Bøger af Adah Blair

The complement system is a part of the immune system which improves the capability of phagocytic cells and antibodies to take out damaged cells and microbes from the organism's body. Complement control proteins, which are found in a higher concentration in the blood plasma as compared to complement proteins, regulate the complement system. Some of the complement control proteins are found on the membranes of self-cells that protect them from attack by the complement system. This system is considered to be focused on killing bacteria that infect the host organism. Furthermore, it acts as an innate immune surveillance system, which has a significant role to play in host homeostasis, defense against pathogens and inflammation. The dysfunction of the complement system is a major reason of diseases caused in the central nervous system, such as neurodegenerative conditions like spinal cord injuries and Alzheimer's disease. C3 glomerulopathy and atypical hemolytic uremic syndrome have been found linked with mutations in the genes of complement regulators specifically factor H. The readers would gain knowledge that would broaden their perspective about the complement system and its immunobiology through this book. It will help the readers in keeping pace with the rapid changes in this area of study.

The part of the immune system, which improves the abilities of antibodies and phagocytic cells that eliminate microbes and destroyed cells from an organism, is known as the complement system. It also promotes inflammation and damages the pathogen's cell membrane. It is a continuous process and hence belongs to the innate immune system. It is non-adaptive and has a lifelong presence. The complement system can be used by antibodies, which are produced by the adaptive immune system. Various small proteins are included in the complement system which synthesize through the liver and circulate as inactive precursors in the blood. There are three biochemical pathways which contribute in the activation of complement system, namely, the alternative complement pathway, the classical complement pathway and the lectin pathway. Such selected concepts that redefine the study of the human complement system have been presented in this book. It aims to serve as a resource guide for students and experts alike and contribute to the growth of research in this area of study. Those in search of information to further their knowledge will be greatly assisted by this book.