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临床试验/NCT06366672
NCT06366672进行中(未招募)早期 1 期

Evaluating the Durability of the Human Immune Response to the JYNNEOS Modified Vaccinia Ankara-Bavarian Nordic (MVA-BN) Vaccine

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年6月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
进行中(未招募)
入组人数
20
试验地点
1
主要终点
Change in magnitude of the MVA-BN antigen-specific antibody response in blood plasma

研究概览

简要总结

This study is designed to evaluate the magnitude and duration of the human adaptive immune response to the JYNNEOS Modified Vaccinia Ankara-Bavarian Nordic (MVA-BN) vaccine in the blood, lung mucosa, skin and bone marrow.

详细描述

Orthopoxvirus vaccination leads to very high magnitude antigen-specific T cell responses and neutralizing antibody responses that can be detected in blood decades after vaccination. Despite a large number of previous studies of human immune responses to Modified Vaccinia Ankara (MVA) vaccination in blood, very few of these previous studies evaluate the human mucosal immune response to MVA in the lung and skin, or the immune response to MVA vaccination in the bone marrow. The development of methods to explore human immune responses in these key immunologic compartments now allows the evaluation of the induction of immune responses in these human tissues using the MVA vaccine system.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18-60 year old otherwise healthy participants

排除标准

  • Prisoners
  • Participants unable to provide full written informed consent
  • Previous receipt of a smallpox or monkeypox vaccine
  • Previous infection with monkeypox
  • Receipt of any vaccine in the 28 days prior to the first study procedure or planned receipt of any vaccine outside of those provided in the current study before completion of the study day 42 visit.
  • Immunocompromise (primary or secondary due to other medical conditions or medications)
  • Previous organ transplant
  • Active malignancy
  • Pregnancy
  • < 4 weeks post-partum or actively breastfeeding
  • Female participants who are not actively on hormonal contraception or do not have an intrauterine device in place
  • Body Mass Index > 40
  • Current smokers
  • History of a known chronic pulmonary, cardiovascular, renal, hepatic, hematologic or metabolic disorder. Participants with isolated treated hypertension as the only cardiovascular disorder may be included in the study.
  • History of a chronic neurologic or neurodevelopmental condition. This does not exclude potential participants with chronic back pain or previous disk herniation/back surgery, only participants with documented weakness, quadriplegia or paraplegia. This exclusion criterion also does not exclude from the study participants with recurrent migraine headaches as the only chronic neurologic condition.
  • Pulse oxygen saturation value of 92% or less on room air at study enrollment or on the day of bronchoscopy
  • Any significant infiltrate or pleural effusion on upright posterior-anterior and lateral chest x-ray imaging performed on the day of bronchoscopy
  • International Normalized Ratio value greater than 1.4 or a Partial Thromboplastin Time value of greater than 40 seconds at study enrollment
  • Platelet count of less than 100,000 at study enrollment

研究组 & 干预措施

MVA-BN vaccinated

Experimental

MVA-BN vaccine administered: day 0 and day 28 Phlebotomy: within 30 days prior to first vaccine dose, day 0, day 14, day 28, day 35, day 42, day 56, day 90, day 110, day 150, day 210, day 395 Research bronchoscopy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Skin punch biopsy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Bone marrow aspiration: within 30 days prior to first vaccine dose, day 56, day 110, day 210, day 395

干预措施: JYNNEOS (Smallpox and Monkeypox Vaccine, Live, Nonreplicating) suspension for subcutaneous injection (Biological)

MVA-BN vaccinated

Experimental

MVA-BN vaccine administered: day 0 and day 28 Phlebotomy: within 30 days prior to first vaccine dose, day 0, day 14, day 28, day 35, day 42, day 56, day 90, day 110, day 150, day 210, day 395 Research bronchoscopy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Skin punch biopsy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Bone marrow aspiration: within 30 days prior to first vaccine dose, day 56, day 110, day 210, day 395

干预措施: Phlebotomy (Procedure)

MVA-BN vaccinated

Experimental

MVA-BN vaccine administered: day 0 and day 28 Phlebotomy: within 30 days prior to first vaccine dose, day 0, day 14, day 28, day 35, day 42, day 56, day 90, day 110, day 150, day 210, day 395 Research bronchoscopy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Skin punch biopsy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Bone marrow aspiration: within 30 days prior to first vaccine dose, day 56, day 110, day 210, day 395

干预措施: Research bronchoscopy (Procedure)

MVA-BN vaccinated

Experimental

MVA-BN vaccine administered: day 0 and day 28 Phlebotomy: within 30 days prior to first vaccine dose, day 0, day 14, day 28, day 35, day 42, day 56, day 90, day 110, day 150, day 210, day 395 Research bronchoscopy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Skin punch biopsy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Bone marrow aspiration: within 30 days prior to first vaccine dose, day 56, day 110, day 210, day 395

干预措施: Skin punch biopsy (Procedure)

MVA-BN vaccinated

Experimental

MVA-BN vaccine administered: day 0 and day 28 Phlebotomy: within 30 days prior to first vaccine dose, day 0, day 14, day 28, day 35, day 42, day 56, day 90, day 110, day 150, day 210, day 395 Research bronchoscopy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Skin punch biopsy: within 30 days prior to first vaccine dose, day 42, day 210, day 395 Bone marrow aspiration: within 30 days prior to first vaccine dose, day 56, day 110, day 210, day 395

干预措施: Bone marrow aspiration (Procedure)

结局指标

主要结局

Change in magnitude of the MVA-BN antigen-specific antibody response in blood plasma

时间窗: Change from day 42 to day 395

Change in magnitude of the MVA-BN antigen-specific T cell response in the blood

时间窗: Change from day 42 to day 395

次要结局

  • Change in magnitude of the MVA-BN antigen-specific antibody response in bronchoalveolar lavage fluid(Change from day 42 to day 395)
  • Change in magnitude of the MVA-BN antigen-specific T cell response in the lower airways(Change from day 42 to day 395)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Philip Mudd

Assistant Professor

Washington University School of Medicine

研究点 (1)

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