Lee Hyeyoung, Ko Geon Young, Lee Jihyun, Bae Hyunjoo, Ryu Ji Hyeong, Jung Jin, Kang Hyunhye, Lee Raeseok, Lee Dong-Gun, Oh Eun-Jee
Department of Laboratory Medicine, International St. Mary's Hospital, College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea.
Department of Medical Sciences, Graduate School of The Catholic University of Korea, Seoul 06591, Republic of Korea.
Vaccines (Basel). 2024 Nov 29;12(12):1350. doi: 10.3390/vaccines12121350.
: Cellular and humoral immunity are key to the immune response against SARS-CoV-2, but the comparability and correlation across different assays remain underexplored. This study compares three T-cell and three antibody assays in two vaccine groups. : This prospective longitudinal cohort study involved 46 naïve healthcare workers: a total of 11 in the homologous mRNA-1273 group (three doses) and 35 in the heterologous ChAd group (two ChAd doses followed by a BNT booster). Blood samples were collected at five time points. Cellular immunity was assessed using ELISPOT and two commercial interferon-gamma release assays: (IGRA)-QuantiFERON SARS-CoV-2 (QF) and Covi-FERON ELISA (CoVF). Humoral immunity was evaluated using total and IgG antibody assays and a surrogate virus neutralization test. : The mRNA-1273 group exhibited stronger and more consistent responses than the ChAd group. The correlations between ELISPOT and IGRA varied from weak to moderate (ρ = 0.300-0.410), while QF-IGRA and CoVF-IGRA showed stronger correlations (ρ = 0.700-0.737). The ELISPOT assay showed substantial agreement with QF [Ag2]-IGRA (k = 0.697-0.774) and CoVF [O-sp]-IGRA (k = 0.641-0.718), and an 80.4% agreement rate (k = 0.608) was found between the QF [Ag2]- and CoVF [O-sp]-IGRA tests. Three antibody assays demonstrated very strong correlations with each other and substantial to near-perfect agreement with ELISPOT (k = 0.866-0.949), QF [Ag2]-IGRA (k = 0.807-0.831), and CoVF [O-sp]-IGRA (k = 0.753-0.777). : SARS-CoV-2-specific cellular and antibody responses vary by platform and vaccine type, highlighting the importance of measuring both T-cell and B-cell responses using multiple assays to comprehensively assess immune status.
细胞免疫和体液免疫是针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)免疫反应的关键,但不同检测方法之间的可比性和相关性仍未得到充分探索。本研究比较了两个疫苗组中的三种T细胞检测方法和三种抗体检测方法。:这项前瞻性纵向队列研究涉及46名未接种过疫苗的医护人员:同源mRNA-1273组(三剂)共有11人,异源ChAd组(两剂ChAd后接种一剂BNT加强针)共有35人。在五个时间点采集血样。使用酶联免疫斑点法(ELISPOT)和两种商用干扰素-γ释放检测方法评估细胞免疫:定量荧光SARS-CoV-2检测(QF)和Covi-FERON酶联免疫吸附测定(CoVF)。使用总抗体和IgG抗体检测方法以及替代病毒中和试验评估体液免疫。:mRNA-1273组比ChAd组表现出更强且更一致的反应。ELISPOT与干扰素-γ释放检测之间的相关性从弱到中等(ρ=0.300-0.410),而QF-干扰素-γ释放检测和CoVF-干扰素-γ释放检测显示出更强的相关性(ρ=0.700-0.737)。ELISPOT检测与QF[Ag2]-干扰素-γ释放检测(κ=0.697-0.774)和CoVF[O-sp]-干扰素-γ释放检测(κ=0.641-0.718)显示出高度一致性,并且在QF[Ag2]-和CoVF[O-sp]-干扰素-γ释放检测之间发现一致性率为80.4%(κ=0.608)。三种抗体检测方法相互之间显示出非常强的相关性,并且与ELISPOT(κ=0.866-0.949)、QF[Ag2]-干扰素-γ释放检测(κ=0.807-0.831)和CoVF[O-sp]-干扰素-γ释放检测(κ=0.753-0.777)显示出高度至近乎完美的一致性。:SARS-CoV-2特异性细胞和抗体反应因检测平台和疫苗类型而异,突出了使用多种检测方法同时测量T细胞和B细胞反应以全面评估免疫状态的重要性。