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231224s2014 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2014.06.002
|2 doi
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|a pubmed24n0797.xml
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|a (PII)S1521-6616(14)00149-1
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|a eng
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| 100 |
1 |
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|a Ballegaard, V
|e verfasserin
|4 aut
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1 |
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|a The lectin pathway of complement
|b advantage or disadvantage in HIV pathogenesis?
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|c 2014
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Completed 30.09.2014
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|a Date Revised 02.08.2014
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2014 Elsevier Inc. All rights reserved.
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|a The pattern recognition molecules of the lectin complement pathway are important components of the innate immune system with known functions in host-virus interactions. This paper summarizes current knowledge of how these intriguing molecules, including mannose-binding lectin (MBL), Ficolin-1, -2 and -3, and collectin-11 (CL-11) may influence HIV-pathogenesis. It has been demonstrated that MBL is capable of binding and neutralizing HIV and may affect host susceptibility to HIV infection and disease progression. In addition, MBL may cause variations in the host immune response against HIV. Ficolin-1, -2 and -3 and CL-11 could have similar functions in HIV infection as the ficolins have been shown to play a role in other viral infections, and CL-11 resembles MBL and the ficolins in structure and binding capacity
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|a Journal Article
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|a Review
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|a Collectin-11
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|a Ficolin-1, -2 and -3
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|a HIV
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|a Innate immunity
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|a Lectin pathway
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|a Mannose-binding lectin (MBL)
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| 700 |
1 |
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|a Haugaard, A K
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Garred, P
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Nielsen, S D
|e verfasserin
|4 aut
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|a Munthe-Fog, L
|e verfasserin
|4 aut
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| 773 |
0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 154(2014), 1 vom: 28. Sept., Seite 13-25
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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| 773 |
1 |
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|g volume:154
|g year:2014
|g number:1
|g day:28
|g month:09
|g pages:13-25
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|u http://dx.doi.org/10.1016/j.clim.2014.06.002
|3 Volltext
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