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Review
. 2016 Mar 7:7:87.
doi: 10.3389/fimmu.2016.00087. eCollection 2016.

Transplantation Tolerance Induction: Cell Therapies and Their Mechanisms

Affiliations
Review

Transplantation Tolerance Induction: Cell Therapies and Their Mechanisms

Joseph R Scalea et al. Front Immunol. .

Abstract

Cell-based therapies have been studied extensively in the context of transplantation tolerance induction. The most successful protocols have relied on transfusion of bone marrow prior to the transplantation of a renal allograft. However, it is not clear that stem cells found in bone marrow are required in order to render a transplant candidate immunologically tolerant. Accordingly, mesenchymal stem cells, regulatory myeloid cells, T regulatory cells, and other cell types are being tested as possible routes to tolerance induction, in the absence of donor-derived stem cells. Early data with each of these cell types have been encouraging. However, the induction regimen capable of achieving consistent tolerance, while avoiding unwanted sided effects, and which is scalable to the human patient, has yet to be identified. Here, we present the status of investigations of various tolerogenic cell types and the mechanistic rationale for their use in tolerance induction protocols.

Keywords: CD34+ cells; HSCT; MDSC; Treg; regulatory mechanisms; regulatory myeloid cells; transplantation tolerance.

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References

    1. Owen RD. Immunogenetic consequences of vascular anastomoses between bovine twins. Science (1945) 102:400–1. 10.1126/science.102.2651.400 - DOI - PubMed
    1. Brent L. The discovery of immunologic tolerance. Hum Immunol (1997) 52:75–81. 10.1016/S0198-8859(96)00289-3 - DOI - PubMed
    1. Billingham RE, Brent L, Medawar PB. Actively acquired tolerance of foreign cells. Nature (1953) 172:603–6. 10.1038/172603a0 - DOI - PubMed
    1. Sharabi Y, Sachs DH. Mixed chimerism and permanent specific transplantation tolerance induced by a nonlethal preparative regimen. J Exp Med (1989) 169:493–502. 10.1084/jem.169.2.493 - DOI - PMC - PubMed
    1. Strober S, Modry DL, Hoppe RT, Pennock JL, Bieber CP, Holm BI, et al. Induction of specific unresponsiveness to heart allografts in mongrel dogs treated with total lymphoid irradiation and antithymocyte globulin. J Immunol (1984) 132:1013–8. - PubMed

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