此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

A Study to Evaluate the Immune Response Features Following Vaccination With a Recombinant Respiratory Syncytial Virus Vaccine (CHO Cells)

The purpose of this study is to elucidate the molecular mechanism by which novel adjuvants enhance the immunogenicity of Respiratory Syncytial Virus (RSV) vaccines by regulating antigen-specific B cell affinity maturation and T cell memory formation.

研究概览

详细说明

Novel adjuvants can effectively induce humoral immunity and generate neutralizing antibodies, as well as activate cellular immunity to clear intracellular pathogens.They mainly include particle-based adjuvants based on molecular agonists, synthetic inorganic/organic particulate materials, and virus-like particle mimetics.This study focuses on the mechanisms by which adjuvants enhance humoral and cellular immunity, analyzes antibody lineages, structural characteristics, and the patterns of T-cell activation, differentiation and memory formation, and elucidates the regulatory effects of adjuvants on antibody breadth and neutralizing activity. This study aims to systematically study the role of RSV adjuvants in enhancing high-affinity antibody responses and CD4⁺/CD8⁺ memory T cell generation through multi-dimensional immune analysis methods, including B Cell Receptor (BCR) / T Cell Receptor (TCR) sequencing, flow cytometry, and single-cell omics, so as to provide theoretical basis and new ideas for improving the sustainability and broad-spectrum immunization effect of novel RSV vaccines. A total of 60 adults aged 20 years and above will be enrolled. All participants will receive a single dose of investigational vaccine.

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Participants must be 20 years of age or older as determined by the investigator at enrollment.
  • Participants must be able to understand study procedures, risks, and benefits, provide voluntary agreement to participate in the study, and sign the informed consent form (ICF).
  • Participants must be willing and able to attend all scheduled follow-up visits and comply with all requirements specified in the study protocol.
  • Females of childbearing potential must use highly effective contraception from 1 month prior to vaccination through 12 months following vaccination.

    • Effective contraceptive methods include: oral contraceptives (excluding emergency contraceptives), contraceptive injections, subcutaneous implants, hormonal patches, intrauterine devices (IUDs), surgical sterilization, true abstinence, and condom use.
    • Methods not considered effective include: rhythm method, withdrawal method, and emergency contraception.

Exclusion Criteria:

*Participants who meet any of the following criteria shall be ineligible for enrollment:

