Immunology Flashcards

1
Q

What are the primary tissues of the immune system?

A

Spleen, thymus, bone marrow

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2
Q

What happens during an infection?

A

Immune system activates to defend the body, several characters working together

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3
Q

What components of the immune system are related to specific immunity?

A

T cells, B cells

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4
Q

What are the players involved in innate immunity?

A

Granulocytes (neutrophils, eosinophils, basophils), macrophages, natural killer cells, complement proteins

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5
Q

What are B and T cells derived from? Where do they develop? What immunity are their responses involved in?

A

progenitor cells in the bone marrow
B cells develop in the bone marrow; T cells develop in the thymus gland
B cell responses related to humoral immunity
T cell responses related to cellular immunity

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6
Q

What is humoral immunity?

A

B cell immunity
Fights bacteria and viruses in body fluids with antibodies from plasma and lymph

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7
Q

What two cells do B cells differentiate into?

A

Antibody producing cells, memory cells

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8
Q

What is the structure of immunoglobulins?

A

one of 5 heavy chains
2 light chains

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9
Q

What are the 5 isotypes of immunoglobulins?

A

IgM, IgD, IgG, IgA, and IgE

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10
Q

What is the role of T cells?

A

Lysis of virally infected cells and rejection of foreign tissue grafts
Can function as “killer”, “helper”, or “suppressor”

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11
Q

What is the significance of the major histocompatibility complex (MHC)?

A

These are the molecules tested in transplant donors/recipients

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12
Q

What are some key features of the innate immune system?

A

Confers broad protection against pathogens and can act without previous exposure to that pathogen
Inflammatory responses is hallmark

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13
Q

What are some clinical features of immunodeficiency?

A

Increased susceptibility to infection
chronic/recurrent infections without explanation
infection with organism of low virulence
infection of unusual severity
autoimmune or inflammatory disease

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14
Q

What are some hallmarks of primary immune deficiency disorders?

A

Predominance of males M:F 5:1
>120 conditions with known genetic causes
most diagnosed in infancy but 40% diagnosed in adolescence or early adulthood

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15
Q

What are the three subgroups of primary immune deficiency disorders?

A

antibody deficiency disorders
combined immune deficiency disorders
other well-defined immune deficiency disorders

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16
Q

What is the most common primary immunodeficiency disease?

A

Selective IgA deficiency

17
Q

What is the underlying mechanism of X-linked agammaglobulinemia?

A

failure of B-cell precursors to mature into B-cells and ultimately plasma cells

18
Q

What is the underlying mechanism of X-linked hyper IgM syndrome?

A

Failure of T- and B-cell interactions

19
Q

What is the underlying mechanism of SCID (severe combined immunodeficiency syndrome)?

A

absence of T-cell and B-cell function

20
Q

APS type 1

A

AR inheritance of mutations in Aire (autoimmune regulator) gene

21
Q

What is newborn screening measuring?

A

TRECs (T-cell receptor excision circles)
severely reduced in all forms of SCID