Higher memory responses in HIV-infected and kidney transplanted patients than in healthy subjects following priming with the pandemic vaccine

PLoS One. 2012;7(7):e40428. doi: 10.1371/journal.pone.0040428. Epub 2012 Jul 27.

Abstract

Background: Memory responses require immune competence. We assessed the influence of priming with AS03-adjuvanted pandemic vaccine (Pandemrix®) on memory responses of HIV patients, kidney recipients (SOT) and healthy controls (HC).

Method: Participants (HIV: 197, SOT: 53; HC: 156) were enrolled in a prospective study and 390/406 (96%) completed it. All had been primed in 2009/2010 with 1 (HC) or 2 (patients) doses of Pandemrix®, and were boosted with the 2010/2011 seasonal influenza vaccine. Geometric mean titres and seroprotection rates were measured 12 months after priming and 4 weeks after boosting. Primary and memory responses were directly compared in 191 participants (HCW: 69, HIV: 71, SOT: 51) followed during 2 consecutive seasons.

Results: Most participants (HC: 77.8%, HIV: 77.6%, SOT: 66%) remained seroprotected at 12 months post-priming. Persisting A/09/H1N1 titers were high in HIV (100.2) and HC (120.1), but lower in SOT (61.4) patients. Memory responses reached higher titers in HIV (507.8) than in HC (253.5) and SOT (136.9) patients. Increasing age and lack of HAART reduced persisting and memory responses, mainly influenced by residual antibody titers. Comparing 2009/2010 and 2010/2011 titers in 191 participants followed for 2 seasons indicated lower post-2010/2011 titers in HC (240.2 vs 313.9), but higher titers in HIV (435.7 vs 338.0) and SOT (136 vs 90.3) patients.

Conclusions: Priming with 2 doses of Pandemrix® elicited persistent antibody responses and even stronger memory responses to non-adjuvanted seasonal vaccine in HIV patients than 1 dose in healthy subjects. Adjuvanted influenza vaccines may improve memory responses of immunocompromised patients.

Trial registration: ClinicalTrials.gov NCT01022905.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology*
  • Female
  • HIV Infections / blood
  • HIV Infections / immunology*
  • Humans
  • Immunocompromised Host
  • Immunologic Memory / drug effects*
  • Influenza Vaccines / administration & dosage*
  • Influenza, Human / blood
  • Influenza, Human / immunology
  • Influenza, Human / prevention & control*
  • Kidney Transplantation / immunology*
  • Male
  • Middle Aged
  • Pandemics*

Substances

  • Antibodies, Viral
  • Influenza Vaccines
  • pandemrix

Associated data

  • ClinicalTrials.gov/NCT01022905

Grants and funding

This work was supported by an Institutional grant of the Centre de Recherche Clinique of the University Hospitals of Geneva and Medical Faculty of Geneva, by the Louis Jeantet Foundation, by the Centre of Vaccinology and in the framework of the Swiss HIV Cohort Study, supported by the Swiss National Science Foundation (grant # 33CS30_134277). MB and Y. Thomas were supported by the Swiss Federal Office of Public Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.