Primary Immunodeficiency
Conditions
Keywords
Diagnostic immunization with rabies vaccine, Primary immunodeficiency
Brief summary
The purpose of this study is to evaluate diagnostic immunization protocol of rabies vaccine for diagnosis the patients with primary immunodeficiency disorders and study humoral and cellular immune response to rabies vaccine in patients with primary immunodeficiency.
Detailed description
Objective Primary objective : To study diagnostic immunization protocol of rabies vaccine for diagnosis the patients with primary immunodeficiency disorders. Secondary objective * To study humoral and cellular immune response to rabies vaccine in patients with primary immunodeficiency. * To study anti-rabies immunization protocol in patients with primary immunodeficiency disorders. Population Case group: Twenty primary immunodeficiency disease patients that are diagnosed, treated and followed at Allergy and Immunology unit, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University. Control group: Twenty healthy subjects who have no underlying disease and age-matched with case patients. Inclusion and exclusion criteria Vaccine : * Verorab® (PVRV; Purified Vero Cell Vaccine) 0.5 ml intramuscular * Standard intramuscular regimen: ESSEN on days 0, 3, 7, 14, 28 and booster at 1 year later on days 360 and 363 Immunological evaluations : 1. Humoral immune response : on 5 ml blood samples will be collected for antibody determination days 0, 14, 28, 90, 360, 367 and 374. Neutralizing antibodies will be determined blindly using the rapid fluorescent focus inhibition test (RFFIT) at Queen Saovabha Memorial Institute. Rabies neutralizing antibody will be reported in IU/ml The protective antibody level are defined rabies neutralizing antibody ≥ 0.5 IU/ml . 2. Cellular mediated immune response : On 5 ml blood samples will be collected for antibody determination days 14, 28, 90, 360, 367 and 374. Lymphocyte proliferation response to rabies antigen will be determined by using 3H-thymidine incorporation assay. The responder criteria are defined as stimulation index (SI index) ≥ 2.0 was considered as evidence of antigen-induced lymphocyte proliferation.
Interventions
BIOLOGICALVerorab® (PVRV; Purified Vero Cell Vaccine)
* Verorab® (PVRV; Purified Vero Cell Vaccine) 0.5 ml intramuscular * Standard intramuscular regimen: ESSEN on days 0, 3, 7, 14, 28 and booster at 1 year later on days 360 and 363
Sponsors
Chulalongkorn University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
12 Months to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* Case group 1. Patient with primary immunodeficiency diseases who follows up at Division of pediatric allergy and immunology unit, King Chulalongkorn Memorial Hospital 2. Subject or father/mother/legally acceptable representative properly informed about the study and having signed the informed consent form. 3. Subject is able to comply with the follow-up schedule of the protocol * Control group 1. Subject is healthy (from history and physical examination) 2. Subject do not has underlying diseases. 3. Subject do not has primary and secondary immunodeficiency diseases 4. Subject is not receiving immunosuppressive therapy or cytotoxic drugs 5. Subject or father/mother/legally acceptable representative properly informed about the study and having signed the informed consent form. 6. Subject is able to comply with the follow-up schedule of the protocol 7. Age more than 12 month old to 60 years old
Exclusion criteria
1. Reported history of previous rabies immunization or Rabies neutralizing antibody (Rabies Nab) \> 0.5 IU/ml 2. Subject is unable to comply with the follow-up schedule of the protocol 3. Pregnancy 4. Body temperature more than 38 degree celcius at screening visit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rabies neutralizing antibody titer (RFFIT test) | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Lymphocyte proliferation response to rabies antigen (3H-Thymidine incorporation assay) | 1 year |
Countries
Thailand
Contacts
Primary ContactNarissara - Suratannon, MD
Outcome results
None listed