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Local immunodiagnosis of pulmonary tuberculosis by enzyme-linked immunospot C. Jafari*, M. Ernst
Local immunodiagnosis of pulmonary tuberculosis by enzyme-linked immunospot C. Jafari*, M. Ernst

... MTB-specific lymphocytes are selectively compartmentalised in the lungs of patients with minimal active pulmonary tuberculosis (PTB). Patients with smear-negative MTB-culture-confirmed PTB were prospectively recruited. Differential cell counts, immunophenotyping with monoclonal antibodies directed a ...
Licentiate thesis from the Department of Immunology,
Licentiate thesis from the Department of Immunology,

... environmental microbes that we face from the moment of birth. The immune system also has to be able to tell pathogenic from non-pathogenic organisms, as organs like the gut are colonized rapidly at birth with a commensal microbial flora. Further, the immune system can mediate homeostasis and elimina ...
Practice Exam 4 - Montgomery College
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... but their role in respiratory viral infections has received little attention. Here we observed that ...
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Type i and type ii Fc receptors regulate innate and adaptive immunity
Type i and type ii Fc receptors regulate innate and adaptive immunity

... Antibodies produced in response to a foreign antigen are characterized by polyclonality, not only in the diverse epitopes to which their variable domains bind but also in the various effector molecules to which their constant regions (Fc domains) engage. Thus, the antibody’s Fc domain mediates diver ...
Innate and adaptive immune responses in the lungs
Innate and adaptive immune responses in the lungs

... IFN-γ (which can activate macrophages to destroy the intracellular bacteria) and other cytokines and chemokines produced by CD4+ T cells are critical in the host is response to Mtb. The infected DC are observed as the primary APC responsible for activating CD4+ T cells as part of the adaptive immune ...
The Role of Th-17 Cells and γδ T-Cells in Modulating the Systemic
The Role of Th-17 Cells and γδ T-Cells in Modulating the Systemic

... activity, another critical component of wound healing, is contingent on iNOS activity. However, in higher concentrations, NO has also been associated with remote organ injury. Chen et al. have implicated iNOS-derived NO in contributing to gastrointestinal dysfunction through increased mucosal permea ...
Regulatory T Cells (Tregs)- Frequently Asked
Regulatory T Cells (Tregs)- Frequently Asked

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Phagocyte



Phagocytes are cells that protect the body by ingesting (phagocytosing) harmful foreign particles, bacteria, and dead or dying cells. Their name comes from the Greek phagein, ""to eat"" or ""devour"", and ""-cyte"", the suffix in biology denoting ""cell"", from the Greek kutos, ""hollow vessel"". They are essential for fighting infections and for subsequent immunity. Phagocytes are important throughout the animal kingdom and are highly developed within vertebrates. One litre of human blood contains about six billion phagocytes. They were first discovered in 1882 by Ilya Ilyich Mechnikov while he was studying starfish larvae. Mechnikov was awarded the 1908 Nobel Prize in Physiology or Medicine for his discovery. Phagocytes occur in many species; some amoebae behave like macrophage phagocytes, which suggests that phagocytes appeared early in the evolution of life.Phagocytes of humans and other animals are called ""professional"" or ""non-professional"" depending on how effective they are at phagocytosis. The professional phagocytes include many types of white blood cells (such as neutrophils, monocytes, macrophages, mast cells, and dendritic cells). The main difference between professional and non-professional phagocytes is that the professional phagocytes have molecules called receptors on their surfaces that can detect harmful objects, such as bacteria, that are not normally found in the body. Phagocytes are crucial in fighting infections, as well as in maintaining healthy tissues by removing dead and dying cells that have reached the end of their lifespan.During an infection, chemical signals attract phagocytes to places where the pathogen has invaded the body. These chemicals may come from bacteria or from other phagocytes already present. The phagocytes move by a method called chemotaxis. When phagocytes come into contact with bacteria, the receptors on the phagocyte's surface will bind to them. This binding will lead to the engulfing of the bacteria by the phagocyte. Some phagocytes kill the ingested pathogen with oxidants and nitric oxide. After phagocytosis, macrophages and dendritic cells can also participate in antigen presentation, a process in which a phagocyte moves parts of the ingested material back to its surface. This material is then displayed to other cells of the immune system. Some phagocytes then travel to the body's lymph nodes and display the material to white blood cells called lymphocytes. This process is important in building immunity, and many pathogens have evolved methods to evade attacks by phagocytes.
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