Chapter 17: Adaptive Specific Host Defenses Flashcards

1
Q

Specificity

A

Refers to the adaptive immune system’s ability to target pathogens.

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1
Q

Memory

A

Refers to its ability to quickly respond to pathogens to which it has previously been exposed.

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2
Q

Primary Response

A

The immune system’s first time responding to a bacteria/virus; where programming for memory and specificity occur.

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3
Q

Secondary Response

A

Is faster and stronger as a result of the body’s memory of the first exposure; also is specific to the pathogen itself.

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4
Q

B Cells

A

Mature in the bone marrow and are responsible for the production of glycoproteins called antibodies, or immunoglobins.

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5
Q

Antibodies

A

Involved in the body’s defense against pathogens and toxins in the extracellular environment.

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6
Q

Humoral Immunity

A

Mechanisms of adaptive specific immunity that involve B cells and antibody production.

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7
Q

T Cells

A

Mature in the thymus; function as the central orchestrator of both innate and adaptive immune responses; responsible for destruction of cells infected with intracellular pathogens.

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8
Q

Cellular Immunity

A

The targeting and destruction of intracellular pathogens by T cells.

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9
Q

Antigens/Immunogens

A

Similar to PAMPs, but unique to a specific pathogen.

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10
Q

Antigenic

A

A molecule that stimulates antibody production.

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11
Q

Haptens

A

Free epitopes that are not part of the complex 3-D structure of a larger antigen.

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12
Q

Antibodies/Immunoglobulins

A

Glycoproteins that are present in both the blood and tissue fluids.

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13
Q

Disulfide Bonds

A

A covalent bond between the sulfhydryl R groups found on two cysteine amino acids.

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14
Q

Heavy Chains

A

The two largest chains on an antibody; identical to each other.

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15
Q

Light Chains

A

The two smaller chains on an antibody; identical to each other.

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16
Q

Fab Region

A

The two ‘arms’ of the Y-shaped antibody molecule; stands for ‘fragment of antigen binding’.

17
Q

Variable Region

A

Serves as the site of antigen binding; the amino acid sequence dictates the 3-D structure, and thus the specific 3-D epitope to which the Fab region is capable of binding.

18
Q

Constant Region

A

Includes the trunk of the Y lower portion of each arm of the Y.

19
Q

Fc Region

A

The trunk of the Y; stands for ‘fragment of crystallization’; the site of complement factor binding and binding to phagocytic cells during antibody-mediated opsonization.

20
Q

Isotype/Class

A

How antibodies are group; determined by the constant region.

21
Q

IgG

A

Most abundant antibody in human blood; penetrates efficiently into tissue spaces, and is the only antibody class with the ability to cross the placental barrier, providing passive immunity to the developing fetus during pregnancy.

22
Q

IgM

A

The first antibody produced and secreted by B cells during the primary and secondary immune responses, making pathogen-specific IgM a valuable diagnostic marker during active or recent infections.

23
Q

IgA

A

The most common and abundant antibody class found in the mucus secretions that protect the mucous membranes; traps pathogens in mucus so that they can later be eliminated form the body.

24
Q

IgD

A

Not secreted by B cells and only trace amounts are detected in serums; a membrane-bound monomer found in the surface of B cells, where it serves as an antigen-binding receptor.

25
Q

IgE

A

The least abundant antibody class in serum; its role in adaptive immunity is restricted to anti-parasitic defenses.

26
Q

Neutralization

A

Involves the binding of certain antibodies (IgG, IgM, or IgA) to epitopes on the surface of pathogens or toxins, preventing their attachment to cells.

27
Q

Opsonization

A

The coating of a pathogen with molecules, such as complement factors, C-reactive protein, and serum amyloid A, to assist in phagocyte binding to facilitate phagocytosis.

28
Q

Agglutination/Aggregation

A

Involves the cross-linking of pathogens by antibodies to create large aggregates.

29
Q

Complement System

A

Promotes the inflammatory response, recruits phagocytes to site of infection, enhances phagocytosis by opsonization, and kills gram-negative bacterial pathogens with the membrane attack complex (MAC).

30
Q

Classical Pathway

A

Requires the initial binding of IgG or IgM antibodies to the surface of a pathogen cell, allowing for recruitment and activation of the C1 complex.

31
Q

Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC)

A

Enhances killing of pathogens that are too large to be phagocytosed.

32
Q

Major Histocompatibility Complex (MHC)

A

A collection of genes encoding for MHC molecules found in the surface of all nucleated cells of the body.

33
Q

Human Leukocyte Antigen (HLA) Genes

A

The MHC genes in humans.

34
Q

MHC I

A

Found on all nucleated cells; they present normal self-antigens as well as abnormal or nonself pathogens to the effector T cells involved in cellular immunity.

35
Q

MHC II

A

Only found on macrophages, dendritic cells, and B cells; they present abnormal or nonself pathogen antigens for the initial activation of T cells.

36
Q

Antigen-Presenting Cells (APCs)

A

Macrophages, dendritic cells, and B cells that have the ability to present antigens specifically for the purpose of activating T cells.

37
Q

T-Cell Independent Activation

A

What the activation of B cells without the cooperation of helper T cells is referred to and occurs when BCRs interact with T-independent antigens.

38
Q

T-Cell Independent Activation

A

What the activation of B cells without the cooperation of helper T cells is referred to and occurs when BCRs interact with T-independent antigens.

39
Q

Plasma Cells

A

Antibody factories that secrete large quantities of antibodies.