Pediatric Clinic, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Research and Innovation Unit, University Hospital of Parma, Parma, Italy.
Front Immunol. 2022 Jun 23;13:933774. doi: 10.3389/fimmu.2022.933774. eCollection 2022.
Inflammatory bowel diseases (IBD), including Crohn's disease, ulcerative colitis, and unclassified inflammatory bowel disease, are a group of chronic, immune mediated conditions that are presumed to occur in genetically susceptible individuals because of a dysregulated intestinal immune response to environmental factors. IBD patients can be considered subjects with an aberrant immune response that makes them at increased risk of infections, particularly those due to opportunistic pathogens. In many cases this risk is significantly increased by the therapy they receive. Aim of this narrative review is to describe the impact of SARS-CoV-2 infection and the immunogenicity of COVID-19 vaccines in patients with IBD. Available data indicate that patients with IBD do not have an increased susceptibility to infection with SARS-CoV-2 and that, if infected, in the majority of the cases they must not modify the therapy in place because this does not negatively affect the COVID-19 course. Only corticosteroids should be reduced or suspended due to the risk of causing severe forms. Furthermore, COVID-19 seems to modify the course of IBD mainly due to the impact on intestinal disease of the psychological factors deriving from the measures implemented to deal with the pandemic. The data relating to the immune response induced by SARS-CoV-2 or by COVID-19 vaccines can be considered much less definitive. It seems certain that the immune response to disease and vaccines is not substantially different from that seen in healthy subjects, with the exception of patients treated with anti-tumor necrosis factor alone or in combination with other immunosuppressants who showed a reduced immune response. How much, however, this problem reduces induced protection is not known. Moreover, the impact of SARS-CoV-2 variants on IBD course and immune response to SARS-CoV-2 infection and COVID-19 vaccines has not been studied and deserves attention. Further studies capable of facing and solving unanswered questions are needed in order to adequately protect IBD patients from the risks associated with SARS-CoV-2 infection.
炎症性肠病(IBD),包括克罗恩病、溃疡性结肠炎和未分类的炎症性肠病,是一组慢性、免疫介导的疾病,据推测它们发生在遗传易感个体中,是由于对环境因素的肠道免疫反应失调所致。IBD 患者可被视为免疫反应异常的个体,他们感染的风险增加,特别是由机会性病原体引起的感染。在许多情况下,这种风险因他们所接受的治疗而显著增加。本综述的目的是描述 SARS-CoV-2 感染和 COVID-19 疫苗在 IBD 患者中的免疫原性。现有数据表明,IBD 患者对 SARS-CoV-2 感染的易感性没有增加,而且,如果感染,在大多数情况下,他们不需要改变现有的治疗方案,因为这不会对 COVID-19 的病程产生负面影响。只有皮质类固醇应该因引起严重形式的风险而减少或暂停。此外,COVID-19 似乎主要通过应对大流行所采取的措施对肠道疾病产生心理影响来改变 IBD 的病程。与 SARS-CoV-2 或 COVID-19 疫苗诱导的免疫反应相关的数据可以认为不太确定。似乎可以肯定的是,疾病和疫苗的免疫反应与健康受试者所见的免疫反应没有实质性差异,除了单独或联合使用抗肿瘤坏死因子治疗的患者,他们的免疫反应减弱。然而,这个问题在多大程度上降低了诱导的保护作用尚不清楚。此外,SARS-CoV-2 变异对 IBD 病程和对 SARS-CoV-2 感染及 COVID-19 疫苗的免疫反应的影响尚未得到研究,值得关注。需要进一步的研究来解决尚未回答的问题,以便为 IBD 患者提供充分的保护,使其免受与 SARS-CoV-2 感染相关的风险。