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Published on: August 14, 2019
Pneumococcal and influenza immunization and human immunodeficiency virus load in children
M Keller1, A Deveikis, M Cutillar-Garcia
1Department of Pediatrics, UCLA School of Medicine, Harbor-UCLA Medical Center, Torrance, CA 90509, USA. keller@humc.edu
Insights
Immunizing children with HIV against influenza and pneumococcal disease is safe. Vaccines, alone or combined, rarely cause significant increases in HIV viral load in children on antiretroviral therapy.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Virology
Background:
- Children with Human Immunodeficiency Virus (HIV) infection are at increased risk for bacterial and viral infections.
- Vaccination is crucial for preventing opportunistic infections in immunocompromised individuals.
Purpose of the Study:
- To evaluate the impact of influenza and pneumococcal vaccinations on plasma HIV viral load in children.
- To assess potential increases in HIV RNA levels following immunization.
Main Methods:
- A cohort of 13 HIV-infected children on combination antiretroviral therapy received pneumococcal vaccine, influenza vaccine, or both.
- Plasma HIV RNA levels were measured pre-immunization and at multiple time points post-immunization.
- T cell activation markers were analyzed in a subset of participants.
Main Results:
- Only one child experienced a significant increase in HIV viral load (>0.5-log) after vaccination.
- No correlation was observed between viral load changes and antibody response to pneumococcal vaccine.
- T cell activation markers showed minimal increases in a few children, with one experiencing a viral load increase.
Conclusions:
- Concomitant or individual administration of pneumococcal and influenza vaccines is generally safe for HIV-infected children on combination antiretroviral therapy.
- Significant increases in HIV plasma RNA are rare following these immunizations.
Objective:
HIV-infected children receiving influenza vaccine, pneumococcal vaccine and both vaccines concurrently were studied to examine the effect of immunization on plasma HIV viral load.
Methods:
Thirteen children received immunizations: pneumococcal vaccine, 5; pneumococcal and influenza vaccines, 7; and influenza vaccine, 1. Most patients (12 of 13) were receiving combination reverse transcriptase inhibitor antiretroviral therapy without protease inhibitors at the time of immunization. Baseline plasma HIV RNA was determined 1 month prior (11 of 13), 2 weeks prior (12 of 13) and on the day of immunization (12 of 13). Plasma HIV RNA was assayed at 2 weeks (11 of 13), 4 weeks (12 of 13) and 3 months (5 of 13) after immunization. T cell activation markers (HLA-DR+, CD38+ and CD45RO+, CD28+) were examined for both CD4+ and CD8+ lymphocytes on the day of immunization and 2 weeks after immunization for 11 children.
Results:
Only one child developed a >0.5-log increase in viral load at any time after immunization. There was no correlation between an increase in viral load and antibody response to pneumococcal vaccine. At least one activation marker increased (> 10%) for two children receiving pneumococcal vaccine and two children receiving pneumococcal and influenza vaccines. One of these children experienced an increase in viral load.
Conclusion:
Immunization with pneumococcal and influenza vaccines, alone or in combination, is rarely associated with a significant increase in HIV plasma RNA in children receiving combination antiretroviral therapy.
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