T lymphocytes
T lymphocytes, commonly known as T cells, are a fundamental component of the body's adaptive immune system. These cells are distinguished for their remarkable ability to target and destroy cells infected by pathogens, such as viruses and some bacteria. Each T cell has a unique receptor on its surface that is designed to bind only to specific antigens—a sort of lock-and-key system. This specificity allows them to recognize and attack infected cells particularly, sparing the body's normal cells.
Once an antigen is recognized, T cells can either directly kill the infected cell, induce the infected cell to die by apoptosis, or perform a helper role by enhancing the immune response of other cells. By doing so, T cells remember past infections, which contributes to a faster and more efficient immune response if the same pathogen is encountered again, thereby providing immunological memory.
Adaptive immunity
Adaptive immunity, also called acquired immunity, is the immune system's second line of defense following innate immunity. It consists of specialized cells and processes that eliminate or prevent pathogenic growth. This type of immunity is characterized by its ability to learn and remember specific pathogens, making it extremely effective in fighting subsequent infections by the same microbe.
It involves both T lymphocytes and B lymphocytes which produce antibodies against pathogens. The adaptive immune response is slower to activate than the innate response but provides a more specialized attack against infections. It's the part of our immune system that adapts and evolves to recognize and better target specific pathogens over time.
Innate immunity
In contrast to adaptive immunity, innate immunity includes the body's initial defenses against pathogens, providing immediate, though non-specific, protection. It involves physical barriers like the skin and mucous membranes, chemical barriers such as stomach acid and enzymes, and cellular defenses including natural killer cells, macrophages, and dendritic cells.
Innate immunity also encompasses inflammation and fever as responses to infection. While it doesn't specifically recognize pathogens, it can rapidly mobilize to prevent the spread of infections and prepare the adaptive immune system to take over the more specialized task of fully eliminating the pathogens.
Antigens
Antigens are substances that can trigger an immune response when detected by the body. They are typically found on the surface of pathogens, such as viruses, bacteria, and parasites, but can also be part of foreign non-pathogenic substances like pollen or transplanted organs.
Protein-based antigens are the main targets of T lymphocytes within the adaptive immunity. The specific recognition of these protein antigens allows for a tailored immune response. This is in contrast to the innate immune system, which responds to a broader range of antigenic markers, such as lipopolysaccharides and glycoproteins that are common among various pathogens.
Glycoproteins
Glycoproteins are molecules that consist of a protein backbone with carbohydrate (sugar) chains attached. This combination creates diverse structures on the surfaces of cells, including those of pathogens. They perform various functions, from cell recognition to providing stability and support on cell surfaces.
In terms of immunity, glycoproteins are important because they are often used by the innate immune system to identify possible threats. White blood cells can bind to these sugar-modified proteins to activate immune responses, like phagocytosis, where cells engulf and destroy pathogens, contributing to the body's first line of defense against infections.
Lipopolysaccharides
Lipopolysaccharides (LPS) are large molecules found on the outer membrane of Gram-negative bacteria. They consist of a lipid component, which anchors them in the bacterial membrane, and a polysaccharide component that extends outward. These substances play a key role in the innate immune system's recognition of bacterial invaders.
Immune cells possess pattern recognition receptors (PRRs) that detect LPS as part of a pathogen-associated molecular pattern (PAMP). Binding of LPS to PRRs, such as Toll-like receptor 4 (TLR4), triggers an alarm within the immune system, launching a swift protective response involving inflammation and fever. This broad targeting mechanism embodies the non-specific nature of the innate immune response.