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|a 9783764374419
|9 978-3-7643-7441-9
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|a 10.1007/3-7643-7441-1
|2 doi
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|a 616.079
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|a Toll-like Receptors in Inflammation
|h [electronic resource] /
|c edited by Luke A.J. O'Neill, Elizabeth Brint.
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|a 1st ed. 2005.
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|a Basel :
|b Birkhäuser Basel :
|b Imprint: Birkhäuser,
|c 2005.
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|a XII, 246 p.
|b online resource.
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|a text
|b txt
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|a computer
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|a online resource
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|a text file
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|a Progress in Inflammation Research,
|x 2296-4525
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|a TLRs as bacterial sensors -- Toll-like receptors and rheumatoid arthritis: is there a connection? -- Toll-like receptor 9 and systemic autoimmune diseases -- Toll-like receptors and airway disease -- Toll-like receptors and vascular disease -- Toll-like receptors and inflammatory bowel disease -- Toll-like receptor signaling in the liver -- Toll-like receptors as key sensors of viral infection -- IRAK-4: A key kinase involved in toll-like receptor signaling and resistance to bacterial infection -- Endogenous regulation of toll-like receptor signalling -- Tuning of inflammatory cytokines and toll-like receptors by TIR8/SIGIRR, a member of the IL-1 receptor family with unique structure and regulation -- Toll-like receptors as pharmacological targets.
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|a Toll-like receptors (TLRs) are critical mediators of the innate immune response in mammals. This family of receptors recognizes a variety of microbial products or motifs and initiates the host response to infection. Examples include TLR4 which recognizes lipopolysaccharide (LPS) from Gram-negative bacteria, TLR3 which recognizes viral double-stranded RNA, and TLR9 which recognizes CpG DNA motifs, found in both viruses and bacteria. All TLRs possess an intracellular region termed the Toll-IL-1 receptor-Resistance (TIR) domain which is essential for signaling from these receptors. The specificity of signaling from individual TLRs arises from differential utilization of adapter proteins. This specificity results in a tailoring of the host defense response depending on the microbe being sensed. TLRs are increasingly being implicated in both infectious and inflammatory diseases, notable examples being sepsis, inflammatory bowel disease, atherosclerosis, and asthma. There is, therefore, great interest in targeting TLRs therapeutically since a disruption of TLR function will result in a decrease in the production of inflammatory mediators. This volume covers our current understanding of TLRs and their role in inflammation. Given the importance of TLRs in the inflammatory process and their emerging role in inflammatory diseases the book is of great interest to researchers working in inflammation and immunology.
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650 |
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|a Immunology.
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|a Diseases.
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|a Medical microbiology.
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|a Cytology.
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|a Pharmacology.
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|a Immunology.
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|a Diseases.
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|a Medical Microbiology.
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|a Cell Biology.
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|a Pharmacology.
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|a O'Neill, Luke A.J.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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700 |
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|a Brint, Elizabeth.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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710 |
2 |
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|a SpringerLink (Online service)
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|t Springer Nature eBook
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776 |
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|i Printed edition:
|z 9783764390785
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|i Printed edition:
|z 9783764372859
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830 |
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|a Progress in Inflammation Research,
|x 2296-4525
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|u https://doi.uam.elogim.com/10.1007/3-7643-7441-1
|z Texto Completo
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|a ZDB-2-SBL
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912 |
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|a ZDB-2-SXB
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|a Biomedical and Life Sciences (SpringerNature-11642)
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950 |
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|a Biomedical and Life Sciences (R0) (SpringerNature-43708)
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