Immune response to small intestinal submucosa (Surgisis) implant in humans: Preliminary observations

被引:82
作者
Ansaloni, Luca
Cambrini, Paolo
Catena, Fausto
Di Saverio, Salomone
Gagliardi, Stefano
Gazzotti, Filippo
Hodde, Jason P.
Metzger, Dennis W.
D'Alessandro, Luigi
Pinna, Antonio Daniele
机构
[1] Univ Bologna, Sant Orsola Malpighi Hosp, Unit Gen Surg, I-40138 Bologna, Italy
[2] Cook Biotech Incorp, W Lafayette, IN USA
[3] Albany Med Coll, Ctr Immunol & Microbial Dis, Albany, NY 12208 USA
关键词
body wall; collagen; galactosyl-alpha(1,3) galactose epitope; extracellular matrix; inguinal hernioplasty; small intestinal submucosa;
D O I
10.1080/08941930701481296
中图分类号
R61 [外科手术学];
学科分类号
摘要
Surgisis IHM is an acellular biomaterial derived from porcine small intestinal submucosa (SIS) that induces site-specific remodeling in the organ or tissue into which it is placed. Previous animal studies have shown that the graft recipient mounts a helper T type 2-restricted immune response to the SIS xenograft without signs of rejection. The aims of this study were to evaluate the immune response to the SIS implant in a small series of humans and to examine the long-term clinical acceptance of the xenograft in these patients. Five consecutive male patients (mean age 56 years, range 34-68) who underwent inguinal hernioplasty with Surgisis IHM were assessed at 2 weeks, 6 weeks, and 6 months after implant for SIS-specific, alpha-1,3-galactose (alpha-gal) epitope and type I collagen specific antibodies. All five patients were also clinically assessed up to 2 years for signs of clinical rejection, hernia recurrence, and other complications. All 5 patients implanted with Surgisis IHM produced antibodies specific for SIS and a-gal with a peak between 2 and 6 weeks after implantation. By 6 months, all patients showed decreasing levels of anti-SIS antibodies. Two patients developed a transient, mild local seroma that resolved spontaneously. None of the patients showed any clinical signs of rejection, wound infection, hernia recurrence, or other complications in the follow-up out to 2 years. Thus, this study showed that in a small series of patients the SIS elicits an antibody response without clinical rejection of the xenograft and minimal postoperative complications.
引用
收藏
页码:237 / 241
页数:5
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