| Literature DB >> 34506905 |
Divyansh Agarwal1, Eline T Luning Prak2, Tina Bharani3, Matthew Everly4, Thi-Sau Migone5, Michael Cancro2, David Allman2, Insuk Choe2, Jane D Kearns2, Jennifer Trofe-Clark6, Ali Naji7, Malek Kamoun8.
Abstract
Pre-existing anti-HLA allo-antibodies (allo-Abs) are a major barrier to successful kidney transplantation, resulting in an elevated risk for antibody-mediated rejection (AMR) and eventual graft loss. The cytokine B lymphocyte stimulator (BLyS) promotes B cell maturation and plasma cell survival; consequently, anti-BLyS therapy represents a potential therapeutic opportunity in diminishing pre-existing allo-Abs. Here we report that in our 1-year pilot trial, BLyS neutralization failed to reduce total anti-HLA allo-Ab levels in highly sensitized candidates awaiting kidney transplant in a clinically meaningful way. Additionally, we performed a post hoc analysis using sera from trial candidates which revealed selective depletion of anti-HLA class I and class II Abs in response to belimumab treatment, restricted to certain allele specificities and IgG subclasses. Altogether, we observed that BLyS blockade only results in selective depletion of anti-HLA Abs recognizing a few discrete HLA allele specificities.Entities:
Keywords: Alloantibody desensitization; B cell depletion; BLyS/BAFF and APRIL; Belimumab; Complement C1q; Human leukocyte antigen; IgG antibody; Immunosuppression; Kidney transplantation
Mesh:
Substances:
Year: 2021 PMID: 34506905 DOI: 10.1016/j.trim.2021.101465
Source DB: PubMed Journal: Transpl Immunol ISSN: 0966-3274 Impact factor: 1.708