An immunological algorithm to predict risk of high-grade rejection in cardiac transplant recipients

Silviu Itescu, Thomas C.M. Tung, Elizabeth M. Burke, Alan D. Weinberg, Donna Mancini, Robert E. Michler, Nicole M. Suciu-Foca, Eric A. Rose

Research output: Contribution to journalArticle

54 Scopus citations

Abstract

Background: Transplant-related coronary-artery disease (TCAD) develops frequently in cardiac-allograft recipients, and limits long-term survival. We examined the relation between this disorder and cumulative frequency of high-grade rejection, and investigated whether concomitant use of three immunological factors at the time of a low-grade endomyocardial biopsy can predict progression to high-grade rejection. Methods: We investigated the relation between the cumulative annual frequency of high-grade rejection and TCAD in 198 recipients of cardiac transplantation between 1992 and 1996 by means of Kaplan-Meier actuarial life-tables. Endomyocardial biopsy, lymphocyte-growth assays, and anti-HLA antibody measurements were compiled over 12 months in 102 patients during their first post-transplant year. We calculated predictive values for high-grade rejection within 90 days by χ2, Kaplan Meier suvival curves, and by multivariable logistic regression analyses. Findings: We found a direct correlation between cumulative annual frequency of rejection and TCAD onset with highest risk in those with more than 0.75 rejections per year (p = 0.0002). After a low-grade endomyocardial biopsy (0 or 1A), one or more donor-recipient HLA-DR matches protected against high-grade rejections (p < 0.001). Among individuals with one or two DR matches, the negative predictive value for progression from a low-grade biopsy to a high-grade rejection was 87% in the presence of a negative lymphocyte-growth assay. Among individuals with no DR matches, the presence of either a positive lymphocyte-growth assay or IgG anti-major-histocompatibility complex (MHC) class II antibodies was independently associated with high probability of progression to rejection (64% and 66%, respectively, p < 0.0005). When both assays were positive, concomitantly with a low-grade endomyocardial biopsy, the positive predictive value for progression to a high-grade rejection was 86% (p < 0.0001). For endomyocardial-biopsy grades 1B or 2, a positive lymphocyte-growth assay alone was associated with high-grade rejection in 100% of cases. Interpretation: Use of an algorithm combining three immunological factors at the time of a low-grade endomyocardial biopsy enables prospective stratification of cardiac transplant recipients into risk categories for progression to high-grade rejection. Low-risk individuals require fewer biopsies, moderate-risk individuals require an ongoing schedule of surveillance biopsies, and high-risk individuals require rational organisation of interventional strategies aimed at preventing rejection. Additional predictive factors are needed to identify moderate-risk individuals who will progress to rejection. Ultimately, successful intervention may have an impact on the subsequent complication of TCAD.

Original languageEnglish (US)
Pages (from-to)263-270
Number of pages8
JournalLancet
Volume352
Issue number9124
DOIs
StatePublished - Jul 25 1998
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'An immunological algorithm to predict risk of high-grade rejection in cardiac transplant recipients'. Together they form a unique fingerprint.

  • Cite this

    Itescu, S., Tung, T. C. M., Burke, E. M., Weinberg, A. D., Mancini, D., Michler, R. E., Suciu-Foca, N. M., & Rose, E. A. (1998). An immunological algorithm to predict risk of high-grade rejection in cardiac transplant recipients. Lancet, 352(9124), 263-270. https://doi.org/10.1016/S0140-6736(98)09475-6