Association between CTL precursor frequency to HLA-C mismatches and HLA-C antigen cell surface expression

Previous studies showed the relevance of the cytotoxic T cell precursor frequency assay (CTLp) for prediction of the outcome of HLA mismatched hematopoietic cell transplantation (HCT). Recently it has been shown that HLA-C cell surface expression is correlated with virus specific cytotoxic T cell re...

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Bibliographic Details
Main Authors: Moshe eIsraeli, Dave L. Roelen, Mary eCarrington, Effie Wang Petersdorf, Frans HJ Claas, Geert W Haasnoot, Machteld eOudshoorn
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-10-01
Series:Frontiers in Immunology
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00547/full
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Summary:Previous studies showed the relevance of the cytotoxic T cell precursor frequency assay (CTLp) for prediction of the outcome of HLA mismatched hematopoietic cell transplantation (HCT). Recently it has been shown that HLA-C cell surface expression is correlated with virus specific cytotoxic T cell responses and viremia control in HIV patients.The aim of the current study was to investigate the association between HLA-C antigen expression and the CTLp frequency to the mismatched HLA-C antigen.In total 115 recipient–donor pairs, for whom a successful CTLp assay was performed, were evaluated for this pilot study. All donor-recipient pairs were matched at 9/10 alleles with a single mismatch at the HLA-C locus. Antigen expression level of the mismatched HLA-C allele for each recipient and donor was based on the MFI values as described by Apps et al (Science, 2013).The cell surface expression of recipient’s mismatched HLA-C antigen was significantly lower among CTLp negative (n=59) compared to CTLp positive (n=56) pairs (154 and 193 MFI units, respectively; p=0.0031). This difference was more pronounced in donor-recipient pairs that were mismatched for amino-acid residue-116 located in the groove of the HLA-C antigen, suggesting the importance of peptide binding in the allo-recognition. Furthermore, in the particular case of low expression of the recipient mismatched HLA-C antigen (MFI<115), CTLp reactivity depended on HLA-C expression level in the donor; the median MFI of donor’s mismatched HLA-C antigen was 114 in CTLp negative cases (n=26), while in CTLp positive cases (n=15) the median MFI of donor’s HLA-C antigen was 193. (P=0.0093).We conclude that the expression level of the donor and recipient mismatched HLA-C antigens affect CTLp outcome. HLA-C antigen expression levels in combination with the CTLp assay may prove useful for the prediction of the clinical outcome of HLA-C mismatched HCT.
ISSN:1664-3224