Physiology of intestinal transplants
Epithelial and hematopoietic cell chimerism in intestinal allografts

https://doi.org/10.1016/j.transproceed.2004.01.107Get rights and content

Abstract

Background

In intestinal transplantation recipient lymphocytes infiltrate the allograft soon after reperfusion. Recently, it has been demonstrated that long-surviving small bowel transplants bear enterocytes of recipient origin. We investigated whether epithelial cells (enterocytes) persisted in long-term allografts based on studies of biopsies.

Methods

The biopsies of four male intestinal transplant recipients of female grafts with a previous graft biopsy positive for recipient enterocytes were examined at least 6 months after previous positive assessment. Using the FISH technique, we searched for Y-chromosome-positive enterocytes in the female allograft.

Results

Recipient male enterocytes were identified in all biopsies at low percentages ranging from 0.18 to 0.26. The lymphocytes within the graft were of both recipient (male) and donor (female) origin.

Conclusion

The four types of cells—enterocytes and lymphocytes of recipient and donor origin—coexist in long-term graft biopsies.

Section snippets

Materials and methods

We studied graft biopsies from four male patients—two adults and two children—who had received a small bowel graft from a female donor. Their respective original diseases were trauma (n = 1), diabetic enteropathy (n = 1), and gastroschesis (n = 2). All patients had undergone a previous graft biopsy that was positive for recipient-derived enterocytes. A time interval of at least 6 months separated the new biopsies from the previous positive ones. We used the FISH technique for the X and Y

Results

Male enterocytes were identified in all graft biopsies. Their percentage was low ranging from 0.18 to 0.26% (average 0.21%). This average value was not significantly different from that in the previous positive biopsies. Although the lamina propria of the same sections was infiltrated mostly by recipient male (XY) lymphocytes, we identified a few female (XX) lymphocytes of donor origin that persisted in the allograft. All positive biopsies were obtained between 300 and 1200 days

Discussion

The FISH technique has been used to demonstrate donor (female) versus recipient (male) origin of cells in transplants. However, it is not sufficient to show whether the cells are epithelial or hematopoietic in origin. Many intraepithelial lymphocytes may be mistaken for enterocytes due to their localization at the epithelial lining. However, use of cytokeratin and CD45 staining resolved these issues. The morphology of the enterocytes, namely, cytokeratin-positive columnar cells with abundant

References (2)

Cited by (7)

  • Evaluation of epithelial chimerism after bone marrow mesenchymal stromal cell infusion in intestinal transplant patients

    2014, Transplantation Proceedings
    Citation Excerpt :

    Patient 3 (postoperative period of 8 months) displayed lower RFU rate compared to patients 1 and 2 (P < .05, Fig 3F). Epithelial chimerism was previously shown to be 0.18% to 0.26% in graft biopsies collected up to 770 days postsurgery in intestinal transplant patients without any BMSC infusion [27]. Likewise, in this study, we show epithelial chimerism of 1.7% in graft biopsies collected 69 months (2070 days) postsurgery in patient 1 without BMSC infusion (Fig 2).

  • Bronchial epithelial cells produce IL-5: Implications for local immune responses in the airways

    2010, Cellular Immunology
    Citation Excerpt :

    BEC populations were cyto-centrifuged onto slides and stained with DAPI and a monoclonal antibody specific for cytokeratin (clone PCK-26; Sigma–Aldrich, St. Louis, MO). Typically, 95% of the cells stained positive for cytokeratin, an epithelial cell marker not expressed by lymphocytes [33]. During our initial characterization, slides were also stained with monoclonal antibodies specific for CD4 (clone RM4-5; eBioscience, San Diego, CA), CD11b (clone M1/70; BD Bioscience, San Jose, CA), and CD8 (clone 53-6.7; BD Bioscience), as well as with anti-major basic protein serum (gift from Dr. Jamie Lee, The Mayo Clinic, Phoenix, AZ), followed by the appropriate secondary antibodies.

  • GI and liver transplantation pathology in childhood

    2014, Pathology of Pediatric Gastrointestinal and Liver Disease
View all citing articles on Scopus
View full text