Immuno 2 Flashcards

(19 cards)

1
Q

What is the primary route by which foreign antigens enter the body?

A

Through the skin, respiratory tract, or gastrointestinal tract. They are captured by APCs and transported to peripheral lymphoid tissues where adaptive immune responses are initiated.

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2
Q

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

A

Macrophages, dendritic cells, and Langerhans cells. Dendritic cells are the most efficient.

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3
Q

What changes occur during dendritic cell maturation?

A

Increased expression of MHC II and chemokine receptors, making them responsive to cytokines and capable of T cell activation.

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4
Q

What are the 4 main subfamilies of chemokines

A

CXC, CC, CX3C, and XC. These proteins interact with G protein-coupled receptors (chemokine receptors) on target cells.

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5
Q

What is the major function of the MHC complex?

A

Cell surface protein. Binds antigens from pathogens and display them on cell surfaces for recognition by T cells. It also determines organ transplant compatibility and autoimmune disease susceptibility.

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6
Q

What are the differences between MHC class I and II molecules?

A

MHC I is found on all cells (excludes RBC and also neurons), presents endogenous antigens
8-10 aa long antigens, and activates CD8 T cells.

MHC II is on APCs, presents exogenous antigens
12-18 aa long
and activates CD4 T cells.

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7
Q

What defines whether a T cell will trigger a cytotoxic or helper response?

A

CD8 T cells interact with MHC I and respond to endogenous antigens. TCR and cell activation leads to killing of infected cells and activation of CD4

CD4 T cells interact with MHC II and respond to exogenous antigens. TCR and cell activation leads to activation of B cells

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8
Q

What are naive vs effector T cells?

A

Naive T cells have not encountered antigen. Effector T cells have been activated, proliferate, and are ready to perform immune functions like cytotoxicity or cytokine release.

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9
Q

What molecules are required for full T cell activation?

A

TCR-MHC interaction
LFA1-ICAM1 adhesion molecules
CD28 B7-1 and B7-2 costimulation.

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10
Q

What happens to CD28 after stimulation

A

Becomes CTLA-4 inhibits further reactivity

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11
Q

What is the role of Th1, Th2, and Th17 CD4+ T cell subsets?

A

Th1: cell-mediated immunity and intracellular pathogens. Th2: antibody production and extracellular parasites. Th17: neutrophil recruitment for extracellular bacteria.

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12
Q

What markers differentiate effector and memory T cells?

A

Effector T cells express CD69, while memory T cells express CD45RA.

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13
Q

What is the role of B cells in adaptive immunity?

A

B cells recognize antigens, present them via MHC II, and produce antibodies after activation by CD4+ T cells.

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14
Q

How do B and T cells interact?

A

B cells present antigens on MHC II to CD4+ T cells in lymph nodes, requiring TCR and CD40/CD40L binding to activate B cells into plasma cells.

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15
Q

What are thymus-dependent and thymus-independent B cell responses?

A

Thymus-dependent requires T cell help and antigen delivery to B cell follicles

Thymus-independent involves TLRs and polysaccharides that cross link B cell receptors and results in short-lived IgM-producing plasma cells.

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16
Q

What influences class switch recombination in B cells?

A

Cytokines from T cells, such as IL-4 (IgE), TGF-beta (IgA), and IFN-gamma (IgG).

17
Q

What signals are needed for CD8+ T cell activation?

A

Recognition of antigen on MHC I and CD28-B7 costimulation. Proliferation requires IL-2.

18
Q

How do CD8+ cytotoxic T cells kill infected cells?

A

By releasing perforin to form membrane pores and granzymes that enter and trigger apoptosis in the target cell.

19
Q

What happens after a primary immune response?

A

90% of cells die, 10% become memory B and T cells. Upon re-exposure, memory responses are faster and stronger. Secondary immune response peaks within 4 days