HIV/AIDS Unit, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, 00149 Rome, Italy.
Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, UCL, London WC1E 6BT, UK.
Viruses. 2022 Aug 3;14(8):1710. doi: 10.3390/v14081710.
The aim was to measure neutralizing antibody levels against the SARS-CoV-2 Omicron (BA.1) variant in serum samples obtained from vaccinated PLWH and healthcare workers (HCW) and compare them with those against the Wuhan-D614G (W-D614G) strain, before and after the third dose of a mRNA vaccine. We included 106 PLWH and 28 HCWs, for a total of 134 participants. Before the third dose, the proportion of participants with undetectable nAbsT against BA.1 was 88% in the PLWH low CD4 nadir group, 80% in the high nadir group and 100% in the HCW. Before the third dose, the proportion of participants with detectable nAbsT against BA.1 was 12% in the PLWH low nadir group, 20% in the high nadir group and 0% in HCW, respectively. After 2 weeks from the third dose, 89% of the PLWH in the low nadir group, 100% in the high nadir group and 96% of HCW elicited detectable nAbsT against BA.1. After the third dose, the mean log2 nAbsT against BA.1 in the HCW and PLWH with a high nadir group was lower than that seen against W-D614G (6.1 log2 (±1.8) vs. 7.9 (±1.1) and 6.4 (±1.3) vs. 8.6 (±0.8)), respectively. We found no evidence of a different level of nAbsT neutralization by BA.1 vs. W-D614G between PLWH with a high CD4 nadir and HCW (0.40 (−1.64, 2.43); p = 0.703). Interestingly, in PLWH with a low CD4 nadir, the mean log2 difference between nAbsT against BA.1 and W-D614G was smaller in those with current CD4 counts 201−500 vs. those with CD4 counts < 200 cells/mm3 (−0.80 (−1.52, −0.08); p = 0.029), suggesting that in this target population with a low CD4 nadir, current CD4 count might play a role in diversifying the level of SARS-CoV-2 neutralization.
目的是测量接种过疫苗的 PLWH 和医护人员(HCW)血清样本中针对 SARS-CoV-2 奥密克戎(BA.1)变异株的中和抗体水平,并与针对武汉-D614G(W-D614G)株的水平进行比较,比较对象为接种 mRNA 疫苗第三针之前和之后的中和抗体水平。我们共纳入了 106 名 PLWH 和 28 名 HCW,共 134 名参与者。接种第三针之前,低 CD4 细胞计数最低组的 PLWH 中,88%的参与者针对 BA.1 的无检测到的 nAbsT,高细胞计数最低组为 80%,HCW 组为 100%。接种第三针之前,低细胞计数最低组的 PLWH 中,12%的参与者针对 BA.1 的有检测到的 nAbsT,高细胞计数最低组为 20%,HCW 组为 0%。接种第三针后 2 周,低细胞计数最低组的 89%的 PLWH、高细胞计数最低组的 100%和 HCW 的 96%产生了针对 BA.1 的有检测到的 nAbsT。接种第三针后,高细胞计数最低组的 HCW 和 PLWH 针对 BA.1 的平均 log2 nAbsT 低于针对 W-D614G 的水平(6.1 log2(±1.8)vs. 7.9(±1.1)和 6.4(±1.3)vs. 8.6(±0.8))。我们发现,高 CD4 细胞计数最低组的 PLWH 和 HCW 之间针对 BA.1 和 W-D614G 的 nAbsT 中和水平没有差异(0.40(-1.64,2.43);p=0.703)。有趣的是,在低 CD4 细胞计数最低组的 PLWH 中,针对 BA.1 和 W-D614G 的 nAbsT 的平均 log2 差值在当前 CD4 计数为 201-500 与计数小于 200 细胞/mm3 的患者中较小(-0.80(-1.52,-0.08);p=0.029),这表明在这个 CD4 细胞计数较低的目标人群中,当前 CD4 计数可能在多样化 SARS-CoV-2 中和水平方面发挥作用。