1/26
A comprehensive set of vocabulary flashcards covering the fundamentals of immunology, including cell types, signaling pathways, and the adaptive immune system mechanisms as described in the lecture notes.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Cluster of differentiation (CD)
Molecules recognized by groups of antibodies, forming a "cluster" numbered from CD1 to CD372.
Mast Cells
Long-lived resident cells found in peripheral tissues (skin, lung, gut) that degranulate to release cytokines, histamines, or other inflammatory mediators in response to allergies.
Eosinophils
Cells found in peripheral tissues (respiratory, gastrointestinal, and genitourinary tracts) that contain pre-formed cytoplasmic granules for defense against parasites such as helminths.
Basophils
Blood granulocytes that are functionally and structurally similar to mast cells and release histamine and heparin to prevent blood clotting.
Neutrophils
Short-lived blood granulocytes with potent antibacterial functions (defensins) that can produce NETS (exploding DNA and chromatin) to trap pathogens.
Monocyte / Macrophages
Long-lived professional APCS and resident tissue cells (e.g., Microglia in the CNS, Kupffer cells in the liver) that secrete cytokines such as TNF−α, IL−1, IL−6, IL−8, and IL−12.
Dendritic Cells
Cells that initiate the adaptive immune response by detecting PAMPS through a range of receptors and activating CD4 and CD8 T cells.
Innate Lymphoid cells (ILCs)
Cells residing in epithelial tissue that produce cytokines; they are divided into five major groups including NK cells, Group 1 ILC (ILC1), ILC2, and ILC3.
Hematopoiesis
The process by which all circulating blood cells arise in the bone marrow.
AIRE (auto immune regulator)
Specialized cells in the thymus medullary epithelial cells (MEC) that produce tissue-specific or peripheral tissue-specific antigens.
Spleen
A highly vascularized abdominal organ containing sinusoids where blood-borne antigens are trapped and processed by abundant phagocytes.
PAMPs (Pathogen-associated molecular patterns)
Molecular patterns expressed by microbes that are recognized by pattern recognition receptors (PRR).
DAMPs (Danger-associated molecular patterns)
Molecules released from damaged or necrotic cells that trigger an immune response.
Toll-like receptors (TLRs)
Membrane-bound receptors specific for different microbial components; for example, TLR−4 recognizes LPS and TLR−5 recognizes bacterial flagellin.
NOD receptors
Cytoplasmic sensors (e.g., NOD1 and NOD2) that recognize bacterial cell wall components such as DAP or MDP and activate NF−κB via the adaptor molecule RIPK2.
NF-kB (NF−κB)
The key signaling pathway for inflammation that induces the expression of inflammatory genes following the degradation of the inhibitor IκB.
Complement System
A cascade of sequential proteolytic cleavage of complement proteins that assists the anti-microbial activity of antibodies; it includes Alternative, Classical, and Lectin pathways.
MAC (Membrane attack complex)
A late-step complement assembly consisting of C5b, C6, C7, C8, and Poly-C9 that forms a pore in the plasma membrane to cause cell lysis.
Epitopes
Also known as antigenic determinants, these are small, often linear parts of pathogens that bind to antigen-specific receptors on T cells.
MHC Class I
Molecules expressed by all nucleated cells that present intracellular antigens to CD8+ cytotoxic T lymphocytes (CTL).
MHC Class II
Molecules expressed only on professional APCS (and some non-professional ones) that present extracellular antigens to CD4+ helper T cells.
Cross-presentation
A process unique to professional APCs where exogenous antigens are processed and presented on MHC class I to activate CD8+ T cells.
V(D)J Recombination
The random rearrangement of Variable (V), Diversity (D), and Joining (J) gene segments mediated by the recombinase enzymes RAG−1 and RAG−2 to create BCR and TCR diversity.
Isotype switching
A T-dependent process where B cells change the constant region of their heavy chain (e.g., from IgM to IgG, IgA, or IgE) based on cytokine signals.
Affinity maturation
The process where B cells undergo somatic hypermutation of Ig V genes followed by selection to increase the affinity of the antibody for a specific antigen.
Chemokines
Cytokines (such as CCL19, CCL21, or CXCL13) that stimulate cytoskeletal changes and coordinate the migration and homing of leukocytes.
Defensins
Hydrophobic pore-forming peptides widely expressed by mucosal epithelial cells and specialized anti-microbial cells (PMNs) to clear infections.