Lecture 1 Flashcards

1
Q

Extracellular Microbes

A

Survive in animals by growing extracellularly, being simply immersed in nutrients

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2
Q

Intracellular Microbes

A

Invade and live and replicate intracellularly within animal cells where they utilize host-cell energy sources

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3
Q

Immunity

A

Set of cooperative defense mechanisms which provide protection from various infectious diseases

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4
Q

Tissue Injury

A

Immunopathology; immune response against microbes that causes “injury”, “collateral damage”

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5
Q

Antigens

A

Noninfectious foreign substances that elicit an immune response; in some pathological conditions, self antigens (Ags) in the body can elicit an autoimmune response; include proteins, carbohydrates, lipids, and nucleic acids

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6
Q

Antibody (Ab)

A

Protein produced by the immune system when it detects antigens

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7
Q

Epitope

A

Portion of an Ag molecule to which an antibody binds; also called an antigenic determinant; the smallest epitope which an antibody can be made is about 3-6 AA or about 5-6 sugar residues

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8
Q

T Cell Receptors

A

Recognize linear AA sequences

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9
Q

Immunogens

A

Ags which can stimulate an immune response; all immunogens are Ags, but not all Ags are immunogens

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10
Q

Haptens

A

Very small Ags that can bind to Abs but they CAN’T initiate an immune response

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11
Q

Innate Immunity

A

First line of defense against infection that works rapidly, gives rise to acute inflammation, some specificity for Ag, and has no memory; also called the “decision-making stage” of immune response

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12
Q

Adaptive Immunity

A

Takes longer to develop, highly specific, and shows memory (remembers Ag it has encountered previously)

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13
Q

Primary Fixed Elements of Immune System

A

Bone marrow, thymus

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14
Q

Secondary Fixed Elements of Immune System

A

Spleen/lymph nodes, mucosal immune tissues

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15
Q

Mobile Elements of Immune System

A

Immune cells, soluble (humoral) components (Abs, complements, acute phase proteins)

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16
Q

Antimicrobial Peptides

A

Small peptides which target pathogenic microorganisms ranging from viruses to parasites

17
Q

Complement

A

System of plasma proteins that enhances (complements) the ability of Abs and phagocytic cells to clear pathogens from an organism

18
Q

Acute Phase Proteins (APPs)

A

Large group of blood proteins whose plasma concentrations change in response to tissue injury, acute infections, burns, or inflammation

19
Q

Cytokines

A

Cell signaling molecules that aid cell-to-cell communication in immune responses; large group of small secreted proteins with diverse structures and functions, which regulate and coordinate many activities of the cells of innate and adaptive immunity

20
Q

Chemokines

A

Subfamily of cytokines secreted by immune cells to induce chemotaxis (movement) in nearby cells; large subset of structurally related cytokines that regulate cell migration and movement

21
Q

Phagocytes

A

Immune cells that have the ability to ingest and digest microbes; include neutrophils and macrophages; secrete cytokines

22
Q

Cellular and Chemical Barriers of Innate Immunity

A

Skin, mucosal epithelia, antimicrobial peptides

23
Q

Blood Proteins of Innate Immunity

A

Complement, acute phase proteins, cytokines, chemokines, and others

24
Q

Cells of Innate Immunity

A

Phagocytes (macrophages, neutrophils), dendritic cells, natural killer cells, innate lymphoid cells

25
Q

Cellular and Chemical Barriers of Adaptive Immunity

A

Lymphocytes in epithelia; Abs secreted at epithelial surfaces

26
Q

Blood Proteins of Adaptive Immunity

A

Abs, cytokines

27
Q

Cells of Adaptive Immunity

A

B and T Lymphocytes

28
Q

Functions of Cytokines

A

Regulate growth and differentiation of all immune cells, activate the effector functions of lymphocytes and phagocytes; acts via a specific signaling receptor expressed on target cells

29
Q

Steps in Functional Responses of Phagocytes

A

Recruitment of the cells to the sites of infection; Recognition of and activation by microbes; Ingestion of the microbes by the process of phagocytosis; Destruction of ingested microbes

30
Q

Neutrophils

A

Also called polymorphonuclear leukocytes because their nucleus is segmented into 3-5 connected lobules; most abundant population of circulating spherical white blood cells; mediate the earliest phases of inflammatory reactions; produced in the bone marrow and arise from precursors that also give rise to mononuclear phagocytes; last in blood for hours or a few days, but only 1-2 days in tissues

31
Q

Mononuclear Phagocyte System

A

Includes circulating monocytes and resident tissue macrophages which play a central roles in innate and adaptive immunity; resident tissue macrophages populate many tissues and have phenotypes depending on the organ and these cells arise from committed precursor cells in the bone marrow, driven by monocyte/macrophage colony stimulating factor (M-CSF)

32
Q

Monocytes

A

Mature monocytes enter the blood circulation and then migrate into tissues, where they further mature into macrophages, especially during inflammation

33
Q

Macrophages

A

Tissue resident macrophages are a heterogenous population of immune cells that fulfill tissue-specific and niche-specific functions; these range from homeostatic functions, immune surveillance, response to infection, and resolution of inflammation

34
Q

Dendritic Cells

A

Cells of innate immunity that comprise a diverse group of professional antigen presenting cells (APCs); share a particular morphology (long surface membrane extensions called dendrites); potent stimulators of T cells to induce the adaptive immunity; can be broadly divided to myeloid (mDCs) and plasmacytoid (pDCs); other DC subpopulations include Langerhan’s cells residing in epidermis of the skin

35
Q

mDCs

A

Derived from monocytes and differentiated from peripheral blood mononuclear cells (PBMCs)

36
Q

Mast Cells, Basophils, and Eosinophils

A

Play roles in innate and adaptive immune responses, protect against helminthes and reactions that cause allergic diseases; share the common feature of having cytoplasmic granules filled with various inflammatory and antimicrobial mediators

37
Q

Location of Mast Cells

A

Common at sites in the body that are exposed to the external environment, such as the skin; found in close proximity to blood vessels, where they can regulate vascular permeability and effector-cell recruitment; although they don’t have direct cell-to-cell contact with local cell populations, mast cells can modulate the behavior of these and other neighboring effector cells through the release of mediators