Cargando…

Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts

INTRODUCTION: Interleukin-6 (IL-6) is an important mediator of inflammation and activation of T cells, B cells, and plasma cells. Excessive IL-6 production is linked to human diseases characterized by unregulated antibody production, including alloimmunity, where persistence of donor-specific antibo...

Descripción completa

Detalles Bibliográficos
Autores principales: Jordan, Stanley C., Ammerman, Noriko, Choi, Jua, Huang, Edmund, Najjar, Reiad, Peng, Alice, Sethi, Supreet, Sandhu, Rana, Atienza, Janet, Toyoda, Mieko, Ge, Shili, Lim, Kathlyn, Gillespie, Matthew, Zhang, Xiaohai, Haas, Mark, Vo, Ashley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039906/
https://www.ncbi.nlm.nih.gov/pubmed/35497778
http://dx.doi.org/10.1016/j.ekir.2022.01.1074
_version_ 1784694229927198720
author Jordan, Stanley C.
Ammerman, Noriko
Choi, Jua
Huang, Edmund
Najjar, Reiad
Peng, Alice
Sethi, Supreet
Sandhu, Rana
Atienza, Janet
Toyoda, Mieko
Ge, Shili
Lim, Kathlyn
Gillespie, Matthew
Zhang, Xiaohai
Haas, Mark
Vo, Ashley
author_facet Jordan, Stanley C.
Ammerman, Noriko
Choi, Jua
Huang, Edmund
Najjar, Reiad
Peng, Alice
Sethi, Supreet
Sandhu, Rana
Atienza, Janet
Toyoda, Mieko
Ge, Shili
Lim, Kathlyn
Gillespie, Matthew
Zhang, Xiaohai
Haas, Mark
Vo, Ashley
author_sort Jordan, Stanley C.
collection PubMed
description INTRODUCTION: Interleukin-6 (IL-6) is an important mediator of inflammation and activation of T cells, B cells, and plasma cells. Excessive IL-6 production is linked to human diseases characterized by unregulated antibody production, including alloimmunity, where persistence of donor-specific antibodies (DSAs), chronic active antibody-mediated rejection (cAMR), and graft loss are noted. Here, we report our experience investigating clazakizumab, a novel IL-6 inhibitor, in treating human leukocyte antigen (HLA)-sensitized patients with cAMR. METHODS: Between February 2018 and January 2019, 10 adults with biopsy-proven cAMR were enrolled in a phase 2, single-center, open-label study. Patients received clazakizumab 25 mg subcutaneously (s.c.) monthly for 12 months, with a 6-month protocol biopsy. Primary end points included patient survival, graft survival, estimated glomerular filtration rate (eGFR), and safety. Secondary end points assessed immune markers (DSAs, IgG, T-regulatory [Treg] cells). At 12 months, stable patients entered a long-term extension (LTE). RESULTS: LTE patients received clazakizumab for >2.5 years. Mean eGFRs showed significant declines from −24 months to study initiation (0 months) (52.8 ± 14.6 to 38.11 ± 12.23 ml/min per 1.73 m(2), P = 0.03). However, after initiation of clazakizumab, eGFR stabilized at (41.6 ± 14.2 and 38.1 ± 20.3 ml/min per 1.73 m(2), at 12 and 24 months, respectively). Banff 2017 analysis of pre- and post-treatment biopsies showed reductions in g+ptc and C4d scores. DSA reductions were seen in most patients. Adverse events (AEs) were minimal, and 2 graft losses occurred, both in patients who discontinued clazakizumab therapy at 6 months and 12 months after study initiation. CONCLUSION: In this small cohort of patients with cAMR, clazakizumab treatment showed a trend toward stabilization of eGFR and reductions in DSA and graft inflammation. No significant safety issues were observed. A randomized, placebo-controlled clinical trial (IMAGINE) of clazakizumab in cAMR treatment is underway (NCT03744910).
format Online
Article
Text
id pubmed-9039906
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-90399062022-04-27 Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts Jordan, Stanley C. Ammerman, Noriko Choi, Jua Huang, Edmund Najjar, Reiad Peng, Alice Sethi, Supreet Sandhu, Rana Atienza, Janet Toyoda, Mieko Ge, Shili Lim, Kathlyn Gillespie, Matthew Zhang, Xiaohai Haas, Mark Vo, Ashley Kidney Int Rep Clinical Research INTRODUCTION: Interleukin-6 (IL-6) is an important mediator of inflammation and activation of T cells, B cells, and plasma cells. Excessive IL-6 production is linked to human diseases characterized by unregulated antibody production, including alloimmunity, where persistence of