Literature DB >> 12810107

What's the difference between CD80 and CD86?

David M Sansom1, Claire N Manzotti, Yong Zheng.   

Abstract

CD28 and CD152 have crucial yet opposing functions in T-cell stimulation, in which CD28 promotes but CD152 inhibits T-cell responses. Intriguingly, they share two ligands, CD80 and CD86, but at present there is no clear model for understanding whether a ligand will promote or inhibit responses. Current perceptions are based around the concept that CD86 is the initial co-stimulatory ligand based on its more abundant and earlier expression pattern; CD80 has a role following antigen-presenting-cell activation. We describe an alternative view in which CD80 is the initial ligand, responsible for maintaining aspects of immune tolerance through interactions with CD152. These inhibitory functions can then be over-ridden by the upregulation of CD86 on dendritic cells as a result of inflammatory stimuli, leading to immune activation.

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Year:  2003        PMID: 12810107     DOI: 10.1016/s1471-4906(03)00111-x

Source DB:  PubMed          Journal:  Trends Immunol        ISSN: 1471-4906            Impact factor:   16.687


  63 in total

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3.  Type I IFN signaling in CD8- DCs impairs Th1-dependent malaria immunity.

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Journal:  J Clin Invest       Date:  2014-05-01       Impact factor: 14.808

Review 4.  Blockade of co-stimulation in chronic inflammatory diseases.

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Journal:  Wien Med Wochenschr       Date:  2014-10-01

5.  Linarin down-regulates phagocytosis, pro-inflammatory cytokine production, and activation marker expression in RAW264.7 macrophages.

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6.  Preferential use of B7.2 and not B7.1 in priming of vaccinia virus-specific CD8 T cells.

Authors:  Shahram Salek-Ardakani; Ramon Arens; Rachel Flynn; Alessandro Sette; Stephen P Schoenberger; Michael Croft
Journal:  J Immunol       Date:  2009-03-01       Impact factor: 5.422

7.  FOXP3 expression is upregulated in CD4T cells in progressive HIV-1 infection and is a marker of disease severity.

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8.  Flt3 Ligand Treatment Attenuates T Cell Dysfunction and Improves Survival in a Murine Model of Burn Wound Sepsis.

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Journal:  Shock       Date:  2017-01       Impact factor: 3.454

9.  ERK and not p38 pathway is required for IL-12 restoration of T cell IL-2 and IFN-gamma in a rodent model of alcohol intoxication and burn injury.

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10.  Differential role for CD80 and CD86 in the regulation of the innate immune response in murine polymicrobial sepsis.

Authors:  Anna Nolan; Hiroshi Kobayashi; Bushra Naveed; Ann Kelly; Yoshihiko Hoshino; Satomi Hoshino; Matthew R Karulf; William N Rom; Michael D Weiden; Jeffrey A Gold
Journal:  PLoS One       Date:  2009-08-12       Impact factor: 3.240

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