Division of Infectious Diseases, University of Toronto, University Health Network, Toronto, Ontario; ; Postdoctoral Scholarship National Council for Scientific and Technological Development (CNPq), University of Campinas, Sao Paulo, Brazil;
Division of Infectious Diseases, University of Toronto, University Health Network, Toronto, Ontario;
Can J Infect Dis Med Microbiol. 2013 Spring;24(1):e7-e10. doi: 10.1155/2013/256756.
Immunocompromised individuals are more susceptible to complications produced by influenza infection. As a result, solid-organ transplant (SOT) recipients were targeted as a priority group to receive AS03-adjuvanted H1N1 influenza vaccine during 2009.
To evaluate seroconversion after one dose of adjuvanted pandemic influenza H1N1 (pH1N1) vaccine in SOT recipients.
Adult SOT recipients were enrolled to receive one 3.75 μg dose of adjuvanted pH1N1 vaccine. Serological status was tested using a hemagglutination inhibition assay before and two and four weeks postvaccination.
The five SOT recipients (one liver, two kidney and two lung transplants) had a median age of 50 years (range 36 to 53 years), and three were male, who were a median time of three years (range two months to 15 years) post-transplant. All patients were on a double or triple immunosuppressive regimen. The prevaccination pH1N1 titre was 1:10 in four patients and 1:40 in one patient. Seroprotection was observed only in one patient, with a rise in titre from 1:40 at baseline to 1:320 at both two and four weeks after vaccination. This lung transplant recipient had documented previous infection with pH1N1.
Results of the present small study call into question whether one dose of adjuvanted pH1N1 vaccine can provide seroprotection in SOT recipients.
免疫功能低下的个体更容易受到流感感染引起的并发症的影响。因此,实体器官移植(SOT)受者被作为优先群体,在 2009 年接种含佐剂的 H1N1 流感疫苗。
评估 SOT 受者接种一剂佐剂季节性流感 H1N1(pH1N1)疫苗后的血清转化率。
纳入成年 SOT 受者接种一剂 3.75μg 佐剂 pH1N1 疫苗。在接种前以及接种后 2 周和 4 周,使用血凝抑制试验检测血清学状态。
5 例 SOT 受者(1 例肝移植、2 例肾移植和 2 例肺移植)的中位年龄为 50 岁(范围 36 至 53 岁),3 例为男性,移植后中位时间为 3 年(范围 2 个月至 15 年)。所有患者均接受双重或三重免疫抑制治疗。4 例患者接种前 pH1N1 滴度为 1:10,1 例为 1:40。仅 1 例患者观察到血清保护,其滴度从基线时的 1:40 升高至接种后 2 周和 4 周时的 1:320。该肺移植受者有 pH1N1 既往感染的记录。
本小型研究的结果对 SOT 受者接种一剂含佐剂 pH1N1 疫苗是否能提供血清保护提出了质疑。