Daratumumab Interferes with Allogeneic Crossmatch Impacting Immunological Assessment in Solid Organ Transplantation.

antibody-mediated rejection crossmatch daratumumab end-stage renal disease flow cytometry human leukocyte antigen (HLA) multiple myeloma transplantation

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
14 Oct 2022
Historique:
received: 11 09 2022
revised: 03 10 2022
accepted: 12 10 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

We report the first case of Daratumumab interference of allogeneic crossmatch tests repeatedly causing aberrant false-positive results, which inadvertently delayed transplant for a waitlisted renal patient with multiple myeloma. Daratumumab is an IgG1κ human monoclonal antibody commonly used to treat multiple myeloma, characterized by cancerous plasma cells and often leads to renal failure requiring kidney transplant, by depleting CD38-expressing plasma cells. In this case study, the patient had end-stage renal disease secondary to multiple myeloma and was continuously receiving Daratumumab infusions. The patient did not have any detectable antibodies to human leukocyte antigens but repeatedly had unexpected positive crossmatch by the flow cytometry-based method with 26 of the 27 potential deceased organ donors, implying donor-recipient immunological incompatibility. However, further review and analysis suggested that the positive crossmatches were likely false-positive as a result of interference from Daratumumab binding to donor cell surface CD38 as opposed to the presence of donor-specific antibodies. The observed intensity of the false-positive crossmatches was also highly variable, potentially due to donor- and/or cell-dependent expression of CD38. The variability of CD38 expression was, therefore, for the first time, characterized on the T and B cells isolated from various tissues and peripheral blood of 78 individuals. Overall, T cells were found to have a lower CD38 expression profile than the B cells, and no significant difference was observed between deceased and living individuals. Finally, we show that a simple cell treatment by dithiothreitol can effectively mitigate Daratumumab interference thus preserving the utility of pre-transplant crossmatch in multiple myeloma patients awaiting kidney transplant.

Identifiants

pubmed: 36294380
pii: jcm11206059
doi: 10.3390/jcm11206059
pmc: PMC9605360
pii:
doi:

Types de publication

Case Reports

Langues

eng

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Auteurs

Chak-Sum Ho (CS)

Gift of Hope Organ & Tissue Donor Network, Itasca, IL 60143, USA.
Department of Medicine, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
Gift of Life Michigan, Ann Arbor, MI 48108, USA.

Kyle R Putnam (KR)

Gift of Life Michigan, Ann Arbor, MI 48108, USA.

Christine R Peiter (CR)

Gift of Life Michigan, Ann Arbor, MI 48108, USA.

Walter F Herczyk (WF)

Gift of Life Michigan, Ann Arbor, MI 48108, USA.

John A Gerlach (JA)

Gift of Life Michigan, Ann Arbor, MI 48108, USA.
Biomedical Laboratory Diagnostics Program, College of Natural Science, Michigan State University, East Lansing, MI 48824, USA.

Yee Lu (Y)

Division of Nephrology, Department of Internal Medicine, University of Michigan Medicine, Ann Arbor, MI 48109, USA.

Erica L Campagnaro (EL)

Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan Medicine, Ann Arbor, MI 48109, USA.

Kenneth J Woodside (KJ)

Division of Nephrology, Department of Internal Medicine, University of Michigan Medicine, Ann Arbor, MI 48109, USA.

Matthew F Cusick (MF)

Department of Pathology, University of Michigan Medicine, Ann Arbor, MI 48109, USA.

Classifications MeSH