  • Axillary body temperature ≥ 37.3 °C.
  • History of respiratory syncytial virus (RSV) infection within 6 months prior to enrollment.
  • New-onset respiratory infection symptoms within 7 days prior to enrollment, including cough, expectoration, dyspnea, wheezing, fever, rhinorrhea, and nasal obstruction.
  • Presence of an acute illness or acute exacerbation of a chronic condition within 3 days prior to enrollment.
  • Use of antipyretics and analgesics (excluding enteric-coated aspirin for the prevention of cardiovascular and cerebrovascular diseases) or antiallergic medications within 3 days prior to enrollment.
  • Known hypersensitivity to any ingredient of the study vaccine, including Quillaja saponaria (QS-21), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), cholesterol, sucrose, sodium dihydrogen phosphate, anhydrous disodium hydrogen phosphate, polysorbate 80, sodium chloride, hydrochloric acid, and sodium hydroxide; history of severe allergic reactions or serious adverse events following any vaccination or drug administration, including anaphylactic shock, allergic laryngeal edema, allergic purpura, thrombocytopenic purpura, local Arthus reaction, and severe urticaria.
  • Pregnant female (positive urine pregnancy test), lactating female, or female with a pregnancy plan within 12 months following vaccination.
  • Congenital asplenia, functional asplenia, or splenectomy due to any cause.
  • Previous or current malignant neoplasm, with the exception of clinically cured carcinoma in situ and papillary thyroid carcinoma.
  • Confirmed diagnosis of an autoimmune disease, including systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, and autoimmune thyroid disease.
  • Confirmed or suspected immunosuppression or immunodeficiency resulting from any cause, including primary or secondary immunocompromise, congenital or acquired immunodeficiency, human immunodeficiency virus (HIV) infection, or treatment with immunosuppressive or cytotoxic agents (e.g., chemotherapy, organ transplantation, or therapy for autoimmune diseases).
  • Any condition that, in the investigator's judgment, would render intramuscular injection unsafe, such as a history of thrombocytopenia or other coagulation disorders.
  • Previous or current serious clinical illness that is not cured (such as serious cardiovascular and cerebrovascular diseases, liver and kidney diseases, respiratory diseases, diabetes with complications, major surgery, etc.) may affect the evaluation of the trial.
  • Previous or current thrombotic diseases.
  • History of untreated tuberculosis or active tuberculosis infection at enrollment.
  • Uncontrolled hypertension defined as systolic blood pressure ≥ 150 mmHg and/or diastolic blood pressure ≥ 100 mmHg on measurement prior to vaccination.
  • History of severe cardiac arrhythmia (e.g., atrial fibrillation).
  • History or family history of convulsions, epilepsy, congenital brain malformation, psychiatric disorders, or other severe neurological conditions associated with cerebral nerve tissue injury, including brain tumor, cerebral hemorrhage, cerebral infarction (excluding lacunar cerebral infarction and cerebral infarction without sequelae), central nervous system infection, and chemical intoxication.
  • History of any cognitive disorder or any moderate or severe condition causing cognitive impairment.
  • Use of any investigational or unlicensed product (medicinal product, vaccine, or medical device) other than the study vaccine within 30 days prior to vaccination, or planned participation in another clinical trial during the study period.
  • Administration of any inactivated vaccine within 14 days prior to vaccination, or any live vaccine within 28 days prior to vaccination.
  • Prior receipt of any RSV vaccine.
  • Administration of immunoglobulin and/or any blood or plasma derivative (e.g., gamma globulin, intravenous immunoglobulin) within 3 months prior to vaccination, or planned administration during the study period.
  • Long-term use (consecutive use > 14 days) of immunosuppressive or other immunomodulatory agents within 3 months prior to vaccination or planned use during the study period. Systemic glucocorticoids ≥ 20 mg prednisone or equivalent daily for ≥ 14 days are considered long-term use. Topical preparations (ointments, eye drops, inhalations, nasal sprays) at doses not exceeding those recommended in the package insert are permitted.
  • Use of long-acting immunomodulatory agents (e.g., infliximab) within 6 months prior to vaccination or planned use during the study period.
  • History of chronic alcohol abuse and/or drug abuse that, in the investigator's judgment, may interfere with study assessments.
  • Planned migration during the study period that would preclude completion of all study procedures.
  • Any other condition that, in the investigator's judgment, may interfere with the validity of study evaluations, with special attention to respiratory infection symptoms.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Vaccine Group
Participants will receive single dose of Recombinant Respiratory Syncytial Virus Vaccine (CHO Cell), by IM injection into the deltoid muscle of the upper arm.
0.5 毫升/剂量

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Neutralizing Antibodies against both the RSV-A and RSV-B subtypes.
大体时间:At pre-vaccination (Day 1), and at 1, 12, and 24 months post-vaccination.
Measured by Virus Neutralization Test.
At pre-vaccination (Day 1), and at 1, 12, and 24 months post-vaccination.
Specific IgG Antibodies to RSV pre-F of both RSV-A and RSV-B subtypes.
大体时间:At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.
Measured by ELISA.
At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.
The Frequency of RSV pre-F Specific Cluster of Differentiation 4+ (CD4+) T Cells or Cluster of Differentiation 8+ (CD8+) T cells Expressing.
大体时间:At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.
Among markers expressed were interleukin-2 (IL-2), cluster of 40 ligand (CD40L), tumor necrosis factor alpha (TNF α) and interferon gamma (IFN γ), in vitro upon stimulation with RSV-PreF peptide preparations. Measured by Intracellular Cytokine Staining (ICS).
At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月2日

初级完成 (估计的)

2028年6月30日

研究完成 (估计的)

2028年8月31日

研究注册日期

首次提交

2026年5月25日

首先提交符合 QC 标准的

2026年5月25日

首次发布 (实际的)

2026年6月1日

研究记录更新

最后更新发布 (实际的)

2026年6月1日

上次提交的符合 QC 标准的更新

2026年5月25日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • MKKCT-900-005

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