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A complete set of vocabulary flashcards covering the components, mechanisms, and recognition pathways of the innate immune system as described in the lecture notes.
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Innate (Nonspecific) Immunity
The first and second lines of host defense, including physical barriers like skin, phagocytic cells, natural killer cells, inflammation, and fever.
Adaptive (Acquired) Immunity
The third line of defense involving specialized lymphocytes (T cells and B cells) and antibodies, characterized by a specific memory response.
PAMPs
Pathogen-associated molecular patterns; molecular structures characteristic of microbial pathogens, such as peptidoglycan or lipopolysaccharide, recognized by the innate immune system.
DAMPs
Damage-associated molecular patterns; endogenous molecules produced by or released from damaged and dying cells.
PRRs
Pattern Recognition Receptors; cellular or soluble receptors that recognize PAMPs and DAMPs.
Toll-like receptors (TLRs)
An evolutionarily conserved family of signaling PRRs expressed on leukocytes and other cell types that play essential roles in innate immune responses.
TLR4
A cell surface receptor that recognizes Gram-negative bacterial Lipopolysaccharide (LPS).
TLR5
A cell surface receptor that recognizes bacterial flagellin.
TLR3, 7, 8, and 9
Endosomal receptors that recognize microbial nucleic acids, such as dsRNA, ssRNA, and unmethylated CpG DNA.
Neutrophils
The most abundant population of circulating white blood cells with a segmented nucleus of 3 to 5 lobules; they mediate the earliest phases of inflammatory responses.
Mast cells
Cells present in the skin and mucosal epithelium that express high-affinity receptors for IgE and contain granules with vasoactive amines like histamine.
Küpffer cells
The specific name for tissue-resident macrophages located in the liver.
Alveolar dust cells
The specific name for tissue-resident macrophages located in the lung.
Dendritic cells
Antigen-presenting cells (APC) that capture antigens and present them to T cells in the lymph nodes to bridge innate and adaptive immunity.
Opsonization
The process of coating a microbe with molecules like antibodies or complement proteins (C3b) to promote phagocytosis.
Phagolysosome
A cytoplasmic body formed by the fusion of a phagosome with a lysosome, where microbes are digested by enzymes.
Respiratory burst
A process in which phagocytes increase oxygen consumption to produce reactive oxygen species (ROS), such as superoxide anion (O2−) and hydrogen peroxide (H2O2), to kill microbes.
Chronic granulomatous disease (CGD)
A genetic defect in phagocyte oxidase components (most commonly gp91) that prevents the production of reactive oxygen species.
Natural Killer (NK) cells
Large granular lymphocytes that kill infected cells or cells lacking MHC class I molecules and secrete cytokines like IFN\text{-}\text{\textgamma}.
Perforin
A protein in NK cell granules that forms pores in the target cell membrane.
Antibody-dependent cell-mediated cytotoxicity (ADCC)
A process where NK cells bind to antibody-coated cells via Fc receptors and destroy them.
Complement System
A group of serum proteins that interact in a cascade (Classical, Alternative, or Lectin pathways) to cause cell lysis, opsonization, and inflammation.
Membrane attack complex (MAC)
The terminal complex of the complement system (C5b, C6, C7, C8, and C9) that causes the lysis of certain pathogens.
C3a and C5a
Peptide mediators (anaphylatoxins) of inflammation and phagocyte recruitment produced during complement activation.
Acute phase proteins
Proteins produced by the liver in response to cytokines like IL-6, including C-reactive protein and mannose-binding lectin.
Acute inflammation
The localized response of tissue to injury or infection, characterized by four symptoms: pain, swelling, redness, and heat.
Interferon-alpha (IFN\text{-}\text{\textalpha}) and Interferon-beta (IFN\text{-}\text{\textbeta})
Type I interferons produced in response to viral infections that induce an antiviral state by blocking viral replication.
Costimulator
A second signal required for lymphocyte activation; for example, the membrane protein B7 on an APC is required to activate naive T cells.