Key result
pAMR is linked to higher inflammatory burden correlating with pAMR grade, C4d, and DSA positivity.
Why the study?
Does the presence of pathologic antibody-mediated rejection correlate with increased myocardial inflammatory burden and specific cell phenotypes in endomyocardial biopsies?
Case-Control (n=65)
Yes
Does the presence of pathologic antibody-mediated rejection correlate with increased myocardial inflammatory burden and specific cell phenotypes in endomyocardial biopsies?
p-value: p=<0.0001
In endomyocardial biopsies, inflammatory burden and specific cell phenotypes strongly correlate with pathologic antibody-mediated rejection grade, C4d, and DSA positivity.
May inform refined biopsy assessment in cardiac transplant surveillance; leaves open whether inflammatory phenotypes predict outcomes or guide therapy.
This multicenter case-controlled pilot study evaluated myocardial inflammatory burden (IB) and phenotype in endomyocardial biopsies (EMBs) with and without pathologic antibody-mediated rejection (pAMR). Sixty-five EMBs from five European heart transplant centers were centrally reviewed as positive (grade 2, n = 28), suspicious (grade 1, n = 7) or negative (n = 30) for pAMR. Absolute counts of total, intravascular (IV) and extravascular (EV) immunophenotyped mononuclear cells were correlated with pAMR grade, capillary C4d deposition, donor specific antibody (DSA) status and acute cellular rejection (ACR). In pAMR+ biopsies, equivalent number of IV CD3+ T lymphocytes (23 ± 4/0.225 mm(2) ) and CD68+ macrophages (21 ± 4/0.225 mm(2) ) were seen. IB and cell phenotype correlated with pAMR grade, C4d positivity and DSA positivity (p < 0.0001). High numbers of IV T lymphocytes were associated with low grade ACR (p = 0.002). In late-occurring AMR EV plasma cells occurring in 34% of pAMR+ EMBs were associated with higher IB. The IB in AMR correlated with pAMR+, C4d positivity and DSA positivity. In pAMR+ equivalent numbers of IV T lymphocytes and macrophages were found. The presence of plasma cells was associated with a higher IB and occurrence of pAMR late after transplantation.
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Fedrigo et al. (2015) conducted a case-control in Antibody-Mediated Rejection in heart transplant (n=65). Pathologic antibody-mediated rejection (pAMR) vs. No pathologic antibody-mediated rejection was evaluated on Correlation of inflammatory burden and cell phenotype with pAMR grade, C4d positivity and DSA positivity (p=<0.0001). Pathologic antibody-mediated rejection in endomyocardial biopsies was associated with higher inflammatory burden, correlating with pAMR grade, C4d positivity, and DSA positivity (p < 0.0001).
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