2 Immunology I - Fundamental Concepts and Innate Immunity

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Vocabulary flashcards covering core concepts of immunology, immune cells, recognition mechanisms, and innate defense pathways based on Ross University School of Veterinary Medicine lecture notes.

Last updated 2:06 PM on 9/28/26
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34 Terms

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Immune system

A system of organs, cells, tissues, and molecules that facilitate resistance against foreign or danger elements (antigens).

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Immune response

A coordinated reaction of the immune system in response to antigens.

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Inflammatory response

A coordinated reaction of the immune system in response to danger signals.

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Immunology

The discipline that studies the immune system, including its structure, organization, function, and evolution.

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Antigen

A molecule or structure that can be recognized by immune system receptors, producing a specific reaction by cells or antibodies.

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Immunogen

An antigen that is recognized by the body as non-self and stimulates an immune response.

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Epitope

The specific, smallest region of an antigen that is recognized and bound by an antibody or an immune cell receptor (BCR or TCR) on lymphocytes.

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Innate immunity

An antigen-independent arm of defense with broad specificity and minimal memory that responds immediately (minutes to hours) using physical barriers, phagocytes, complement, and inflammation.

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Adaptive immunity

An antigen-dependent arm of defense with high specificity for specific epitopes and significant memory that generates a delayed response (days to weeks) via T lymphocytes, B lymphocytes, and antibodies.

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Humoral immunity

Immunity mediated by macromolecules in solution found in extracellular fluids (body fluids/humors), such as complement, antimicrobial peptides, and antibodies.

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Cellular immunity

Immunity involving various cells that participate directly in the immune response, including macrophages, dendritic cells, neutrophils, mast cells, NK cells, B cells, and T cells.

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<p>Neutrophils</p>

Neutrophils

Polymorphonuclear granulocytes with multilobed nuclei and neutral (slightly pink) granules that provide antimicrobial defense (especially during acute bacterial infections) via phagocytosis, degranulation, and NET formation.

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Heterophils

Antimicrobial granulocytes found in birds and reptiles instead of neutrophils that perform immune defense and form heterophil extracellular traps (HETs).

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<p>Eosinophils</p>

Eosinophils

Granulocytes with lobed nuclei and prominent pink-to-red (eosinophilic) granules that participate in defense against parasites (helminths) and in allergic reactions.

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Eosinophilia

An increase in the number of eosinophils in peripheral blood, commonly associated with helminth parasite infections or allergic responses.

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<p>Basophils</p>

Basophils

Granulocytes with a bilobed nucleus and large purple (basophilic) granules involved in allergic reactions, inflammation, and defense against parasites.

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<p>Mast cells</p>

Mast cells

Tissue sentinel cells containing prominent secretory granules that release vasoactive amines (histamine, serotonin), lipid mediators, and cytokines to induce vasodilation, increase vascular permeability, and amplify inflammation.

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<p>Macrophages</p>

Macrophages

Large mononuclear cells derived from monocytes that function in immune surveillance, antimicrobial phagocytosis, release of inflammatory mediators, tissue repair, and limited antigen presentation.

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<p>Dendritic cells</p>

Dendritic cells

Specialized antigen-presenting cells that capture, process, and present antigens to T lymphocytes, bridging innate and adaptive immune responses.

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Natural Killer (NK) cells

Innate lymphocytes that identify virus-infected or abnormal/mutated host cells exhibiting reduced MHC Class I expression and release cytotoxic lytic granules to induce apoptosis.

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Cytokines

Small proteins that signal cells to engage in functions such as cell growth, activation, differentiation, and polarization.

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Interleukins

A class of cytokines that function specifically in communication between white blood cells and other immune cells.

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Chemokines

A class of cytokines that induce chemotaxis, directing cell movement toward chemical signals.

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Pathogen-Associated Molecular Patterns (PAMPs)

Conserved molecular structures shared by groups of pathogens (or microbes/MAMPs) that are distinct from host self-molecules and recognized as non-self.

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Damage-Associated Molecular Patterns (DAMPs)

Endogenous molecules released by damaged, injured, or necrotic host cells (or extracellular matrix breakdown) that signal danger to initiate inflammation.

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Pattern Recognition Receptors (PRRs)

Molecules located on the cell surface, inside endosomes/phagolysosomes, or in the cytosol of host cells that bind PAMPs and DAMPs to induce innate immune responses.

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Phagocytosis

The process by which specialized phagocytes (neutrophils, macrophages, dendritic cells) engulf and ingest large particles such as bacteria, dead cells, or debris into a phagosome for destruction.

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Phagolysosome

A cytoplasmic body formed by the fusion of a phagosome (containing an ingested microbe) with a lysosome, exposing the pathogen to oxidative and enzymatic killing mechanisms.

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Respiratory burst

An oxygen-dependent intracellular killing mechanism in phagocytes characterized by a sudden increase in oxygen and glucose consumption to produce Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS).

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Complement System

A collection of over 30 circulating plasma proteins and membrane proteins that circulate as inactive zymogens and activate in a cascade sequence to mediate opsonization, inflammation, and cell lysis.

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Classical pathway

A complement activation pathway triggered by antigen-antibody complexes (IgG or IgM bound to antigen).

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Lectin pathway

A complement activation pathway triggered when carbohydrate-binding plasma proteins, such as mannose-binding lectin (MBL), bind to microbial carbohydrates.

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Alternative pathway

A complement activation pathway triggered spontaneously on microbial surfaces due to the absence of host regulatory proteins, operating independently of antibodies.

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Membrane Attack Complex (MAC)

A structure formed by complement proteins C5b, C6, C7, C8, and multiple C9 molecules that inserts into microbial cell membranes, creating cylindrical pores that induce osmotic lysis.