Department of Rheumatology and Clinical Immunology, University General Hospital, Faculty of Medicine, School of Health Sciences, University of Thessaly, Viopolis, 41110, Larissa, Greece.
Institute of Immunology, EUROIMMUN, Lubeck, Germany.
Immunol Res. 2020 Feb;68(1):39-47. doi: 10.1007/s12026-020-09124-w.
Helicobacter pylori (Hp) is a likely trigger of systemic sclerosis (SSc), but systemic antigen-specific antibody (Ab) responses in a well-defined cohort of SSc patients have not been thoroughly assessed. Line immunoassay and immunoblotting testing Abs against 15 Hp antigens were performed in 91 SSc patients and 59 demographically matched healthy controls (HCs). Results were validated in an independent cohort of 35 SSc patients. Anti-Hp positivity was detected in 67% SSc patients vs 76.3% HCs. Among anti-Hp (+) individuals, anti-p67-FSH was less frequent in SSc than HCs (p = 0.016), whereas reactivity to the remaining 14 Hp antigens did not differ between patients and HCs. Anti-p67 Abs were less frequent in diffuse cutaneous SSc (dcSSc) compared with HCs (p = 0.018). Anti-p57 and anti-p33 Ab levels were lower in SSc vs HCs (p = 0.007 and p = 0.035, respectively). Anti-p57 and anti-p33 Ab levels were lower in limited cutaneous SSc (lcSSc) (p = 0.010) and dcSSc (p = 0.024), respectively, compared with HCs. Anti-p50 and anti-p17 Ab titers tended to be higher in dcSSc than in lcSSc. Sera from the independent SSc cohort showed comparable results. Anti-VacA Abs were more frequent in pulmonary arterial hypertension (p = 0.042), and anti-p30 Abs were more frequent in calcinosis (p = 0.007), whereas anti-VacA Ab levels were higher in lung fibrosis (p = 0.02). In conclusion, anti-Hp Abs are neither more frequent nor elevated in SSc compared with healthy population, the only exception being the higher frequency and levels of anti-VacA Abs in pulmonary hypertension and lung fibrosis, respectively. These results suggest that Hp is unlikely to be involved in the development of SSc.
幽门螺杆菌(Hp)可能是系统性硬化症(SSc)的触发因素,但尚未对明确队列的 SSc 患者的系统抗原特异性抗体(Ab)反应进行彻底评估。对 91 例 SSc 患者和 59 名年龄匹配的健康对照者(HCs)进行了针对 15 种 Hp 抗原的线免疫分析和免疫印迹检测 Ab。结果在 35 例 SSc 患者的独立队列中得到了验证。67%的 SSc 患者抗-Hp 阳性,而 76.3%的 HCs 阳性。在抗-Hp(+)个体中,抗-p67-FSH 在 SSc 中比 HCs 中更为少见(p=0.016),而对其余 14 种 Hp 抗原的反应性在患者和 HCs 之间没有差异。与 HCs 相比,弥漫性皮肤 SSc(dcSSc)中抗-p67 Abs 更为少见(p=0.018)。与 HCs 相比,抗-p57 和抗-p33 Ab 水平在 SSc 中较低(p=0.007 和 p=0.035)。与 HCs 相比,局限性皮肤 SSc(lcSSc)(p=0.010)和 dcSSc(p=0.024)中抗-p57 和抗-p33 Ab 水平较低。dcSSc 中抗-p50 和抗-p17 Ab 滴度高于 lcSSc。来自独立 SSc 队列的血清显示出类似的结果。抗-VacA Abs 在肺动脉高压中更为常见(p=0.042),抗-p30 Abs 在钙沉积症中更为常见(p=0.007),而抗-VacA Ab 水平在肺纤维化中更高(p=0.02)。总之,与健康人群相比,抗-Hp Ab 在 SSc 中既不更常见也不升高,唯一的例外是肺动脉高压和肺纤维化中抗-VacA Ab 的频率和水平分别升高。这些结果表明 Hp 不太可能参与 SSc 的发生。