Institute of Biomedical Engineering, National Tsing Hua University, Hsinchu, Taiwan.
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital at Linkou, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Front Cell Infect Microbiol. 2024 Mar 20;14:1358967. doi: 10.3389/fcimb.2024.1358967. eCollection 2024.
The aim of this study is to investigate changes in TNF-related apoptosis-inducing ligand (TRAIL) and gamma interferon-induced protein 10 (IP-10) after COVID-19 vaccination in pregnant women and to explore their association with neutralizing antibody (Nab) inhibition.
The study evaluated 93 pregnant women who had previously received two (n=21), three (n=55) or four (n=17) doses of COVID-19 vaccine. Also we evaluated maternal blood samples that were collected during childbirth. The levels of TRAIL, IP-10 and Nab inhibition were measured using enzyme-linked immunosorbent assays (ELISA).
Our study revealed four-dose group resulted in lower TRAIL levels when compared to the two-dose and three-dose groups (4.78 vs. 16.07 vs. 21.61 pg/ml, p = 0.014). The two-dose group had reduced IP-10 levels than the three-dose cohort (111.49 vs. 147.89 pg/ml, p=0.013), with no significant variation compared to the four-dose group. In addition, the four-dose group showed stronger Nab inhibition against specific strains (BA.2 and BA.5) than the three-dose group. A positive correlation was observed between TRAIL and IP-10 in the two-dose group, while this relationship was not found in other dose groups or between TRAIL/IP-10 and Nab inhibition. As the doses of the COVID-19 vaccine increase, the levels of TRAIL and IP-10 generally increase, only by the fourth dose, the group previously vaccinated with AZD1222 showed lower TRAIL but higher IP-10. Despite these changes, more doses of the vaccine consistently reinforced Nab inhibition, apparently without any relation to TRAIL and IP-10 levels. The variation may indicate the induction of immunological memory in vaccinated mothers, which justifies further research in the future.
本研究旨在探讨 COVID-19 疫苗接种后孕妇肿瘤坏死因子相关凋亡诱导配体(TRAIL)和γ干扰素诱导蛋白 10(IP-10)的变化,并探讨其与中和抗体(Nab)抑制的关系。
该研究评估了 93 名先前接受过两剂(n=21)、三剂(n=55)或四剂(n=17)COVID-19 疫苗接种的孕妇的母亲血液样本。使用酶联免疫吸附试验(ELISA)测量 TRAIL、IP-10 和 Nab 抑制水平。
我们的研究表明,与两剂和三剂组相比,四剂组的 TRAIL 水平较低(4.78 对 16.07 对 21.61pg/ml,p=0.014)。两剂组的 IP-10 水平低于三剂组(111.49 对 147.89pg/ml,p=0.013),与四剂组相比无显著差异。此外,四剂组对特定株(BA.2 和 BA.5)的 Nab 抑制作用更强。两剂组中观察到 TRAIL 与 IP-10 之间存在正相关,而其他剂量组或 TRAIL/IP-10 与 Nab 抑制之间不存在这种关系。随着 COVID-19 疫苗剂量的增加,TRAIL 和 IP-10 的水平通常会升高,只有在第四剂接种 AZD1222 的组中,TRAIL 水平较低,但 IP-10 水平较高。尽管存在这些变化,但更多剂量的疫苗持续加强了 Nab 抑制作用,显然与 TRAIL 和 IP-10 水平无关。这种变化可能表明接种母亲体内诱导了免疫记忆,这为未来的进一步研究提供了依据。