de Fallois J, Baatz S, Krüger BM, Dilz LM, Boldt A, Beck J, Bornemann-Kolatzki K, Petzold F, Daniel C, Amann KU, Kowald J (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 17
Article Number: 1867833
DOI: 10.3389/fimmu.2026.1867833
With the advent of CD38 antibody therapy, an effective treatment option for antibody-mediated rejection (ABMR) appears achievable. However, a subset of patients remains refractory. We report a kidney transplant recipient with persistent microvascular inflammation in kidney allograft biopsy after six months of CD38 antibody treatment, necessitating rescue therapy. Persistent detection of peripheral CD38-negative class-switched memory B cells prompted additional deep B-cell depletion using a humanized, glycoengineered, IgG1 monoclonal antibody targeting the type-II epitope of CD20. Follow-up kidney biopsy demonstrated histological resolution of microvascular inflammation, while normalization of donor-derived cell-free DNA was consistent with remission of ABMR. In this case of CD38 antibody-refractory ABMR, adjunctive type-II-CD20 antibody therapy had a favorable response. This highlights the potential contribution of additional effector cells to refractory ABMR, such as CD38-negative class-switched memory B cells. These findings suggest a potential role for individualized, multimodal B-cell–directed immunomodulatory strategies that may improve outcomes in selected patients with treatment-refractory ABMR, thus contributing to sustained allograft survival.
APA:
de Fallois, J., Baatz, S., Krüger, B.M., Dilz, L.M., Boldt, A., Beck, J.,... Kowald, J. (2026). Type-II-CD20-targeted therapy for CD38 antibody-refractory antibody-mediated rejection after kidney transplantation: a case report. Frontiers in Immunology, 17. https://doi.org/10.3389/fimmu.2026.1867833
MLA:
de Fallois, Jonathan, et al. "Type-II-CD20-targeted therapy for CD38 antibody-refractory antibody-mediated rejection after kidney transplantation: a case report." Frontiers in Immunology 17 (2026).
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