CMV Modulation of the Immune System in ANCA-associated Vasculitis (CANVAS)

Professor Lorraine Harper

Status and phase

Unknown

Phase 2

Conditions

ANCA Associated Vasculitis

CMV Infection

Treatments

Drug: Valaciclovir

Study type

Interventional

Funder types

Other

Identifiers

NCT01633476

2012-001970-28 (EudraCT Number)

097962/Z/11/Z (Other Grant/Funding Number)

CMV-001

Details and patient eligibility

About

The purpose of this study is to determine whether Cytomegalovirus (CMV) reactivation in ANCA-associated vasculitis (AAV) patients can be effectively and safely reduced using an antiviral agent (valaciclovir) and whether this in turn improves the function of the immune system thereby also improving the body's ability to fight other infections.

The primary hypothesis is that repeated episodes of CMV reactivation in AAV patients drive the expansion and functional impairment of CMV-specific T-cells, with increased susceptibility to infection. Inhibition of CMV replication with valaciclovir will block further stimulation of CMV specific T-cells and increase the functional capacity of the immune system.

Full description

Infection is the commonest cause of death in patients with ANCA-associated vasculitis (AAV). The investigators have shown that the expansion of CD4+CD28- T-cells present in patients with AAV is driven by CMV and this expansion is associated with increased infection risk. It is suggested that these cells are driven by CMV reactivation and express markers of T-cell exhaustion with reduced cytokine production and inhibitory receptor expression. However the phenotype of CMV-specific T cells in those with extreme expansions of CD4+CD28- T-cells has not been explored.

The investigators aim to investigate the phenotype of CMV-specific T-cells comparing those patients with extreme expansions of CD4+CD28- T-cells to those with smaller expansions and relate this to CMV reactivation. The investigators will monitor CMV reactivation in urine and blood monthly by qPCR. This will be correlated with the expansion of CD4+CD28- T-cells and the phenotype of these cells, specifically looking at cytokine production and inhibitory receptor expression. The investigators will identify CMV-specific T-cells by MHC class II tetramers or by stimulating with CMV lysate. The investigators will proceed to undertake a randomised controlled trial with valaciclovir or no treatment to investigate whether the reduction of CMV reactivation improves the phenotype of CD4+CD28- T-cells in these patients.

Enrollment

38 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Documented diagnosis of Wegener's granulomatosis (now called Granulomatosis with Polyangiitis), microscopic polyangiitis or renal limited vasculitis according to Chapel Hill Consensus Conference criteria.
In stable remission (no documented clinical disease activity) for at least 6 months prior to entry.
On maintenance immunosuppression with prednisolone, mycophenolate mofetil or azathioprine alone or in combination (maximum 2 agents).
Documented evidence of CMV infection (CMV-specific immunoglobulin G detected in peripheral blood).
Documentation that female patients of child bearing potential are not pregnant and using an appropriate form of contraception.
Written informed consent for study participation

Exclusion criteria

Stage 5 chronic kidney disease (eGFR<15ml/minute/1.73m2).
Other significant chronic infection (HIV, HBV, HCV, TB).
B-cell or T-cell depleting therapy within 12 months.
Treatment with anti-CMV therapies in last month
Underlying medical conditions, which in the opinion of the Investigator place the patient at unacceptably high risk for participating in the study.
Inability to fully or appropriately participate in the study.