill them using perforin and granzyme B.

28
Q

What are the clinical implications of a deficiency in CD40 or CD40L?

A

Deficiency leads to absent T-dependent antibody responses and increased susceptibility to infections.

29
Q

What is the role of cytokines in the differentiation of T helper cells?

A

Cytokines influence the differentiation of naive T cells into specific subsets (Th1, Th2, Th17) based on the pathogen.