A Randomized, Double-blind, Placebo-controlled Study to Determine the Immune Effects of Multiple Doses of Vitamin D3 in Patients With Allergic Rhinitis/Rhino-conjunctivitis Caused by Birch Pollen and in Healthy Control Subjects.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 44
- 试验地点
- 1
- 主要终点
- change in IL-10 production from baseline
研究概览
简要总结
Low Vitamin D3 (VD3) levels have been reported to be associated with the risk of allergic diseases like asthma. VD3 has been demonstrated in vitro, ex vivo and in animal models to program the immune system towards anti-inflammatory immune responses. VD3 co-administered with allergen may be a promising adjuvant to improve the onset and efficacy of allergen immunotherapy (AIT). A clinical trial will be performed to compare the immune effects, the tolerability and safety of multiple doses of aVD3 analogue (registered for the intravenous route) administered by the subcutaneous (s.c.) route in subjects with allergic rhinitis and healthy controls.
The overall aim is to provide additional (in vivo) support for the use of VD3 as an adjuvant in allergen-specific immunotherapy, on top of the existing pre-clinical evidence demonstrating that antigen-presenting cells educate the adaptive immune system towards an anti-inflammatory response when allergen is seen in the presence of VD3.
详细描述
Low Vitamin D3 (VD3) levels have been reported to be associated with the risk of allergic diseases like asthma. In addition, VD3 has been demonstrated in vitro, ex vivo (skin-explants) and in animal models to program the immune system towards anti-inflammatory immune responses, dominated by regulatory T-cells (Treg) producing Interleukin (IL)-10. In response to allergens, healthy individuals by default have such a protective immune response against innocuous allergens, whereas allergic subjects develop an inflammatory Th2-type response. VD3 co-administered with allergen may be a promising adjuvant to improve the onset and efficacy of allergen immunotherapy (AIT), by helping the allergic immune system to divert towards an allergen-specific response dominated by regulatory T cells (Treg) and IL-10. A clinical trial will be performed to compare the immune effects, the tolerability and safety of multiple doses of a VD3 analogue (Zemplar® 5 μg/ml - Abbvie, registered for the intravenous route) administered by the subcutaneous (s.c.) route in subjects with allergic rhinitis and healthy controls. Primary and secondary outcomes will be compared at baseline and at several time points during the study to investigate whether 1) the healthy controls at baseline have a more anti-inflammatory systemic cellular immune response to polyclonal stimuli and to allergens compared to birch pollen allergic subjects, and 2) whether s.c.VD3 analogue can skew these responses in allergic subjects towards a profile more resembling the one observed in healthy controls. The overall aim is to provide additional (in vivo) support for the use of VD3 as an adjuvant in allergen-specific immunotherapy, on top of the existing pre-clinical evidence demonstrating that antigen-presenting cells educate the adaptive immune system towards an anti-inflammatory response when allergen is seen in the presence of VD3.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •A history of allergen-specific immunotherapy (SCIT or SLIT) with any allergen(s) within the 5 years before inclusion/screening visit.
- •Treatment with parenteral Vitamin D3 analogue in the year before inclusion
- •Significant, ongoing nasal symptoms caused by other allergens at study onset
- •A history of Hypercalcemia, Hypophosphatemia or vitamin D toxicity
- •Any vaccination within one week before randomization
- •Treatment with experimental products within the last 3 months or during the study or biologicals (including anti-IgE or TNF- α treatment) within the last 6 months or during the study
- •Severe immune disorders (including auto-immune diseases) and/or diseases requiring immunosuppressive drugs
- •Uncontrolled asthma or other active respiratory diseases
- •Malignancies or any malignant disease during the previous 5 years
- •Severe uncontrolled diseases that could increase the risk for subjects participating in the study, including but not limited to: cardiovascular insufficiency, any severe or unstable lung diseases, endocrine diseases, clinically significant renal or hepatic diseases, or hematological disorders
- •Active inflammation or infection of the target organs (nose, eyes or lower airways) at the start of the study
- •Use of preparations containing calcium or magnesium such as thiazide, diuretics, antacides.
- •Use of systemic steroids within 4 weeks before screening and during the study
- •Daily use of ketoconazole cream or immunosuppressive creams at planned injection site less than 7 days before or during the study
- •Pregnancy, lactation or inadequate contraceptive measures for women of child-bearing age (adequate contraceptive measures will be the use of a contraceptive device or -pill)
- •Any clinically significant abnormal laboratory parameter at screening
- •Any physical or mental condition that precludes compliance or participation in a clinical trial
- •Subjects who are employees or students of the institution or 1st grade relatives or partners of the investigators
研究组 & 干预措施
Paricalcitol (Vitamin D3)
paricalcitol, (Zemplar® 5 μg/ml Abbvie), will be administered via the subcutaneous route 4 times at 0.5 ml (registered dose of 5 μg/ml, thus 2.5 μg per sub-cutaneous injection). The minimum time interval between two injections is 4 days, which is a significantly lower frequency than the prescribed maximum of 3 times a week or every other day.
干预措施: Paricalcitol (Drug)
Placebo
Placebo, the same constituents as Zemplar (propylene glycol 30% (v/v) alcohol 20% (v/v)) but no paricalcitol, same dosage as verum-arm.
干预措施: Placebo (for paricalcitol) (Drug)
结局指标
主要结局
change in IL-10 production from baseline
时间窗: baseline and follow-up visit (between 5-7 weeks)
Compare the change in IL-10 production as marker of the induction of a more anti-inflammatory systemic immune response, at baseline and at follow-up (between 5-7 weeks) comparing birch pollen allergic subjects and healthy controls in a placebo-controlled design.
次要结局
- Change in IgE responses to birch pollen compared to baseline(Baseline compared to 4 weeks of treatment)
- To evaluate the number of patients that reported adverse events with Zemplar compared to placebo. This includes adverse measurements in blood safety biochemistry/haematology parameters, urinalysis, vital signs and ECG, lung function compared to placebo.(Throughout the study and follow-up (a maximum total of 8 weeks))
- changes in percentage Th1 cells characterized by the expression of CD4, CXCR3, CCR6 and T-bet, compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- changes in percentage Th2 cells characterized by the expression of CD4, CRTh2, CCR4 and Gata-3, compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- changes in percentage Th17/Th22 cells characterized by the expression of CD4, CCR6, CCR4, CCR10 and RORc2 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- changes in percentage Treg cells characterized by the expression of CD4, CD25, CD127, and Foxp3 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- changes in percentage B cells characterized by the expression of CD19, CD5, CD20, CD27, and CD38 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- changes in percentage antigen presenting cells characterized by the expression of CD11c, HLA-DR, CD14, CD16, CD1c, CD141, CD123, CD19, CD163, CD68, CD86 and CD83 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to enhance T-cell proliferation compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-5 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-13 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-17 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-10 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IFN-y compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-21 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce TGF-b compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with Bet v 1, to produce IL-22 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to enhance T-cell proliferation compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-5 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-13 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-17 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IFN-y, compared to baseline(Baseline compared to 4 weeks of treatment)
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IFN-y compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-10 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-21 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce IL-22 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated polyclonally (anti-CD3/anti-CD28), to produce TGF-b compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IFN-y compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-4 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-9 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-13 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-17A compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-21 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
- Changes in the ability of PBMCs stimulated with PMA/Ionomycin, to produce IL-22 compared to baseline(baseline and follow-up visit (between 5-7 weeks))
研究者
Laurian Jongejan
Project manager
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)