immune_memory_flashcards

1
Q

Front

A

Back

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2
Q

What is immune memory?

A

Feature of adaptive immune system - pool of antigen specific cells following infection with enhanced ability to respond to a second infection.

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3
Q

What cells are involved in presenting peptides to T lymphocytes to initiate an acquired immune response?

A

Antigen presenting cells (APCs - macrophages, B lymphocytes, Langerhans cells, dendritic cells).

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4
Q

What are the markers for memory T cells and naïve T cells?

A

CD45 RO = memory T cells, CD45 RA = naïve T cells.

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5
Q

How long do memory cells remain following an infection?

A

Memory cells remain for a long time following infection.

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6
Q

Do memory cells continue to proliferate after infection?

A

Yes, they continue to proliferate at a low rate.

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7
Q

What is the response of memory cells to subsequent exposure to an antigen?

A

Rapid and robust response, easier to activate than naïve cells.

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8
Q

What influences the migration and adhesion of memory T cells?

A

Different cell surface markers.

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9
Q

Can memory T cells access non-lymphoid tissue?

A

Yes, they can access non-lymphoid tissue (the sites of microbe entry).

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10
Q

Where are central memory cells found?

A

In lymph nodes & tonsils - roll along and extravasate in High Endothelial Venules (HEVs).

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11
Q

Where are effector memory cells found?

A

In liver, lungs, and gut.

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12
Q

What markers do central memory cells express?

A

CCR7+ and CD62L high (allow entry/migrate via HEVs to peripheral lymph nodes).

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13
Q

What markers do effector memory cells express?

A

CCR7-ve and CD62L low (therefore not found in lymph nodes).

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14
Q

What do central memory cells produce?

A

IL-2 (to support other cells).

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15
Q

What do effector memory cells produce?

A

Perforin and IFN-γ.

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16
Q

Which population has more central memory cells, CD4 or CD8?

A

More central memory in CD4 population.

17
Q

Which population has more effector memory cells, CD4 or CD8?

A

More effector memory in CD8 population.

18
Q

Describe the process of immune memory development after exposure to a pathogen.

A

Exposure to pathogen → Antigen(s) stimulation of specific T and B lymphocytes → Expansion → Some lymphocytes become effector cells and some become memory cells → Immunologic memory develops (long lived, up to 65 years).

19
Q

What are the steps involved in the expansion of specific T and B lymphocytes?

A

Antigen stimulation of specific T and B lymphocytes leads to their expansion.

20
Q

What do some lymphocytes become after the expansion?

A

Effector cells and memory cells.

21
Q

What type of immunoglobulins do B cells produce in the memory response?

A

IgG and some IgM.

22
Q

What happens to B cells stimulated by an antigen?

A

Expansion/isotype switching (due to cytokines provided by T helper cells) → Plasma cells producing antibody/memory cells.

23
Q

What type of cells can memory B cells differentiate into?

A

Memory cells that can differentiate into plasma cells (long lived).

24
Q

What is the response of memory B cells compared to the first exposure?

A

Quicker response, more antibodies, higher affinity antibodies, more IgG, and generally better antibodies.

25
Q

Describe the Mantoux Test procedure.

A

Inject 0.1 ml of 5 tuberculin (purified protein derivative) units intradermally, examine arm 48-72 hrs after.

26
Q

What indicates a positive Mantoux Test result?

A

Induration (swelling that can be felt) of at least 10 mm in diameter (erythema around not measured).

27
Q

What does a positive Mantoux Test imply?

A

Previous exposure to tuberculin protein, which could represent previous BCG exposure.