Stiehm E Richard, Roberts Robert L, Kaplan Michael S, Corren Jonathan, Jaracz Eileen, Rico M Joyce
Mattel Children's Hospital, University of California-Los Angeles, California 90095, USA.
J Am Acad Dermatol. 2005 Aug;53(2 Suppl 2):S206-13. doi: 10.1016/j.jaad.2005.04.064.
We sought to determine the effect of treatment with topical tacrolimus on B- and T-cell immunity including the primary antibody response to pneumococcal polysaccharide vaccine in children with atopic dermatitis.
In this open-label, noncomparative study, 23 children aged 2 to 12 years with moderate to severe atopic dermatitis were treated with tacrolimus 0.03% ointment twice daily for 7 weeks, immunized with a 23-valent pneumococcal polysaccharide vaccine after 3 weeks of treatment, and had their antibody response measured (for 12 pneumococcal serotype antigens present in the vaccine) before and 4 weeks after vaccination. None had received pneumococcal vaccine before the study. Patient antibody and cellular immune responses were assessed at each study visit (baseline, week 3, and week 7).
No significant changes in complete blood cell count, lymphocyte subsets, CD4/CD8 ratio, immunoglobulin levels, antibody titers to tetanus and Haemophilus influenzae , or lymphoproliferative responses were noted during the tacrolimus ointment treatment period. Tacrolimus blood levels were 1 ng/mL or less in all 23 children. Protective pneumococcal titers to all 12 serotypes were observed in 2 of 23 (9%) children prevaccination and in 16 of 23 (70%) children postvaccination. All 6 children who had protective titers to 0 to 5 of the 12 serotypes developed protective titers to an additional 5 to 11 serotypes. Of the patients, 91% had a greater than 4-fold increase in titer for at least 4 of 12 pneumococcal serotypes.
Topical application of tacrolimus ointment does not affect the serologic response to pneumococcal vaccine or interfere with preexisting T- and B-cell immune responses.
我们试图确定局部应用他克莫司治疗对特应性皮炎患儿B细胞和T细胞免疫的影响,包括对肺炎球菌多糖疫苗的初次抗体反应。
在这项开放标签、非对照研究中,23名2至12岁的中重度特应性皮炎患儿每天两次外用0.03%他克莫司软膏,持续7周,治疗3周后接种23价肺炎球菌多糖疫苗,并在接种前和接种后4周测量其抗体反应(针对疫苗中存在的12种肺炎球菌血清型抗原)。在研究前,所有患儿均未接种过肺炎球菌疫苗。在每次研究访视(基线、第3周和第7周)时评估患者的抗体和细胞免疫反应。
在他克莫司软膏治疗期间,全血细胞计数、淋巴细胞亚群、CD4/CD8比值、免疫球蛋白水平、破伤风和流感嗜血杆菌抗体滴度或淋巴细胞增殖反应均无显著变化。所有23名儿童的他克莫司血药浓度均为1 ng/mL或更低。23名儿童中有2名(9%)在接种疫苗前对所有12种血清型均有保护性肺炎球菌滴度,23名儿童中有16名(70%)在接种疫苗后有保护性滴度。12种血清型中对0至5种血清型有保护性滴度的所有6名儿童,对另外5至11种血清型也产生了保护性滴度。在患者中,91%的患者对12种肺炎球菌血清型中的至少4种血清型的滴度有大于4倍的升高。
局部应用他克莫司软膏不影响对肺炎球菌疫苗的血清学反应,也不干扰现有的T细胞和B细胞免疫反应。