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Sex-dependent differences in plasma cytokine responses to hantavirus infection
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk mikrobiologi, Infektionssjukdomar.
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk mikrobiologi, Infektionssjukdomar.
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk mikrobiologi, Infektionssjukdomar. (Clas Ahlm)
2008 (engelsk)Inngår i: Clinical and Vaccine Immunology, ISSN 1556-6811, E-ISSN 1556-679X, Vol. 15, nr 5, s. 885-887Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

There are often sex differences in susceptibility to infectious diseases and in level of mortality after infection. These differences probably stem from sex-related abilities to mount proper or unwanted immune responses against an infectious agent. We report that hantavirus-infected female patients show significantly higher plasma levels of interleukin-9 (IL-9), fibroblast growth factor 2, and granulocyte-macrophage colony-stimulating factor and lower levels of IL-8 and gamma interferon-induced protein 10 than male patients. The results demonstrate that a virus infection can induce sex-dependent differences in acute immune responses in humans. This finding may, at least partly, explain the observed sex differences in susceptibility to infectious diseases and in mortality following infection.

sted, utgiver, år, opplag, sider
2008. Vol. 15, nr 5, s. 885-887
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-23368DOI: 10.1128/CVI.00035-08PubMedID: 18353922Scopus ID: 2-s2.0-46249105042OAI: oai:DiVA.org:umu-23368DiVA, id: diva2:223632
Tilgjengelig fra: 2009-06-13 Laget: 2009-06-13 Sist oppdatert: 2023-03-23bibliografisk kontrollert
Inngår i avhandling
1. Study of pathogenesis and immune response in human Puumala virus infection
Åpne denne publikasjonen i ny fane eller vindu >>Study of pathogenesis and immune response in human Puumala virus infection
2013 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Hantaviruses can cause two severe human diseases: hemorrhagic fever with renal syndrome (HFRS) and hantavirus cardiopulmonary syndrome (HCPS). Hantaviruses are spread to humans mainly through inhalation of infectious virions, secreted from infected rodents. The human diseases are characterized by an increased capillary leakage syndrome. Hantaviruses are known to infect endothelial cells, but they are non-cytopathogenic. The mechanism behind human disease is not well understood, but an overactive immune response is implicated in the pathogenesis. The aim of my thesis has been to investigate parts of innate and adaptive immune responses in Puumala virus-infected patients.

In paper I we found a sex difference in the cytokine profile during acute infection. Females had significantly higher plasma levels of IL-9, FGF-2, GM-CSF and lower levels of IL-8 and IP-10 compared to males. These differences may affect the activation and function of the immune response.

In paper II we studied the phenotype and kinetics of NK cells. We observed that CD56dim NK cells were elevated during acute infection and that these, predominantly NKG2C+ NK cells, remained elevated for at least two months after symptom debut. Our novel finding of a prolonged NK cell response, implicates that NK cells may possess adaptive immunity features. 

In paper III we observed a vigorous cytotoxic T cell (CTL) response during acute infection, which contracted in parallel with decrease in viral load. The CTL response was not balanced by an increase in regulatory T cells. The T cells expressed inhibitory immunoregulatory receptors, known to dampen intrinsic T cell activity. 

In paper IV, we found that a low IgG response in patients was significantly associated with more severe disease, while the viral load did not affect the outcome. Our findings support the use of passive immunization as a treatment alternative for hantavirus-infected patients.

In conclusion, my thesis contributes to an increased knowledge about the immune response in hantavirus-infected patients. The findings, combined with future studies, will hopefully lead to a better understanding of the pathogenesis and possible treatment alternatives.

sted, utgiver, år, opplag, sider
Umeå: Umeå universitet, 2013. s. 60
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 1577
Emneord
Hantavirus, puumala virus, immune response, viral load, NK cells, T cells, cytokines, disease severity
HSV kategori
Forskningsprogram
infektionssjukdomar
Identifikatorer
urn:nbn:se:umu:diva-76706 (URN)978-91-7459-681-6 (ISBN)
Disputas
2013-09-20, E04, byggnad 6E, Norrlands Universitetssjukhus, Umeå, 09:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2013-08-30 Laget: 2013-07-11 Sist oppdatert: 2018-06-08bibliografisk kontrollert

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