A Phase I Trial of Epstein-Barr Virus Gp350 Vaccine for Children With Chronic Kidney Disease Awaiting Transplantation

被引:96
作者
Rees, Lesley [2 ]
Tizard, E. Jane [3 ]
Morgan, Andrew J. [4 ]
Cubitt, W. David [5 ]
Finerty, Susan [4 ]
Oyewole-Eletu, Titilade A. [2 ,10 ]
Owen, Karen [6 ]
Royed, Collin [2 ,11 ]
Stevens, Servi J. [7 ,9 ]
Shroff, Rukshana C. [2 ]
Tanday, Manjit K.
Wilson, A. Douglas [4 ]
Middeldorp, Jaap M. [7 ]
Amlot, Peter L. [8 ]
Steven, Neil M. [1 ]
机构
[1] Univ Birmingham, Sch Canc Sci, Canc Res UK Clin Trials Unit, Birmingham B15 2TT, W Midlands, England
[2] Great Ormond St Hosp Sick Children NHS Trust, London, England
[3] Bristol Royal Hosp Children, Renal Unit, Bristol, Avon, England
[4] Univ Bristol, Dept Cellular & Mol Med, Bristol, Avon, England
[5] Great Ormond St Hosp Sick Children NHS Trust, Dept Virol, London, England
[6] Canc Res UK, Drug Dev Off, London, England
[7] Vrije Univ Amsterdam, Med Ctr, Dept Pathol, Amsterdam, Netherlands
[8] UCL, Royal Free & Univ Coll Med Sch, Dept Immunol & Mol Pathol, London, England
[9] Univ Limburg, Acad Hosp Maastricht, Dept Clin Genet, Maastricht, Netherlands
[10] Bridge Hlth Ctr, Canterbury, Kent, England
[11] Oxford Radcliffe Hosp NHS Trust, Oxford, England
关键词
Post transplant lymphoproliferative disease; Epstein-Barr Virus; Vaccination; QUANTITATIVE COMPETITIVE PCR; UNFRACTIONATED WHOLE-BLOOD; DNA LOAD; LYMPHOPROLIFERATIVE DISORDERS; INFECTIOUS-MONONUCLEOSIS; RISK; LYMPHOMAS; EXPRESSION; RECIPIENTS; ANTIGEN;
D O I
10.1097/TP.0b013e3181b9d918
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Vaccination against Epstein-Barr virus (EBV), inducing an antibody response to the envelope glycoprotein gp350, might protect EBV-negative children with chronic kidney disease from lymphoproliferative disease after transplantation. Methods. A phase I trial recruited children with chronic kidney disease to two successive cohorts given three injections of 12.5 mu g (n=6) and 25 mu g (n=10) recombinant gp350/alhydrogel vaccine over 6 to 8 weeks. Results. One in each cohort acquired wild EBV before the week 28 evaluation. Both doses were similarly immunogenic, inducing an IgG response in all 13 evaluable patients. Neutralizing antibodies were detected in four recipients (1/4 in the 12.5 mu g and 3/9 in the 25 mu g cohort). Median time from first vaccination to transplantation was 24 weeks. Immune responses declined rapidly and were unlikely to affect posttransplant events. Discussion. The vaccine was immunogenic but a prolonged vaccine schedule up to time of transplantation or improved adjuvants are required in future trials to reduce posttransplant EBV load and risk of lymphoproliferative disease.
引用
收藏
页码:1025 / 1029
页数:5
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