Improved plasmablast response after repeated pneumococcal revaccinations following primary immunization with 13-valent pneumococcal conjugate vaccine or 23-valent pneumococcal polysaccharide vaccine in patients with chronic lymphocytic leukemia

被引:0
作者
Kattstrom, Magdalena [1 ,6 ]
Uggla, Bertil [1 ]
Tina, Elisabet [2 ]
Kimby, Eva [3 ]
Noren, Torbjorn [4 ]
Athlin, Simon [5 ]
机构
[1] Orebro Univ, Fac Med & Hlth, Dept Med, Sect Hematol, SE-70185 Orebro, Sweden
[2] Orebro Univ, Fac Med & Hlth, Dept Clin Res Lab, Orebro, Sweden
[3] Karolinska Inst, Dept Med, Unit Hematol, Stockholm, Sweden
[4] Orebro Univ, Fac Med & Hlth, Dept Lab Med, Clin Microbiol, Orebro, Sweden
[5] Orebro Univ, Fac Med & Hlth, Sch Med Sci, SE-70185 Orebro, Sweden
[6] Orebro Univ Hosp, Hematologmottagningen, VO Med, S-70185 Orebro, Sweden
关键词
ADULTS; 50; YEARS; INITIAL VACCINATION; IMMUNODEFICIENCY; IMMUNOGENICITY; IMMUNE; SAFETY;
D O I
10.1016/j.vaccine.2023.04.016
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: Patients with chronic lymphocytic leukemia (CLL) show an immune dysfunction with increased risk of infections and poor response to vaccination. Streptococcus pneumoniae is a common cause of morbidity and mortality in CLL patients. In a previous randomized clinical trial, we found a superior immune response in CLL patients receiving conjugated pneumococcal vaccine compared to nonconjugated vaccine. The response to revaccination in CLL patients is scarcely studied. In this study, early humoral response to repeated revaccinations with pneumococcal vaccines was evaluated, by determination of B cell subsets and plasmablast dynamics in peripheral blood.Method: CLL patients (n = 14) and immunocompetent controls (n = 31) were revaccinated with a 13valent pneumococcal conjugate vaccine (PCV13) after previous primary immunization (3-6 years ago) with PCV13 or a 23-valent pneumococcal polysaccharide vaccine (PPSV23). Eight weeks after the first revaccination, all CLL patients received a second revaccination with PCV13 or PPSV23. B cell subsets including plasmablasts were analyzed in peripheral blood by flow cytometry, before and after the first and the second revaccination. Results: None of the CLL patients, but all controls, had detectable plasmablasts at baseline (p < 0.001). After the first revaccination with PCV13, the plasmablast proportions did not increase in CLL patients (p = 0.13), while increases were seen in controls (p < 0.001). However, after a second revaccination with PCV13 or PPSV23, plasmablasts increased compared to baseline also in CLL patients (p < 0.01). If no response was evident after first revaccination, only a second revaccination with PCV13 increased plasmablasts in contrast to PPSV23 revaccination. Patients with hypogammaglobulinemia and ongoing/previous CLL specific treatment responded poorly, also to a second revaccination.Conclusion: In CLL patients, pneumococcal revaccination induced minor early plasmablast response compared to controls, but the response improved using a strategy of repeated doses with of conjugated T cell dependent pneumococcal vaccine.(c) 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
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页码:3128 / 3136
页数:9
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