TLR3 agonism re-establishes CNS immune competence during α4-integrin deficiency

Rehana Z. Hussain, Petra C. Cravens, Richard Doelger, Brianne Dentel, Emily Herndon, Nicolas Loof, Peter Tsai, Darin Okuda, Michael K. Racke, Olaf Stuve

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


Objective: Natalizumab blocks α4-integrin-mediated leukocyte migration into the central nervous system (CNS). It diminishes disease activity in multiple sclerosis (MS), but carries a high risk of progressive multifocal encephalopathy (PML), an opportunistic infection with JV virus that may be prompted by diminished CNS immune surveillance. The initial host response to viral infections entails the synthesis of type I interferons (IFN) upon engagement of TLR3 receptors. We hypothesized that TLR3 agonism reestablishes CNS immune competence in the setting of α4-integrin deficiency. Method: We generated the conditional knock out mouse strain Mx1.Cre+α4-integrinfl/fl, in which the α4-integrin gene is ablated upon treatment with the TLR3 agonist poly I:C. Adoptive transfer of purified lymphocytes from poly I:C-treated Mx1.Cre+α4-integrinfl/fl donors into naive recipients recapitulates immunosuppression under natalizumab. Active experimental autoimmune encephalomyelitis (EAE) in Mx1.Cre+α4-integrinfl/fl mice treated with poly I:C represents immune-reconstitution. Results: Adoptive transfer of T cells from poly I:C treated Mx1.Cre+α4-integrinfl/fl mice causes minimal EAE. The in vitro migratory capability of CD45+ splenocytes from these mice is reduced. In contrast, actively-induced EAE after poly I:C treatment results in full disease susceptibility of Mx1.Cre+ α4-integrinfl/fl mice, and the number and composition of CNS leukocytes is similar to controls. Extravasation of Evans Blue indicates a compromised blood-brain barrier. Poly I:C treatment results in a 2-fold increase in IFNβ transcription in the spinal cord. Interpretation: Our data suggest that TLR3 agonism in the setting of relative α4-integrin deficiency can reestablish CNS immune surveillance in an experimental model. This pathway may present a feasible treatment strategy to treat and prevent PML under natalizumab therapy and should be considered for further experimental evaluation in a controlled setting.

Original languageEnglish (US)
Pages (from-to)1543-1561
Number of pages19
JournalAnnals of Clinical and Translational Neurology
Issue number12
StatePublished - Dec 2018

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology


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