Rheumatology Division, Faculdade de Medicina, Hospital das Clinicas HCFMUSP, Universidade de Sao Paulo, Sao Paulo, SP, 01246-903, Brazil.
Pediatric Rheumatology Unit, Faculdade de Medicina, Hospital das Clinicas HCFMUSP, Universidade de Sao Paulo, Sao Paulo, SP, 01246-903, Brazil.
Clin Rheumatol. 2023 Sep;42(9):2419-2425. doi: 10.1007/s10067-023-06666-w. Epub 2023 Jun 12.
Influenza A (H3N2) virus is the major cause of morbidity/mortality due to seasonal influenza over 50 years. Data about the safety/immunogenicity of influenza A/Singapore (H3N2) vaccine are scarce in primary Sjögren syndrome (pSS).
Twenty-one consecutive pSS patients and 42 HC (healthy control individuals) were immunized with influenza A/Singapore/INFIMH-16-0019/2016 (H3N2)-like virus. Rates of SP (seroprotection) and SC (seroconversion), GMT (geometric mean titers), FI-GMT (factor increase in GMT), ESSDAI (EULAR Sjögren's Syndrome Disease Activity Index), and adverse events were appraised before and 4 weeks post-vaccination.
pSS and HC had similar mean age (51.2 ± 14.2 vs. 50.6 ± 12.1 years, p = 0.886). Pre-vaccination SP rates were high in pSS and HC (90.5% vs. 71.4%, p = 0.114), and GMT were higher in pSS [80.0 (52.4-160.0) vs. 40.0 (20.0-80.0), p = 0.001]. The percentage of influenza vaccination in the preceding two years was elevated and similar in pSS and HC (94.1% vs. 94.6%, p = 1.000). GMT values augmented in both groups four weeks after vaccination and persisted higher in the first group [160.0 (80.0-320.0) vs. 80.0 (40.0-80.0), p < 0.001] with equivalent FI-GMT [1.4 (1.0-2.8) vs. 1.4 (1.0-2.0), p = 0.410]. Both groups had low and similar SC rates (19.0% vs. 9.5%, p = 0.423). ESSDAI values persisted steadily during the study (p = 0.313). No serious adverse events have occurred.
The novel demonstration that the influenza A/Singapore (H3N2) vaccine induces a different pattern of immunogenicity from other influenza A constituents in pSS, featured by a desirable high pre- and post-vaccination immunogenicity, is in line with reported differences in immune responses between strains in trivalent vaccines and may be related to pre-existing immunity.
gov: #NCT03540823. Key Points • This prospective study demonstrated a robust pre- and post-vaccination immunogenicity to influenza A/Singapore/INFIMH-16-0019/2016 (H3N2)-like virus in primary Sjögren's syndrome (pSS). • This high immunogenicity pattern may be related to pre-existing immunization, or else it is related to immunogenicity differences of each strain. • This vaccine had an adequate safety profile in pSS, with no impact on disease activity.
甲型流感(H3N2)病毒是导致 50 岁以上季节性流感发病和死亡的主要原因。在原发性干燥综合征(pSS)患者中,关于甲型流感/A 新加坡(H3N2)疫苗的安全性/免疫原性的数据很少。
21 例连续的 pSS 患者和 42 例 HC(健康对照个体)接种了甲型流感/A 新加坡/INFIMH-16-0019/2016(H3N2)样病毒。评估接种前和接种后 4 周 SP(血清保护)和 SC(血清转化率)、GMT(几何平均滴度)、FI-GMT(GMT 增加因子)、ESSDAI(EULAR 干燥综合征疾病活动指数)和不良反应的发生率。
pSS 和 HC 的平均年龄相似(51.2±14.2 岁 vs. 50.6±12.1 岁,p=0.886)。接种前 pSS 和 HC 的 SP 率均较高(90.5% vs. 71.4%,p=0.114),GMT 也较高[80.0(52.4-160.0)比 40.0(20.0-80.0),p=0.001]。pSS 和 HC 在前两年的流感疫苗接种率均较高且相似(94.1% vs. 94.6%,p=1.000)。GMT 值在两组接种后 4 周均升高,且第一组持续升高[160.0(80.0-320.0)比 80.0(40.0-80.0),p<0.001],FI-GMT 也相似[1.4(1.0-2.8)比 1.4(1.0-2.0),p=0.410]。两组的 SC 率均较低且相似(19.0% vs. 9.5%,p=0.423)。ESSDAI 值在研究期间保持稳定(p=0.313)。未发生严重不良事件。
新型甲型流感/A 新加坡(H3N2)疫苗在 pSS 中诱导的免疫原性与其他甲型流感成分不同,表现为理想的高接种前和接种后免疫原性,这与三价疫苗中菌株间免疫反应的差异一致,可能与预先存在的免疫有关。
gov:#NCT03540823。关键点 • 本前瞻性研究显示,原发性干燥综合征(pSS)患者对甲型流感/A 新加坡/INFIMH-16-0019/2016(H3N2)样病毒具有强大的接种前和接种后的免疫原性。 • 这种高免疫原性模式可能与预先存在的免疫有关,或者与每种菌株的免疫原性差异有关。 • 该疫苗在 pSS 中的安全性良好,对疾病活动无影响。