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临床试验/NCT06027801
NCT06027801招募中不适用

Iron Fortified Food to Improve Japanese Encephalitis and Typhoid Fever Vaccine Immunogenicity: a Randomized Controlled Trial in Iron Deficient Thai Women

University of Oxford1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2023年9月6日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
150
试验地点
1
主要终点
Immunoglobulin G (IgG) concentrations against Salmonella Typhi

研究概览

简要总结

Iron deficiency (ID) anaemia (IDA) is a global public health problem, with the highest prevalence in Africa and in South-East Asia. While immunization programs have achieved high global coverage, vaccines often underperform in low- and middle-income countries (LMIC). The cause remains uncertain, but undernutrition, including ID, likely plays a role. Our recent in vitro and in vivo studies have shown the importance of iron status in adaptive immunity and vaccine response. Hypoferremia blunted T cell, B cell, and neutralizing antibody responses to influenza virus infection in mice, allowing the virus to persist. Iron deficient anaemic Kenyan women receiving intravenous iron at time of vaccination had a better immune response to the first dose of the ChAdOx Coronavirus 19 (COVID-19) vaccine and yellow fever vaccine. Japanese encephalitis and typhoid fever are endemic in Thailand. Vaccines are available but show variable efficacy. Whether ID impairs adult vaccine response to the live attenuated Japanese encephalitis (JE) and the Typhoid Vi polysaccharide (Vi-PS) vaccine and whether iron repletion via iron fortification improves vaccine response is uncertain.

The objective of this study is to assess whether IDA in Thai women impairs immune response to the JE and the Typhoid Vi-PS vaccine and whether fortification iron improves their response.

In this double-blind randomized controlled trial, IDA women will be assigned to two study groups: group 1 (fortification group) will receive iron-fortified biscuits (15mg iron as ferrous fumarate) for 56 days; group 2 (control group) will receive non-fortified biscuits for 56 days. All women will receive live attenuated JE and Typhoid Vi-PS vaccine on study day 28. Vaccine response will be measured 28 days after vaccination (on day 56) in both groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 49 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Participant is willing and able to give informed consent for participation in the trial.
  • Female aged 18-49 years.
  • Diagnosed with anaemia (i.e. hemoglobin (Hb) concentration <12 g/dl), but no severe anaemia (Hb <8 g/dl), and iron deficiency (ZnPP >40 µmol/mol)
  • Anticipated residence in the area for the study duration

排除标准

  • Pregnant (confirmed by rapid test during screening and at time of vaccination), lactating or planning pregnancy during the trial.
  • Blood transfusion or intravenous iron treatment within 4 months of study start
  • Major chronic infectious disease (e.g., tuberculosis, HIV+, hepatitis)
  • Major chronic non-infectious disease (e.g., Type 1 or 2 diabetes, cancer)
  • Treatment with supplemental iron two weeks prior to enrolment
  • JE or typhoid vaccine within the past two years

结局指标

主要结局

Immunoglobulin G (IgG) concentrations against Salmonella Typhi

时间窗: day 56 (4 weeks after vaccination)

Immunoglobulin A (IgA) concentrations against Salmonella Typhi

时间窗: day 56 (4 weeks after vaccination)

Neutralizing antibodies against Japanese encephalitis

时间窗: day 56 (4 weeks after vaccination)

次要结局

  • zinc protoporphyrin (ZnPP) concentration (µmol/mol heme)(day 56)
  • plasma ferritin (PF) concentration (µg/L)(day 56)
  • Hemoglobin concentration (g/dL)(day 56)
  • alpha-glycoprotein (AGP) concentration (g/L)(day 56)
  • retinol-binding protein concentration (µmol/L)(day 56)
  • serum iron (SFe) concentration (ng/µl)(day 56)
  • total iron binding capacity (µg/dL)(day 56)
  • transferrin saturation (TSAT) (%)(day 56)
  • soluble transferrin receptor (sTfR) concentration (mg/L)(day 56)
  • C-reactive protein (CRP) concentration (mg/L)(day 56)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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