Cross-Reactivity of Virus-Specific CD8+ T Cells Against Allogeneic HLA-C: Possible Implications for Pregnancy Outcome

Author
Anita van der Zwan, Ellen van der Meer-Prins, Paula van Miert, Heleen van den Heuvel, Jacqueline Anholts, Dave Roelen, Frans Claas, Sebastiaan Heidt
Keywords
Abstract

<p>Heterologous immunity of virus-specific T cells poses a potential barrier to transplantation tolerance. Cross-reactivity to HLA-A and -B molecules has broadly been described, whereas responses to allo-HLA-C have remained ill defined. In contrast to the transplant setting, HLA-C is the only polymorphic HLA molecule expressed by extravillous trophoblasts at the maternal-fetal interface during pregnancy. Uncontrolled placental viral infections, accompanied by a pro-inflammatory milieu, can alter the activation status and stability of effector T cells. Potential cross-reactivity of maternal decidual virus-specific T cells to fetal allo-HLA-C may thereby have detrimental consequences for the success of pregnancy. To explore the presence of cross-reactivity to HLA-C and the other non-classical HLA antigens expressed by trophoblasts, HLA-A and -B-restricted CD8+ T cells specific for Epstein-Barr virus, Cytomegalovirus, Varicella-Zoster virus, and Influenza virus were tested against target cells expressing HLA-C, -E, and -G molecules. An HLA-B<sup>*</sup>08:01-restricted EBV-specific T cell clone displayed cross-reactivity against HLA-C<sup>*</sup>01:02. Furthermore, cross-reactivity of HLA-C-restricted virus-specific CD8+ T cells was observed for HCMV HLA-C<sup>*</sup>06:02/TRA CD8+ T cell lines and clones against HLA-C<sup>*</sup>03:02. Collectively, these results demonstrate that cross-reactivity against HLA-C can occur and thereby may affect pregnancy outcome.</p>

Year of Publication
2018
Journal
Frontiers in immunology
Volume
9
Number of Pages
2880
Date Published
01/2018
ISSN Number
1664-3224
DOI
10.3389/fimmu.2018.02880
Alternate Journal
Front Immunol
PMCID
PMC6291497
PMID
30574149
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Reactivity
Human
Category
ELISA
Analyte
IFN-γ