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常规 13 价肺炎球菌结合疫苗在推荐年龄范围外用于血液系统恶性肿瘤和实体瘤患者的免疫原性和安全性。

Immunogenicity and safety of routine 13-valent pneumococcal conjugate vaccination outside recommended age range in patients with hematological malignancies and solid tumors.

机构信息

Department of Pediatrics, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, Chiba, Japan.

出版信息

Vaccine. 2022 Feb 23;40(9):1238-1245. doi: 10.1016/j.vaccine.2022.01.056. Epub 2022 Feb 4.

DOI:10.1016/j.vaccine.2022.01.056
PMID:35125220
Abstract

Hematological malignancy and solid tumor are major risks for invasive pneumococcal disease. Thirteen-valent pneumococcal conjugate vaccine (PCV13) is recommended for immunocompromised patients aged 6 years and older and adults who had not received the vaccine previously. However, vaccination for these individuals is not publicly subsidized in Japan. We measured pneumococcal serotype-specific IgGs (Pn-IgGs) and opsonophagocytic activities (Pn-OPAs) against PCV13 serotypes (1, 3, 5, 6A, 7F, and 19A) in patients with hematological malignancies and solid tumors who were outside the recommended age range for routine vaccination at baseline and at 1 and 6 months after the first dose of PCV13. Pneumococcal serotype-specific memory B cells (Pn-MBCs) against serotype 3 were measured from a portion of the study samples. Thirty-seven patients (30 in the young patient group and 7 in the adult patient group) completed the study. Pn-IgGs were significantly elevated at 1 month post-vaccination and persisted in protection level for 6 months after the first vaccination against all six serotypes measured except serotype 3. Pn-OPAs were significantly elevated and persisted as well against all six serotypes. Pn-MBCs were measured in 10 patients, and 90% of them had at least one detectable Pn-MBC, and 70% of them showed an increased frequency of Pn-MBCs against serotype 3. No serious adverse events were observed up to 1 month after vaccination. PCV13 is thus safe and immunogenic, including against serotype 3, in patients with hematological malignancies and solid tumors outside the recommended age range for routine vaccination.

摘要

血液系统恶性肿瘤和实体瘤是侵袭性肺炎球菌病的主要危险因素。13 价肺炎球菌结合疫苗(PCV13)推荐用于 6 岁及以上免疫功能低下的患者和以前未接种过疫苗的成年人。然而,在日本,这些人群的疫苗接种未得到公共补贴。我们在基线时以及 PCV13 第一剂接种后 1 个月和 6 个月时,测量了不符合常规接种推荐年龄范围的血液系统恶性肿瘤和实体瘤患者对 PCV13 血清型(1、3、5、6A、7F 和 19A)的肺炎球菌血清型特异性 IgG(Pn-IgG)和调理吞噬活性(Pn-OPA)。从部分研究样本中测量了针对血清型 3 的肺炎球菌血清型特异性记忆 B 细胞(Pn-MBC)。37 名患者(年轻患者组 30 名,成年患者组 7 名)完成了该研究。接种后 1 个月,Pn-IgG 显著升高,并在第一次接种后 6 个月内持续保持对所有 6 个测量血清型(除血清型 3 外)的保护水平。Pn-OPA 也显著升高并持续存在。在 10 名患者中测量了 Pn-MBC,其中 90%的患者至少有一种可检测的 Pn-MBC,其中 70%的患者对血清型 3 的 Pn-MBC 频率增加。接种后 1 个月内未观察到严重不良事件。因此,PCV13 对推荐常规接种年龄范围之外的血液系统恶性肿瘤和实体瘤患者是安全且具有免疫原性的,包括针对血清型 3。

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