A Study to Evaluate the Immune Response Features Following Vaccination With a Recombinant Respiratory Syncytial Virus Vaccine (CHO Cells)
2026年5月25日 更新者:MAXVAX Biotechnology Limited Liability Company
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.
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (推定)
60
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:LiangHao Zhang
- 電話番号:+86 18971498772
- メール:lianghao.zhang@maxvax.cn
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
はい
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
1回の投与につき0.5 mL
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Neutralizing Antibodies against both the RSV-A and RSV-B subtypes.
時間枠: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.
時間枠: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.
時間枠: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.
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年6月2日
一次修了 (推定)
2028年6月30日
研究の完了 (推定)
2028年8月31日
試験登録日
最初に提出
2026年5月25日
QC基準を満たした最初の提出物
2026年5月25日
最初の投稿 (実際)
2026年6月1日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月1日
QC基準を満たした最後の更新が送信されました
2026年5月25日
最終確認日
2026年5月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- MKKCT-900-005
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いいえ
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いいえ
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