AI Article Synopsis

  • Antibody mediated rejection (ABMR) significantly affects organ transplant outcomes, primarily due to anti-HLA IgG donor-specific antibodies (DSA), while the presence of IgE antibodies is also being studied.
  • A cohort of 105 solid organ transplant recipients was evaluated for pre-existing and post-transplant anti-HLA IgE antibodies using specific assays.
  • Results showed low frequencies of pre-existing anti-HLA IgE antibodies (10% in kidney, 4.4% in other organs), mostly in patients with previous transplants and correlated with IgG positivity, indicating potential function in rejection processes.

Article Abstract

Introduction: Antibody mediated rejection (ABMR) is a major factor limiting outcome after organ transplantation. Anti-HLA donor-specific antibodies (DSA) of the IgG isotype are mainly responsible for ABMR. Recently DSA of the IgE isotype were demonstrated in murine models as well as in a small cohort of sensitized transplant recipients. In the present study, we aimed to determine the frequency of pre-existing and anti-HLA IgE antibodies in a cohort of 105 solid organ transplant recipients.

Methods: We prospectively measured anti-HLA IgE antibodies in a cohort of kidney (n=60), liver, heart and lung (n=15 each) transplant recipients before and within one-year after transplantation, employing a single-antigen bead assay for HLA class I and class II antigens. Functional activity of anti-HLA IgE antibodies was assessed by an mediator release assay. Antibodies of the IgG1-4 subclasses and Th1 and Th2 cytokines were measured in anti-HLA IgE positive patients.

Results: Pre-existing anti-HLA IgE antibodies were detected in 10% of renal recipients (including 3.3% IgE-DSA) and in 4.4% of non-renal solid organ transplant recipients (heart, liver and lung cohort). Anti-HLA IgE occurred only in patients that were positive for anti-HLA IgG, and most IgE positive patients had had a previous transplant. Only a small fraction of patients developed anti-HLA IgE antibodies (1.7% of kidney recipients and 4.4% of non-renal recipients), whereas no IgE-DSA was detected. IgG subclass antibodies showed a distinct pattern in patients who were positive for anti-HLA IgE. Moreover, patients with anti-HLA IgE showed elevated Th2 and also Th1 cytokine levels. Serum from IgE positive recipients led to degranulation of basophils , demonstrating functionality of anti-HLA IgE.

Discussion: These data demonstrate that anti-HLA IgE antibodies occur at low frequency in kidney, liver, heart and lung transplant recipients. Anti-HLA IgE development is associated with sensitization at the IgG level, in particular through previous transplants and distinct IgG subclasses. Taken together, HLA specific IgE sensitization is a new phenomenon in solid organ transplant recipients whose potential relevance for allograft injury requires further investigation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507692PMC
http://dx.doi.org/10.3389/fimmu.2023.1179036DOI Listing

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