Skip to content

Antibody Response in People living with HIV Comparing CD4 T-cell Levels more than 200 vs. lower or equal 200 cells/mm3 after mRNA COVID-19 Vaccine Booster

Antibody Response in People living with HIV Comparing CD4 T-cell Levels more than 200 vs. lower or equal 200 cells/mm3 after mRNA COVID-19 Vaccine Booster

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20240708002
Enrollment
61
Registered
2024-07-08
Start date
2023-04-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antibody response HIV Covid vaccine immunogenicity Antibody response SARS-CoV-2 AntiSARS-CoV vaccine HIV/AIDs CD4 level Surrogate virus neutralization test

Interventions

CD4 level is lower or equal than 200 cells/mL.,CD4 level is more than 200 cells/mL.
Prevention,Prevention
Lower CD4 group,Higher CD4 group

Sponsors

Thai AIDS society
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Individuals living with HIV aged 18 years and above 2. on stable antiretroviral regimen for at least three months 3. Received at least two doses of the primary COVID-19 vaccine more than three months prior to enrollment in the study

Exclusion criteria

Exclusion criteria: 1. virologic failure, defined as an HIV viral load exceeding 200 copies/mL 2. high-level immunosuppression, such as the use of prednisolone at doses exceeding 20 mg/day methotrexate at doses exceeding 0.4 mg/kg/week, or previous administration of rituximab or TNF-alpha blockers within the past year 3. active autoimmune disease 4. contraindications for COVID-19 vaccination 5. previous administration of monoclonal antibodies, JAK inhibitors, or convalescent plasma for COVID-19 6. receipt of any other vaccination within 15 days prior to enrollment 7. self-reported history of SARS-CoV-2 infection in the 3 months prior to enrollment.

Design outcomes

Primary

MeasureTime frame
AntiRBDIgG 1 month AU/mL

Secondary

MeasureTime frame
sVNT 1 month percent

Countries

Thailand

Contacts

Public ContactNapon Hiranburana

Faculty of Medicine, Chulalongkorn University

napon.hir@gmail.com0816409087

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026