Colombo Delia, Chimenti Sergio, Grossi Paolo, Marchesoni Antonio, Di Nuzzo Sergio, Griseta Vito, Gargiulo Anna, Parodi Aurora, Simoni Lucia, Bellia Gilberto
Novartis Farma Italia, Origgio (Va), Italy.
Policlinico Tor Vergata, Rome, Italy.
Biomed Res Int. 2014;2014:941767. doi: 10.1155/2014/941767. Epub 2014 Apr 3.
We have prospectively evaluated psoriatic arthritis (PsA) patients for (1) seropositivity for former viral infections and seroconversion and (2) efficacy of cyclosporine A (CsA) alone or in combination with other immunosuppressants in a time period of 12 months. Screening included HBV antibodies and antigens, HCV antibodies and RNA, HSV 1-2, HZV, EBV, and CMV IgG, and IgM, HHV-6 DNA, and HIV 1-2 antibodies. PsA was evaluated by the Psoriasis Area Severity Index (PASI), the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), and the Visual Analogue Scale (VAS). At baseline, 126 (56%) out of 225 evaluable patients had 2 or more seropositivities indicative of former infections, and 31 patients (13.8%) presented seropositivity for HCV, HBV, HSV-1 and -2, HHV-6, EBV, or parvovirus infection; one of them, positive for HBAg, was treated with lamivudine, while the remaining 30 received no specific treatment. None of the 31 patients developed virus reactivation. A reduction (P < 0.001) of PASI, BASDAI, and VAS scores was observed at 6 and 12 months. The treatment of PsA with CsA as monotherapy or in combination was safe and effective. In vitro experiments and clinical findings, including those from our study, suggest that CsA as monotherapy or in combination with biologics might be the treatment of choice in PsA HCV-positive patients.
我们前瞻性地评估了银屑病关节炎(PsA)患者,以确定(1)既往病毒感染的血清阳性率和血清转化情况,以及(2)环孢素A(CsA)单独使用或与其他免疫抑制剂联合使用在12个月内的疗效。筛查项目包括乙肝病毒抗体和抗原、丙肝病毒抗体和RNA、单纯疱疹病毒1-2型、带状疱疹病毒、EB病毒、巨细胞病毒IgG和IgM、人疱疹病毒6型DNA以及人类免疫缺陷病毒1-2型抗体。通过银屑病面积和严重程度指数(PASI)、巴斯强直性脊柱炎疾病活动指数(BASDAI)和视觉模拟量表(VAS)对PsA进行评估。在基线时,225例可评估患者中有126例(56%)有2种或更多种提示既往感染的血清阳性,31例患者(13.8%)出现丙肝病毒、乙肝病毒、单纯疱疹病毒1型和2型、人疱疹病毒6型、EB病毒或细小病毒感染的血清阳性;其中1例乙肝表面抗原阳性患者接受了拉米夫定治疗,其余30例未接受特殊治疗。这31例患者均未发生病毒再激活。在6个月和12个月时观察到PASI、BASDAI和VAS评分降低(P<0.001)。CsA单药治疗或联合治疗PsA安全有效。体外实验和临床研究结果,包括我们的研究结果,表明CsA单药治疗或与生物制剂联合使用可能是PsA丙肝病毒阳性患者的首选治疗方法。