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Completed

NCT Number: NCT01135082

Pneumococcal Conjugate Vaccine (PCV) in HIV- Infected Children

The purpose of this study is to evaluate the immunogenicity and safety of 7 - valent pneumococcal conjugated vaccine in HIV - infected children, and assess the predictive factors for protective antibody responses after receiving the vaccine.

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Key information

Conditions

HIV

Age range

2 month–9 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

HIV-NAT, The Thai Red Cross AIDS Research Center, Bangkok, Thailand

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About this study

S. pneumoniae is an important cause of severe invasive bacterial disease in human immunodeficiency disease (HIV) infected children. The incidence of pneumococcal bacteremia cases requiring hospitalization among Thai children aged < 5 years had a range of 10.6-28.9 cases per 100,000 persons.[1]

Children infected with HIV have a markedly increased risk for pneumococcal infection compared with those who are not HIV-infected. HIV-infected children had rates of invasive pneumococcal disease (IPD) that were 2.8 and 12.6 times the rate among HIV-negative children aged <5 and <3 years, respectively. Incidence of IPD is 6.1 cases/100 patient-years among HIV-infected children through age 7 years [2]

Recent important strategy in prevention of invasive pneumococcal disease (IPD) is an implementation of pneumococcal conjugate vaccine (PCV), which can induce immunity starting from 2 months of age. In a small study of 5-valent PCV among children < 2 years of age, serotype-specific IgG antibodies (ELISA) response after 3 doses was found to be immunogenic among both groups.[3] The Pediatric AIDS Clinical Trials Group Study 292 show that the immunologic responses to 7- valent PCV were similar for all serotypes among asymptomatic and symptomatic HIV - infected children.[4] The study of quantitative and qualitative antibody responses to 9 - valent PCV in HIV-infected children in South Africa shows similar quantitative antibody responses but poorer qualitative antibody responses to the pneumococcal conjugate vaccine when compared to HIV-negative children.[5].

In Thailand, 7 - valent PCV (Prevnar® ) was available in 2003. It is recommended for young children and highly recommended for high risk children such as HIV-infected children, congenital heart disease or premature infants. However, one of the major obstacles for large scale implementation is cost issue. There is no previous study about immunogenicity, safety or efficacy of 7 - valent PCV in HIV -infected Thai children, the objective of this study is to assess the safety and immunogenicity of a 7 - valent PCV vaccine among HIV - infected compared with HIV - exposed children.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV - infected children
  • HIV infected individuals
  • Age between 2 months to 9 years
  • Signed written informed consent
  • HIV - exposed negative children
  • Maternal HIV infection, documented prior to delivery.
  • Age between 2 months to 9 years
  • Signed written informed consent

Exclusion criteria

  • Active opportunistic infection
  • History of hypersensitivity to pneumococcal conjugate vaccine or diphtheria toxoid
  • Using oral steroid or immunosuppressive drugs
  • Received pneumococcal conjugate vaccine, or pnuemococal polysaccharide vaccine

Treatment and study plan

valent pneumococcal conjugated vaccine

Biological

Dosage: 0.5 ml per dose Administration: intramuscular injection Location: left deltoid area x 1 injection Frequency: depend on first dose of vaccination. If 2-6 months of age, vaccination at month 0, 2, and 4. If 7-23 months of age, vaccination at month 0 and 2. If 2-9 years of age, vaccination at month 0. If patient is HIV positive, vacciation months 0 and 2 if age is 2-9 years.

Primary outcomes

  1. immunogenicity

    Time frame: 28 days

    Proportion of children with PCV serotype - specific IgG antibody at 28 days after completion of primary series of vaccination.

Secondary outcomes

  1. Safety

    Time frame: 28 days

    Number of adverse events after PCV administration

  2. compare serotype

    Time frame: 28 days

    Compare proportion of PCV serotype - specific IgG antibody in HIV - infected children by baseline clinical staging, CD4 and viral load.

Sponsors and collaborators

Lead sponsor

The HIV Netherlands Australia Thailand Research Collaboration

Other

Collaborators

  • King Chulalongkorn Memorial Hospital

Registry information

Official study title

The Immunogenicity and Safety of Pneumococcal Conjugate Vaccine in Human Immunodeficiency Virus - Infected Children

Important dates

Study start
2010
Primary completion
2010
Study completion
2011
First posted
Jun 2, 2010
Registry last updated
Sep 4, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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