Abstract

OBJECTIVES:To investigate the expression levels of surface markers of activation (CD38 and HLA-DR), inhibition (PD-1, TIGIT and CD57) and co-stimulation (CD28 and CD127) on CD4+ T cells of children/adolescents with vertical HIV infection (HI patients) and HIV-uninfected (HU) controls vaccinated with the meningococcal C conjugate vaccine (MCC).METHODS:HI patients (n=12), aged 8-17 years, were immunized with two MCC injections, while HU controls (n=9), aged 5.3-10.7 years, received a single MCC dose (as per national recommendation at the time of this study, a single MCC vaccine dose should be given for healthy children and youth aged 1-18 years). The HI patients were categorized according to the combined antiretroviral therapy (cART) treatment. Blood samples were obtained before vaccination, after priming, and after the administration of a booster dose of vaccine to determine the serum bactericidal antibody (SBA) titers and the expression levels of surface markers on CD4+ T cells by flow cytometry. The levels of serum cytokines, IL-4 and CXCL-13 were also measured using Luminex kits.RESULTS:The co-expression of the TIGIT-HLA-DR-CD38 molecules increased in the CD4+ T cells of HI patients/no-cART who also showed a lower frequency of CD127+CD28+ CD4+ T cells than HI patients/cART and HU group subjects. There were significant negative correlations between the frequency of exhausted CD4+ T cells and the SBA response. IL-4 levels were higher in HI patients/cART and positively correlated with SBA titers but negatively associated with the expression of exhaustion markers. Moreover, the CXCL-13 levels were positively correlated with the exhausted CD4+ T cells.CONCLUSION:The results of our study suggest that the co-expression of exhaustion markers and/or loss of co-stimulatory molecules influence the SBA response in HI patients.

Highlights

  • The use of meningococcal C conjugate (MCC) vaccine has positively influenced meningococcal disease epidemiology throughout the world [1]

  • In 2006, the Brazilian Ministry of Health recommended that all patients under 13 years of age with human immunodeficiency virus (HIV) infection should be immunized with a single dose of the MCC vaccine

  • We have previously shown that the poor antibody responses in combined antiretroviral therapy (cART)-treated children and adolescents with HIV infection were associated with a high frequency of CD38+HLADR+ CD4+ T cells [9]

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Summary

Introduction

The use of meningococcal C conjugate (MCC) vaccine has positively influenced meningococcal disease epidemiology throughout the world [1]. In 2006, the Brazilian Ministry of Health recommended that all patients under 13 years of age with human immunodeficiency virus (HIV) infection should be immunized with a single dose of the MCC vaccine. In 2011, Brazil incorporated the MCC vaccine into the routine immunization program, with doses administered at 3 and 5 months of age, with a booster dose at 12 months. In 2014, there was a recommendation for two doses of MCC in children above 12 months of age with HIV infection and adult HIV patients, who were not previously vaccinated [3]. To measure protection against meningococcal disease, the serum bactericidal antibody (SBA) assay is the method of choice [6]

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