Pneumococcal conjugate vaccine triggers a better immune response than pneumococcal polysaccharide vaccine in patients with chronic lymphocytic leukemia A randomized study by the Swedish CLL group

被引:46
|
作者
Svensson, Tobias [1 ]
Kattstrom, Magdalena [2 ]
Hammarlund, Ylva [3 ]
Roth, Daniel [4 ]
Andersson, P-O [5 ]
Svensson, Magnus [6 ]
Nilsson, Ingmar [7 ]
Rombo, Lars [6 ]
Cherif, Honar [1 ]
Kimby, Eva [8 ,9 ]
机构
[1] Uppsala Univ, Dept Med Sci, Sect Hematol, Uppsala, Sweden
[2] Orebro Univ Hosp, Dept Med, Sect Hematol, Orebro, Sweden
[3] Falun Cent Hosp, Dept Med, Falun, Sweden
[4] Lund Univ Hosp, Fac Med, Inst Clin Sci, Lund, Sweden
[5] South Alvsborg Hosp, Dept Med, Sect Hematol, Boras, Sweden
[6] Eskilstuna Hosp, Dept Med, Eskilstuna, Sweden
[7] Karlstad Hosp, Dept Med, Karlstad, Sweden
[8] Karolinska Inst, Dept Med, Unit Hematol, Huddinge, Sweden
[9] Karolinska Univ Hosp, Huddinge, Sweden
关键词
Chronic lymphocytic leukemia (CLL); Pneumococcal vaccine; Polysaccharide vaccine; Protein-conjugate vaccine; Immunogenicity; STREPTOCOCCUS-PNEUMONIAE; OPSONOPHAGOCYTIC ASSAY; ANTIBODY-RESPONSES; PROTEIN-CONJUGATE; ADULTS; HYPOGAMMAGLOBULINEMIA; IMMUNOGENICITY; INFECTIONS; SEROTYPES; DISEASE;
D O I
10.1016/j.vaccine.2018.05.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: To determine if patients with untreated chronic lymphocytic leukemia (CLL) benefit from vaccination with a 13-valent pneumococcal conjugated vaccine (PCV13), Prevenar13 (R), compared to a 23-valent pneumococcal polysaccharide vaccine (PPSV23), Pneumovax (R), in terms of immune response. Background: Streptococcus pneumoniae causes substantial morbidity in patients with CLL, a group known to respond poorly to polysaccharide vaccines. Comparative studies with conjugated vaccines are lacking. Methods: 128 treatment naive CLL patients from eight hematology clinics in Sweden were randomized to vaccination with PCV13 (n = 63) or PPSV23 (n = 65) after stratification by IgG level and CLL clinical stage (Rai). Blood samples for evaluation of immune response were obtained at baseline, and at one and six months after vaccination. Analyses for each of the 12 pneumococcal serotypes common for PCV13 and PPSV23 were performed by opsonophagocytic assay (OPA) and enzyme-linked immunosorbent assay (ELISA). Results: PCV13 elicited a superior immune response than PPSV23 in 10/12 serotypes one month after vaccination and in 5/12 serotypes six months after vaccination, measured as OPA geometric mean titers (GMTs). Geometric mean concentrations of serotype-specific IgG antibodies elicited by PCV13 as measured by ELISA, were higher than those elicited by PPSV23 in half of the common serotypes, both after one and six months. PPSV23 did not trigger a better immune response than PCV13 for any of the serotypes, regardless of analysis method or time point of analysis. Negative predictive factors for vaccination response were hypogammaglobulinemia and long disease duration. Both vaccines were well tolerated. Conclusions: In patients with previously untreated CLL, the efficacy of PCV13 in terms of immune response is superior to PPSV23 for most serotypes common for the two vaccines. We therefore propose that PCV13 should be included in vaccination programs against Streptococcus pneumoniae for CLL patients and administered as early as possible during the course of the disease. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3701 / 3707
页数:7
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