Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| The University of Hong Kong | OTHER |
Not provided
Not provided
Not provided
Not provided
A recent randomized controlled trial (RCT) from our group has demonstrated safety and immune response (both humoral and cell-mediated) of the live-attenuated herpes zoster (HZ) vaccine (Zostavax) in stable systemic lupus erythematosus (SLE) patients with a previous history of HZ or varicella infection. An important research question is whether the immunogenicity of the HZ vaccine in SLE patients is long-lasting. There is no information in the literature regarding the long-term immunogenicity and safety of Zostavax in SLE patients. This prompts the current extension study which is planned to evaluate the long-term immunogenicity and efficacy of Zostavax in our original patient cohort.
A recent RCT from our group has demonstrated safety and immune response (both humoral and cell-mediated) of the live-attenuated Zostavax in stable SLE patients with a previous history of HZ or varicella infection. An important research question is whether the immunogenicity of the HZ vaccine in SLE patients is long-lasting. There is no information in the literature regarding the long-term immunogenicity and safety of the HZ vaccine, Zostavax, in SLE patients.
Patients who had completed the original RCT and had been followed for 5 years since HZ vaccination or placebo injection were invited to participate in this extension study. Blood samples will be taken for a repeat assessment of the humoral and cell-mediated response to VZV at 5 years.
Outcomes of interest Primary outcome Difference between the two groups in the proportion of patients who have a persistent and 50% increase in IgG to VZV (humoral response to Zostavax) at 5 years compared to baseline Secondary outcomes
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Vaccine | Those SLE patients who had been given herpes zoster vaccine in our original RCT |
| |
| Placebo | Those SLE patients who had been given placebo vaccination in our original RCT |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Immunogenicity | Diagnostic Test | anti-VZV IgG titer and cell-mediated immunity (VZV-stimulated T cell spots) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Humoral immune response to vaccine | percentage and absolute change in anti-VZV IgG titer from baseline | 5 years after vaccination |
| Measure | Description | Time Frame |
|---|---|---|
| Cell-mediated immune response to vaccine | percentage and absolute change in VZV-stimulated T cell response (T cell spots) from baseline | 5 years after vaccination |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
systemic lupus erythematosus (SLE) patients
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Chi Chiu Mok | Tuen Mun Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Medicine, Tuen Mun Hospital | Hong Kong | 000 | China |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D006562 | Herpes Zoster |
| ID | Term |
|---|---|
| D000073618 | Varicella Zoster Virus Infection |
| D006566 | Herpesviridae Infections |
| D004266 | DNA Virus Infections |
| D014777 | Virus Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D000071497 | Immunogenicity, Vaccine |
| ID | Term |
|---|---|
| D000087506 | Vaccine Development |
| D008919 | Investigative Techniques |
| D055633 | Immune System Phenomena |
Not provided
Not provided
Not provided
Not provided
Not provided
| D007239 | Infections |