Tick-borne encephalitis is associated with low levels of interleukin-10 in cerebrospinal fluid

References

• Lindquist L, Vapalahti O. Tick-borne encephalitis. Lancet. 2008; 371: 1861–71.
   PubMed Web of Science ®Google Scholar
• Günther G, Haglund M, Lindquist L, Forsgren M, Sköldenberg B. Tick-borne encephalitis in Sweden in relation to aseptic meningo-encephalitis of other etiology: a prospective study of clinical course and outcome. J Neurol. 1997; 244: 230–8.
   PubMed Web of Science ®Google Scholar
• Haglund M, Forsgren M, Lindh G, Lindquist L. A 10-year follow-up study of tick-borne encephalitis in the Stockholm area and a review of the literature: need for a vaccination strategy. Scand J Infect Dis. 1996; 28: 217–24.
   PubMed Web of Science ®Google Scholar
• Günther G, Haglund M, Lindquist L, Sköldenberg B, Forsgren M. Intrathecal production of neopterin and beta 2 microglobulin in tick-borne encephalitis (TBE) compared to meningoencephalitis of other etiology. Scand J Infect Dis. 1996; 28: 131–8.
   PubMed Web of Science ®Google Scholar
• Mosmann TR, Coffman RL. TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol. 1989; 7: 145–73.
   PubMed Web of Science ®Google Scholar
• Strle K, Zhou JH, Shen WH, Broussard SR, Johnson RW, Freund GG, et al.. Interleukin-10 in the brain. Crit Rev Immunol. 2001; 21: 427–49.
   PubMed Web of Science ®Google Scholar
• Ramilo O, Saez-Llorens X, Mertsola J, Jafari H, Olsen KD, Hansen EJ, et al.. Tumor necrosis factor alpha/cachectin and interleukin 1 beta initiate meningeal inflammation. J Exp Med. 1990; 172: 497–507.
   PubMed Web of Science ®Google Scholar
• Teranishi T, Hirano T, Arima N, Onoue K. Human helper T cell factor(s) (ThF). II. Induction of IgG production in B lymphoblastoid cell lines and identification of T cell-replacing factor-(TRF) like factor(s). J Immunol. 1982; 128: 1903–8.
   PubMed Web of Science ®Google Scholar
• Aurelius E, Andersson B, Forsgren M, Sköldenberg B, Strannegard Ö. Cytokines and other markers of intrathecal immune response in patients with herpes simplex encephalitis. J Infect Dis. 1994; 170: 678–81.
   PubMed Web of Science ®Google Scholar
• Heinz FX, Roggendorf M, Hofmann H, Kunz C, Deinhardt F. Comparison of two different enzyme immunoassays for detection of immunoglobulin M antibodies against tick-borne encephalitis virus in serum and cerebrospinal fluid. J Clin Microbiol. 1981; 14: 141–6.
   PubMed Web of Science ®Google Scholar
• Glimåker M, Abebe A, Johansson B, Ehrnst A, Olcen P, Strannegård O. Detection of enteroviral RNA by polymerase chain reaction in faecal samples from patients with aseptic meningitis. J Med Virol. 1992; 38: 54–61.
   PubMed Web of Science ®Google Scholar
• Samuelsson A, Skoog E, Forsgren M. Aspects on the serodiagnosis of enterovirus infections by ELISA. Serodiagn Immunother Infect Dis. 1990; 4: 395–406.
   Google Scholar
• Glimåker M, Johansson B, Olcen P, Ehrnst A, Forsgren M. Detection of enteroviral RNA by polymerase chain reaction in cerebrospinal fluid from patients with aseptic meningitis. Scand J Infect Dis. 1993; 25: 547–57.
   PubMed Web of Science ®Google Scholar
• Casas I, Powell L, Klapper PE, Cleator GM. New method for the extraction of viral RNA and DNA from cerebrospinal fluid for use in the polymerase chain reaction assay. J Virol Methods. 1995; 53: 25–36.
   PubMed Web of Science ®Google Scholar
• Aurelius E, Johansson B, Sköldenberg B, Staland A, Forsgren M. Rapid diagnosis of herpes simplex encephalitis by nested polymerase chain reaction assay of cerebrospinal fluid. Lancet. 1991; 337: 189–92.
   PubMed Web of Science ®Google Scholar
• Aurelius E, Johansson B, Sköldenberg B, Forsgren M. Encephalitis in immunocompetent patients due to herpes simplex virus type 1 or 2 as determined by PCR or type-specific antibody assays of cerebrospinal fluid. J Med Virol. 1991; 27: 591–4.
   Google Scholar
• Forsgren M, Skoog E, Jeansson S, Olofsson S, Giesecke J. Prevalence of antibodies to herpes simplex virus in pregnant women in Stockholm in 1969, 1983 and 1989: implications for STD epidemiology. Int J STD AIDS. 1994; 5: 113–6.
   PubMed Web of Science ®Google Scholar
• Huang S, Hendriks W, Althage A, Hemmi S, Bluethmann H, Kamijo R, et al.. Immune response in mice that lack the interferon-gamma receptor. Science. 1993; 259: 1742–5.
   PubMed Web of Science ®Google Scholar
• Cardell S, Sander B, Moller G. Helper interleukins are produced by both CD4 and CD8 splenic T cells after mitogen stimulation. Eur J Immunol. 1991; 21: 2495–500.
   PubMed Web of Science ®Google Scholar
• de Waal Malefyt R, Haanen J, Spits H, Roncarolo MG, te Velde A, Figdor C, et al.. Interleukin 10 (IL-10) and viral IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression. J Exp Med. 1991; 174: 915–24.
   PubMed Web of Science ®Google Scholar
• Gallo P, Sivieri S, Rinaldi L, Yan XB, Lolli F, De Rossi A, et al.. Intrathecal synthesis of interleukin-10 (IL-10) in viral and inflammatory diseases of the central nervous system. J Neurol Sci. 1994; 126: 49–53.
   PubMed Web of Science ®Google Scholar
• Maggi E, Mazzetti M, Ravina A, Annunziato F, de Carli M, Piccinni MP, et al.. Ability of HIV to promote a TH1 to TH0 shift and to replicate preferentially in TH2 and TH0 cells. Science. 1994; 265: 244–8.
   PubMed Web of Science ®Google Scholar
• Swarup V, Ghosh J, Duseja R, Ghosh S, Basu A. Japanese encephalitis virus infection decrease endogenous IL-10 production: correlation with microglial activation and neuronal death. Neurosci Lett. 2007; 420: 144–9.
   PubMed Web of Science ®Google Scholar
• Moskophidis D, Frei K, Lohler J, Fontana A, Zinkernagel RM. Production of random classes of immunoglobulins in brain tissue during persistent viral infection paralleled by secretion of interleukin-6 (IL-6) but not IL-4, IL-5, and gamma interferon. J Virol. 1991; 65: 1364–9.
   Web of Science ®Google Scholar
• Glimåker M, Kragsbjerg P, Forsgren M, Olcen P. Tumor necrosis factor-alpha (TNF alpha) in cerebrospinal fluid from patients with meningitis of different etiologies: high levels of TNF alpha indicate bacterial meningitis. J Infect Dis. 1993; 167: 882–9.
   PubMed Web of Science ®Google Scholar