Scalvini Davide, Schiepatti Annalisa, Maimaris Stiliano, Cosentini Emanuele, Muscia Roberta, Gregorio Virginia, Roda Elisa, Fassio Federico, Baiardi Paola, Locatelli Carlo Alessandro, Biagi Federico
Dipartimento di Medicina Interna e Terapia Medica, University of Pavia.
Istituti Clinici Scientifici Maugeri, IRCCS, Gastroenterology Unit of Pavia Institute.
Eur J Gastroenterol Hepatol. 2023 Feb 1;35(2):167-173. doi: 10.1097/MEG.0000000000002484. Epub 2022 Nov 29.
Data are lacking on the immunogenicity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in patients affected by coeliac disease, Whipple's disease and other noncoeliac enteropathies (NCE), characterised by primary or drug-related immunosuppression. We aimed to assess humoral response to SARS-CoV-2 vaccination in these patients compared to controls.
Between December 2021 and January 2022, IgG anti-SARS-CoV-2 spike protein antibodies were measured in serum samples of coeliac disease, Whipple's disease and NCE patients attending our gastroenterology outpatient clinic for follow-up, who had received their first SARS-CoV-2 vaccination dose 3-6-9 (±1) months prior. Humoral response was compared with healthy controls (vaccinated healthcare workers undergoing serological screening), matched for gender, age, and time from first vaccine dose at sample collection.
A total of 120 patients [107 coeliac disease; 10 Whipple's disease; 2 common-variable immunodeficiency (CVID); 1 idiopathic villous atrophy; 77 F, 42 ± 16 years] and 240 matched controls (154 F, 43 ± 14 years) were enrolled. At 3, 6 and 9 months, humoral response in coeliac patients was not impaired compared to controls. Inadequate humoral response to vaccination was significantly more common among Whipple's disease patients than controls ( P < 0.001). Patients on immunosuppressive therapy had markedly lower IgG anti-SARS-CoV-2 antibody titres (median 14 vs. 520 BAU/mL, P < 0.001). As expected, patients with CVID showed no humoral response to vaccination.
Humoral immunogenicity of SARS-CoV-2 vaccines was not reduced in coeliac disease patients compared to controls, although it was in Whipple's disease and CVID patients. Post-vaccination humoral response should be monitored in patients with Whipple's disease and chronic enteropathies on immunosuppressive therapy in order to schedule vaccine booster doses.
对于乳糜泻、惠普尔病和其他非乳糜泻性肠病(NCE)患者,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗的免疫原性数据缺乏,这些疾病的特征为原发性或药物相关免疫抑制。我们旨在评估这些患者与对照组相比对SARS-CoV-2疫苗接种的体液反应。
在2021年12月至2022年1月期间,对在我们胃肠病门诊接受随访的乳糜泻、惠普尔病和NCE患者的血清样本中IgG抗SARS-CoV-2刺突蛋白抗体进行检测,这些患者在3 - 6 - 9(±1)个月前接种了第一剂SARS-CoV-2疫苗。将体液反应与健康对照组(接受血清学筛查的接种疫苗医护人员)进行比较,对照组在性别、年龄以及样本采集时距第一剂疫苗接种的时间方面进行匹配。
共纳入120例患者[107例乳糜泻;10例惠普尔病;2例普通变异型免疫缺陷(CVID);1例特发性绒毛萎缩;77例女性,42±16岁]和240例匹配的对照组(154例女性,43±14岁)。在3个月、6个月和9个月时,乳糜泻患者的体液反应与对照组相比未受损。惠普尔病患者中疫苗接种后体液反应不足的情况显著多于对照组(P<0.001)。接受免疫抑制治疗的患者IgG抗SARS-CoV-2抗体滴度明显较低(中位数14 vs. 520 BAU/mL,P<0.001)。正如预期的那样,CVID患者对疫苗接种无体液反应。
与对照组相比,SARS-CoV-2疫苗在乳糜泻患者中的体液免疫原性未降低,尽管在惠普尔病和CVID患者中降低了。对于惠普尔病患者和接受免疫抑制治疗的慢性肠病患者,应监测疫苗接种后的体液反应,以便安排疫苗加强剂量。