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Immunological response to Brucella

dc.contributor.authorCoelho, Ana Cláudia
dc.contributor.authorCoelho, Adosinda
dc.contributor.authorQuintas, Helder
dc.contributor.authorSimões, João
dc.date.accessioned2020-04-01T13:37:36Z
dc.date.available2020-04-01T13:37:36Z
dc.date.issued2019
dc.description.abstractThis chapter describes the immunological response to Brucella. The host immune response to Brucella is divided into innate and adaptive immunity. Protection against Brucella infection requires cell-mediated immunity, which includes CD4+ and CD8+ T lymphocytes, Th1-type cytokines such as IFN-γ and tumor necrosis factor-alpha (TNF-α), and activated macrophages and dendritic cells. Neutrophils, CD8+ and γδ T cells are part of the secondary innate immune response and migrate in the early stages of the infection to contribute to resolve the infection. Cytokine expression is necessary for development of a protective immune response. Brucella induces minimal production of pro-inflammatory cytokines. TNF-α, IL-12, and IFN-γ are the primary cytokines critical for defense against Brucella. In brucellosis, immune response mechanisms are divided in three primary mechanisms: (1) in the first step, it inhibits the intracellular survival of Brucella, IFN-γ produced by CD4+, CD8+, and T cells which activate macrophages, enhancing their bactericidal capacity; (2) secondly, cytotoxic CD8+ T cells directly kill infected macrophages, and T cells; and (3) thirdly, B lymphocytes secrete antibodies, in the endocytic compartments opsonization of Brucella and occur by immunoglobulin (Ig) G2a and IgG3 to increase phagocytosis which is useful for diagnosis of disease. The humoral antibody response consists in an early production of IgM against Brucella LPS for 3 to 4 weeks and rises gradually during the course of acute infection, followed by a gradual increase in IgG and IgA, beginning 7 to 14 days after infection. The dominant IgG isotype is IgG2. Antibodies against Brucella are proteins that cause agglutination, complement fixation, and precipitation when reacted with their homologous antigens. These antibodies have the potential to produce cross-reactions and this inevitably results in false positive serological tests.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationCoelho, Ana Claudia; Coelho, Adosinda; Quintas, Helder; Simões, João (2019) Immunological response to Brucella. In J.C. Simões; M.J. Saavedra and P.A. Hunter (Eds.) Brucellosis in Goats and Sheep: an endemic and re-emerging old zoonosis in the 21st century. New York: Nova Science Publisher. p. 127-137. ISBN 978-1-53614-962-3pt_PT
dc.identifier.isbn978-1-53614-962-3
dc.identifier.urihttp://hdl.handle.net/10198/21353
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherNova Science Publisherspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCell-mediated immunitypt_PT
dc.subjectBrucellapt_PT
dc.subjectCytokine expressionpt_PT
dc.subjectHost immune responsept_PT
dc.titleImmunological response to Brucellapt_PT
dc.typebook part
dspace.entity.typePublication
oaire.citation.conferencePlaceNew Yorkpt_PT
oaire.citation.endPage137pt_PT
oaire.citation.startPage127pt_PT
oaire.citation.titleBrucellosis in Goats and Sheep: an endemic and re-emerging old zoonosis in the 21st centurypt_PT
person.familyNameQuintas
person.givenNameHélder
person.identifier1486884
person.identifier.ciencia-id6018-8BBD-80AB
person.identifier.orcid0000-0002-6934-1669
person.identifier.scopus-author-id35796342900
rcaap.rightsrestrictedAccesspt_PT
rcaap.typebookPartpt_PT
relation.isAuthorOfPublication068e74bc-656d-4fd1-93ed-f7346baa3b69
relation.isAuthorOfPublication.latestForDiscovery068e74bc-656d-4fd1-93ed-f7346baa3b69

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