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37 Cards in this Set

  • Front
  • Back
B-cell co-receptor
a complex of the CD19, TAPA-1, and CR2 polypeptides that associates with the B-cell receptor and augments its response to specific antigen.
B-1 cells
the minority population of B cells. They express the CD5 glycoprotein and make antibodies of broad specificities. They are also known as CD5 B cells.
B-2 cells
the majority population of B cells. They do not express the CD5 glycoprotein and make antibodies of narrow specificities.
B7
co-stimulatory molecules present on the surface of professional antigen-presenting cells.
Bare lymphocyte syndromes
genetically determined diseases in which MHC class I or II molecules are not expressed on cells. They can be caused by various different regulatory gene defects, and their effect is severe immunodeficiency.
C-reactive protein (CRP)
an acute-phase protein that binds to phosphocholine, a surface constituent of various bacteria. CRP binds bacteria, opsonizing them for uptake by phagocytes.
C1 inhibitor (C1INH)
a regulatory protein in plasma that inhibits the activity of activated completment component C1. C1INH deficiency causes the disease hereditary angioneurotic edema, in which spontaneous complement activation causes episodes of epiglottal swelling and suffocation.
C3 convertases
proteolytic enzymes that are formed during complement activation and cleave complement component C3 to C3b and C3a, thereby enabling C3b to bond covalently to antigens.
C4-binding protein (C4BP)
a regulatory protein in plasma that inactivates the classical C3 convertase by binding to C4b and displacing C2b
Calcineurin
a cytosolic serine/threonine phosphatase that contributes to T-cell activation. The immunosuppressive drugs cyclosporin A and tacrolimus act by inhibiting calcineurin.
Carcinoma
cancer of epithelial cells
CCL2
a chemokine produced by activated T cells that attracts macrophages into a site of infection.
CCL21
a chemokine made by vascular endothelial cells and which is involved in extravasation of leukocytes.
CD2
an adhesion molecule of T cells that binds to the LFA-3 adhesion molecule of antigen-presenting cells. Also called LFA-2
CD3 complex
a complex of signaling molecules that associates with T-cell receptors. It consists of CD3gamma, delta, and epsilon chains, and zeta chains.
CD4
a cell-surface glycoprotein on some T cells that recognize antigens presented by MHC class II molecules. CD4 binds to MHC class II molecules on the antigen-presenting cell and acts as a co-receptor to augment the T cell's response to antigen.
CD4 T cells
subset of T cells that express the CD4 co-receptor and recognize peptide antigens presented by MHC class II molecules.
CD8
a cell-surface glycoprotein on some T cells that recognize antigens presented by MHC class I molecules.
CD19
a component of the B-cell co-receptor
CD21
another name for CR2. A component of the B-cell receptor
CD28
the low-affinity receptor on T cells that interacts with B7 co-stimulatory molecules to promote T-cell activation.
CD40 ligand
on T cells triggers B-cell proliferation
CD81
a component of the B-cell receptor that is also a cellular receptor for hepatitis C virus. Also called TAPA-1
CAMs
cell adhesion molecules: cell-surface proteins that enable cells to bind to each other.
Cell-mediated immunity
any adaptive immune response in which antigen-specific effector T cells dominate. It is defined operationally as all adaptive immunity that cannot be transferred to a naive recipient with serum antibody.
Chediak-Higashi syndrome
a genetic disease in which phagocytes malfunction. Their lysosomes fail to fuse properly with phagosomes, and killing of ingested bacteria is impaired.
Chronic granulomatous disease
an immunodeficiency disease in which multiple granulomas form as a result of defective elimination of bacteria by phagocytic cells. It is caused by a defect in the NADPH oxidase system of enzymes, which generates the superoxide radical involved in bacterial killing.
Classical pathway of complement activation
one of three pathways of complement activation; activated by antibody bound to antigen, and involves complement components C1, C4, and C2 in the generation of the C3 and C5 convertases.
Clonal deletion
the elimination of immature lymphocytes that bind to self antigens. Clonal deletion is the main mechanism that produces self-tolerance.
Clonal selection
the central principle of adaptive immunity. It is the mechanism by which adaptive immune responses derive only from individual antigen-specific lymphocytes, which are stimulated by the antigen to proliferate and differentiate into antigen-specific effector cells.
Complement
a set of plasma proteins that act in a cascade of reactions to attack extracellular forms of pathogens. As a result of complement activation, pathogens become coated with complement components, which can either kill the pathogen directly or cause its engulfment and destruction by phagocytes.
Complement control protein modules (CCP)
family of structurally similar protein modules found in many of the proteins that regulate complement activity
Conjugate vaccine
a vaccine made from capsular polysaccharides bound to an immunogenic protein such as tetanus toxoid. The protein provides peptide epitopes that stimulate CD4 T cells to help B cells specific for the polysaccharide.
CTLA-4
a high-affinity inhibitory receptor on T cells that interacts with B7 co-stimulatory molecules.
CXCL8 (formerly IL-8)
a chemokine involved in the extravasation of neutrophils
Clyclosporin A
an immunosuppressive drug that specifically prevents T-cell activation and effector function.
Cytotoxins
proteins made by cytotoxic T cells that participate in the destruction of target cells. Perforins, granzymes or fragmentins, and granulysin are examples of cytotoxins.