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Pre-transplant donor-specific Interferon-gamma-producing cells and acute rejection of the kidney allograft.

Authors :
Slavcev A
Rybakova K
Svobodova E
Slatinska J
Honsova E
Skibova J
Viklicky O
Striz I
Source :
Transplant immunology [Transpl Immunol] 2015 Oct; Vol. 33 (2), pp. 63-8. Date of Electronic Publication: 2015 Aug 05.
Publication Year :
2015

Abstract

Background: Our retrospective study included a cohort of 47 patients who underwent living donor kidney transplantation.The pre-transplant frequencies of donor-specific Interferon-gamma (IFN-γ) producing cells were define dusing enzyme-linked immunosorbent spot (ELISpot) assay and correlated with incidence of acute cellular(ACR), antibody-mediated rejection (AMR) and kidney graft survival up to one year after transplantation.<br />Results: We found a statistically significant correlation between the frequencies of IFN-γ-producing cells and the number of mismatches in HLA antigens between patients and their respective donors – for Class I – A and B (r = 0.399, p b 0.01) and for Class I and Class II antigens – A, B and DR (r = 0.409, p b 0.01). No significant relationship was observed between the numbers of IFN-γ-secreting cells and incidence of acute rejection (neither ACR, nor AMR). However, there was a trend of elevated frequencies of IFN-γ-producing cells in patients who developed ACR or AMR in comparison with kidney recipients free of rejection (91 ± 82 and 114 ± 75 vs. 72 ± 70/5 × 10(4) peripheral blood mononuclear cells respectively). Patients with concurrent acute cellular and antibody-mediated rejection had also higher numbers of IFN-γ-producing memory/effector cells compared to patients with cellular rejection only.<br />Conclusion: Pre-transplant determination of the numbers of IFN-γ-producing donor-specific memory cells using the ELISpot technique may provide clinically relevant results when evaluating the risk of development of acute cellular and antibody-mediated rejection. These frequencies are influenced by the degree of HLA mismatching between patients and their respective kidney donors.

Details

Language :
English
ISSN :
1878-5492
Volume :
33
Issue :
2
Database :
MEDLINE
Journal :
Transplant immunology
Publication Type :
Academic Journal
Accession number :
26254561
Full Text :
https://doi.org/10.1016/j.trim.2015.07.007