MAGT1缺乏症成功接种抗sars - cov -2刺突蛋白抗体

IF 2.3 Q1 OTORHINOLARYNGOLOGY Allergy & Rhinology Pub Date : 2021-11-24 eCollection Date: 2021-01-01 DOI:10.1177/21526567211056239
Maaz Jalil, Marija Rowane, Jayanth Rajan, Robert Hostoffer
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引用次数: 1

摘要

背景:针对严重急性呼吸综合征冠状病毒(SARS-CoV-2)的新型信使RNA疫苗在解决冠状病毒病-2019 (COVID-19)大流行中至关重要。检测针对SARS-CoV-2刺突蛋白(S)的中和抗体(nab)证实具有高灵敏度和特异性的免疫原性。最近对原发性和继发性免疫缺陷队列的研究很少显示足够的或降低的抗体反应。我们描述了首次报道的镁转运蛋白1 (MAGT1)基因缺陷疫苗接种后抗sars - cov - 2s抗体的成功应答,镁转运蛋白1 (MAGT1)基因缺陷更常被认为是x连锁免疫缺陷伴镁缺陷、eb病毒感染和肿瘤(XMEN)。病例介绍:我们报告了一名30岁男性,患有选择性抗多糖抗体缺乏,外周血CD5 + /CD19 + b细胞优势(97%),MAGT1突变,CD16 + CD56 +自然杀伤细胞和/或CD8 + t细胞受体减少,2组,成员D表达。他最初的免疫学评估显示,所有疫苗接种后抗体滴度均为血清阴性,但临床对蛋白质抗原破伤风和白喉抗类毒素有足够的反应。在该办公室就诊时,建议进行COVID-19疫苗接种和相关血清学抗体检测。第一次BNT162b2 mRNA COVID-19疫苗剂量前后抗sars - cov -2免疫球蛋白(Ig)M和IgG抗体以及核衣壳抗体均为阴性。第二次给药后S蛋白总抗体出现反应。讨论:最近的文献充分记录了普通人群接种covid -19疫苗后的强烈免疫后遗症。很少有研究评估免疫缺陷患者的COVID-19疫苗抗体反应。文献中为数不多的研究,如本病例,在大多数原发性免疫缺陷(PID)患者中,大多数抗s抗体检测阳性,支持免疫缺陷患者接种mRNA COVID-19疫苗的安全性和有效性,尽管需要更大规模的研究。结论:在首次报道的covid -19疫苗接种后反应性抗s抗体病例中,我们证明了在PID MAGT1缺陷中成功接种疫苗。
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Successful Anti-SARS-CoV-2 Spike Protein Antibody Response to Vaccination in MAGT1 Deficiency.

Background: Novel messenger RNA vaccines against severe acute respiratory syndrome coronavirus (SARS-CoV-2) have been vital in resolving the coronavirus disease-2019 (COVID-19) pandemic. Detection of neutralizing antibodies (NAbs) against the SARS-CoV-2 spike protein (S) confirms immunogenicity with high sensitivity and specificity. Few recent studies with primary and secondary immunodeficient cohorts present adequate or reduced antibody response. We describe the first reported successful response to anti-SARS-CoV-2 S antibody post-vaccination in magnesium transporter 1 (MAGT1) gene deficiency, more commonly recognized as x-linked immunodeficiency with magnesium defect, Epstein-Barr Virus infection, and neoplasia (XMEN).

Case presentation: We present a 30-year-old male with selective anti-polysaccharide antibody deficiency, peripheral blood CD5  +  /CD19  +  B-cell predominance (97%), MAGT1 mutation, and reduced CD16  +  CD56  +  natural killer- and/or CD8  +  T-cell receptor, Group 2, Member D expression. His initial immunological evaluation revealed all seronegative post-vaccination antibody titers but clinically adequate response to protein antigens tetanus and diphtheria anti-toxoids.COVID-19 vaccination and associated serology antibody testing was recommended at this office visit. Anti-SARS-CoV-2 immunoglobulin (Ig)M and IgG antibodies before and after the first BNT162b2 mRNA COVID-19 vaccine doses, as well as nucleocapsid antibody, were negative. S protein total antibody was reactive after the second dose.

Discussion: Robust immunological sequelae post-COVID-19 vaccination in the general population are well-documented in the recent literature. Few studies have evaluated COVID-19 vaccination antibody response in immunodeficient patients. The majority positive anti-S antibody detection in most primary immunodeficient (PID) patients among the few studies in the literature, such as the present case, support the safety and efficacy of mRNA COVID-19 vaccination in immunodeficient patients, although larger scale studies are needed.

Conclusion: We demonstrate successful vaccination in the PID MAGT1 deficiency in this first reported case of reactive anti-S antibody post-COVID-19 vaccination.

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来源期刊
Allergy & Rhinology
Allergy & Rhinology OTORHINOLARYNGOLOGY-
CiteScore
3.30
自引率
4.50%
发文量
11
审稿时长
15 weeks
期刊最新文献
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