Retroviral Immunology Laboratory, London, NW1 1AT, UK.
Retroviral Immunology Laboratory, London, NW1 1AT, UK; National Heart and Lung Institute, Imperial College London, London, SW3 6LY, UK.
Semin Immunol. 2021 Jun;55:101507. doi: 10.1016/j.smim.2021.101507. Epub 2021 Oct 25.
Coronaviruses are evolutionarily successful RNA viruses, common to multiple avian, amphibian and mammalian hosts. Despite their ubiquity and potential impact, knowledge of host immunity to coronaviruses remains incomplete, partly owing to the lack of overt pathogenicity of endemic human coronaviruses (HCoVs), which typically cause common colds. However, the need for deeper understanding became pressing with the zoonotic introduction of three novel coronaviruses in the past two decades, causing severe acute respiratory syndromes in humans, and the unfolding pandemic of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This renewed interest not only triggered the discovery of two of the four HCoVs, but also uncovered substantial cellular and humoral cross-reactivity with shared or related coronaviral antigens. Here, we review the evidence for cross-reactive B cell memory elicited by HCoVs and its potential impact on the puzzlingly variable outcome of SARS-CoV-2 infection. The available data indicate targeting of highly conserved regions primarily in the S2 subunits of the spike glycoproteins of HCoVs and SARS-CoV-2 by cross-reactive B cells and antibodies. Rare monoclonal antibodies reactive with conserved S2 epitopes and with potent virus neutralising activity have been cloned, underscoring the potential functional relevance of cross-reactivity. We discuss B cell and antibody cross-reactivity in the broader context of heterologous humoral immunity to coronaviruses, as well as the limits of protective immune memory against homologous re-infection. Given the bidirectional nature of cross-reactivity, the unprecedented current vaccination campaign against SARS-CoV-2 is expected to impact HCoVs, as well as future zoonotic coronaviruses attempting to cross the species barrier. However, emerging SARS-CoV-2 variants with resistance to neutralisation by vaccine-induced antibodies highlight a need for targeting more constrained, less mutable parts of the spike. The delineation of such cross-reactive areas, which humoral immunity can be trained to attack, may offer the key to permanently shifting the balance of our interaction with current and future coronaviruses in our favour.
冠状病毒是进化上成功的 RNA 病毒,常见于多种禽类、两栖类和哺乳类宿主。尽管它们无处不在且具有潜在影响,但宿主对冠状病毒的免疫机制仍不完全清楚,部分原因是地方性人类冠状病毒(HCoV)缺乏明显的致病性,这些病毒通常会引起普通感冒。然而,随着过去二十年三种新型冠状病毒的人畜共患引入,导致人类出现严重急性呼吸综合征,以及由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)大流行,对更深入了解的需求变得迫在眉睫。这种新的兴趣不仅引发了对其中两种 HCoV 的发现,还揭示了与共享或相关冠状病毒抗原的大量细胞和体液交叉反应性。在这里,我们回顾了 HCoV 引起的交叉反应性 B 细胞记忆的证据及其对 SARS-CoV-2 感染结果令人费解的变异性的潜在影响。现有数据表明,交叉反应性 B 细胞主要针对 HCoV 和 SARS-CoV-2 的刺突糖蛋白 S2 亚单位中的高度保守区域和抗体靶向。已经克隆了少数与保守 S2 表位反应且具有强大病毒中和活性的单克隆抗体,强调了交叉反应性的潜在功能相关性。我们在冠状病毒异源体液免疫的更广泛背景下讨论了 B 细胞和抗体的交叉反应性,以及针对同源再感染的保护性免疫记忆的局限性。鉴于交叉反应性的双向性质,针对 SARS-CoV-2 的前所未有的当前疫苗接种运动预计将影响 HCoV 以及试图跨越物种屏障的未来人畜共患冠状病毒。然而,对疫苗诱导的抗体具有中和抗性的 SARS-CoV-2 新变体突出表明,需要针对刺突中更受限、更不易变的部分进行靶向。这些交叉反应区域的划定,即体液免疫可以针对这些区域进行训练,可能为永久改变我们与当前和未来冠状病毒相互作用的平衡提供关键。