With all the uncertainty of COVID-19, we hope you are safe and in good health. Ozgene is still here to meet your research needs.

Alloimmunogenicity of an isolated MHC allele is affected by the context of MHC mismatch in a murine model.

 Back to publications

2019

Transfusion. 2019 Feb;59(2):744-753. doi: 10.1111/trf.15109. Epub 2019 Jan 25.

Alloimmunogenicity of an isolated MHC allele is affected by the context of MHC mismatch in a murine model.

KE Hudson;ASL Wong;AL Richards;LM Kapp;JC Zimring

BloodworksNW Research Institute, Seattle, Washington. Department of Laboratory Medicine, University of Washington School of Medicine, Seattle, Washington. Department of Medicine, Division of Hematology, University of Washington School of Medicine, Seattle, Washington.

Service type: Knock-in mice

Abstract

BACKGROUND: Humoral alloimmunization to human leukocyte antigen (HLA) can represent a barrier to solid-organ transplantation, can lead to a refractory state in patients requiring platelet transfusion, and can also contribute to transfusion-related acute lung injury (TRALI). While exposure to HLA-mismatched cells/tissues are generally required for HLA alloimmunization, the effect of the extent of major histocompatibility complex (MHC) mismatch between donor and recipient is poorly understood. STUDY DESIGN AND METHODS: A novel mouse was generated that allows the expression of a single MHC Class I alloantigen, Kd . Alloimmune responses to Kd were studied in C57BL/6 mice transfused with splenocytes from different donor mice, allowing the analysis of responses to Kd as an isolated alloantigen, or in the context of additional mismatched MHC molecules. Advanced tools were utilized to study responses to Kd , including T-cell receptor transgenic mice that recognize the immunodominant Kd peptide presented by C57BL/6 mice to CD4+ T cells. RESULTS: A single MHC Class I alloantigen mismatch is less immunogenic than when the same alloantigen is encountered in the context of additional mismatched MHC alloantigens. This difference is due, at least in part, to induction of CD4+ helper T cells, as the effect is overcome by increasing either mature CD4+ T-cell help through immunization or by increasing the precursor frequency of naïve CD4+ T cells by adoptive transfer from T-cell receptor transgenic donors. CONCLUSION: These findings indicate that the immunogenicity of a single alloantigen can be affected by the context in which it is encountered, demonstrating the potential for cooperative effects between different mismatched MHC alloantigens.

View Publication