Fc fragment
Fc fragment refers to the crystallizable fragment of an antibody. It is the tail region of an antibody that interacts with cell surface receptors called Fc receptors and some proteins of the complement system. This interaction is crucial for the antibody's ability to mediate immune responses such as phagocytosis and antibody-dependent cell-mediated cytotoxicity (ADCC). The Fc fragment is composed of the constant regions of the heavy chains of the antibody.
Structure[edit | edit source]
The Fc region is composed of two heavy chains that contribute to its two-lobed structure. Each heavy chain in the Fc region contains two or three constant domains (CH domains) depending on the antibody class. The Fc regions of different antibody classes have distinct structures and functions, reflecting their roles in the immune response. The structure of the Fc region allows it to bind to various receptors and proteins, facilitating the antibody's effector functions.
Function[edit | edit source]
The primary function of the Fc fragment is to mediate the interaction of antibodies with Fc receptors on the surface of certain immune cells, such as natural killer cells, macrophages, and neutrophils. This interaction triggers a range of immune responses aimed at eliminating the antigen. The Fc fragment also plays a role in the classical pathway of the complement system activation, leading to the lysis of target cells.
Clinical Significance[edit | edit source]
The Fc fragment is significant in both diagnostic and therapeutic contexts. In therapeutics, engineering the Fc region of monoclonal antibodies can enhance their efficacy and reduce side effects. This has led to the development of antibody therapies with modified Fc regions for improved interaction with immune cells or reduced effector function, depending on the therapeutic goal.
Antibody Classes[edit | edit source]
Different antibody classes (IgG, IgA, IgM, IgE, and IgD) have distinct Fc regions, which determine their distribution within the body and their specific roles in the immune response. For example, IgG antibodies, with their well-defined Fc region, are known for their ability to cross the placenta and provide passive immunity to the fetus.
Research and Development[edit | edit source]
Research into the Fc fragment and its interactions with Fc receptors is ongoing, with the aim of developing more effective immunotherapies. This includes the design of antibodies with enhanced ability to recruit immune cells to tumor sites or to modulate immune responses in autoimmune diseases.
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Contributors: Prab R. Tumpati, MD