Exp Clin Endocrinol Diabetes 1989; 93(2/03): 147-150
DOI: 10.1055/s-0029-1210848
Original

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Islet Cell Transplantation in Type I Diabetes Mellitus: Evaluation of Humoral Immune Response

Y. Y. Kondratiev1 , Natalja V. Sadovnikova1 , Galina N. Petrova2 , V. P. Fedotov1 , V. N. Bljumkin2 , S. N. Ignatenko2 , Y. A. Pankov1
  • 1Institute for Experimental Endocrinology and Hormone Chemistry, Academy of Medical Sciences, Moscow, USSR
  • 2Research Institute of Transplantology and Artificial Organs, Ministry of Health, Moscow, USSR
Further Information

Publication History

1988

Publication Date:
16 July 2009 (online)

Summary

Four males and three females ranging in age from 20 to 35 years and afflicted with complicated Type I-diabetes for more than 8 years underwent islet cell allotransplantation (ATx, 6 cases) and xenotransplantation (XTx, 1 case). Precultured islet cells derived from human or bovine fetal pancreata were injected into the m. rectus abdominis. Immunosuppression was not applied.

Plasma C-peptide and islet cell surface antibodies (ICSA) were continually measured both before and until the twentienth week following islet cell transplantation. All recipients were subdivided as “responsive” (RR, 3 males) or “non-responsive” (NRR, 1 male and 3 females), according to the dynamics of their ICSA levels. All 3 RR (lXTx and 2 ATx) showed a peak of ICSA two weeks after cell injection. Subsequent ICSA levels had the tendency to either diminish or increase. Heterogeneity of preoperative antibody level, especially in NRR, was also observed. No associations between ICSA and ATx or XTx, age at diabetes onset, or duration of the disease was found. Only one RR with XTx had a reduced daily insulin requirement and a significant C-peptide response similar to the dynamics of ICSA levels. A greater mass of available bovine islet cells might be responsible for this effect.