donor-specific antibodies (DSAs), chronic active antibody-mediated rejection (cAMR), and graft loss are noted. Here, we report our experience investigating clazakizumab, a novel IL-6 inhibitor, in treating human leukocyte antigen (HLA)-sensitized patients with cAMR. METHODS: Between February 2018 and January 2019, 10 adults with biopsy-proven cAMR were enrolled in a phase 2, single-center, open-label study. Patients received clazakizumab 25 mg subcutaneously (s.c.) monthly for 12 months, with a 6-month protocol biopsy. Primary end points included patient survival, graft survival, estimated glomerular filtration rate (eGFR), and safety. Secondary end points assessed immune markers (DSAs, IgG, T-regulatory [Treg] cells). At 12 months, stable patients entered a long-term extension (LTE). RESULTS: LTE patients received clazakizumab for >2.5 years. Mean eGFRs showed significant declines from −24 months to study initiation (0 months) (52.8 ± 14.6 to 38.11 ± 12.23 ml/min per 1.73 m(2), P = 0.03). However, after initiation of clazakizumab, eGFR stabilized at (41.6 ± 14.2 and 38.1 ± 20.3 ml/min per 1.73 m(2), at 12 and 24 months, respectively). Banff 2017 analysis of pre- and post-treatment biopsies showed reductions in g+ptc and C4d scores. DSA reductions were seen in most patients. Adverse events (AEs) were minimal, and 2 graft losses occurred, both in patients who discontinued clazakizumab therapy at 6 months and 12 months after study initiation. CONCLUSION: In this small cohort of patients with cAMR, clazakizumab treatment showed a trend toward stabilization of eGFR and reductions in DSA and graft inflammation. No significant safety issues were observed. A randomized, placebo-controlled clinical trial (IMAGINE) of clazakizumab in cAMR treatment is underway (NCT03744910). Elsevier 2022-02-09 /pmc/articles/PMC9039906/ /pubmed/35497778 http://dx.doi.org/10.1016/j.ekir.2022.01.1074 Text en © 2022 International Society of Nephrology. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Clinical Research
Jordan, Stanley C.
Ammerman, Noriko
Choi, Jua
Huang, Edmund
Najjar, Reiad
Peng, Alice
Sethi, Supreet
Sandhu, Rana
Atienza, Janet
Toyoda, Mieko
Ge, Shili
Lim, Kathlyn
Gillespie, Matthew
Zhang, Xiaohai
Haas, Mark
Vo, Ashley
Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title_full Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title_fullStr Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title_full_unstemmed Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title_short Evaluation of Clazakizumab (Anti–Interleukin-6) in Patients With Treatment-Resistant Chronic Active Antibody-Mediated Rejection of Kidney Allografts
title_sort evaluation of clazakizumab (anti–interleukin-6) in patients with treatment-resistant chronic active antibody-mediated rejection of kidney allografts
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039906/
https://www.ncbi.nlm.nih.gov/pubmed/35497778
http://dx.doi.org/10.1016/j.ekir.2022.01.1074
work_keys_str_mv AT jordanstanleyc evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT ammermannoriko evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT choijua evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT huangedmund evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT najjarreiad evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT pengalice evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT sethisupreet evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT sandhurana evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT atienzajanet evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT toyodamieko evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT geshili evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT limkathlyn evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT gillespiematthew evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT zhangxiaohai evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT haasmark evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts
AT voashley evaluationofclazakizumabantiinterleukin6inpatientswithtreatmentresistantchronicactiveantibodymediatedrejectionofkidneyallografts