Jagne Ya Jankey, Jobe Dawda, Darboe Alansana, Danso Madikoi, Barratt Natalie, Gomez Marie, Wenlock Rhys, Jarju Sheikh, Sylva Ellen Lena, Touray Aji Fatou, Toure Fatoumata, Kumado Michelle, Saso Anja, Zafred Domen, Nicklin Martin, Sayers Jon, Hornsby Hailey, Lindsey Benjamin, Sesay Abdul Karim, Temperton Nigel, Kucharski Adam, Hodgson David, de Silva Thushan, Kampmann Beate
Vaccines and Immunity Theme, Medical Research Council Unit, The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Division of Clinical Medicine, School of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Commun Med (Lond). 2025 May 16;5(1):178. doi: 10.1038/s43856-025-00902-x.
The reported number of SARS-CoV-2 cases and deaths are lower in Africa compared to many high-income countries. However, in African cohorts, detailed characterisation of SARS-CoV-2 mucosal and T cell immunity are limited. We assessed the SARS-CoV-2-specific immune landscape in The Gambia during the presence of the pre-Delta variant in July 2021.
A cross-sectional assessment of SARS-CoV-2 immunity in 349 unvaccinated individuals from 52 Gambian households was performed between March-June 2021. SARS-CoV-2 spike (S) and nucleocapsid (N) specific binding antibodies were measured by ELISA, variant-specific serum neutralizing-antibodies (NAb) by viral pseudotype assays and nasal fluid IgA by mesoscale discovery assay. SARS-CoV-2 T-cell responses were evaluated using ELISpot assay.
We show that adjusted anti-Spike antibody seroprevalence is 56.7% (95% confidence interval (CI) 49.0-64.0), with lower rates in children <5 years (26.2%, 13.9-43.8) and 5-17 years (46.4%, 36.2-56.7) compared to adults 18-49 years (78.4%, 68.8-85.8). Among spike-seropositive individuals, NAb titres are highest against Alpha variant (median IC50 110), with 27% showing pre-existing Delta variant titres >1:50. T-cell responses are higher in spike-seropositive individuals, although 34% of spike-seronegative individuals show responses to at least one antigen pool. We observe strong correlations within SARS-CoV-2 T-cell, mucosal IgA, and serum NAb responses.
High SARS-CoV-2 seroprevalence in The-Gambia induce mucosal and blood immunity, reducing Delta and Omicron impact. Children are relatively protected from infection. T-cell responses in seronegative individuals may indicate either pre-pandemic cross-reactivity or individuals with a T-cell dominated response to SARS-CoV-2 infection with absent or poor humoral responses.
与许多高收入国家相比,非洲报告的新冠病毒病例数和死亡数较低。然而,在非洲人群中,对新冠病毒黏膜免疫和T细胞免疫的详细表征有限。我们评估了2021年7月德尔塔变异株出现之前冈比亚的新冠病毒特异性免疫情况。
2021年3月至6月期间,对来自52个冈比亚家庭的349名未接种疫苗的个体进行了新冠病毒免疫的横断面评估。通过酶联免疫吸附测定(ELISA)检测新冠病毒刺突蛋白(S)和核衣壳蛋白(N)特异性结合抗体,通过病毒假型试验检测变异株特异性血清中和抗体(NAb),通过中尺度发现试验检测鼻液中的IgA。使用酶联免疫斑点试验(ELISpot)评估新冠病毒T细胞反应。
我们发现,调整后的抗刺突抗体血清阳性率为56.7%(95%置信区间(CI)49.0 - 64.0),5岁以下儿童(26.2%,13.9 - 43.8)和5 - 17岁儿童(46.4%,36.2 - 56.7)的阳性率低于18 - 49岁成年人(78.4%,68.8 - 85.8)。在刺突蛋白血清阳性个体中,针对阿尔法变异株的中和抗体滴度最高(中位数IC50为110),27%的个体显示存在的德尔塔变异株滴度>1:50。刺突蛋白血清阳性个体的T细胞反应较高,尽管34%的刺突蛋白血清阴性个体对至少一个抗原池有反应。我们观察到新冠病毒T细胞、黏膜IgA和血清中和抗体反应之间存在强相关性。
冈比亚较高的新冠病毒血清阳性率诱导了黏膜免疫和血液免疫,降低了德尔塔和奥密克戎变异株的影响。儿童相对不易感染。血清阴性个体中的T细胞反应可能表明大流行前的交叉反应性,或者是对新冠病毒感染以T细胞为主导反应且体液反应缺失或较弱的个体。