4.6 Article

Drak2 contributes to West Nile virus entry into the brain and lethal encephalitis

Journal

JOURNAL OF IMMUNOLOGY
Volume 181, Issue 3, Pages 2084-2091

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.181.3.2084

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Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIAID NIH HHS [R01 AI032947, R01 AI041440, R01 AI055749-05, AI072060, R01 AI055749, R01 AI053091-05, N01AI50031, R01 AI053091, R01 AI072060, AI053091, R01 AI072060-01A2, AI055749] Funding Source: Medline
  3. NIA NIH HHS [1K99AG029726-01, R00 AG029726, 4R00AG029726, K99 AG029726, K99 AG029726-01, R00 AG029726-02] Funding Source: Medline

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Death-associated protein kinase-related apoptosis-inducing kinase-2 (Drak2), a member of the death-associated protein family of serine/threonine kinases, is specifically expressed in T and B cells. In the absence of Drak2, mice are resistant to experimental autoimmune encephalomyelitis due to a decrease in the number of cells infiltrating the CNS. In the present study, we investigated the role of Drak2 in West Nile virus (WNV)-induced encephalitis and found that Drak2(-/-) mice were also more resistant to lethal WNV infection than wild-type mice. Although Drak2(-/-) mice had an increase in the number of IFN-gamma-producing T cells in the spleen after infection, viral levels in the peripheral tissues were not significantly different between these two groups of mice. In contrast, there was a reduced viral load in the brains of Drak2(-/-) mice, which was accompanied by a decrease in the number of Drak2(-/-) CD4(+) and CD8(+) T cells in the brain following WNV infection. Moreover, we detected viral Ags in T cells isolated from the spleen or brain of WNV-infected mice. These results suggest that following a systemic infection, WNV might cross the blood brain barrier and enter the CNS by being carried by infected infiltrating T cells.

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