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Mannan-binding lectin modulates the response to HSV-2 infection.

Gadjeva, M (författare)
Paludan, S R (författare)
Thiel, S (författare)
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Slavov, V (författare)
Ruseva, M (författare)
Eriksson, Kristina, 1962 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för reumatologi och inflammationsforskning,Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Löwhagen, Gun-Britt, 1942 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för särskilda specialiteter, Avdelningen för dermatologi och venereologi,Institute of Selected Clinical Sciences, Department of Dermatology and Venereology
Shi, L (författare)
Takahashi, K (författare)
Ezekowitz, A (författare)
Jensenius, J C (författare)
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 (creator_code:org_t)
2004-09-27
2004
Engelska.
Ingår i: Clinical and experimental immunology. - : Oxford University Press (OUP). - 0009-9104 .- 1365-2249. ; 138:2, s. 304-11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Viruses have developed numerous strategies to escape recognition by the immune system. However, some viruses such as herpes simplex virus-2 (HSV-2) are recognized by initiators of the complement system, e.g. mannan-binding lectin (MBL). To study the effects of MBL deficiency during viral infection we have chosen a model of generalized HSV-2 infection. We infected MBL-A and MBL-C double knock-out mice (DKO) with HSV-2 via the intraperitoneal (i.p.) route. DKO mice cleared HSV-2 from the liver less efficiently than the comparable wild-type animals. The impairment to effectively neutralize HSV-2 correlated with compromised liver function as measured by increased plasma levels of alanine-amino transferase. No differences in the viral burden were found in other organs such as spleen or brain. Thus, MBL-mediated protection was limited to the effects of preservation of liver homeostasis. Reconstitution with recombinant human MBL before and during the HSV-2 infection dramatically lowered the viral titres in the liver. Taken together, the data show that MBL modulates the response to HSV-2 in mice by affecting neutralization of the virus. To analyse if MBL plays a role in establishment and progression of human HSV-2 infection we analysed MBL levels in the serum samples from asymptomatic (virus-exposed people who have never displayed symptoms of HSV-2 infection) and symptomatic HSV-2 patients (people with recurrent HSV-2 infections). We found that the frequency of the MBL deficiency (<100 ng/ml) was higher in the symptomatic group and significantly different from that in the asymptomatic group (P = 0.0369). This suggests that lack of MBL-mediated complement activation increases susceptibility to viral infection.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

Adult
Aged
Alanine Transaminase
blood
Animals
Brain
immunology
Female
Herpes Genitalis
immunology
Herpes Simplex
blood
immunology
Herpesvirus 2
Human
immunology
Homeostasis
immunology
Humans
Liver
immunology
Male
Mannose-Binding Lectin
blood
immunology
Mice
Mice
Knockout
Middle Aged
Recombinant Proteins
immunology
Recurrence
Spleen
immunology
Viral Load
methods
Viral Proteins
immunology

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