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  2. Pathogen-associated molecular pattern - Wikipedia

    en.wikipedia.org/wiki/Pathogen-associated...

    Pathogen-associated molecular patterns (PAMPs) are small molecular motifs conserved within a class of microbes, but not present in the host. [1] They are recognized by toll-like receptors (TLRs) and other pattern recognition receptors (PRRs) in both plants and animals. [ 2 ]

  3. Pattern recognition receptor - Wikipedia

    en.wikipedia.org/wiki/Pattern_recognition_receptor

    The microbe-specific molecules that are recognized by a given PRR are called pathogen-associated molecular patterns (PAMPs) and include bacterial carbohydrates (such as lipopolysaccharide or LPS, mannose), nucleic acids (such as bacterial or viral DNA or RNA), bacterial peptides (flagellin, microtubule elongation factors), peptidoglycans and ...

  4. Immunological memory - Wikipedia

    en.wikipedia.org/wiki/Immunological_memory

    In addition to the formed antibodies in the body there remains a small number of memory T and B cells that make up the cellular component of the immunological memory. They stay in blood circulation in a resting state and at the subsequent encounter with the same antigen these cells are able to respond immediately and eliminate the antigen.

  5. Damage-associated molecular pattern - Wikipedia

    en.wikipedia.org/wiki/Damage-associated...

    In contrast to the noninfectious inflammatory response produced by DAMPs, pathogen-associated molecular patterns (PAMPs) initiate and perpetuate the infectious pathogen-induced inflammatory response. [6] Many DAMPs are nuclear or cytosolic proteins with defined intracellular function that are released outside the cell following tissue injury. [7]

  6. Antibody opsonization - Wikipedia

    en.wikipedia.org/wiki/Antibody_opsonization

    1) Antibodies (A) and pathogens (B) circular in the blood. 2) The antibodies bind to pathogens with complementary antigen sequences, engaging in opsonization (2a), neutralisation (2b), and agglutination (2c). 3) A phagocyte (C) approaches the pathogen, and Fc region (D) of the antibody binds to one of the Fc receptors (E) on the phagocyte.

  7. Danger model - Wikipedia

    en.wikipedia.org/wiki/Danger_model

    Function of T helper cells: Antigen-presenting cells present antigens on their Class II MHC molecules . Helper T cells recognize these by expressing the CD4 co-receptor . The activation of a resting helper T cell causes it to release cytokines and other signals (green arrows) that stimulate the activity of macrophages , killer T cells , and B ...

  8. Complement system - Wikipedia

    en.wikipedia.org/wiki/Complement_system

    Scheme of the complement system. The complement system, also known as complement cascade, is a part of the humoral, innate immune system and enhances (complements) the ability of antibodies and phagocytic cells to clear microbes and damaged cells from an organism, promote inflammation, and attack the pathogen's cell membrane. [1]

  9. Macrophage - Wikipedia

    en.wikipedia.org/wiki/Macrophage

    Both complement proteins and antibodies can bind to antigens and opsonize them. Macrophages have complement receptor 1 (CR1) and 3 (CR3) that recognize pathogen-bound complement proteins C3b and iC3b, respectively, as well as fragment crystallizable γ receptors (FcγRs) that recognize the fragment crystallizable (Fc) region of antigen-bound ...