A phase 1/2 study of an adjuvanted varicella-zoster virus subunit vaccine in autologous hematopoietic cell transplant recipients

被引:120
|
作者
Stadtmauer, Edward A. [1 ]
Sullivan, Keith M. [2 ]
Marty, Francisco M. [3 ,4 ]
Dadwal, Sanjeet S. [5 ]
Papanicolaou, Genovefa A. [6 ]
Shea, Thomas C. [7 ]
Mossad, Sherif B. [8 ]
Andreadis, Charalambos [9 ]
Young, Jo-Anne H. [10 ]
Buadi, Francis K. [11 ]
El Idrissi, Mohamed [12 ]
Heineman, Thomas C. [13 ]
Berkowitz, Elchonon M. [13 ]
机构
[1] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Duke Univ, Med Ctr, Durham, NC USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Boston, MA 02115 USA
[5] City Hope Natl Med Ctr, Duarte, CA USA
[6] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[7] Univ North Carolina Hosp, Chapel Hill, NC USA
[8] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[9] Univ Calif Med Ctr, San Francisco, CA USA
[10] Univ Minnesota, Minneapolis, MN USA
[11] Mayo Clin, Rochester, MN USA
[12] GlaxoSmithKline Vaccines, Wavre, Belgium
[13] GlaxoSmithKline Vaccines, King Of Prussia, PA USA
关键词
HERPES-ZOSTER; GLYCOPROTEIN-E; ACYCLOVIR PROPHYLAXIS; IMMUNE-RESPONSES; RISK-FACTORS; INFECTION; PATHOGENESIS; IMMUNOGENICITY; COMPLICATIONS; PREVENTION;
D O I
10.1182/blood-2014-04-573048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recombinant herpes zoster (HZ) vaccines may be an alternative to the live-attenuated HZ vaccine for immunocompromised individuals. This was a phase 1/2, randomized, observer-blind, placebo-controlled study in adults with multiple myeloma, non-Hodgkin lymphoma (B-or T-cell), Hodgkin lymphoma, or acute myeloid leukemia who had undergone autologous hematopoietic stem-cell transplant 50 to 70 days earlier. Subjects (N = 121) were randomized 1:1:1:1 to receive (at months 0, 1, 3) three doses of 50 mu g varicella-zoster virus glycoprotein E (gE) adjuvanted with AS01(B), 3 doses of gE adjuvanted with AS01(E), 1 dose of saline followed by 2 doses of gE/AS01(B), or 3 doses of saline. One month after the last dose (6 months after transplant), frequencies of CD4(+) T cells expressing >= 2 activation markers after induction with gE and anti-gE antibody concentrations were higher with all gE/AS01 regimens than with saline. Both responses persisted up to 1 year in subjects vaccinated with gE/AS01. Immune responses were higher in the gE/AS01(B) 3-dose group than in the gE/AS01(B) 2-dose group but not higher than in the gE/AS01(E) 3-dose group. One serious adverse event (pneumonia) was considered vaccine related. Both formulations and both schedules were immunogenic and well tolerated in this population. This study was registered at www.clinicaltrials.gov as #NCT00920218.
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页码:2921 / 2929
页数:9
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