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Immunology

The immune defence mechanisms by which an organism combats viral infections can be divided into two systems. On the one hand, there are the unspecific, non-adaptive immune reactions, which recognize and eliminate invading foreign pathogens. This so-called natural or innate immune system becomes prim...

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Autores principales: Modrow, Susanne, Falke, Dietrich, Truyen, Uwe, Schätzl, Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122902/
http://dx.doi.org/10.1007/978-3-642-20718-1_7
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author Modrow, Susanne
Falke, Dietrich
Truyen, Uwe
Schätzl, Hermann
author_facet Modrow, Susanne
Falke, Dietrich
Truyen, Uwe
Schätzl, Hermann
author_sort Modrow, Susanne
collection PubMed
description The immune defence mechanisms by which an organism combats viral infections can be divided into two systems. On the one hand, there are the unspecific, non-adaptive immune reactions, which recognize and eliminate invading foreign pathogens. This so-called natural or innate immune system becomes primarily active after a virus has overcome the external physical protection barriers of the body (skin, mucous membranes). It consists of dendritic cells, granulocytes, monocytes, macrophages and natural killer cells (NK cells). They have proteins that serve as receptors, e.g. Toll-like receptors (TLRs) and complement receptors, for specific structures of pathogens and for the soluble products of the innate immune system (acute-phase proteins, factors of the complement system, cytokines, chemokines and interferons). The effects and functions of cytokines, chemokines and interferons will be discussed separately in Chap. 8. The specific, adaptive immune response is the second line of defence, and is developed only during or after the establishment of an infection. It includes antibody-producing B cells – the humoral immune system – as well as T-helper (T(H)) cells and cytotoxic T lymphocytes, which collectively constitute the cellular defence system. The adaptive immune reactions can selectively recognize certain pathogen types or subtypes, and in the case of a reinfection, they are able to recognize the pathogens again and eliminate them. They are long-lasting and a subset of stimulated lymphocytes transform into memory cells during their development, which confers on the organism an efficient protective immunity against infections with the same pathogen. The systems of the specific and non-specific immune responses are in close contact with each other, particularly via cytokines, chemokines and interferons. An immune response is generally triggered by antigens. These may be the infectious pathogens, individual protein components or sugar structures. The immune system recognizes these as foreign, and thus can distinguish between endogenous and exogenous components. However, the antigens must be of a certain size to trigger different immune responses. Molecules with a molecular mass of less than 3–4 kDa are usually incapable of doing that.
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spelling pubmed-71229022020-04-06 Immunology Modrow, Susanne Falke, Dietrich Truyen, Uwe Schätzl, Hermann Molecular Virology Article The immune defence mechanisms by which an organism combats viral infections can be divided into two systems. On the one hand, there are the unspecific, non-adaptive immune reactions, which recognize and eliminate invading foreign pathogens. This so-called natural or innate immune system becomes primarily active after a virus has overcome the external physical protection barriers of the body (skin, mucous membranes). It consists of dendritic cells, granulocytes, monocytes, macrophages and natural killer cells (NK cells). They have proteins that serve as receptors, e.g. Toll-like receptors (TLRs) and complement receptors, for specific structures of pathogens and for the soluble products of the innate immune system (acute-phase proteins, factors of the complement system, cytokines, chemokines and interferons). The effects and functions of cytokines, chemokines and interferons will be discussed separately in Chap. 8. The specific, adaptive immune response is the second line of defence, and is developed only during or after the establishment of an infection. It includes antibody-producing B cells – the humoral immune system – as well as T-helper (T(H)) cells and cytotoxic T lymphocytes, which collectively constitute the cellular defence system. The adaptive immune reactions can selectively recognize certain pathogen types or subtypes, and in the case of a reinfection, they are able to recognize the pathogens again and eliminate them. They are long-lasting and a subset of stimulated lymphocytes transform into memory cells during their development, which confers on the organism an efficient protective immunity against infections with the same pathogen. The systems of the specific and non-specific immune responses are in close contact with each other, particularly via cytokines, chemokines and interferons. An immune response is generally triggered by antigens. These may be the infectious pathogens, individual protein components or sugar structures. The immune system recognizes these as foreign, and thus can distinguish between endogenous and exogenous components. However, the antigens must be of a certain size to trigger different immune responses. Molecules with a molecular mass of less than 3–4 kDa are usually incapable of doing that. 2013-08-12 /pmc/articles/PMC7122902/ http://dx.doi.org/10.1007/978-3-642-20718-1_7 Text en © Springer-Verlag Berlin Heidelberg 2013 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Modrow, Susanne
Falke, Dietrich
Truyen, Uwe
Schätzl, Hermann
Immunology
title Immunology
title_full Immunology
title_fullStr Immunology
title_full_unstemmed Immunology
title_short Immunology
title_sort immunology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122902/
http://dx.doi.org/10.1007/978-3-642-20718-1_7
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AT schatzlhermann immunology